Uma Brothers

LBS Marg, Mumbai, Maharashtra

Curcumin is a diarylheptanoid. About two centuries ago, isolation of a “yellow coloring-matter” from the rhizomes of curcuma longa (turmeric) & was named curcumin.  Turmeric's other two curcuminoids are desmethoxycurcumin and bis-desmethoxy- curcumin. The curcuminoids are natural phenols that are responsible for the yellow color of turmeric. Curcumin can exist in several tautomeric forms, including a 1, 3-diketo form and two equivalent enol forms. The enol form is more energetically stable in the solid phase and in organic solvents, while in water the 1, 3-diketo dominates.
Curcumin can be used for boron quantification in the curcumin method. It reacts with boric acid to form a red-color compound, rosocyanine. Curcumin is a bright-yellow color powder and may be used as a food coloring. Curcumin is powerful anti-inflammatory effects and is a very strong antioxidant. Combat cancer stem cells and enhance heart health and inhibit the formation of ldl (bad) cholesterol.
It Is Orange Crystalline Powder With Its Melting Point Of 183 °C. It Is Slightly Soluble In Hot Water

SYNONYMS: 2', 2' DIFLUORODEOXYCYTIDINE, CAS NUMBER: 122111-03-9, MOLECULAR FORMULA: C9H11F2N3O4 .HCL, MOLECULAR WEIGHT: 263.2.36.5

 

IT IS WHITE TO OFF WHITE CRYSTALLINE POWDER WITH MELTING RANGE 168.6°C. SOLUBLE IN WATER, SLIGHTLY SOLUBLE IN METHANOL, ALMOST INSOLUBLE IN  ETHANOL OR POLAR ORGANIC SOLVENTS. ALSO AVAILABLE AS GEMCITABINE ELAIDATE AND GEMCITABINE DIPHOSPHATE

           

STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP

 

PACKING: OFFERED IN EXPORT WORTHY PACKING OR AS PER OUR CUSTOMER REQUIREMENTS

SYNONYMS: 2-TERT-BUTYL-4-METHOXYPHENOL; 2, 6-DITERT-BUTYL-4-METHYLPHENOL -– CAS NUMBER: 128-37-0, MOL. FORMULA: C15H24O, MOL. WEIGHT: 220.35. IT IS WHITE CRYSTALLINE POWDER WITH ITS MELTING RANGE OF 69°C -73°C. IT IS INSOLUBLE IN WATER.

SYNONYMS: METHYL (2S)-2-(2-CHLOROPHENYL)-2-(6, 7-DIHYDRO-4H-THIENO[3, 2-C]PYRIDIN-5-YL)ACETATE

CAS NUMBER: 113665-84-2, MOL. FORMULA: C16H18NS2CIO6, MOL. WEIGHT: 419.90

IT IS WHITE TO OFF WHITE CRYSTALLINE POWDER. IT IS FREELY SOLUBLE IN METHANOL, PRACTICALLY INSOLUBLE IN ETHER WITH ITS MELTING POINT OF 184ºC.

STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP – ALSO AVAILABLE AS CLOPIDOGREL HYDROGEN SULPHATE

 

PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS

SYNONYMS: 2-(2, 4-DIFLUOROPHENYL)-1, 3-BIS(1, 2, 4-TRIAZOL-1-YL)PROPAN-2-OL, CAS NO: 86386-73-4, MOLECULAR FORMULA: C13H12F2N6O, MOLECULAR WEIGHT: 306.3.

FLUCONAZOLE IS A WHITE CRYSTALLINE POWDER, SLIGHTLY SOLUBLE IN WATER AND SALINE WITH MELTING RANGE OF 138°C TO 140 °C.

STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP

 

PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS

SYNONYMS: MAGNESIUM; 5-METHOXY-2-[(4-METHOXY-3, 5-DIMETHYLPYRIDIN-2-YL) METHYLSULFINYL] BENZIMIDAZOL-1-IDE

CAS NUMBER: 217087-09-7, MOL. WEIGHT: C34H36MGN6O6S2, MOL. WEIGHT: 7767.4

IT IS WHITE TO SLIGHTLY COLOURED POWDER WHICH IS SOLUBLE IN METHANOL, SLIGHTLY SOLUBLE IN WATER, INSOLUBLE IN HEPTANE AND ITS MELTING RANGE IS 137ºC TO 142ºC.

STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP – ALSO AVAILABLE AS ESOMEPRAZOLE MAGNESIUM TRIHYDRATE, ESOMEPRAZOLE MAGNESIUM PELLETS

 

PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS

standard: offered of pharmaceutical grade bp/usp/ep

packing: offered in export worthy packing of 25 kilos or as per our customer requirements

Diacerein (inn), also known as diacetylrhein, is a slow-acting medicine of the class anthraquinone used to treat joint diseases such as osteoarthritis (swelling and pain in the joints). It works by inhibiting interleukin-1 beta. A 2005 cochrane review found diacerein to be slightly, but significantly, more effective than placebo in improving pain and slowing the progress of osteoarthritis in the hip and knee. synonyms: 4, 5-diacetyloxy-9, 10-dioxoanthracene-2-carboxylic acidcas number: 13739-02-1, mol. Formula: c19h12o8, mol.weight: 368.29diacerein is a yellow crystalline solid. It is soluble in water (partly), dmso, and methanol with melting range of 217c to 218c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

Ornidazole Is A Nitroimidazole Antiprotozoal Agent Used In Ameba And Trichomonas Infections. It Is Partially Plasma-Bound And Also Has Radiation-Sensitizing Action. Ornidazole Is An Anti-Infective; Used To Treat Selected Protozoan Infections. It Has Been Investigated For Use In Crohn's Disease After Bowel Resection.
Ornidazole is crystalline solid powder. It is soluble in chloroform and methanol with melting range of 85°c to 90°c.

We are offering glipizide is an oral hypoglycemic agent which is rapidly absorbed and completely metabolized. Glipizide is a sulfonylurea. The chemical classification of glipizide is sulfonylurea compounds.Glipizide is a short-acting, second-generation sulfonylurea with hypoglycemic activity. Glipizide is rapidly absorbed, has a very quick onset of action and a short half-life. This agent is extensively metabolized in the liver and the metabolites as well as the unchanged form are excreted in the urine. synonyms: n-[2-[4-(cyclohexylcarbamoylsulfamoyl) phenyl] ethyl]-5-methylpyrazine-2-carboxamidecas number: 29094-61-9, mol. Formula: c21h27n5o4s, mol.weight: 445.54glipizide is a white crystalline powder. It is soluble in water (partly), chloroform, dmf, dmso (48 mgml), and methanol with melting range of 200c to 103c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering artesunate. Artesunate is a water-soluble, semi-synthetic derivative of the sesquiterpine lactone artemisinin with anti-malarial, anti-shistosomiasis, antiviral, and potential anti-neoplastic activities. Upon hydrolysis of artesunate's active endoperoxide bridge moiety by liberated heme in parasite-infected red blood cells, reactive oxygen species and carbon-centered radicals form, which have been shown to damage and kill parasitic organisms. Additionally, in vitro studies demonstrate that this agent induces dna breakage in a dose-dependent manner. Artesunate has also been shown to stimulate cell differentiation, arrest the cell cycle in the g1 and g2m phases, inhibit cell proliferation, and induce apoptosis through mitochondrial and caspase signaling pathways. Artemisinin is isolated from the plant artemisia annua. Artesunate is part of the artemisinin group of drugs that treat malaria. It is a semi-synthetic derivative of artemisinin that is water-soluble and may therefore be given by injection. synonyms: dihydroartemisinine -12-alpha-succinate cas number: 88495-63-0 mol. Formula: c19h28o8, mol.weight: 384.42 artesunate is a fine-white crystalline powder.soluble in dmso (25 mgml) and ethanol (25 mgml) with melting range of 131c - 135c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering cisplatin.Cisplatin is a potent platinum-based anti-neoplastic agent that is believed to form inter intrastrand dna adducts which activate signaling pathways culminating in apoptosis. The compound has also been shown to induce apoptosis through caspase-3 activation and xiap expression also shown to cause immunosuppression which is thought to be followed by an increase in the host immune response. Platinated dna adducts also enhance poisoning of dna topoisomerase I by camptothecin (sc-200871). Cisplatin was the first member of a class of anticancer drugs, which now include carboplatin (sc-202093) and oxaliplatin (sc-202270) that form dna adducts resulting in apoptosis; however, these molecules also bind other biological molecules such as enzymes which might play a role in their mechanism of action. synonyms: azane; dichloroplatinum (2+)cas number: 15663-27-1, mol. Formula: cl2h6n2pt, mol.weight: 300.05cisplatin is a yellow crystalline powder. It is soluble in dmso (25 mgml), water (0.25 g100ml) at 25 c, ethanol (

We are offering brimonidine tartrate.Brimonidine tartrate is a quinoxaline derivative and adrenergic alhpa-2 receptor agonist that is used to manage intraocular pressure associated with open-angle glaucoma and ocular hypertension.Brimonidine tartrate is the tartrate salt form of brimonidine, an imidazole derivative and selective alpha-2 adrenergic receptor agonist. Upon ocular administration, brimonidine tartrate acts on the blood vessels causing them to constrict which leads to a decrease in the production of aqueous humor. Brimonidine tartrate also enhances the outflow of aqueous humor. This drug is used in the treatment of glaucoma to reduce intraocular pressure. synonyms: 5-bromo-n-(4, 5-dihydro-1h-imidazol-2-yl)quinoxalin-6-amine;(2r, 3r)-2, 3-dihydroxybutanedioic acidcas number: 79570-19-7, mol. Formula: c15h16brn5o6, mol.weight: 442.22brimonidine is a off-white to pale-yellow powder. It is soluble in both water (0.6 mgml) and in the product vehicle (1.4 mgml) at ph 7.7.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering drotaverine.Drotaverine hydrochloride is an antispasmodic, and an analogue of papaverine. Is an antispasmodic drug, used to enhance cervical dilation during childbirth.Drotaverine hydrochloride is structurally related to papaverine, is a selective inhibitor of phosphodiesterase 4, and has no anticholinergic effects. synonyms: (3e)-3-(6h-benzo[c] [1] benzoxepin-11-ylidene)-n, n-dimethylpropan-1-amine; hydrochloridecas number: 985-12-6, mol. Formula: c24h32clno4, mol.weight: 433.97drotaverine hydrochloride is a pale-yellow crystalline solid. It is soluble in dmso, methanol and water with melting range of 197c to 200c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering clarithromycin.Clarithromycin is a semisynthetic macrolide antibiotic derived from erythromycin that is active against a variety of microorganisms. It can inhibit protein synthesis in bacteria by reversibly binding to the 50s ribosomal subunits. This inhibits the translocation of aminoacyl trans- fer-rna and prevents peptide chain elongation. Clarithromycin is a macrolide antimicrobial.the mechanism of action of clarithromycin is as a cytochrome p450 3a4 inhibitor, cytochrome p450 3a inhibitor, and p-gly coprotein inhibitor. The chemical classification of clarithromycin is macrolides.Clarithromycin is a semisynthetic 14-membered ring macrolide antibiotic. Clarithromycin binds to the 50s ribosomal subunit and inhibits rna-dependent protein synthesis in susceptible organisms. Clarith romy- cin has been shown to eradicate gastric malt (mucosa-associated lymphoid tissue) lymphomas, presumably due to the eradication of tumorigenic helicobacter pylori infection. This agent also acts as a biological response modulator, possibly inhibiting angiogenesis and tumor growth through alterations in growth factor expression synonyms: (3r, 4s, 5s, 6r, 7r, 9r, 11r, 12r, 13s, 14r)-6-[(2s, 3r, 4s, 6r)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-12, 13-dihydroxy-4-[(2r, 4r, 5s, 6s)-5-hydroxy-4-methoxy-4, 6-dimethyloxan-2-yl]oxy-7-methoxy-3, 5, 7, 9, 11, 13-hexamethyl-oxacyclotetradecane-2, 10-dionecas number: 81103-11-9, mol. Formula: c38h69no13, mol.weight: 747.95clarithromycin is a colourless crystalline needles powder. It is soluble in ethanol (

We are offering disopyramide phosphate is a class I anti-arrhythmic agent (one that interferes directly with the depolarization of the cardiac membrane and thus serves as a membrane-stabilizing agent) with a depressant action on the heart similar to that of guanidine. It also possesses some anticholin- ergic and local anesthetic properties.Disopyramide phosphate is a class ia antiarrhythmic agent with cardiac depressant properties. Disopyramide phosphate exerts its actions by blocking both sodium and potassiumchannels in cardiac membrane during phase 0 of the action potential. This slows the impulse conduction through the av node and prolongs the duration of the action potential of normal cardiac cells in atrial and ventricular tissues. disopyramide prolongs the qt interval and causes a widening of the qrs complex. It also possesses some anticholinergic and local anaesthetic properties. Disopyramide phosphate is used in the treatment of supraventricular tachycardia. synonyms: 4-[di (propan-2-yl) amino]-2-phenyl-2-pyridin-2-ylbutanamide; phosphoric acidcas number: 22059-60-5, mol. Formula: c21h32n3o5p, mol.weight: 437.47disopyramide phosphate is in solid form. It is freely soluble in water, and the free base (pka 10.4) has an aqueous solubility of 1 mgml with melting point of 94c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering furosemide is a benzoic-sulfonamide-furan. It is a diuretic with fast onset and short duration that is used for edema and chronic renal in- sufficiency. Furosemide is a loop diuretic. The physiologic effect of furosemide is by means of increased diuresis at loop of henle.Furosemide is a sulfamoylanthranilic acid derivative, also known as frusemide, and potent loop diuretic. Furosemide is widely used to treat hypertension and edema. This agent is highly bound to albumin and is largely excreted unchanged in the urine. synonyms: 4-chloro-2-(furan-2-ylmethylamino)-5-sulfamoylbenzoic acidcas number: 54-31-9, mol. Formula: c12h11cln2o5s, mol.weight: 330.74furosemide is white to light yellow crystal powder. It is soluble in dmso (66 mgml at 25 c), ethanol (

We are offering aceclofenac.Aceclofenac is a non-steroidal anti-inflammatory drug analog of diclofenac. It is used for the relief of pain and inflammation in rheumatoid arthritis, osteoarthritis and ankylosing spondylitis. It is a cytokine inhibitor. Aceclofenac works by blocking the action of a substance in the body called cyclo-oxygenase. Cyclo-oxygenase is involved in the production of prostaglandins (chemicals in the body) which cause pain, swelling and inflammation. Aceclofenac is the glycolic acid ester of diclofenac. synonyms: 2-[2-[2-(2, 6-dichloroanilino) phenyl] acetyl] oxyacetic acidcas number: 89796-99-6 mol. Formula: c16h13cl2no4, mol.weight: 354.18aceclofenac is a white crystalline .it is soluble in ethanol and acetone, insoluble in water with melting range of 149c to 153c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering pyrazinamide is a pyrazine that is used therapeutically as an antitu bercular agent. Pyrazinamide is an antimycobacterial. Pyrazinamide is a synthetic pyrazinoic acid amide derivative with bactericidal property. pyrazinamide is particularly active against slowly multiplying intra cellular bacilli (unaffected by other drugs) by an unknown mechanism of action. Its bactericidal action is dependent upon the presence of bacterial pyrazinamidase, which removes the amide group to produce active pyrazinoic acid. Pyrazinamide is an important component of multidrug therapy for tuberculosis. synonyms: pyrazine-2-carboxamidecas number: 98-96-4, mol. Formula: c5h5n3o, mol.weight: 123.11pyrazinamide is white to white crystalline powder. It is soluble in water (50 mgml), methanol (13.8 mgml at 25 c), ethanol (5.7 mgml at 25 c), chloroform (7.4 mgml at 25 c), and dmso with melting range of 189c to 191c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering quinine.Quinine is an alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood. synonyms: (r)-[(2s, 5r)-5-ethenyl-1- azabicyclo [2.2.2] octan-2-yl]-(6-methoxyquinolin-4-yl) methanolcas number: 130-95-0, mol. Formula: c20h24n2o2, mol.weight: 324.42quinine is white to light yellow crystal powder. It is soluble chloroform, alcohol and water with melting range of 173c to 175c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering vecuronium bromide is the bromide salt form of vecuronium, a synthetic steroid derivative of the naturally occurring alkaloids of curare with a muscle relaxant property. Vecuronium bromide competes with acetyl- choline for the nicotinic receptors at the neuromuscular junction of skeletal muscles, thereby inhibiting the action of acetylcholine and blocking the neural transmission without depolarizing the postsynaptic membrane. This leads to skeletal muscle relaxation and paralysis.Monoquaternary homolog of pancuronium a non-depolarizing neuromuscular blocking agent with shorter duration of action than pancuronium. Its lack of significant cardiovascular effects and lack of dependence on good kidney function for elimination as well as its short duration of action and easy reversibility provide advantages over, or alternatives to, other established neuromuscular blocking agents. synonyms: [(2s, 3s, 5s, 8r, 9s, 10s, 13s, 14s, 16s, 17r)-17-acetyloxy-10, 13-dimethyl-16-(1-methylpiperidin-1-ium-1-yl)-2-piperidin-1-yl-2, 3, 4, 5, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl] acetate;bromidecas number: 50700-72-6, mol. Formula: c34h57brn2o4, mol.weight: 637.73vecuronium bromide is white solid. It is soluble in water, dmso (128 mgml at 25 c), and ethanol (128 mgml at 25 c) with melting range of 227.2c to 228.9c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering tegaserod.Tegaserod is a serotonin-4 receptor antagonist. The mechanism of action of tegaserod is as a serotonin 4 receptor antagonists. Its use was also approved to treat chronic idiopathic constipation. synonyms: 1-[[(z)-(5-methoxyindol-3-ylidene) methyl] amino]-2-pentylguanidinecas number: 145158-71-0, mol. Formula: c16h23n5o, mol.weight: 301.39tegaserod is a soluble in water (slightly) with melting point of 198.15c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We offer high quality Chlorhexidine Gluconate. Carefully formulated Chlorhexidine Gluconate has innumerous applications. Thus, we make sure that our Chlorhexidine Gluconate is completely free from germs. We are counted among the leading Exporters and Suppliers of Chlorhexidine Gluconate. The Chlorhexidine Gluconate is available at market leading prices. Specifications :

• Relative density : 1.06 to 1.07
• Ph : dilute 5.0ml to 100.0 ml with carbon dioxide free water
• The Ph of the solution is 5.5 to 7.0
• Chloroaniline : to comply with BP test
• Assay : Chlor Hexidine Digluconate solution is an aqueous solution which contains not less than 190 g/1 and not more than 210g/1 of 1, 1 - Hexamethylenebis [5 - (4 - Chlorophenyl - Biguanide] Di (d - Digluconate)
• Color test : absorbance not more than 0.03 at 480 NM

Applications :

• Chlorhexidine is present in oral rinses and skin cleansers, and in small quantities it is used as a preservative.
• It is also used as a surgical scrub, surgical hand wash, hand rub, as a wound wash.
• It is also used in some acne skin washes.
• It is also used as part of a treatment for athlete's foot. It is also used in the combination of cetrimide which is very effective in cleaning surgical instruments.
• This combination is also used to clean and wash the wounds as antiseptic.
• It is effective on both gram-positive and gram-negative bacteria, although it is less effective with some gram-negative bacteria.

Suitable for animals :

• It is used as a topical disinfectant of wounds.
• It is more effective in killing bacteria than both Povidone-Iodine and saline
• It has residual effects up to 6 hours. Skin and wound cleaner. It is also more beneficial to wound healing than using saline solutions alone. It is commonly used to manage skin infections in dogs.

Packing :

• It is available in export worthy packing of 200 kg barrels or as per our customers requirements

We are offering zuclopenthixol.Zuclopenthixol is a thioxanthene with therapeutic actions similar to the phenothiazine antipsychotics. It is an antagonist at d1 and d2 dopamine receptors. Zuclopenthixol, also known as zuclopentixol or zuclopen- thixolum, is an antipsychotic agent. Zuclopenthixol is a thioxanthene-based neuroleptic with therapeutic actions similar to the phenothiazine antipsychotics. It is an antagonist at d1 & d2 dopamine receptors. Major brands of zuclopenthixol are cisordinol, acuphase, and clopixol. This drug is a liquid. This compound belongs to the thioxanthenes. These are organic polycyclic compounds containing a thioxanthene moiety, which is an aromatic tricycle derived from xanthene by replacing oxygen atom with a sulfur atom. Known drug targets of zuclopenthixol include 5-hydroxytryptamine receptor 2a, d (1b) dopamine receptor, d (2) dopamine receptor, d (1a) dopamine receptor, and alpha-1a adrenergic receptor. synonyms: 2-[4-[(3z)-3-(2-chlorothioxanthen-9-ylidene) propyl] piperazin-1-yl] ethanolcas number: 53772-83-1, mol. Formula: c22h25cln2os, mol.weight: 400.96zuclopenthixol is a pale yellow low melting solid. It is slightly soluble in water with melting point of 50c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering enbucrilate.Enbucrilate is also known as n-butyl-2-cyanoacrylate or butyl cyanoacrylate.Butyl 2-cyanoacrylate is a tissue adhesive that is applied as a monomer to moist tissue and polymerizes to form a bond. It is slowly biodegradable and used in all kinds of surgery, including dental. synonyms: butyl 2-cyanoprop-2-enoatecas number: 6606-65-1, mol. Formula: c8h11no2, mol.weight: 153.17844enbucrilate is a clear colorless liquid with a sharp, irritating odor. It is soluble in acetone, methyl ethyl ketone, nitromethane, and methylene chloride it is insoluble in water.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering lamivudine.Lamivudine is a reverse transcriptase inhibitor and zalcitabine analog in which a sulfur atom replaces the 3' carbon of the pentose ring. It is used to treat hiv disease. Lamivudine is a hepatitis b virus nucleoside analog reverse transcriptase inhibitor and human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor. The mechanism of action of lamivudine is as a nucleoside reverse transcriptase inhibitor. The chemical classification of lamivudine is nucleoside analog.Lamivudine is a synthetic nucleoside analogue with activity against hepatitis b virus (hbv) and hiv. Intracellularly, lamivudine is phosphorylated to its active metabolites, lamiduvinetriphosphate (l-tp) and lamiduvine monophosphate (l-mp). In hiv, l-tp inhibits hiv-1 reverse transcriptase (rt) via dna chain termination after incorporation of the nucleoside analogue into viral dna. In hbv, incorporation of l-mp into viral dna by hbv polymerase results in dna chain termination; l-tp is a weak inhibitor of mammalian dna polymerases alpha and beta, and mitochondrial dna polymerase. synonyms: 4-amino-1-[(2r, 5s)-2-(hydroxymethyl)-1, 3-oxathiolan-5-yl] pyrimidin-2-onecas number: 134678-17-4, mol. Formula: c8h11n3o3s, mol.weight: 229.26lamivudine is white crystalline powder. It is soluble in water (46 mgml at 25 c), dmso (46 mgml at 25 c), methanol, and ethanol (

We are offering pyridostigmine bromide is a cholinesterase inhibitor with a slightly longer duration of action than neostigmine. It is used in the treatment of myasthenia gravis and to reverse the actions of muscle relaxants.Pyridostigmine bromide is the bromide salt form of pyridostigmine, a quaternary ammonium carbamate derivative & an acetylcholinesterase inhibitor. Pyridostigmine bromide binds reversibly to acetylcholine- sterase active sites in the peripheral nervous system, thereby preventing the breakdown of acetylcholine. This leads to an accumu- lation of acetylcholine at cholinergic synapses and facilitates transmission of impulses across the neuromuscular junction. Mediated through muscarinic receptors, this agent increases contraction of bronchial and intestinal smooth muscle and the exocrine glands secretions, while it causes paralysis of the skeletal muscles mediated through nicotinic receptors. In addition, pyridostigmine is used as a reversible blocking agent to prevent organophosphates from binding to the acetylcholinesterase receptors and thereby protect the nervous system from the effects of nerve agents such as soman. synonyms: (1-methylpyridin-1-ium-3-yl) n, n-dimethylcarbamate; bromidecas number: 101-26-8, mol. Formula: c9h13brn2o2, mol.weight: 261.12pyridostigmine bromide is white or practically white, crystalline powder. It is soluble in water, alcohol, practically insol in ether, acetone benzene with melting range of 152c to 154c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering rivastigmine is a carbamate-derived reversible cholinesterase inhibitor that is selective for the central nervous system and is used for the treatment of dementia in alzheimer disease and parkinson disease.Rivastigmine is a cholinesterase inhibitor. The mechanism of action of rivastigmine is as a cholinesterase inhibitor. synonyms: [3-[(1s)-1-(dimethylamino) ethyl] phenyl] n-ethyl-n-methylcarbamatecas number: 123441-03-2, mol. Formula: c14h22n2o2, mol.weight: 250.34rivastigmine is a white powder. It is soluble in 10 mm in dmso with melting range of 123c tp 125c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering indomethacin.Indomethacin is a non-steroidal anti-inflammatory agent (nsaid) that inhibits the enzyme cyclooxygenase necessary for the formation of prostaglandins and other autacoids. It also inhibits the motility of polymorphonuclear leukocytes. Indomethacin is a nonsteroidal anti-inflammatory drug. The mechanism of action of indomethacin is as a cyclooxygenase inhibitor. The chemical classification of indomethacin is nonsteroidal anti-inflammatory compounds.Indomethacin is a synthetic nonsteroidal indole derivative with anti-inflammatory activity and chemopreventive properties. As a nonsteroidal anti-inflammatory drug indomethacin inhibits the enzyme cyclooxygenase, thereby preventing cyclooxygenase-mediated dna adduct formation by heterocyclic aromatic amines. This agent also may inhibit the expression of multidrug-resistant protein type 1, resulting in increased efficacies of some antineoplastic agents in treating multi-drug resistant tumors. In addition, indomethacinactivates phosphatases that inhibits the migration and proliferation of cancer cells and downregulates survivin, which may result in tumor cell apoptosis. synonyms: 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl] acetic acidcas number: 53-86-1, mol. Formula: c19h16clno4, mol.weight: 357.79indomethacin is a white crystalline solid powder. It is soluble in ethanol (25 mgml), dmso (25 mgml) solutions are yellow in color with melting range of 155c to 162c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering mebendazole.Mebendazole is a benzimidazole that acts by interfering with carbohydrate metabolism and inhibiting polymerization of microtubules. Mebendazole is an antihelminthic.Mebendazole is a synthetic benzimidazole derivate and anthelmintic agent. Mebendazole interferes with the reproduction and survival of helminths by inhibiting the formation of their cytoplasmic microtubules, thereby selectively and irreversibly blocking glucose uptake. This results in a depletion of glycogen stores and leads to reduced formation of atp required for survival and reproduction of the helminth. This eventually causes the helminths death. synonyms: methyl n-(6-benzoyl-1h-benzimidazol-2-yl) carbamatecas number: 31431-39-7, mol. Formula: c16h13n3o3, mol.weight: 295.29mebendazole is a white amorphous powder. It is soluble in formic acid practically insoluble in ethanol, ether and chloroform with melting point of 288.5c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering amoxicillin trihydrate is a broad-spectrum semisynthetic antibiotic similar to ampicillin except that its resistance to gastric acid permits higher serum levels with oral administration.Amoxicillin is a broad-spectrum, semisynthetic aminopenicillin antibiotic with bactericidal activity. Amoxicillin binds to and inactivates penicillin-binding protein (pbp) 1a located on the inner membrane of the bacterial cell wall. Inactivation of pbps interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This interrupts bacterial cell wall synthesis and results in the weakening of the bacterial cell wall and causes cell lysis. synonyms: (2s, 5r, 6r)-6-[[(2r)-2-amino-2-(4-hydroxyphenyl) acetyl] amino]-3, 3-dimethyl-7-oxo-4-thia-1- azabicyclo [3.2.0] heptane-2-carboxylic acid; trihydratecas number: 61336-70-7 mol. Formula: c16h25n3o8s, mol.weight: 419.45amoxicillin trihydrate is a white to off-white solid. It is soluble in water with melting point of 200c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering bambuterol is a long acting beta-adrenoceptor agonist used in the treatment of asthma. It is a prodrug of terbutaline.Bambuterol hydrochloride acts as a bronchodilator. It inhibits plasma bche (cholinesterase) during metabolism prolongs suxamethonium-induced neuromuscular blockade. Bambuterol hydrochloride is an activator of 2-ar. synonyms: [3-[2-(tert-butylamino)-1-hydroxyethyl]-5-(dimethyl carbamoyloxy) phenyl] n, n-dimethylcarbamate; hydrochloridecas number: 81732-46-9, mol. Formula: c18h30cln3o5, mol.weight: 403.9bambuterol is a white solid powder. It is soluble in water (33 mgml), dmso, and methanol with melting range of 222c to 224c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering lactulose is a synthetic disaccharide used in the treatment of constipation & hepatic encephalopathy. It has also been used in the diagnosis of gastrointestinal disorders.Lactulose is a disaccharide (sugar) synthesized from fructose & galactose, lactulose is used to treat constipation and some liver diseases. Nondigestible in mammals, lactulosepasses unabsorbed down to the large intestine where resident bacteria consume it and produce lactic, acetic and formic acids, which draw fluid into the bowel to soften the stool (laxative effect). Acidification of the colon contents attracts ammonia from the bloodstream, assisting stool excretion; helpful in liver failure when ammonia cannot be detoxified. synonyms: (2s, 3r, 4s, 5r, 6r)-2-[(2r, 3s, 4s, 5r)-4, 5-dihydroxy-2, 5-bis(hydroxymethyl)oxolan-3-yl]oxy-6-(hydroxymethyl)oxane-3, 4, 5-triolcas number: 4618-18-2, mol. Formula: c12h22o11, mol.weight: 342.3lactulose is white powder. It is soluble in water (76.4%) at 30 c, water (81%) at 60 c & water (>86%) at 90c with melting range of 167c to 169c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering mupirocin.Mupirocin is a topically used antibiotic from a strain of pseudomonas fluorescens. It has shown excellent activity against gram-positive staphylococci and streptococci. The antibiotic is used primarily for the treatment of primary and secondary skin disorders, nasal infections, and wound healing. Mupirocin is a rna synthetase inhibitor antibacterial. The mechanism of action of mupirocin is as a rna synthetase inhibitor.Mupirocin is a natural crotonic acid derivative extracted from pseudomonas fluorescens. Mupirocin inhibits bacterial protein synthesis by specific reversible binding to bacterial isoleucyl trna synthase. synonyms: 9-[(e)-4-[(2s, 3r, 4r, 5s)-3, 4-dihydroxy-5-[[(2s, 3s)-3-[(2s, 3s)-3-hydr oxybutan-2-yl] oxiran-2-yl] methyl] oxan-2-yl]-3-methylbut-2-enoyl] oxynonanoic acidcas number: 186826-86-8, mol. Formula: c21h25clfn3o4, mol.weight: 437.89mupirocin is a white crystalline solid. It is soluble in ethanol, methanol, dmf, dmso ( 10 mgml), and water (limited) with melting range of 75c to 78c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering nicorandil.Nicorandil is a derivative of the niacinamide that is structurally combined with an organic nitrate. It is a potassium-channel opener that causes vasodilatation of arterioles & large coronary arteries. it is nitrate-like properties produce venous vasodilation through stimulation of guanylate cyclase. Nicorandil is a vasodilatory drug used to treat angina.Nicorandil is a small molecule katp (kir6) channel opener, producing relaxation of coronary vascular smooth muscle. Specific binding of nicorandil to the c-terminus of the sur2b k (atp) channel generates k+ flux and hyperpolarization of the surface membrane, producing consequent closure of voltage-dependent ion channels and reduction of intracellular free ca2+. Nicorandil stimulates guanylate cyclase and increases cyclic gmp levels in correlation with the activation of k (atp) channels. Nicorandil is also described to suppress mitochondrial permeability transition triggered by oxidative stress resulting from ischemia-reperfusion, preventing mitochondrial calcium uptakeoverload and oxidative damage. Nicorandil has also been shown to serve as a nitric oxide donor. synonyms: 2-(pyridine-3-carbonylamino) ethyl nitratecas number: 65141-46-0, mol. Formula: c8h9n3o4, mol.weight: 211.17nicorandil is a white solid powder. It is soluble in water (4 mgml), dmso (>25 mgml), ethanol, ether, and methanol with melting range of 92c to 93c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering pheniramine maleate is antihistamine with anticholinergic properties used to treat allergicconditions such as hay fever or urticaria. Its relatively strong sedative effects, and may sometimes be used off-label as an over-the-counter sleeping pill in a similar manner to other sedating antihistamines such as diphenhydramine. Pheniramine is also commonly found in eyedrops used for the treatment of allergic conjunctivitis.Pheniramine is generally sold in combination with other medications, rather than as a stand-alone drug, although some formulations are available containing pheniramine by itself. One of this histamine h1 antagonist with little sedative action. Pheniramine maleate is used in treatment of hay fever, rhinitis, allergic dermatoses, and pruritus. synonyms: (z)-but-2-enedioic acid; n, n-dimethyl-3-phenyl-3-pyridin-2-ylpropan-1-aminecas number: 132-20-7, mol. Formula: c20h24n2o4, mol.weight: 356.42pheniramine maleate is a white powder with a faint amine-like odor. It is soluble in water with melting point of 107c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering simethicone is a poly (dimethylsiloxane) which is a polymer of 200-350 units of dimethylsiloxane, along with added silica gel. It is used as an antiflatulent, surfactant, and ointment base. Simethicone is an orally administered anti-foaming agent used to reduce bloating, discomfort or pain caused by excessive gas mainly swallowed air, with small amounts of hydrogen and methane in the stomach or intestines. synonyms: dioxosilane; methoxy-dimethyl-trimethylsilyloxysilanecas number: 9016-00-6, mol. Formula: c5h6si, mol.weight: 94.18simethicone is a colorless odorless liquid, floats on water. It is insoluble in water with melting point of -35c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering voglibose.Voglibose is a valiolamine derivative & inhibitor of alpha-glucosidase with antihyperglycemic activity. Voglibose binds to & inhibits alpha-glucosidase, an enteric enzyme found in the brush border of the small intestines that hydrolyzes oligosaccharides & disaccharides into- glucose & other monosaccharides. This prevents the breakdown of larger carbohydrates into glucose & decreases the rise in post- prandial blood glucose levels. Voglibose is an alpha-glucosidase inhibitor used for lowering post-prandial blood glucose levels in people with diabetes mellitus. Voglibose is orally active maltase-glucoamylase (-glucosidase) inhibitor (ic50 values are 3.9 & 6.4 nm at sucrase & maltase respectively). It increases glucagon-like peptide 1 (glp-1) secretion and also decreases food consumption in obob mice. Voglibose reduces plasma concentration of glucose, triglycerides and insulin in wistar fatty rats additionally, voglibose exhibits antidiabetic and antiobesity activity in vivo. synonyms: (1s, 2s, 3r, 4s, 5s)-5-(1, 3-dihydroxypropan-2-ylamino)-1-(hydroxymethyl) cyclohexane-1, 2, 3, 4-tetrolcas number: 83480-29-9, mol. Formula: c10h21no7, mol.weight: 267.28voglibose is a colourless crystalline solid powder. It is soluble to 100 mm in water and to 75 mm in dmso with melting range of 163c to 168c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering pamidronate disodium is the disodium salt of the synthetic bisphospho- nate pamidronate. Although its mechanism of action is not completely understood, pamidronate appears to adsorb to calcium phosphate crystals in bone, blocking their dissolution by inhibiting osteoclast-mediated bone resorption. This agent does not inhibit bone mineralization and formation.Pamidronate disodium salt is a bisphosphonate compound, which inhibits farnesyl diphosphate synthase & bone resorption. Studies suggest that pamidronate disodium salt stimulates polymorphonuclear leukocyte and platelet derived nitric oxide production. It is believed that this nitric oxide production can lead to a negative feedback mechanism, which could restrict the inflammatory process and reduce bone resorption. Furthermore, bisphosphonates induce endothelial cell death, cancer cell apoptosis, and nuclear factor-b pathway activation, via the endothelial protein c receptor. synonyms: disodium; [3-amino-1-hydroxy-1-[hydroxy (oxido) phosphoryl] propyl] hydroxyphosphinate; pentahydratecas number: 57248-88-1, mol. Formula: c3h9nna2o7p2.xh2o, mol.weight: 279.03pamidronate disodium is white crystalline powder. It is soluble in water: 28 mgml with melting point of 300c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering pindolol is a moderately lipophilic beta blocker (adrenergic beta-antagonists). It is non-cardioselective and has intrinsic sympathomimetic actions, but little membrane-stabilizing activity. A moderately lipophilic beta blocker (adrenergic beta-antagonists). It is non-cardioselective and has intrinsic sympathomimetic actions, but little membrane-stabilizing activity. Pindolol is a sr-1asr-1b antagonist with similar affinity for each subtype. Pindolol acts as a partial agonist at mouse and human 3-ar (3-adrenoceptors). Pindolol is an inhibitor of 1-ar. synonyms: 1-(1h-indol-4-yloxy)-3-(propan-2-ylamino) propan-2-olcas number: 13523-86-9, mol. Formula: c14h20n2o2, mol.weight: 248.32pindolol is a white to off-white crystalline powder. It is soluble in 0.1 m naoh (0.2 mgml), dmso (100 mm), methanol, and ethanol (with heating, 25 mm) insoluble in water with melting range of 167c to 171c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering linezolid.Linezolid is an oxazolidinone and acetamide derived anti-bacterial agent and protein synthesis inhibitor that is used in the treatment of gram-positive bacterial infections of the skin and respiratory tract. Linezolid is an oxazolidinone antibacterial. The chemical classification of linezolid is oxazolidinones.Linezolid is a synthetic oxazolidinone derivative; linezolid selectively inhibits an early step in bacterial protein synthesis and affects blood pressure through monoamine oxidase inhibition. It is effective against gram-positive organisms, including methicillin-resistant staphylococcus aureus strains, coagulase-negative staphylococci, vancomycin-resistant enterococci, and penicillin-resistant streptococcus pneumoniae strains. synonyms: n-[[(5s)-3-(3-fluoro-4-morpholin-4-ylphenyl)-2-oxo-1, 3-oxazolidin-5-yl] methyl] acetamidecas number: 165800-03-3, mol. Formula: c16h20fn3o4, mol.weight: 337.35linezolid is a white crystalline powder. It is soluble in water (

We are offering ritonavir.Ritonavir is an hiv protease inhibitor that works by interfering with the reproductive cycle of hiv. It also inhibits cytochrome p-450 cyp3a. It is a cytochrome p450 3a inhibitor and protease inhibitor. The mechanism of action of ritonavir is as a hiv protease inhibitor, cytochrome p450 3a inhibitor, cytochrome p450 2d6 inhibitor, cytochrome p450 2c19 inducer, cytochrome p450 3a inducer, p-glycoprotein inhibitor, breast cancer resistance protein inhibitor, and cytochrome p450 3a4 inhibitor.Ritonavir is a peptidomimetic agent that inhibits both hiv-1 and hiv-2 proteases. Ritonavir is highly inhibited by serum proteins but boosts the effect of other hiv proteases by blocking their degradation by cytochrome p450. synonyms: 1, 3-thiazol-5-ylmethyl n-[(2s, 3s, 5s)-3-hydroxy-5-[[(2s)-3-methyl-2-[[methyl-[(2-propan-2-yl-1, 3-thiazol-4- yl) methyl] carbamoyl]amino] butanoyl]amino]-1, 6-diphenylhexan-2-yl]carbamatecas number: 155213-67-5, mol. Formula: c37h48n6o5s2, mol.weight: 720.96ritonavir is a white powder. It is freely soluble in methanol and ethanol; soluble in isopropanol practically insoluble in water with melting range of 120c tp 122c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering zinc sulfate monohydrate.Zinc sulfate monohydrate can be used in electrolytes for zinc plating. It can be used as a mordant in dyeing. It can also be used in medicine as an astringent and emetic. Zinc sulfate monohydrate can be used to supply zinc in animal feeds, fertilizers, and agricultural sprays. synonyms: sulfuric acid zinc salt monohydrate;zinc sulfate-1-hydrate;zinc sulfate monohydrate;zinc sulfate;zinc sulphate h2o;zinc sulphate monohydrate;sulfuricacid, zincsalt(1:1), monohydrate;zincfertilizercas number: 7446-19-7, mol. Formula: h2o5szn, mol.weight: 179.47zinc sulfate monohydrate is a white powder or granules. It is soluble in water with melting point of 100c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering vincristine.Vincristine is an antitumor alkaloid isolated from vinca rosea. vincristine is an antitumor vinca alkaloid isolated from vinca rosea. It is marketed under several brand names, many of which have different formulations such as marqibo (liposomal injection) and vincasar. vincristine is indicated for the treatment of acute leukaemia, malignant lymphoma, hodgkin's disease, acute erythraemia, and acute panmyelosis. Vincristine sulfate is often chosen as part of polychemotherapy because of lack of significant bone-marrow suppression (at recommended doses) and of unique clinical toxicity (neuropathy). synonyms: vincristine;vincaleukoblastine, 22-oxo-;lcr;leucristine; vleurocristine (7ci, 8ci);vincaleukoblastine, 22-oxo- (9ci);vincristine (base andor unspecified salts);vincristine , vcr, nsc-67574, oncovincas number: 57-22-7, mol. Formula: c46h56n4o10, mol.weight: 824.96vincristine is a white crystalline solid. It is soluble in water, 2.27 mgl at 25 deg c (est) with melting range of 218c to 220c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering ribavirin is a nucleoside antimetabolite antiviral agent that blocks nucleic acid synthesis and is used against both rna and dna viruses. Ribavirin is a nucleoside analog antiviral. The chemical classification of ribavirin is nucleoside analog.Ribavirin is a synthetic nucleoside analog of ribofuranose with activity against hepatitis c virus and other rna viruses. Ribavirin is incorporated into viral rna, thereby inhibiting viral rna synthesis, inducing viral genome mutations, and inhibiting normal viral replication. synonyms: 1-[(2r, 3r, 4s, 5r)-3, 4-dihydroxy-5-(hydroxymethyl) oxolan-2-yl]-1, 2, 4-triazole-3-carboxamidecas number: 36791-04-5, mol. Formula: c8h12n4o5, mol.weight: 244.2ribavirin is a colourless solid. It is soluble in water (20 mgml), dmso (49 mgml at 25 c), ethanol (

We are offering tenofovir.Tenofovir is an adenine analog reverse transcriptase inhibitor with antiviral activity against hiv-1 and hepatitis b. It is used to treat hiv infections and chronic hepatitis b, in combination with other antiviral agents, due to the emergence of antiviral drug resistance when it is used alone. Tenofovir anhydrous is a human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor and hepatitis b virus nucleoside analog reverse transcriptase inhibitor. The mechanism of action of tenofovir anhydrous is as a nucleoside reverse transcriptase inhibitor. The chemical classification of tenofovir anhydrous is nucleoside analog. synonyms: [(2r)-1-(6-aminopurin-9-yl) propan-2-yl] oxymethylphosphonic acidcas number: 147127-20-6, mol. Formula: c9h14n5o4p, mol.weight: 287.21tenofovir is a white crystalline solid. It is soluble in dmso (10 mm), 1.1 eq.naoh (100 mm), water (2 mgml at 25 c), and ethanol (

We are offering zonisamide.Zonisamide is an anti-epileptic agent. The mechanism action of zonisamide is as a carbonic anhydrase inhibitor & p-glycoprotein inhibitor. The physiologic effect ofzonisamide is by means of decreased central nervous system disorganized electrical activity. The chemical classi- fication of zonisamide is sulfonamides. Zonisamide is a sulfonamide derivative with an anticonvulsant property the exact mechanism of action remains to be elucidated. zonisamide appears to block sodium & calciumchannels, thereby stabilizing neuronal membranes and suppressing neuronal hyper-synchronization. Although zonisamide shows affinity for the gamma-aminobutyric acid (gaba)benzodiazepine receptor ionophore complex, it does not potentiate the synaptic activity of gaba. In addition, this agent also facilitates both dopaminergic and serotonergic neurotransmission. synonyms: (1, 2-benzoxazol-3-ylmethanesulfonamidecas number: 68291-97-4, mol. Formula: c8h8n2o3s, mol.weight: 212.23zonisamide is an off-white solid powder. It is soluble in water (10 mm), dmso (100 mm), 1.1eq naoh (100 mm), ethanol (25 mm), methanol, and ethyl acetate with melting range of 162c to 167c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering dutasteride capsules.Dutasteride is a 5-alpha-reductase inhibitor that is reported to inhibit both type-1 and type2 isoforms of the enzyme and is used to treat benign prostatic hyperplasia.dutasteride is a 5-alpha reductase inhibitor. The mechanism of action of dutasteride is as a 5-alpha reductase inhibitor.Dutasteride is a synthetic 4-azasteroid compound. Dutasteride competitively & specifically binds to isoenzymes 1 and 2 of 5 alpha-reductase, forming stable enzyme complexes and inhibiting the conversion of testosterone to 5 alpha-dihydrotestosterone (dht); the reduction in dht activity may mitigate or prevent enlargement of the prostate gland. The type 2 5alpha-reductase isoenzyme is primarily active in the reproductive tissues, while the type 1 isoenzyme is also active in skin and the liver. synonyms: (1s, 3as, 3bs, 5ar, 9ar, 9bs, 11as)-n-[2, 5-bis(trifluoromethyl)phenyl]-9a, 11a-dimethyl-7-oxo-1, 2, 3, 3a, 3b, 4, 5, 5a, 6, 9b, 10, 11-dodecahydroindeno[5, 4-f]quinoline-1-carboxamidecas number: 164656-23-9, mol. Formula: c27h30f6n2o2, mol.weight: 528.53dutasteride is a white crystalline solid. It is soluble in ethanol (44 mgml), methanol (64 mgml), polyethylene glycol 400 (3 mgml), and dmso (62 mgml at 25 c 117mm) insoluble in water with melting range of 247c to 248c.Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering repaglinide is a glinide. The mechanism of action of repaglinide is as a potassium channel antagonist. Repaglinide is a nonsulfonylurea insulin secretagogue belonging to the melgitinide class with hypo glycemic activity. Repaglinide is rapidly absorbed and has a rapid onset and short duration of action. This agent is metabolized in the liver by cyp2c8 and cyp3a4 and its metabolites are excreted in the bile. Repaglinide has a half-life of one hour. synonyms: 2-ethoxy-4-[2-[[(1s)-3-methyl-1-(2-piperidin-1-ylphenyl) butyl] amino]-2-oxoethyl] benzoic acidcas number: 135062-02-1, mol. Formula: c27h36n2o4, mol.weight: 452.59repaglinide is a white to off-white solid. It is soluble to 100 mm in dmso and to 100 mm in ethanol with melting range of 130c to 131c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements

We are offering cefixime is a third-generation cephalosporin antibiotic that is stable to hydrolysis by beta-lactamases. Cefixime, an antibiotic, is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases, may be susceptible to cefixime.the antibacterial effect of cefixime results from inhibition of mucopeptide synthesis in the bacterial cell wall. synonyms: (6r, 7r)-7-[[(2e)-2-(2-amino-1, 3-thiazol-4-yl)-2-(carboxymeth- oxyimino) acetyl] amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acid cas number: 79350-37-1, mol. Formula: c16h15n5o7s2, mol.weight: 453.45 cefixime is a pale yellow solid powder. It is soluble in water, dmso, and methanol with melting range of 218cto 225c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements