Mumbai, Maharashtra, India GST : 27AGPPS8689E1ZF Verified Supplier
Our Complete range of products are Famotidine, fexofenadine hydrochloride tablet, Irbesartan, valacyclovir and nelfinavir.
SYNONYMS : 3-[[2-(DIAMINOMETHYLIDENEAMINO)-1, 3-THIAZOL-4-YL] METHYL SULFANYL]-N'-SULFAMOYLPROPANIMIDAMIDE CAS NUMBER: 76824-35-6, MOL. FORMULA: C8H15N7O2S3 MOL. WEIGHT: 337.43 IT IS WHITE TO PALE YELLOW COLOUR CRYSTALS WITH MELTING RANGE OF 163°C -164 °C. FREELY SOLUBLE IN GLACIAL ACETIC ACID, SLIGHTLY SOLUBLE IN METHANOL, VERY SLIGHTLY SOLUBLE IN WATER, AND PRACTICALLY INSOLUBLE INETHANOL STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
SYNONYMS: 2-(4-(1-HYDROXY-4-(4-(HYDROXYDIPHENYLMETHYL) PIPERIDIN-1-YL) BUTYL) PHENYL)- 2-METHYLPROPANOIC ACID HYDROCHLORIDE CAS NO: 153439-40-8, MOLECULAR WEIGHT IS 538.13, MOLECULAR FORMULA: C32H40CINO4 FEXOFENADINE HYDROCHLORIDE IS A WHITE TO OFF-WHITE CRYSTALLINE POWDER WITH MELTING RANGE OF 195°C TO 197 °C. IT IS FREELY SOLUBLE IN METHANOL AND ETHANOL, SLIGHTLY SOLUBLE IN CHLOROFORM & WATER, & INSOLUBLE IN HEXANE. STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
SYNONYMS: 2-N-BUTYL-3-((2'-(1H-TETRAZOL-5-YL) BIPHENYL-4-YL) METHYL)-1, 3-DIAZASPIRO(4, 4) NON-1-EN-4-ONE CAS NUMBER: 138402-11-6 , MOL.WEIGHT: 428.52 MOLECULAR FORMULA: C25H28N6O IT IS AVAILABLE IN WHITE CRYSTALLINE POWDER WITH MELTING RANGE 180-181 °C. STANDARD: OFFERED OF PHARMACEUTICAL GRADE BP/USP/EP PACKING: OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
We are offering valacyclovir. Valacyclovir is a herpes simplex virus nucleoside analog dna polymerase inhibitor, herpes zoster virus nucleoside analog dna polymerase inhibitor & herpesvirus nucleoside analog dna polymerase inhibitor. The mechanism of action of valacyclovir is as a dna polymerase inhibitor. The chemical classification of valacyclovir is nucleoside analog. Valacyclovir is the hydrochloride salt of the l-valyl ester of the antiviral drug acyclovir. Orally administered, valacyclovir is rapidly converted to acyclovir which inhibits viral dna replication after further conversion to the nucleotide analog acyclovir triphosphate by viral thymidine kinase, cellular guanyl cyclase, and a number of other cellular enzymes.acyclovir triphosphate competitively inhibits viral dna polymerase; incorporates into and terminates the growing viral dna chain; and inactivates viral dna polymerase. The greater antiviral activity of acyclovir against herpes simplex virus (hsv) compared with varicella-zoster virus (vzv) is due to its more efficient phosphorylation by hsv thymidine kinase. synonyms: 2-[(2-amino-6-oxo-3h-purin-9-yl) methoxy] ethyl (2s)-2-amino-3-methylbutanoate cas number: 124832-26-4, mol. Formula: c13h20n6o4, mol.weight: 324.34 valacyclovir is white solid powder. It is soluble in water 2239 mgl at 25 deg c (est) with melting range of 170°c to 172°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering nelfinavir is a potent hiv protease inhibitor. It is used in combination with other antiviral drugs in the treatment of hiv in both adults and children. Nelfinavir is a protease inhibitor. The mechanism of action of nelfinavir is as a hiv protease inhibitor. Nelfinavir is a synthetic antiviral agent that selectively binds to and inhibits human immunodeficiency virus (hiv) protease. Nelfinavir has activity against hiv 1 and 2. Nelfinavir mesylate is an inhibitor of hsp90. synonyms: (3s, 4as, 8as)-n-tert-butyl-2-[(2r, 3r)-2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-phenylsulfanylbutyl]-3, 4, 4a, 5, 6, 7, 8, 8a-octahydro-1h-isoquinoline-3-carboxamide cas number: 159989-64-7, mol. Formula: c32h45n3o4s, mol.weight: 567.78 nelfinavir is a white to off-white amorphous powder. It is soluble in water very soluble in methanol, ethanol, and acetonitrile. Practically insoluble in soybean oil, mineral oil with melting point of 349.84°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering torasemide. Torasemide is a loop diuretic. The physiologic effect of torsemide is by means of increased diuresis at loop of henle. Torasemide is an anilinopyridine sulfonylurea belonging to the class of loop diuretics. Torsemide has a prolonged duration of action compared to other loop diuretics, is extensively protein bound in plasma and has a relatively long half-life. synonyms: 1-[4-(3-methylanilino) pyridin-3-yl] sulfonyl-3-propan-2-ylurea cas number: 56211-40-6, mol. Formula: c16h20n4o3s, mol.weight: 348.42 torasemide is white crystalline solid powder. It is soluble in water >52.3 [ugml] with melting range of 163°c to 164°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
Atenolol is a cardioselective beta-1 adrenergic blocker possessing properties and potency similar to propranolol, but without a negative inotropic effect. Atenolol is a synthetic isopropylamino-propanol derivative used as an antihypertensive, hypotensive and antiarrhythmic atenolol acts as a peripheral, cardioselective beta blocker specific for beta-1 adrenergic receptors, without intrinsic sympathomimetic effects. It reduces exercise heart rates and delays atrioventricular conduction, with overall oxygenrequirements decreasing. Atenolol Is A white To Off-White Powder. It Is Soluble In Water (25 Mm), Dmso (18 Mg/Ml), Ethanol (3.4 Mg/Ml), Methanol (50 Mg/Ml), And Water (26.5 Mg/Ml At 37 °C) With Melting Range Of 146°C - 148°C.
We are offering leflunomide. Leflunomide is an antirheumatic agent. Leflunomide is a derivative of isoxazole used for its immunosuppressive and anti-inflammatory properties. As a prodrug, leflunomide is converted to an active metabolite, a77 1726, which blocks dihydroorotate dehydrogenase, a key enzyme of de novo pyrimidine synthesis, thereby preventing the expansion of activated t lymphocytes. This agent also inhibits various protein tyrosine kinases, such as protein kinase c (pkc), thereby inhibiting cell proliferation. synonyms: 5-methyl-n-[4-(trifluoromethyl) phenyl]-1, 2-oxazole-4-carboxamide cas number: 75706-12-6, mol. Formula: c12h9f3n2o2, mol.weight: 270.21 leflunomide is off white crystalline solid. It is soluble in dmso (54 mgml at 25 °c), ethanol (54 mgml at 25 °c), and water (
We are offering oxaliplatin. Oxaliplatin is a second generation potent platinum-based anti-neoplastic agent that is believed to form inters- and intrastrand dna adducts which activate signaling pathways culminating in apoptosis. The development of oxaliplatin was inspired from the efficacy of its progenitor, cisplatin (sc-200896), and the first of this class of anti-neoplastic agents. Oxaliplatin displays higher cytotoxicity and lower nephrotoxicity than cisplatin (sc-200896) or carboplatin (sc-202093), and shows antitumor activity in cell lines with acquired cisplatin (sc-200896) resistance. The enhanced activity of oxaliplatin compared to other members of this class is attributed to the bulky diaminocyclohexane ligand in the major groove that might limit the flexibility of the oxaliplatin-dna adduct, and interfere with dna repair enzymes differently. synonyms: (1r, 2r)-cyclohexane-1, 2-diamine; oxalic acid; platinum cas number: 61825-94-3, mol. Formula: c8h14n2o4pt, mol.weight: 397.29 oxaliplatin is white crystalline solid powder. It is soluble in water (7.9 mgml), methanol (slightly), and dmso (50 mm) insoluble in ethanol with melting point of 245°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering indinavir. Indinavir is a potent and specific hiv protease inhibitor that appears to have good oral bioavailability.indinavir anhydrous is a protease inhibitor. The mechanism of action of indinavir anhydrous is as a hiv protease inhibitor. Indinavir anhydrous is an anhydrous formulation of indinavir, a synthetic hydroxyaminopentane amide agent that selectively inhibits the protease of both human immunodeficiency virus 1 and 2. The incorporation of a basic amine into the hydroxyethylene backbone improves its aqueous solubility and its oral bioavailability. synonyms: (2s)-1-[(2s, 4r)-4-benzyl-2-hydroxy-5-[[(1s, 2r)-2-hydroxy-2, 3-dihydro-1h-inden-1-yl] amino]-5-oxopentyl]-n-tert-butyl-4-(pyridin-3-ylmethyl) piperazine-2-carboxamide cas number: 150378-17-9, mol. Formula: c36h47n5o4, mol.weight: 613.79 indinavir is a white crystalline solid powder. It is soluble in water (0.02 mgml) (unbuffered) with melting range of 153°c to 154°c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering famciclovir is a herpes simplex virus nucleoside analog dna polymerase inhibitor. The mechanism of action of famciclovir is as a dna polymerase inhibitor and dna polymerase inhibitor. The chemical classification of famciclovir is nucleoside analog. Famciclovir is a diacetyl 6-deoxy prodrug analog of the antiviral agent penciclovir. Orally administered, famciclovir in vivo is converted to penciclovir triphosphate, which is active against the herpes viruses, including herpes simplex 1 and 2 and varicella-zoster. This agent inhibits the replication of viral dna by interfering competitively with dna polymerase. synonyms: [2-(acetyloxymethyl)-4-(2-aminopurin-9-yl) butyl] acetate cas number: 104227-87-4, mol. Formula: c14h19n5o4, mol.weight: 321.33 famciclovir is off-white powder. It is solubility in water (25 deg c): > 25% wv initially; rapidly precipitates as sparingly soluble monohydrate (2-3% wv) with melting range of 102°c to 104°c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering isoniazid. Antibacterial agent used primarily as a tuberculostatic. Isoniazid remains the treatment of choice for tuberculosis. Isoniazid is an antimycobacterial. Isoniazid is a synthetic derivative of nicotinic acid with antimyco bacterial properties. Although mechanism of action is still unclear, isoniazid appears to block the synthesis of mycolic acids, major components of the mycobacterial cell wall.this agent is only active against actively growing mycobacteria because, as a pro-drug, it requires activation in susceptible mycobacterial species. Isoniazid also interferes with mycobacterial metabolism of vitamin b6. Resistance occurs due to decreased bacterial wall penetration. synonyms: pyridine-4-carbohydrazide cas number: 54-85-3, mol. Formula: c6h7n3o, mol.weight: 137.14 isoniazid is a white crystalline powder. It is soluble in water (50 mgml), ethanol (27 mgml at 25 °c), dmso (27 mgml at 25 °c), and methanol with melting range of 171°c to 173°c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering naproxen. Naproxen is an anti-inflammatory agent with analgesic & antipyretic properties. Both the acid & its sodium salt are used in the treatment of rheumatoid arthritis & other rheumatic or musculoskeletal disorders, dysmenorrhea & acute gout. Naproxen is a nonsteroidal antiinflam- matory drug. The mechanism of action of naproxen is as a cyclooxy- genase inhibitor. The chemical classification of naproxen is nonsteroidal anti-inflammatory compounds. Naproxen is a propionic acid derivative and a non-steroidal antiinflam- matory drug with anti-inflammatory, antipyretic & analgesic activities. Naproxen inhibits the activity of the enzymes cyclo-oxygenase I and ii, resulting in a decreased formation of precursors of prosta- glandins & thromboxanes. The resulting decrease in prostaglandin synthesis is responsible for the therapeutic effects of naproxen. naproxen also causes a decrease in the formation of thromboxane a2 synthesis, by thromboxane synthase, thereby inhibiting platelet aggregation. synonyms: (2s)-2-(6-methoxynaphthalen-2-yl) propanoic acid cas number: 22204-53-1, mol. Formula: c14h14o3, mol.weight: 230.26 naproxen is a white to light yellow crystal powder. It is soluble in water (>3 mgml) at 25 °c, pbs ph 7.2, sol., ethanol, dmso, dmf (100 mgml), chloroform, dichloromethane, ether, ethyl acetate, methanol, and thf with melting range of 152°c to 154°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering tolnaftate. Tolnaftate is a synthetic antifungal agent. Tolnaftate is a thiocar- bamate derivative with either fungicidal or fungistatic property. tolnaftate is a selective, reversible and non-competitive inhibitor of membrane-bound squalene-2, 3- epoxidase, and an enzyme involved in the biosynthesis of ergosterol. Inhibition leads to the accumulation of squalene and a deficiency in ergosterol, an essential component of fungal cell walls, thereby increasing membrane permeability, disrupting cellular organization and causing cell death. In addition, this agent may also distort the hyphae and stunts mycelial growth in susceptible fungi. synonyms: o-naphthalen-2-yl n-methyl-n-(3-methylphenyl) carbamothioate cas number: 2398-96-1, mol. Formula: c19h17nos, mol.weight: 307.41 tolnaftate is white crystalline powder. It is soluble in water 0.0000702 mgml at 25 °c with melting range of 110.5°c to 111.5°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering valdecoxib. Valdecoxib is a sulfonamide derivative and non-steroidal anti-inflammatory drug (nsaid) with anti-inflammatory, analgesic, and antipyretic activities. Valdecoxib selectively binds to and inhibits cyclooxygenase (cox)-2, thereby preventing the conversion of arachidonic acid into prostaglandins, which are involved in the regulation of pain, inflammation, and fever. This nsaid does not inhibit cox-1 at therapeutic concentrations and therefore does not interfere with blood coagulation. synonyms: 4-(5-methyl-3-phenyl-1, 2-oxazol-4-yl) benzenesulfonamide cas number: 181695-72-7, mol. Formula: c16h14n2o3s, mol.weight: 314.36 valdecoxib is white crystalline powder. It is soluble in dmso (63 mgml at 25° c), ethanol (18 mgml at 25° c), methanol, acetone, and water (0.5 mgml) with melting range of 170°c to 172°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering nitazoxanide. Nitazoxanide is an antiprotozoal. Nitazoxanide is a synthetic benzamide with antiprotozoal activity. Nitazoxanide exerts its antiprotozoal activity by interfering with the pyruvate ferredoxinflavodoxin oxidore- ductase dependent electron transfer reaction which is essential to anaerobic energy metabolism. Pfor enzyme reduces nitazoxanide thereby impairing the energy metabolism. However, interference with the pfor enzyme-dependent electron transfer reaction may not be the only pathway by which nitazoxanide exhibits antiprotozoal activity. nitazoxanide is active against giardia lamblia & cryptosporidium parvum. synonyms: [2-[(5-nitro-1, 3-thiazol-2-yl) carbamoyl] phenyl] acetate cas number: 55981-09-4, mol. Formula: c12h9n3o5s, mol.weight: 307.28 nitazoxanide is white crystalline powder. It is soluble in methanol with melting range of 198°c to 200°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering lomustine. Lomustine is an alkylating agent of value against both hematologic malignancies and solid tumors. Lomustine is an alkylating drug. The mechanism of action of lomustine is as an alkylating activity. Lomustine is a nitrosourea with antineoplastic activity. lomustine alkylates and crosslinks dna, thereby inhibiting dna and rna synthesis. This agent also carbamoylates dna and proteins resulting in inhibition of dna & rna synthesis and disruption of rna processing. Lomustine is lipophilic and crosses the blood-brain barrier. synonyms: 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea cas number: 13010-47-4, mol. Formula: c9h16cln3o2, mol.weight: 233.7 lomustine is a white to yellow powder. It is soluble in ethanol (47 mgml at 25 °c), chloroform, water (
Ketorolac Tromethamine Is A Pyrrolizine Carboxylic Acid Derivative Structurally Related To Indomethacin. It Is A Non-Steroidal Anti-Inflammatory Agent Used For Analgesia For Postoperative Pain And Inhibits Cyclooxygenase Activity. Ketorolac Tromethamine is The tromethamine salt Of ketorolac, A Synthetic Pyrrolizine Carboxylic Acid derivative With Anti-Inflammatory, Analgesic & Antipyretic Properties.Ketorolac Tromethamine, A Non-Selective Inhibitor Of The Cyclooxygenases (COX), Inhibits Both Cox-1 & Cox-2 Enzymes. This Agent Exerts Its Anti-Inflammatory Effect By Preventing Conversion Of arachidonic Acid to Prostaglandins At Inflammation Site Mediated Through Inhibition Of Cox-2, Which Is Undetec- Table In Most Tissues But Is Up-Regulated At The Inflammation Sites. Since Cox-1 Is Expressed Virtually In All Tissues, Inhibition Of Cox-1 Enzyme By This Agent Prevents Normal State Production Of Prostaglandins, Which Plays Housekeeping Roles In The Protection Of The Gastrointestinal Tract, Regulating Renal Blood Flow, And Functioning In Platelet Aggregation. As A Result, Inhibition Of Cox-1 Is Usually Associated With Adverse Effects Such As Gastrointestinal Toxicity And Nephrotoxicity. Ketorolac Tromethamine is Off-white to Pale Yellow Solid. It is Soluble in Ethanol (~7 Mg/ml), Dmf (~50 Mg/ml), Dmso (~7 Mg/ml), Water (15 Mg/ml), and Methanol with Melting Range of 160°C to 162°C.
We are offering olanzapine. Olanzapine is an atypical antipsychotic. Olanzapine is a synthetic derivative of thienobenzodiazepine with antipsychotic, antinausea & antiemetic activities. As a selective monoaminergic antagonist, olanza- pine binds with high affinity binding to the following receptors: seroton- inergic, dopaminergic, muscarinic m1-5, histamine h1, and alpha-1-adre- nergic receptors; it binds weakly to gamma-aminobutyric acid type a, benzodiazepine & beta-adrenergic receptors. The antinausea & antiemetic effects of this agent appear to be due to the blockade of 5-ht2 and 5-ht3 receptors for serotonin. Although its exact mechanism of action in schiz ophrenia is unknown it has been proposed that olanzapine antipsychotic activity is mediated through antagonism to dopamine d2 recep- tors with rapid ligand-receptor dissociation kinetics that help to minimize extrapyramidal symptoms. Olanzapine may also stimulate appetite. synonyms: 2-methyl-4-(4-methylpiperazin-1-yl)-5h- thieno [3, 2-c] [1, 5] benzodiazepine cas number: 132539-06-1, mol. Formula: c17h20n4s, mol.weight: 312.43 olanzapine is yellow crystalline powder. It is soluble in water, 39.88 mgl at 25 deg c (est) practically insoluble in water with melting point of 195°c. standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements
We are offering lisinopril. Lisinopril anhydrous is an angiotensin converting enzyme inhibitor. The mechanism of action of lisinopril anhydrous is as an angiotensin-converting enzyme inhibitor. One of the angiotensin-converting enzyme inhibitors (ace inhibitors), orally active, that has been used in the treatment of hypertension and congestive heart failure. Lisinopril anhydrous is the anhydrous form of the long-acting angiotensin-converting enzyme (ace) inhibitor lisinopril with antihyper- tensive activity. Lisinopril, a synthetic peptide derivative, competitively binds to and inhibits ace, thereby blocking the conversion of angiotensin I to angiotensin ii. This prevents the potent vasoconstrictive actions of angiotensin ii and results in vasodilation. Lisinopril also decreases angiotensin ii-induced aldosterone secretion by the adrenal cortex, which leads to an increase in sodium excretion and subsequently increases water outflow. synonyms: (2s)-1-[(2s)-6-amino-2-[[(1s)-1-carboxy-3-phenylpropyl] amino] hexanoyl] pyrrolidine-2-carboxylic acid cas number: 83915-83-7, mol. Formula: c21h31n3o5, mol.weight: 405.49 lisinopril is a white to off-white crystalline powder. It is soluble in methanol with melting range of 169°c to 172°c. Standard: offered of pharmaceutical grade bpuspep packing: offered in export worthy packing of 25 kilos or as per our customer requirements