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CAS:157810-81-6
Molecular Formula:C36H49N5O8S
Indinavirsulfate(Subjecttopatentfree); Mk-639,Crixivan; Crixivan; Indinavir Sulphate; Mk-639; Indigowoadrootextract; Indinavir (Sulfate); Idv; (1(1S,2R),5(S))-2,3,5-Trideoxy-N-(2,3-Dihydro-2-Hydroxy-1H-Inden-1-Yl)-5-(2-(((1,1-Dimethylethyl)Amino)Carbonyl)-4-(3-Pyridinylmethyl)-1-Piperazinyl)-2-(Phenylmethyl)-D-Erythro-Pentonamide Sulfate
Brief Introduction
Indinavir sulfate is a protease inhibitor of human immunodeficiency virus (HIV). HIV protease is an enzyme found in infectious HIV, which can cleave the precursor of viral polymeric protein into a single functional protein. Indinavir can bind to the active site of the protease and inhibit its activity. This inhibition blocked the cleavage of viral polyproteins, leading to the formation of immature non infectious virus particles. Indinavir sulfate is used in combination with other antiretroviral drugs for the treatment of HIV-1 infection in adults and children.
CAS:160738-57-8
Molecular Formula:C22H28FN3O7
Gatifloxacin Hcl; Gatifloxacinacid; 1-Cyclopropyl-6-Fluoro-8-Methoxy-7-; (3-Methylpiperazin-1-Yl)-4-Oxo-1,4-
Brief Introduction
This product is used as an antibacterial agent.
Brief Introduction
Netoglitazone is an agent belonging to the glitazone class of antidiabetic agents with antihyperglycemic activity. Netoglitazone exerts both peroxisome proliferator-activated receptor (PPAR) alpha and gamma agonist activity. Netoglitazone decreases bone formation and increases marrow adipocyte formation in vivo.
CAS:16188-61-7
Molecular Formula:C19H21N3O
Talastina; Talastinum; 4-Benzyl-2-(2-Dimethylamino-Aethyl)-2H-Phthalazin-1-On; Talastinum [Inn-Latin]; Talastine; Talastina [Inn-Spanish]; 4-Benzyl-2-(2-Dimethylamino-Ethyl)-1-Oxo-1.2-Dihydro-Phthalazin; 4-Benzyl-2-(2-Dimethylamino-Ethyl)-2H-Phthalazin-1-One; Talastine (Inn); Unii-49Ab2Pa48B; 49Ab2Pa48B
Brief Introduction
Talastine is a member of phthalazines.
CAS:162635-04-3
Molecular Formula:C56H87NO16
Ccl-779; Temsirolimus (~); Rapamycin 42-[3-Hydroxy-2-(Hydroxymethyl)-2-Methylpropanoate; Rapamycin 42-Ester With 3-Hydroxy-2-(Hydroxymethyl)-2-Methylpropionic Acid; (1R,2R,4S)-4-{(2R)-2-[(3S,6R,7E,9R,10R,12R,14S,15E,17E,19E,21S,23S,26R,27R,34As)-9,27-Dihydroxy-10,21-Dimethoxy-6,8,12,14,20,26-Hexamethyl-1,5,11,28,29-Pentaoxo-1,4,5,6,9,10,11,12,13,14,21,22,23,24,25,26,27,28,29,31,32,33,34,34A-Tetracosahydro-3H-23,27-Epoxypyrido[2,1-C][1,4]Oxazacyclohentriacontin-3-Yl]Propyl}-2-Methoxycyclohexyl 3-Hydroxy-2-(Hydroxymethyl)-2-Methylpropanoate; [14C]-Temsirolimus; 42-[3-Hydroxy-2-(Hydroxymethyl)-2-Methylpropanoate]Rapamycin; Rapamycin (42-[3-Hydroxy-2-(Hydroxymethyl)-2-Methylpropanoate]; Temsirolimus (Torisel); Temsirolimus (Cci-779,Torisel)
Brief Introduction
Teisirolimus, also known as sirolimus ester, is a targeted antitumor drug developed by Wyeth medicine (now incorporated into Pfizer medicine) for the treatment of progressive renal cancer. It is also the first targeted therapeutic drug for the treatment of renal cancer, and it is the only drug specifically inhibiting mTOR kinase on the market.
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