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A isoquinolinone derivative as PARP-1/PARP-2 inhibitors. Form: Pale Beige Solid Melting Point: 234-236 degrees C Solubility: DMSO, Methanol
A intermediate in the synthesis of Tilduronic Acid, a biphosphonate bone resorption inhibitor. Form: Yellow Oil Solubility: Dichloromethane, Ethyl Acetate
A intermediate in the synthesis of a metabolite of Docetaxel, an antineoplastic. Form: White Solid Solubility: Chloroform,
A IMP-1 metallo-b-lactamase inhibitor. Melting Point: 41-43 degrees C Solubility: Chloroform, Dichloromethane, Ethyl Acetate, Methanol Storage and Stability:...
A Hydroxysuccinimide derivative. Form: Light Yellow Solid Melting Point: 88-90 degrees C Solubility: DMSo, Ethanol, Methanol
A hydroxylated psoralen that inhibits neutrophil infiltration and brain edema induced by focal cerebral ischemia-reperfusion injury in rats. A potentially...
A hydroxylated psoralen that acts as a potent inhibitors of debenzylation activity of CYP3A4 enzyme with an IC50 value of 24.92 and 42.93 microM,...
A hydroxylated metabolite of Iloperidone. Form: Off-White to Pale Yellow Solid Melting Point: 136-137 degrees C Solubility: Chloroform, Methanol (Sparingly)
A hydroxylated labeled metabolite of Iloperidone. Form: Off-White Solid Melting Point: 135-138 degrees C Solubility: Chloroform, Methanol
A hydroxycarboxylic acid as additive enhancing topical actions of therapeutic agents.
A hydrazine derivative that is a non-selective and irreversible monoamine oxidase inhibitor (MAOI) and also inhibits GABA-transaminase (GABA-T), markedly...
A human urinary organophosphate flame retardant metabolite. Form: Clear Colorless Oil Solubility: Chloroform
A human labeled metabolite of Ibuprofen. Form: White to Off-White Solid Melting Point: 124-126 degrees C Solubility: DMSO, Methanol
A HMG-CoA reductase inhibitor. It has been shown to be effective in reducing cholesterol synthesis in vivo, and thereby in lowering cholesterol levels in...
A histamine H2-receptor antagonist. It is used to inhibit gastric acid secretion; an antiulcer agent. Form: White Solid Melting Point: 147-149 degrees C...
A highly water soluble Clindamycin prodrug. Form: White Solid Melting Point: 187-192 degrees C Solubility: DMSO
A highly toxic semi-volatile organic compound and a suspected human carcinogen. It induces liver tumors in rats after chronic exposure to low doses. Form:...
A highly specific aldose reductase inhibitor that has been shown to enhance HeLa cell sensitivity to chemotherapeutic drugs. Form: Pale Pink Solid Melting...
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