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A labeled (R)-enantiomer of Amlodipine. A dihydropyridine calcium channel blocker; activity resides mainly in the (-)-isomer. Form: White Solid Melting...
A key intermediate of cephem compounds. Form: White Solid Melting Point: 153-155 degrees C Solubility: DMSO, Ethyl Acetate
A key intermediate in the manufacturing of Cephalosporin compounds. Form: White Solid Melting Point: 215-220 degrees C Solubility: DMSO (Sparingly)
A key intermediate in production of HCV (Hepatitis C virus) antivirals. Form: Pale Yellow Solid Solubility: Aqueous Sodium Hydroxide
A key intermediate in production of HCV (Hepatitis C virus) antivirals. Form: Pale Yellow Solid Solubility: Aqueous Sodium Hydroxide
A key intermediate for the preparation of Vitamin D metabolites and analogs. Form: White Solid Melting Point: 105-107 degrees C Solubility: Chloroform
A key intermediate for Diltiazem synthesis. Form: Off-White Solid Melting Point: 202-203 degrees C Solubility: DMSO
A key component of antipsychotic and antihistaminic drugs. Form: Pale Yellow Solid Melting Point: 184-186 degrees C Solubility: Chloroform, Methanol
A key chiral intermediate used for synthesis of a vasopeptidase inhibitor Form: Off-White Solid Melting Point: 238-241 degrees C Solubility: Water
A ketolide antibiotic, used to treat respiratory infections Form: Pale Beige Solid Melting Point: 88-91 degrees C Solubility: DMSO, Methanol
A isotopically labeled metabolite of Losartan, a nonpeptide angiotensin II AT1-receptor antagonist. Form: Yellow Solid Melting Point: 105-110 degrees C...
A isotope Labeled resveratrol analog with a variety of pharmacology action, including Form: Transparent Oil Solubility: Dichloromethane, Ethyl Acetate
A isothiazolidin-3-one derivative as antimicrobial. It was tested for inhibition of PCAF activity. 5-Chloroisothiazolinones showed the most potent inhibition...
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,...
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