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Filtered Search Results
eMolecules 3-BROMO-2-CHLORO-6-FLUOROPYRIDINE | 1211578-75-4 | MFCD18257575 | 1g
AstaTech | 3-BROMO-2-CHLORO-6-FLUOROPYRIDINE | 1g | 475589658 | F30308 | 95.000 | 1211578-75-4 | MFCD18257575 | 210.430 | C5H2BrClFN
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380687 ATORVASTATIN ACETONI 50MG
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5000381820 ATORVASTATIN ETHYL E 25MG
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5000381939 ATORVASTATIN METHYL 25MG
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5000380323 ATORVASTATIN ACETONI 100MG
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5000380319 ATORVASTATIN 3-DEOXY 100MG
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5000380399 ATORVASTATIN ETHYL E 50MG
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5000665692 N-DESETHYL SUNITINIB 25MG
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5000664948 NEMONOXACIN MALATE 10MM/1ML
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5000665745 N-DESETHYL SUNITINIB 100MG
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Selleck Chemical LLC Sacubitril hemicalcium salt S4426-100mg
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Sacubitril (AHU-377) hemicalcium salt a component of the heart failure medicine LCZ696 is a potent inhibitor of neprilysin (neutral endopeptidase NEP)
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5000303184 L-GULONO-1 4-LACTONE 5G
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Cayman Chemical Atorvastatin calcium salt hy
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An HMG-CoA reductase inhibitor (IC50s = 73, 102, and 0.6 nM for HepG2 cells, human fibroblasts, and rat hepatocytes, respectively)
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AdipoGen Sunitinib . malate (25 mg)
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Chemical. CAS: 341031-54-7. Formula: C22H27FN4O2 . C4H6O5. MW: 398.5 . 134.1. Potent ATP-competitive and cell permeable multi-targeted receptor tyrosine kinase (RTK) inhibitor targeting VEGFR and PDGFR-beta. Inhibits FLK1 (Ki=9nM), PDGFRbeta (Ki=8nM) and FLT3. It is at least 10-fold selective for FLK1 and PDGFRbeta over a variety of tyrosine kinases in a panel, including EGFR, Cdk2, Met, IGFR-1, Abl and Src. Inhibits the cellular receptor phosphorylation of FLT3, RET and CSF-1R. Also shown to inhibit c-Kit. Exhibits potent antiangiogenic and antitumor activity in multiple xenograft models.
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Cayman Chemical SBromoenol lactone
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A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
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