| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V5041 | NSC139021 (ERGi-USU) | 1147-56-4 | NSC139021 (also known as ERGi-USU) is a novel, potent and highly selective inhibitor for the growth of ERG-positive cancer cells with IC50s ranging from 30 to 400 nM. |
|
V4835 | EphB1-IN-10 | 2097512-73-5 | EphB1-IN-10 is a novel, potent, selective and irreversible/covalent inhibitor of receptor tyrosine kinase EphB1. |
|
V4863 | GSK-3008348 | 1629249-33-7 | GSK-3008348 (GSK3008348), an investigational drug, is a novel and potent integrin alpha(v)beta6 antagonist thatis being developed by GlaxoSmithKline Research and Development Limited (the Sponsor, a pharmaceutical company based in the UK) for the treatment of Idiopathic Pulmonary Fibrosis (IPF). |
|
V5016 | NSC-41589 | 6310-41-4 | NSC-41589 is N-[2-(methylsulfanyl) phenyl]acetamide. |
|
V4594 | U83836E | 137018-55-4 | U83836E is a novel and potent lipid peroxidation (LP) inhibitor. |
|
V4802 | ZD 7155 | 151801-76-2 | EXP-3174 (also known as losartan aarboxylic acid), a physiologically active metabolite of losartan produced by cytochrome P450 isoforms in the liver, is a non-peptide, potent angiotensin II (AII) receptor, type 1 (AT1) antagonist, which inhibits the AII induced cellular responses. |
|
V2167 | BC-DXI-843 | 2421117-98-6 | BC-DXI-843 is a potent and specificAIMP2-DX2inhibitor with anIC50of 0.92 μM, more than 100-fold selectivity over AIMP2 (IC50>100 μM) in a luciferase assay. |
|
V2171 | Isocanadine | 6656-19-5 | Isocanadine is an isomer of canadine. |
|
V4597 | Sufugolix (TAK013) | 308831-61-0 | Sufugolix (formerly known as TAK-013) is a novel, highly potent,non-peptide, selective and orally bioavailable luteinizing hormone-releasing hormone (LHRH) receptor antagonist with anticancer activity. |
|
V4560 | Alendronate sodium hydrate | 121268-17-5 | Alendronate sodium hydrate, the sodium salt of alendronate, is a novel and potent farnesyl diphosphate synthase inhibitor withIC50of 460 nM. |