About 6 results found for searched term "K-604" (0.121 seconds)
Cat.No. | Name | Target |
---|---|---|
M2664 | Eletriptan hydrobromide | 5-HT Receptor |
UK-116044 | ||
Eletriptan is a selective 5-HT1B and 5-HT1D receptor agonist with Ki of 0.92 nM and 3.14 nM, respectively. | ||
M8694 | K-604 | Others |
K-604 inhibits against acyl-coenzyme A (acyl-CoA):cholesterol O-acyltransferase-1 (ACAT1, SOAT1) activitiy in a selective (IC50 = 450 nM vs. | ||
M22305 | Eletriptan | Others |
UK 116044 | ||
Eletriptan | ||
M6589 | CGP 60474 | CDK |
CGP60474 is a highly effective anti-endotoxin compound, It is an effective cyclin-dependent kinase (CDK) inhibitor (IC50 of CDK1/B, CDK2/E, CDK2/ A, CDK4/D, CDK5/ P25, CDK7/H and CDK9/T are 26, 3, 4, 216, 10, 200 and 13 nM, respectively). CGP60474 is a selective and ATP-competitive PKC inhibitor. | ||
M8623 | RSV604 (A-60444) | RSV |
A-60444; RSV-604 | ||
RSV604 (A-60444) is a cell-permeable, non-cytotoxic (CC50 >50 μM) benzodiazepine derivative that is reported to target respiratory syncytial virus (RSV) nucleoprotein (N), with a Kd of 1.6 μM. RSV604 displays submicromolar activity against numerous clinical isolates of both the A and B subtypes of RSV (average EC50s=0.8 μM). | ||
M30365 | AS604872 | Prostaglandin Receptor |
AS604872 is an orally active, potent and selective prostaglandin F2α receptor (FP) antagonist with a Ki of 35 nM in humans, 158 nM in rats and 323 nM in mice. AS604872 inhibits contractions and delays labour. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.