akash.verma@cenmed.com
(732) 447-1115-
78020-50A general competitive antagonist of mGlu receptors (KB values = 115, 88, and 77 µM for mGlu1a, mGlu2, and mGlu4a receptors, respectively). -
9001871-5An internal standard for the quantification of CMPF by GC- or LC-MS. -
10012431-25A potent and selective inhibitor of MEK1/2 (IC50 = 10-100 nM). -
10135-25ICI 192605 is a potent antagonist of the thromboxane A<sub>2</sub> receptor (TP) that blocks contraction of isolated guinea pig trachea induced by U-46619 (Item No. 16450 K<sub>d</sub> = 0. -
10135-10ICI 192605 is a potent antagonist of the thromboxane A<sub>2</sub> receptor (TP) that blocks contraction of isolated guinea pig trachea induced by U-46619 (Item No. 16450 K<sub>d</sub> = 0. -
78020-5A general competitive antagonist of mGlu receptors (KB values = 115, 88, and 77 µM for mGlu1a, mGlu2, and mGlu4a receptors, respectively). -
17260-5A reversible, ATP-competitive inhibitor of CK1&delta and CK1? (IC<sub>50</sub> = ~1 µM for both), as well as CK1&alpha (IC<sub>50</sub> = 16 µM) at 1 µM, inhibits cytokinesis in primary mouse embryo fibroblasts used to -
10135-5ICI 192605 is a potent antagonist of the thromboxane A<sub>2</sub> receptor (TP) that blocks contraction of isolated guinea pig trachea induced by U-46619 (Item No. 16450 K<sub>d</sub> = 0. -
16800-500A potent, selective, and orally bioavailable inhibitor of PI3K&gamma and PI3K&delta (IC<sub>50</sub>s = 0.24 and 50 nM, respectively) has profound effects in collagen-induced and adjuvant-induced arthritis, ovalbumin-induced asthma, and systemic -
17649-500A potent, cell-permeable inhibitor of the tyrosine kinase activity of the epidermal growth factor (EGF) receptor (IC<sub>50</sub> = 0.45 nM) effective in cells, blocking tyrosine phosphorylation induced by either EGF or heregulin (IC<sub>50</sub>s -
10135-1ICI 192605 is a potent antagonist of the thromboxane A<sub>2</sub> receptor (TP) that blocks contraction of isolated guinea pig trachea induced by U-46619 (Item No. 16450 K<sub>d</sub> = 0. -
10012431-1A potent and selective inhibitor of MEK1/2 (IC50 = 10-100 nM).
