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is a potent inhibitor of the Rho-associated ROCK kinases with anti-invasive and antitumor activities in breast cancer
Smiles: CC1C(=S)SSC=1C1C=NC=CN=1
4-benzodiazepin-3-yl]urea
Small-molecule allosteric inhibitors of BAX
Smiles: COC1C=C(CCC2=CC(NC(=O)C3C=CC(=CC=3)N3C[C@H](C)N[C@H](C)C3)=NN2)C=C(C=1)OC
Propranolol D7 hydrochloride Catalog No.:M15330-2 is a potent inhibitor ofPropranolol D7 hydrochloride is a deuterium labeled Propranolol hydrochloride. Propranolol hydrochloride is a nonselective adrenergic receptor (AR) antagonist, has high affinity for the 1AR and 2AR with Ki values of 1. 8 nM and 0. 8 nM, respectively. Propranolol hydrochloride inhibits [3H] DHA binding to rat brain membrane preparation with an IC50 of 12 nM. Propranolol hydrochloride is used for the study of hypertension, pheochromocytoma, myocardial
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