
CAS 871543-07-6
:Formule :C16H23Cl2N3O2S
InChI :InChI=1S/C16H21N3O2S.2ClH/c1-12-9-18-11-14-5-3-6-15(16(12)14)22(20,21)19-8-4-7-17-10-13(19)2;;/h3,5-6,9,11,13,17H,4,7-8,10H2,1-2H3;2*1H/t13-;;/m0../s1
Code InChI :BFOPDSJOLUQULZ-GXKRWWSZSA-N
SMILES :C[C@H]1CNCCCN1S(=O)(=O)C2=CC=CC3=C2C(=CN=C3)C.Cl.Cl
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7 produits trouvés.
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H-1152 (dihydrochloride)
CAS :Formule :C16H23Cl2N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :392.3437H-1152 dihydrochloride
CAS :H-1152 dihydrochlorideFormule :C16H23Cl2N3O2SDegré de pureté :99.5%Masse moléculaire :392.34H-1152 Dihydrochloride
CAS :Produit contrôléStability Hygroscopic
Applications ROCK Inhibitor. A cell-permeable isoquinolinesulfonamide compound that acts as a highly specific, potent, and ATP-competitive inhibitor of G-protein Rho-associated kinase (ROCK: Ki=1.6nM). Exhibits a much weaker affinity for other serine/threonine kinases (Ki=630nM for PKA 9.27 mMfor PKC, and 10.1mM for MLCK). Shown to selectively block lysophosphatidic acid-induced, but not PDBu-induced, phosphorylation of myristoylated alanine-rich C kinase substrate MARCKS (IC50=2.5nM) in NT-2 cells.
References Ikenoya, M., et al.: J. Neurochem., 81, 9 (2002), Sasaki, Y., et al.: Pharmacol. Ther., 93, 225 (2002)Formule :C16H21N3O2S·2ClHCouleur et forme :NeatMasse moléculaire :392.34H-1152 2HCl
CAS :(S)-4-Methyl-5-((2-methyl-1,4-diazepan-1-yl)sulfonyl)isoquinoline dihydrochlorideFormule :C16H23Cl2N3O2SDegré de pureté :99%Masse moléculaire :392.34H 1152 dihydrochloride
CAS :Inhibitor of Rho-kinase
Formule :C16H23Cl2N3O2SDegré de pureté :Min. 95%Masse moléculaire :392.34 g/molH-1152 dihydrochloride
CAS :H-1152 2HCl: ROCK inhibitor, IC50=12 nM, Ki=1.6 nM. Blocks PKA, PKC, PKG, Aurora A, CaMKII with higher IC50s.Formule :C16H23Cl2N3O2SDegré de pureté :99.85%Couleur et forme :White SolidMasse moléculaire :392.34






