Name: RWJ-56110 dihydrochloride
Rating: 5 (10 reviews)

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HIT ID:HIT214321285
Cas No:2387505-58-8
常用名:RWJ-56110 dihydrochloride
IUPAC:(2S)-4-amino-N-benzyl-2-[(2S)-2-[({1-[(2,6-dichlorophenyl)methyl]-3-[(pyrrolidin-1-yl)methyl]-1H-indol-6-yl}carbamoyl)amino]-3-(3,4-difluorophenyl)propanamido]butanamide hydrochloride
IUPAC:(2S)-4-amino-N-benzyl-2-[(2S)-2-[({1-[(2,6-dichlorophenyl)methyl]-3-[(pyrrolidin-1-yl)methyl]-1H-indol-6-yl}carbamoyl)amino]-3-(3,4-difluorophenyl)propanamido]butanamide hydrochloride
InChI key:GAWPESFUHHEDBS-GVGVJZOBSA-N

分子式:C41H44Cl3F2N7O3
分子量:827.2
氢键供体数 (HBD):
氢键受体数 (HBA):
LogP:
SMILES:Cl.NCC[C@H](NC(=O)[C@H](Cc1ccc(F)c(F)c1)NC(=O)Nc1ccc2c(CN3CCCC3)cn(Cc3c(Cl)cccc3Cl)c2c1)C(=O)NCc1ccccc1
SMILES:Cl.NCC[C@H](NC(=O)[C@H](Cc1ccc(F)c(F)c1)NC(=O)Nc1ccc2c(CN3CCCC3)cn(Cc3c(Cl)cccc3Cl)c2c1)C(=O)NCc1ccccc1

RWJ-56110 dihydrochloride is a potent, selective, peptide-mimetic inhibitor of PAR-1 activation and internalization (binding IC50=0.44 uM) and shows no effect on PAR-2, PAR-3, or PAR-4. RWJ-56110 dihydrochloride inhibits the aggregation of human platelets induced by both SFLLRN-NH2 (IC50=0.16 μM) and thrombin (IC50=0.34 μM), quite selective relative to U46619 . RWJ-56110 dihydrochloride blocks angiogenesis and blocks the formation of new vessels in vivo. RWJ-56110 dihydrochloride induces cell apoptosis[1][2].

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