1209002-43-6

VMY-1-103 Chemical Structure
1209002-43-6

Chemical Structure

VMY-1-103

  • CAS. Nr.: 1209002-43-6
  • Formula:C34H42ClN9O4S
  • Molecular Weight:708.27

IUPAC Name: (R)-2-chloro-N-(2-(5-(dimethylamino)naphthalene-1-sulfonamido)ethyl)-4-((2-((1-hydroxy-3-methylbutan-2-yl)amino)-9-isopropyl-9H-purin-6-yl)amino)benzamide

InChIKey: NJNQGMFCZFMREY-MHZLTWQESA-N

SMILES: O=C(NCCNS(=O)(C1=C2C=CC=C(N(C)C)C2=CC=C1)=O)C3=CC=C(NC4=C5N=CN(C(C)C)C5=NC(N[C@@H](CO)C(C)C)=N4)C=C3Cl

Biological Activity: VMY-1-103 is an inhibitor for cyclin/Cdk complex, that arrests the cell cycle at G1 phase. VMY-1-103 reduces mitochondrial membrane potential, induces p53 phosphorylation and and PARP cleavage, activates caspase-3, and thus induces apoptosis in prostate cancer cell LNCaP[1].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-17548
VMY-1-103 VMY-1-103 is an inhibitor for cyclin/Cdk complex, that arrests the cell cycle at G1 phase. VMY-1-103 reduces mitochondrial membrane potential, induces p53 phosphorylation and and PARP cleavage, activates caspase-3, and thus induces apoptosis in prostate cancer cell LNCaP.
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