330676-02-3

KH7 Chemical Structure
330676-02-3

Chemical Structure

KH7

  • CAS No.: 330676-02-3
  • Formula:C17H15BrN4O2S
  • Molecular Weight:419.30

IUPAC Name: (E)-2-((1H-benzo[d]imidazol-2-yl)thio)-N'-(5-bromo-2-hydroxybenzylidene)propanehydrazide

InChIKey: WILMXUAKQKGGCC-DJKKODMXSA-N

SMILES: CC(SC1=NC2=CC=CC=C2N1)C(N/N=C/C3=CC(Br)=CC=C3O)=O

Biological Activity: KH7 is a soluble adenylyl cyclase (sAC)-specific inhibitor, with IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays[1]. KH7 is also a cAMP inhibitor[2].

Cat. No. Product Name Purity Description Pricing
HY-103194
KH7 99.0% KH7 is a soluble adenylyl cyclase (sAC)-specific inhibitor, with IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibitor.
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HY-103194R
KH7 (Standard) ≥98% KH7 (Standard) is the analytical standard of KH7 (HY-103194). This product is intended for research and analytical applications. KH7 is a soluble adenylyl cyclase (sAC)-specific inhibitor, with IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibitor.
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