696628-90-7

M6766 Chemical Structure
696628-90-7

Chemical Structure

M6766

  • CAS No.: 696628-90-7
  • Formula:C19H16N6S
  • Molecular Weight:360.44

IUPAC Name: 11-((1-methyl-1H-tetrazol-5-yl)thio)-7,8,9,10-tetrahydrobenzo[4,5]imidazo[1,2-b]isoquinoline-6-carbonitrile

InChIKey: HLGLCOORMAFZSN-UHFFFAOYSA-N

SMILES: CN1C(SC2=C3CCCCC3=C(C4=NC5=CC=CC=C5N42)C#N)=NN=C1

Biological Activity: M6766 is a selective endoplasmic reticulum oxidoreductase 1α (ERO1α) inhibitor with an IC50 of 1.4 μM and a KD of 1.1 μM. M6766 also inhibits ERO1β with an IC50 of 7.2 μM. M6766 binds to the flavin adenine dinucleotide-binding pocket in ERO1α. M6766 inhibits granule secretion, αIIbβ3 integrin activation, Ca2+ mobilization, and platelet aggregation. M6766 can be used for the research of neurological disease, such as ischemic stroke[1].

Cat. No. Product Name Purity Description Pricing
HY-175593
M6766 99.43% M6766 is a selective endoplasmic reticulum oxidoreductase (ERO1α) inhibitor with an IC50 of 1.4 μM and a KD of 1.1 μM. M6766 also inhibits ERO1β with an IC50 of 7.2 μM. M6766 binds to the flavin adenine dinucleotide-binding pocket in ERO1α. M6766 inhibits granule secretion, αIIbβ3 integrin activation, Ca2+ mobilization, and platelet aggregation. M6766 can be used for the research of neurological disease, such as ischemic stroke.
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