2843690-50-4

I-0436650 Chemical Structure
2843690-50-4

Chemical Structure

I-0436650

  • CAS No.: 2843690-50-4
  • Formula:C22H22ClN9S
  • Molecular Weight:479.99

InChIKey: VUJLHBJEBKDVNJ-HXUWFJFHSA-N

SMILES: ClC1=C(N2C=CC=N2)N=CC=C1SC3=NC=C(N4CCC5(CC4)[C@@H](C6=CC=NN6C5)N)N=C3

Biological Activity: I-0436650 is an orally active SHP2 inhibitor with an IC50 of 4 nM and a Kd value of 0.3 nM. I-0436650 binds allosterically to the channel between the C-SH2, N-SH2 and PTP catalytic domains, locking the protein in an inactive closed conformation. I-0436650 potently inhibits ERK phosphorylation and suppresses MAPK pathway activity. I-0436650 exhibits antiproliferative activity in EGFR- and RAS-dependent cells. I-0436650 can be used in the research of RAS-driven cancers, EGFR-mutated cancers and RTK-driven cancers[1].

Cat. No. Product Name Purity Description Pricing
HY-189075
I-0436650 I-0436650 is an orally active SHP2 inhibitor with an IC50 of 4 nM and a Kd value of 0.3 nM. I-0436650 binds allosterically to the channel between the C-SH2, N-SH2 and PTP catalytic domains, locking the protein in an inactive closed conformation. I-0436650 potently inhibits ERK phosphorylation and suppresses MAPK pathway activity. I-0436650 exhibits antiproliferative activity in EGFR- and RAS-dependent cells. I-0436650 can be used in the research of RAS-driven cancers, EGFR-mutated cancers and RTK-driven cancers.
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