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YM-201636 inhibits preferentially PtdIns5P rather than PtdIns(3
Solubility: DMSO : 145 mg/mL (142
decrease the phosphorylation of mitogen-activated protein kinases (MAPKs)
ACMC-20f6dm
Smiles: CC1=NC=C(C=C1C1=CC(OC)=C(OC)C(=C1)OC)C1C=CC(=CC=1)N1CCNCC1
ON-01910 selective p38α PROTAC YM-201636 inhibits preferentially PtdIns5P ratherON 01910 is a synthetic benzyl styryl sulfone analogue with potential antineoplastic activity. Polo like kinase 1 inhibitor ON 01910. Na inhibits polo like kinase1 (Plk1), inducing selective G2 M arrest followed by apoptosis in a variety of tumor cells while causing reversible cell arrest at the G1 and G2 stage without apoptosis in normal cells. This agent may exhibit synergistic antitumor activity in combination with other chemotherapeutic agents.
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