ZZM-1220

For research use only. Not for therapeutic Use.

  • CAT Number: I040280
  • Molecular Formula: C25H29N5O3
  • Molecular Weight: 447.53
  • Purity: ≥95%
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ZZM-1220(CAT: I040280) is a covalent small-molecule inhibitor targeting the histone lysine methyltransferases G9a and GLP, with IC₅₀ values of 458 nM and 924 nM, respectively. It effectively inhibits dimethylation of histone H3 at lysine 9 (H3K9me2) in cellular systems, leading to epigenetic reprogramming. ZZM-1220 exhibits potent antitumor activity in triple-negative breast cancer (TNBC) models by inducing apoptosis and causing cell cycle arrest at the G2/M phase. This compound is a valuable tool for studying histone methylation, chromatin regulation, and epigenetic mechanisms involved in aggressive cancers.


Synonyms

N-[3-[6,7-dimethoxy-4-[(1-methylpiperidin-4-yl)amino]quinazolin-2-yl]phenyl]prop-2-enamide

Molecular Formula C25H29N5O3
Purity ≥95%
IUPAC Name N-[3-[6,7-dimethoxy-4-[(1-methylpiperidin-4-yl)amino]quinazolin-2-yl]phenyl]prop-2-enamide
InChI InChI=1S/C25H29N5O3/c1-5-23(31)26-18-8-6-7-16(13-18)24-28-20-15-22(33-4)21(32-3)14-19(20)25(29-24)27-17-9-11-30(2)12-10-17/h5-8,13-15,17H,1,9-12H2,2-4H3,(H,26,31)(H,27,28,29)
InChIKey RIYCTRNTJJXYCH-UHFFFAOYSA-N
SMILES CN1CCC(CC1)NC2=NC(=NC3=CC(=C(C=C32)OC)OC)C4=CC(=CC=C4)NC(=O)C=C
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