Asciminib Hydrochloride
The hydrochloride salt of asciminib that blocks the BCR-ABL1 oncoprotein through a novel allosteric mechanism, offering an option for patients with CML whose leukemia has resisted other tyrosine kinase inhibitors.
分子量
486.3000 g/mol
TPSA
103.00 Ų
作用機序
Selectively inhibits specific receptor tyrosine kinases involved in tumor cell proliferation, angiogenesis, and survival signaling. By blocking ATP binding to the kinase domain, it prevents phosphorylation cascades that drive cancer cell growth.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Selectively inhibits specific receptor tyrosine kinases involved in tumor cell proliferation, angiogenesis, and survival signaling. By blocking ATP binding to the kinase domain, it prevents phosphorylation cascades that drive cancer …
2D構造
Cite this structure
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SMILES
Cl.O=C(Nc1ccc(OC(F)(F)Cl)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cc[nH]n2)c1
InChI
InChI=1S/C20H18ClF2N5O3.ClH/c21-20(22,23)31-15-3-1-13(2-4-15)26-19(30)12-9-16(17-5-7-25-27-17)18(24-10-12)28-8-6-14(29)11-28;/h1-5,7,9-10,14,29H,6,8,11H2,(H,25,27)(H,26,30);1H/t14-;/m1./s1
Molecular Formula
C20H19Cl2F2N5O3
HBD / HBA
4 / 8
回転可能結合数
6
重原子数
32
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
The hydrochloride salt of asciminib that blocks the BCR-ABL1 oncoprotein through a novel allosteric mechanism, offering an option for patients with CML whose leukemia has resisted other tyrosine kinase inhibitors.
Selectively inhibits specific receptor tyrosine kinases involved in tumor cell proliferation, angiogenesis, and survival signaling. By blocking ATP binding to the kinase domain, it prevents phosphorylation cascades that drive cancer cell growth.
Yes, Asciminib Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4297220. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 133082086. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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