Mobocertinib Succinate
A succinate salt form of mobocertinib, an EGFR inhibitor designed to treat non-small cell lung cancer with EGFR exon 20 insertion mutations. It selectively targets these mutations to block tumor cell growth.
Molecular Weight
703.8000 g/mol
TPSA
188.00 Ų
Mechanism of Action
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 Structure
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SMILES
C=CC(=O)Nc1cc(Nc2ncc(C(=O)OC(C)C)c(-c3cn(C)c4ccccc34)n2)c(OC)cc1N(C)CCN(C)C.O=C(O)CCC(=O)O
InChI
InChI=1S/C32H39N7O4.C4H6O4/c1-9-29(40)34-24-16-25(28(42-8)17-27(24)38(6)15-14-37(4)5)35-32-33-18-22(31(41)43-20(2)3)30(36-32)23-19-39(7)26-13-11-10-12-21(23)26;5-3(6)1-2-4(7)8/h9-13,16-20H,1,14-15H2,2-8H3,(H,34,40)(H,33,35,36);1-2H2,(H,5,6)(H,7,8)
Molecular Formula
C36H45N7O8
HBD / HBA
4 / 13
Rotatable Bonds
16
Heavy Atoms
51
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.
Frequently Asked Questions
A succinate salt form of mobocertinib, an EGFR inhibitor designed to treat non-small cell lung cancer with EGFR exon 20 insertion mutations. It selectively targets these mutations to block tumor cell growth.
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, Mobocertinib Succinate 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). CHEMBL4802239. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 146026179. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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