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Capmatinib hydrochloride

Capmatinib hydrochloride Structure
CAS No.
1865733-40-9
Chemical Name:
Capmatinib hydrochloride
Synonyms
INC-280 2HCl.H2O;INCB28060 2HCl.H2O;NVP-INC280 2HCl.H2O;Capmatinib 2HCl.H2O;Capmatinib HCl hydrate;Capmatinib hydrochloride;Capmatinib hydrochloride Hydrate;Capmatinib HCl hydrate (INCB-28060;Capmatinib dihydrochloride hydrate;Capmatinib Hydrochloride Hydrate (INCB28060)
CBNumber:
CB04848242
Molecular Formula:
C23H20ClFN6O2
Molecular Weight:
466.9
MOL File:
1865733-40-9.mol
Modify Date:
2024/11/15 19:19:13

Capmatinib hydrochloride Properties

form Solid
color White to light yellow
InChIKey XCHIKTXPDQTRMI-UHFFFAOYSA-N
SMILES C(C1C=CC2N=CC=CC=2C=1)C1=CN=C2N=CC(C3C=CC(C(=O)NC)=C(F)C=3)=NN12.Cl.O

Capmatinib hydrochloride Chemical Properties,Uses,Production

Description

Capmatinib dihydrochloride hydrate is a orally active,reversible MET tyrosine kinase inhibitor that received approval for advanced non-small cell lung cancer(NSCLC) harboring MET exon 14 skipping mutationa. Capmatinib dihydrochloride hydrate can inhibit phosphorylation of c-MET as well as c-MET pathway downstream effectors such as ERK1/2, AKT, FAK, GAB1, and STAT3/5. Capmatinib dihydrochloride hydrate potently inhibits c-MET-dependent tumor cell proliferation and migration and effectively induces apoptosis. Antitumor activity. Capmatinib dihydrochloride hydrate is largely metabolized by CYP3A4 and aldehyde oxidase[1-3].

Origin

Capmatinib was first reported in 2011 by Liu et al., who showed that in both in vivo and in vitro mice studies using human cell lines, capmatinib had a 10,000-fold selectivity for c-met over a large panel of human kinase. They showed that capmatinib can block the c-MET phosphorylation and activation of downstream targets, including HGF. They further showed that activated c-met upregulates cancer-promoting EGFR and HER-3 pathways. Baltschukat et al. further investigated capmatinib in NSCLC[4].

Mechanism of action

Tabrecta (capmatinib) is a kinase inhibitor that targets MET, including the mutant variant produced by exon 14 skipping. MET exon 14 skipping results in a protein with a missing regulatory domain that reduces its negative regulation, leading to increased downstream MET signaling.

Toxicity evaluation

Effects During Pregnancy and Lactation No information is available on the clinical use of capmatinib during breastfeeding. Because capmatinib is 96% bound to plasma proteins, the amount in milk is likely to be low. The manufacturer recommends that breastfeeding be discontinued during capmatinib therapy and for 1 week after the last dose.

References

[1] HSUROBERT NagasakaMisako BenjaminDavid J. The Development and Role of Capmatinib in the Treatment of MET-Dysregulated Non-Small Cell Lung Cancer-A Narrative Review.[J]. Cancers, 2023. DOI:10.3390/cancers15143561.
[2] LIUXIANGDONG. A novel kinase inhibitor, INCB28060, blocks c-MET-dependent signaling, neoplastic activities, and cross-talk with EGFR and HER-3.[J]. Clinical Cancer Research, 2011. DOI:10.1158/1078-0432.CCR-11-1157.
[3] BALTSCHUKATSABRINA. Capmatinib (INC280) Is Active Against Models of Non-Small Cell Lung Cancer and Other Cancer Types with Defined Mechanisms of MET Activation.[J]. Clinical Cancer Research, 2019. DOI:10.1158/1078-0432.CCR-18-2814.
[4] HsuRobert, NagasakaMisako, BenjaminDavid J. "The Development and Role of Capmatinib in the Treatment of MET-Dysregulated Non-Small Cell Lung Cancer-A Narrative Review." Cancers 15 14 (2023).

Capmatinib hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Capmatinib hydrochloride Suppliers

Global( 45)Suppliers
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Jinan Million Pharmaceutical Co., Ltd 0531-68659554 +8613031714605 China 252 58 Inquiry
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TargetMol Chemicals Inc. United States 38470 58 Inquiry
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +8615195660023 China 23046 58 Inquiry
Wuhan Topule Biopharmaceutical Co., Ltd +8618327326525 China 8467 58 Inquiry
Capmatinib hydrochloride Capmatinib hydrochloride Hydrate Capmatinib HCl hydrate (INCB-28060 Capmatinib 2HCl.H2O INC-280 2HCl.H2O INCB28060 2HCl.H2O NVP-INC280 2HCl.H2O Capmatinib Hydrochloride Hydrate (INCB28060) S114,SNU-5,ATP competitive,Balb/c nu/nu mice,U-87MG,INCB-28060 dihydrochloride,orally active,Capmatinib dihydrochloride,Capmatinib 2HCl.H-2O,Capmatinib 2HCl.H2O,INC280 dihydrochloride,Apoptosis,inhibit,Inhibitor,c-Met/HGFR,H441 2-fluoro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide dihydrochloride monohydrate Capmatinib dihydrochloride hydrate Capmatinib HCl hydrate 1865733-40-9 C23H17FN6O2HClH2O