Dabrafenib Mesylate
The mesylate salt form of dabrafenib, a BRAF V600E/K inhibitor used for treating metastatic melanoma, NSCLC, and anaplastic thyroid cancer with BRAF mutations. The mesylate salt improves the compound's pharmaceutical properties.
الوزن الجزيئي
615,7000 g/mol
TPSA
210,00 Ų
المجالات العلاجية
آلية العمل
Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CC(C)(C)c1nc(-c2cccc(NS(=O)(=O)c3c(F)cccc3F)c2F)c(-c2ccnc(N)n2)s1.CS(=O)(=O)O
InChI
InChI=1S/C23H20F3N5O2S2.CH4O3S/c1-23(2,3)21-30-18(19(34-21)16-10-11-28-22(27)29-16)12-6-4-9-15(17(12)26)31-35(32,33)20-13(24)7-5-8-14(20)25;1-5(2,3)4/h4-11,31H,1-3H3,(H2,27,28,29);1H3,(H,2,3,4)
Molecular Formula
C24H24F3N5O5S3
HBD / HBA
3 / 14
الروابط القابلة للدوران
6
الذرات الثقيلة
40
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.
الأسئلة الشائعة
The mesylate salt form of dabrafenib, a BRAF V600E/K inhibitor used for treating metastatic melanoma, NSCLC, and anaplastic thyroid cancer with BRAF mutations. The mesylate salt improves the compound's pharmaceutical properties.
Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.
Yes, Dabrafenib Mesylate 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). CHEMBL2105729. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 44516822. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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