Short description: Investigational cancer drug
Belvarafenib |
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| Other names | HM95573
GDC5573
RG6185 |
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Routes of administration | By mouth |
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4-amino-N-[1-(3-chloro-2-fluoroanilino)-6-methylisoquinolin-5-yl]thieno[3,2-d]pyrimidine-7-carboxamide
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| Chemical and physical data |
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| Formula | C23H16ClFN6OS |
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| Molar mass | 478.93 g·mol−1 |
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| 3D model (JSmol) | |
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CC1=C(C2=C(C=C1)C(=NC=C2)NC3=C(C(=CC=C3)Cl)F)NC(=O)C4=CSC5=C4N=CN=C5N
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InChI=InChI=1S/C23H16ClFN6OS/c1-11-5-6-13-12(7-8-27-22(13)30-16-4-2-3-15(24)17(16)25)18(11)31-23(32)14-9-33-20-19(14)28-10-29-21(20)26/h2-10H,1H3,(H,27,30)(H,31,32)(H2,26,28,29) Key:KVCQTKNUUQOELD-UHFFFAOYSA-N
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Belvarafenib (developed by Hanmi Pharmaceuticals and Genentech) is a small molecule RAF dimer (type II) inhibitor[1] which shows anti-tumor clinical activity in cancer patients with BRAFV600E- and NRAS- mutations.[2]
References
- ↑ "Melanoma with genetic alterations beyond the BRAFV600 mutation: management and new insights". Current Opinion in Oncology 34 (2): 115–122. March 2022. doi:10.1097/CCO.0000000000000817. PMID 35050937.
- ↑ "Belvarafenib, a novel pan-RAF inhibitor, in solid tumor patients harboring BRAF, KRAS, or NRAS mutations: Phase I study.". Journal of Clinical Oncology 37 (15 suppl): 3000. 31 May 2019. doi:10.1200/JCO.2019.37.15_suppl.3000.
 | Original source: https://en.wikipedia.org/wiki/Belvarafenib. Read more |