Molecular docking analysis reveals differential binding affinities of multiple classes of selective inhibitors towards cancer-associated KRAS mutants
KRAS is the most frequently mutated oncogene in solid cancers, and inhibitors that specifically target the KRAS-G12C mutant were recently approved for clinical use. The limited availability of experimental data pertaining to the sensitivity of KRAS-non-G12C mutants towards RAS inhibitors made it dif...
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Published in | 3 Biotech Vol. 12; no. 12; p. 343 |
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Main Authors | , , , , , , , |
Format | Report |
Language | English |
Published |
01.12.2022
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Online Access | Get full text |
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