EGFR mutant-IN-2 (Compound D51) is a selective inhibitor targeting the EGFR mutant variants, specifically EGFRL858R/T790M/C797S and EGFRdel19/T790M/C797S, with IC50 values of 14 nM and 62 nM, respectively. This compound demonstrates significant antitumor activity alongside favorable pharmacokinetic properties and in vivo stability, making it a valuable tool for research in cancer therapeutics. Its ability to effectively inhibit challenging EGFR mutations underscores its potential application in studying resistance mechanisms and developing targeted treatments.
EGFR mutant-IN-2 (Compound D51) is a selective inhibitor targeting the EGFR mutant variants, specifically EGFRL858R/T790M/C797S and EGFRdel19/T790M/C797S, with IC50 values of 14 nM and 62 nM, respectively. This compound demonstrates significant antitumor activity alongside favorable pharmacokinetic properties and in vivo stability, making it a valuable tool for research in cancer therapeutics. Its ability to effectively inhibit challenging EGFR mutations underscores its potential application in studying resistance mechanisms and developing targeted treatments.
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