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|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|DETD-35||DETD-35 is a derivative of plant sesquiterpene lactone that inhibits Mek-Erk signaling and induces reactive oxygen species generation, which may lead to apoptosis in tumor cells (PMID: 27048951).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|BRAF V600E||melanoma||sensitive||DETD-35||Preclinical - Cell line xenograft||Actionable||In a preclinical study, DETD-35 inhibited proliferation and colony formation of melanoma cells harboring BRAF V600E in culture and reduced tumor size in xenograft models (PMID: 27048951).||27048951|
|PTEN loss||melanoma||sensitive||DETD-35||Preclinical - Cell line xenograft||Actionable||In a preclinical study, DETD-35 treatment resulted in reduced tumor size in cell line xenograft models of Zelboraf (vemurafenib)-resistant melanoma harboring PTEN loss (PMID: 27048951).||27048951|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status||Covered Countries||Other Countries|