MW 183.16 Da, Purity >99%. Novel, nontoxic and selective p53 inducer. Antitumor agent. Promotes tumor cell apoptosis in a mutant p53-dependent manner (IC50 = 10 μM) and prolongs survival. Active in vivo and in vitro.
AHDC, ALDC, ALDH 1, ALDH 11, ALDH class 1, ALDH class 2, ALDH-E1, ALDH-E2, ALDHI, ALDM, ALHDII, Acetaldehyde dehydrogenase 1, Acetaldehyde dehydrogenase 2, Aldehyde dehydrogenase 1, Aldehyde dehydrogenase 1 family member A1, Aldehyde dehydrogenase 1 soluble, Aldehyde dehydrogenase 1A1, Aldehyde dehydrogenase 2 family, Aldehyde dehydrogenase 2 family (mitochondrial), Aldehyde dehydrogenase cytosolic, Aldehyde dehydrogenase liver cytosolic, Aldehyde dehydrogenase mitochondrial, Aldh, DKFZp686C2056, DNA helicase, DNA helicase, RecQ like type 3, Exonuclease WRN, HGNC 12791, Liver mitochondrial ALDH, MGC1806, MGC2318, Mitochondrial aldehyde dehydrogenase 2, Nucleus encoded mitochondrial aldehyde dehydrogenase 2, OTTHUMP00000225301, PUMB 1, RALDH 1, RECQL 2, RECQL 3, RecQ protein-like 2, RecQ-like type 3, RecQ3, Retinal dehydrogenase 1, Retinaldehyde dehydrogenase 1, WRN_HUMAN, Werner syndrome ATP-dependent helicase, Werner syndrome helicase, Werner syndrome protein, Werner syndrome, RecQ helicase like
MW 183.16 Da, Purity >99%. Novel, nontoxic and selective p53 inducer. Antitumor agent. Promotes tumor cell apoptosis in a mutant p53-dependent manner (IC50 = 10 μM) and prolongs survival. Active in vivo and in vitro.
Soluble in water to 100 mM,.
Soluble in ethanol to 100 mM.
Soluble in DMSO to 100 mM.
Novel, nontoxic and selective p53 inducer. Antitumor agent. Promotes tumor cell apoptosis in a mutant p53-dependent manner (IC50 = 10 μM) and prolongs survival. Active in vivo and in vitro.
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2D chemical structure image of ab145862, MIRA-1, p53 inducer
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