Drug intelligence / Profile preview

sardomozide

Development stage
Preclinical
Lead developer
Novartis
Modality
Small Molecules
Administration
Intperitoneal, Intravenous, Oral
01

Overview

Sardomozide (SAM486) is a potent, selective, and competitive small molecule inhibitor of S-adenosylmethionine decarboxylase 1 (AMD1/SAMDC), a key rate-limiting enzyme in the polyamine biosynthesis pathway. Originally developed by Ciba-Geigy (which later became Novartis) under the code name CGP 48664, sardomozide prevents the conversion of S-adenosylmethionine to decarboxylated S-adenosylmethionine, thereby depleting intracellular pools of spermidine and spermine. This depletion leads to cell cycle arrest and apoptosis in rapidly proliferating cells. Sardomozide has been evaluated in preclinical and early-phase clinical trials for various malignancies, including melanoma, non-Hodgkin lymphoma, and solid tumors, and continues to be investigated in preclinical combination regimens for neuroblastoma and non-small cell lung cancer (NSCLC).

Other names
4-(aminoiminomethyl)-2,3-dihydro-1H-inden-1-one-diaminomethylenehydrazone4-amidinoindan-1-one 2'-amidinohydrazonesardomozide dihydrochloride
02

Targets

AMD1 (S-adenosylmethionine decarboxylase)

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