Information ND646 ND-646 is an allosteric inhibitor of the ACC (Acetyl-coA carboxylase) enzymes that prevents ACC subunit dimerization to suppress fatty acid synthesis with IC50 of 3.5 nM and 4.1 nM for hACC1 and hACC2, respectively. Targets hACC1 (Cell-free assay); hACC2 (Cell-free assay) 3.5 nM; 4.1 nM In vitro ND-646 inhibits FASyn in vitro and induces apoptosis in NSCLC cells. AMPK phosphorylation sites can be used as a biomarker to monitor ACC engagement by ND-646. In vivo Chronic ND-646 treatment of xenograft and genetically engineered mouse models of NSCLC inhibits tumor growth. When administered as a single agent or in combination with the standard-of-care drug carboplatin, ND-646 markedly suppresses lung tumor growth in the Kras;Trp53−/− (also known as KRAS p53) and Kras;Stk11−/− (also known as KRAS Lkb1) mouse models of NSCLC. Cell Research(from reference) Cell lines：A549 cells Concentrations：7 nM, 21 nM, 62 nM, 185 nM, 555 nM, 1666 nM, 5000 nM Incubation Time：24 hrs
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ND646
CAS number：1434639-57-2 molecular formula：C28H32N4O7S
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| Chinese alias | - | ||
| English alias | Thieno[2,3-d]pyrimidine-3(2H)-acetamide,1,4-dihydro-1-[(2R)-2-(2-methoxyphenyl)-2-[(tetrahydro-2H-pyran-4-yl)oxy]ethyl]-α,α,5-trimethyl-6-(2-oxazolyl)-2,4-dioxo- | ||
| CAS number | 1434639-57-2 | molecular formula | C28H32N4O7S |
| molecular weight | 568.64 g/mol | Exact mass | ≥98% |
| PSA | 166.000 Ų | logp | 2.600 |
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