NAcM-OPT 是一种口服生物可利用的 cullin neddylation 1 (DCN1) 抑制剂，有效抑制 DCN1-UBE2M 相互作用。
货号:ajcx38694
CAS:2089293-61-6
分子式:C23H29Cl2N3O
分子量：434.4
溶解度:DMSO : 125 mg/mL (287.75 mM; Need ultrasonic)
纯度：98%
存储：Store at -20°C
库存：现货

Background:

NAcM-OPT is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor, which potently inhibits the DCN1-UBE2M interaction[1].

NAcM-OPT (Compound 67) is orally bioavailable, well tolerated in mice, and currently used to study the effects of acute pharmacologic inhibition of the DCN1-UBE2M interaction on the NEDD8/CUL pathway[1].

[1]. Hammill JT, et al. Discovery of an Orally Bioavailable Inhibitor of Defective in Cullin Neddylation 1 (DCN1)-Mediated Cullin Neddylation. J Med Chem. 2018 Apr 12;61(7):2694-2706.