中文名称:

A66

中文同义词:

A66, 一种高活性的P110Α特异性抑制剂;AKT2抑制剂(CCT128930);(2S)-N1-(2-叔丁基-4-甲基[4,5-联噻唑]-2-基)-1,2-吡咯烷二甲酰胺;A66,P110Α抑制剂

英文名称:

A66

英文同义词:

CCT128930;(2S)-N1-[2-(tert-Butyl)-4-methyl[4,5-bithiazol]-2-yl]-1,2-pyrrolidinedicarboxamide;CS-435;(2S)-N1-(5-(2-tert-butylthiazol-4-yl)-4-methylthiazol-2-yl)pyrrolidine-1,2-dicarboxamide;(2S)-N1-[2-(tert-Butyl)-4-methyl[4,5-bithiazol]-2-yl]-1,2-pyrrolidinedicarboxamide A 66;A66, 98%, a potent and specific p110α inhibitor;(2S)-N1-[2-(1,1-Dimethylethyl)-4-methyl[4,5-bithiazol]-2-yl]-1,2-pyrrolidinedicarboxamide;A 66;A-66

CAS号:

1166227-08-2

分子式:

C17H23N5O2S2

分子量:

393.53

EINECS号:

相关类别:

信号转导通路激酶抑制剂;小分子抑制剂;小分子抑制剂，天然产物;细胞生物学试剂;Inhibitors;Akt;mTOR;PI3K;PI3K/Akt/mTOR

Mol文件:

1166227-08-2.mol

密度 

1.354

储存条件 

Sealed in dry,Store in freezer, under -20°C

酸度系数(pKa)

6.27±0.70(Predicted)

生物活性

A66是一种有效的，特异性的p110α抑制剂，IC50为32 nM，作用于p110α比作用于其他I型PI3K亚型选择性高100倍以上。

体外研究

In addition to the wild-type p110α, A66 also potently inhibits the oncogenic forms of p110α such as p110α E545K and p110α H1047R with IC50 of 30 nM and 43 nM, respectively. Unlike PIK-75, A66 displays >100 fold selectivity for p110α over other class-I PI3K isoforms. Among the class-II PI3Ks, class-III PI3K and PI4Ks, A66 only exhibits limited cross-reactivity with the class-II PI3K PI3KC2β and the PI4Kβ isoform of PI4K with IC50 of 462 nM and 236 nM, respectively. A66 exhibits no inhibitory activity against other lipid kinases or the related kinases DNA-PK and mTOR. A66 has a higher degree of specificity compared with PIK-75 when tested at 10 μM against two large panels of 110 protein kinases and 318 kinases. Inhibition of p110α alone by A66 treatment is sufficient to block insulin signalling to Akt/PKB in certain cell lines that harbor H1047R mutations in PIK3CA and have high levels of p110α and class-Ia PI3K activity. A66 treatment at 0.7 μM induces a 75-80% reduction in focus formation by the highly transforming p85α iSH2 mutants KS459delN, DKRMN-S560del, and K379E, and reduces the phosphorylation of Akt on T308 by all p85 mutants.

体内研究

A single dose of A66 at 100 mg/kg induces a profound reduction in the phosphorylation of Akt/PKB and p70 S6 kinase, but not of ERK, in SK-OV-3 tumour tissue in vivo at both 1 hour and 6 hours after dosing. A66 dosed at 100 mg/kg once daily (QD) for 21 days or 75 mg/kg twice daily (BID) for 16 days induces a significant delay in growth of SK-OV-3 xenografted tumors with average TGI of 45.9% and 29.9%, respectively, which is even greater than that induced by the well-established pan-PI3K inhibitor BEZ-235. QD dosing of A66 in the HCT-116 xenograft model also induces a significant reduction in tumour volume with TGI of 77.2%, but causes a non-significant reduction in tumor volume in the U87MG xenograft model. Administration of A66 at 10 mg/kg in male CD1 mice induces significant impairments in the ITT (insulin tolerance test) and GTT (glucose tolerance test), and an increase in glucose production during a PTT (pyruvate tolerance test), almost to the same level as the pan-PI3K inhibitors.

特征

A66 is highly selective for p110α isoform.

靶点

p110α 32 nM (IC 50 ) p110α E545K 30 nM (IC 50 ) p110α H1047R 43 nM (IC 50 ) p110γ 3480 nM (IC 50 ) PI3K-C2β 462 nM (IC 50 ) PI4Kβ 236 nM (IC 50 )

p110α 32 nM (IC 50 )

p110α E545K 30 nM (IC 50 )

海关编码 

29341000