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Saridegib
N-[(3R,3'R,3'aS,4aR,6'S,6aR,6bS,7'aR,9S,12aS,12bS)-3',6',11,12b-tetramethylspiro[1,2,3,4,4a,5,6,6a,6b,7,8,10,12,12a-tetradecahydronaphtho[2,1-a]azulene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-3-yl]methanesulfonamide
化合物简介
Saridegib also known as IPI-926 is an experimental drug candidate undergoing clinical trials for the treatment of various types of cancer, including hard to treat hematologic malignancies such as myelofibrosis and ligand-dependant tumors such as chondrosarcoma. IPI-926 exhibits its pharmacological effect by inhibition of the G protein-coupled receptor smoothened, a component of the hedgehog signaling pathway. Chemically, it is a semi-synthetic derivative of the alkaloid cyclopamine. The process begins with cyclopamine extracted from harvested Veratrum californicum which is taken through a series of alterations resulting in an analogue of the natural product cyclopamine, making IPI-926 the only compound in development/testing that is not fully synthetic.
基本信息
CAS:1037210-93-7
中文别名:
英文别名:UNII-JT96FPU35X;IP9 FREE BASE;IPI 926;SARIDEGIB;FIN-5;
分子式:C29H48N2O3S
分子量:504.768
精确质量:504.339
Psa:75.81
Logp:6.8293
中文别名:
英文别名:UNII-JT96FPU35X;IP9 FREE BASE;IPI 926;SARIDEGIB;FIN-5;
分子式:C29H48N2O3S
分子量:504.768
精确质量:504.339
Psa:75.81
Logp:6.8293
编号系统
UNII:JT96FPU35X
物化性质
储存条件:2-8℃
安全信息
生产方法及用途
合成路线
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参考文献
WO2008/83248 A2, ; Page/Page column 59 ;
上游原料
下游产品
图谱
1H NMR : Predict
13C NMR : Predict






