(4-(2-Hydroxy-2-Methylpropyl)Piperidin-1-Yl)(5-Methoxy-1H-Indol-2-Yl)Methanone (4-(2-羟基-2-甲基丙基)哌啶-1-基)(5-甲氧基-1H-吲哚-2-基)甲酮

CAS 1126084-37-4 MFCD30532740

化学结构图

1126084-37-4
SMILES: COc1ccc2[nH]c(C(=O)N3CCC(CC(C)(C)O)CC3)cc2c1

化学属性

Mol. Weight330.42
Appearance Solid powder
SolubilitySoluble in DMSO, not in water

别名和识别编码

Chemical Name Translation(4-(2-羟基-2-甲基丙基)哌啶-1-基)(5-甲氧基-1H-吲哚-2-基)甲酮
Chemical Name(4-(2-Hydroxy-2-Methylpropyl)Piperidin-1-Yl)(5-Methoxy-1H-Indol-2-Yl)Methanone
FormulaC19H26N2O3
Synonym ASP9521; ASP-9521; ASP 9521. AKR1C3 inhibitor ; 17HSD5 inhibitor
IUPAC Name(4-(2-hydroxy-2-methylpropyl)piperidin-1-yl)(5-methoxy-1H-indol-2-yl)methanone.
InChIKeyOXSCPDKUZWPWFR-UHFFFAOYSA-N
InChIInChI=1S/C19H26N2O3/c1-19(2,23)12-13-6-8-21(9-7-13)18(22)17-11-14-10-15(24-3)4-5-16(14)20-17/h4-5,10-11,13,20,23H,6-9,12H2,1-3H3
Canonical SMILESO=C(N1CCC(CC(C)(O)C)CC1)C(N2)=CC3=C2C=CC(OC)=C3
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产品应用

  • ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid dehydrogenase type 5 (17βHSD5; AKR1C3). ASP9521 has demonstrated anti-tumour activity in in vitro and in vivo preclinical models. ASP9521 inhibited conversion of androstenedione (AD) into testosterone (T) by recombinant human or cynomolgus monkey AKR1C3 in a concentration-dependent manner (IC50,human: 11 nmol/L; IC50,monkey: 49 nmol/L). ASP9521 showed >100-fold selectivity for AKR1C3 over the isoform AKR1C2. In LNCaP-AKR1C3 cells, ASP9521 suppressed AD-dependent PSA production and cell proliferation. In patients with mCRPC, ASP9521 demonstrated dose-proportional increase in exposure over the doses evaluated, with an acceptable safety and tolerability profile. However, the novel androgen biosynthesis inhibitor showed no relevant evidence of clinical activity.

安全信息

Storage condition Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

系列性分类


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