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(S)-ethyl 4-(1H-indazole-7-carboxamido)spiro[chroman-2,4'-piperidine]-1'-carboxylate

中文名称
——
中文别名
——
英文名称
(S)-ethyl 4-(1H-indazole-7-carboxamido)spiro[chroman-2,4'-piperidine]-1'-carboxylate
英文别名
ethyl (S)-4-(1H-indazole-7-carboxamido)spiro[chromane-2,4'-piperidine]-1'-carboxylate;ethyl (4S)-4-(1H-indazole-7-carbonylamino)spiro[3,4-dihydrochromene-2,4'-piperidine]-1'-carboxylate
(S)-ethyl 4-(1H-indazole-7-carboxamido)spiro[chroman-2,4'-piperidine]-1'-carboxylate化学式
CAS
——
化学式
C24H26N4O4
mdl
——
分子量
434.495
InChiKey
OXJLFUFFFCPXHH-IBGZPJMESA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    96.6
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

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文献信息

  • Modulators of indoleamine 2,3-dioxygenase
    申请人:GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
    公开号:US10906924B2
    公开(公告)日:2021-02-02
    Provided are IDO inhibitor compounds of Formula I and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and methods for their use in the prevention and/or treatment of diseases.
    本文提供了式 I 的 IDO 抑制剂化合物及其药学上可接受的盐、它们的药物组合物、它们的制备方法以及它们用于预防和/或治疗疾病的方法。
  • DNA-Encoded Library Technology-Based Discovery, Lead Optimization, and Prodrug Strategy toward Structurally Unique Indoleamine 2,3-Dioxygenase-1 (IDO1) Inhibitors
    作者:Wieslaw M. Kazmierski、Bing Xia、John Miller、Martha De la Rosa、David Favre、Richard M. Dunham、Yoshiaki Washio、Zhengrong Zhu、Feng Wang、Makda Mebrahtu、Hongfeng Deng、Jonathan Basilla、Liping Wang、Ghotas Evindar、Lijun Fan、Alison Olszewski、Ninad Prabhu、Christopher Davie、Jeffrey A. Messer、Vicente Samano
    DOI:10.1021/acs.jmedchem.9b01799
    日期:2020.4.9
    We report the discovery of a novel indoleamine 2,3-dioxygenase-1 (IDO1) inhibitor class through the affinity selection of a previously unreported indole-based DNA-encoded library (DEL). The DEL exemplar, spiro-chromane 1, had moderate IDO1 potency but high in vivo clearance. Series optimization quickly afforded a potent, low in vivo clearance lead 11. Although amorphous 11 was highly bio-available, crystalline 11 was poorly soluble and suffered disappointingly low bio-availability because of solubility-limited absorption. A prodrug approach was deployed and proved effective in discovering the highly bio-available phosphonooxymethyl 31, which rapidly converted to 11 in vivo. Obtaining crystalline 31 proved problematic, however; thus salt screening was performed in an attempt to circumvent this obstacle and successfully delivered greatly soluble and bio-available crystalline tris-salt 32. IDO1 inhibitor 32 is characterized by a low calculated human dose, best-in-class potential, and an unusual inhibition mode by binding the IDO1 heme-free (apo) form.
  • MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE
    申请人:GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
    公开号:US20200165280A1
    公开(公告)日:2020-05-28
    Provided are IDO inhibitor compounds of Formula I and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and methods for their use in the prevention and/or treatment of diseases.
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