(R)-9-(benzyloxy)-3-(3-fluorophenyl)-N-(1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)-8-methoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxamide | 1428796-00-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: (R)-9-(benzyloxy)-3-(3-fluorophenyl)-N-(1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)-8-methoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxamide
• 英文别名: 3-(3-fluorophenyl)-N-[(2R)-1-hydroxy-3-(1H-indol-3-yl)propan-2-yl]-8-methoxy-9-phenylmethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-carboxamide
• CAS: 1428796-00-2
• 化学式: C₃₈H₃₄FN₃O₄
• 分子量: 615.704
• InChiKey: YZOFMOQPXWEFJG-GDLZYMKVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  46
• 可旋转键数：
  10
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  88.5
• 氢给体数：
  3
• 氢受体数：
  5

文献信息

• [EN] FSH RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DU RÉCEPTEUR DE LA FSH
  申请人：MSD OSS BV

  公开号：WO2013041458A1

  公开（公告）日：2013-03-28

  The invention relates to FSH receptor antagonist according to general formula (I) or a pharmaceutically acceptable salt thereof and to a pharmaceutical composition containing the same. The compounds can be used for the treatment and prevention of endometriosis, for the treatment and prevention of pre-menopausal and peri-menopausal hormone-dependent breast cancer, for contraception, and for the treatment of uterine fibroids and other menstrual-related disorders.

  该发明涉及根据通式（I）或其药学上可接受的盐的FSH受体拮抗剂，以及含有该拮抗剂的药物组合物。这些化合物可用于治疗和预防子宫内膜异位症，治疗和预防绝经前和绝经期激素依赖性乳腺癌，避孕以及治疗子宫肌瘤和其他与月经有关的疾病。
• FSH RECEPTOR ANTAGONISTS
  申请人：MSD Oss B.V.

  公开号：US20140350043A1

  公开（公告）日：2014-11-27

  The invention relates to FSH receptor antagonist according to general formula (I) or a pharmaceutically acceptable salt thereof and to a pharmaceutical composition containing the same. The compounds can be used for the treatment and prevention of endometriosis, for the treatment and prevention of pre-menopausal and peri-menopausal hormone-dependent breast cancer, for contraception, and for the treatment of uterine fibroids and other menstrual-related disorders.

  本发明涉及一种FSH受体拮抗剂，其通式为（I）或其药学上可接受的盐，并且涉及一种含有该化合物的制药组合物。该化合物可用于治疗和预防子宫内膜异位症，治疗和预防绝经前和绝经期激素依赖性乳腺癌，避孕以及治疗子宫肌瘤和其他与月经相关的疾病。
• FSH receptor antagonists
  申请人：Merck Sharp & Dohme B.V.

  公开号：US10155259B2

  公开（公告）日：2018-12-18

  The invention relates to FSH receptor antagonist according to general formula I or a pharmaceutically acceptable salt thereof and to a pharmaceutical composition containing the same. The compounds can be used for the treatment and prevention of endometriosis, for the treatment and prevention of pre-menopausal and peri-menopausal hormone-dependent breast cancer, for contraception, and for the treatment of uterine fibroids and other menstrual-related disorders.

  本发明涉及通式 I 的 FSH 受体拮抗剂 或其药学上可接受的盐，以及含有这些化合物的药物组合物。这些化合物可用于治疗和预防子宫内膜异位症、治疗和预防绝经前和围绝经期激素依赖性乳腺癌、避孕、治疗子宫肌瘤和其他月经相关疾病。
• US9127007B2
  申请人：——

  公开号：US9127007B2

  公开（公告）日：2015-09-08