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2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-N-(1,2-oxazol-3-yl)-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-carboxamide 1',1'-dioxide | 1448040-68-3

中文名称
——
中文别名
——
英文名称
2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-N-(1,2-oxazol-3-yl)-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-carboxamide 1',1'-dioxide
英文别名
2-cyclopropyl-1-(4-fluorophenyl)sulfonyl-N-(1,2-oxazol-3-yl)-1',1'-dioxospiro[2H-indole-3,4'-thiane]-5-carboxamide
2-cyclopropyl-1-[(4-fluorophenyl)sulfonyl]-N-(1,2-oxazol-3-yl)-1,2,2',3',5',6'-hexahydrospiro[indole-3,4'-thiopyran]-5-carboxamide 1',1'-dioxide化学式
CAS
1448040-68-3
化学式
C25H24FN3O6S2
mdl
——
分子量
545.612
InChiKey
IVPADIXRRPMRFG-UHFFFAOYSA-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):
    2.9
  • 重原子数:
    37
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    143
  • 氢给体数:
    1
  • 氢受体数:
    9

反应信息

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文献信息

  • SPIROINDOLINE DERIVATIVES AS GONADOTROPIN- RELEASING HORMONE RECEPTOR ANTAGONISTS
    申请人:Bayer Intellectual Property GmbH
    公开号:US20140357655A1
    公开(公告)日:2014-12-04
    Spiroindoline derivatives, process for their preparation and pharmaceutical compositions thereof, their use for the treatment and/or prophylaxis of diseases, and their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, especially sex-hormone-related diseases in both men and women, in particularly those selected from the group of endometriosis, uterine fibroids, polycystic ovarian disease, hirsutism, precocious puberty, gonadal steroid-dependent neoplasia such as cancers of the prostate, breast and ovary, gonadotrope pituitary adenomas, sleep apnea, irritable bowel syndrome, premenstrual syndrome, benign prostatic hypertrophy, contraception and infertility (e.g., assisted reproductive therapy such as in vitro fertilization). The present application relates in particular to spiroindoline derivatives as gonadotropin-releasing hormone (GnRH) receptor antagonists.
    螺内酰吲哚生物,其制备方法和药物组合物,用于治疗和/或预防疾病,以及用于制造治疗和/或预防疾病的药物,特别是男女性激素相关疾病,尤其是选择自子宫内膜异位症,子宫肌瘤,多囊卵巢综合症,多毛症,性早熟,性腺类固醇依赖性肿瘤,如前列腺癌,乳腺癌和卵巢癌,性腺激素释放激素依赖性垂体腺瘤,睡眠呼吸暂停,肠易激综合症,经前综合症,良性前列腺增生,避孕和不育症(例如,体外受精等辅助生殖疗法)。本申请特别涉及螺内酰吲哚生物作为促性腺激素释放激素(GnRH)受体拮抗剂。
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