7-Bromobenzo[b]thiophene-3-carboxylic acid | 19075-62-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻吩类
• 英文名称: 7-Bromobenzo[b]thiophene-3-carboxylic acid
• 英文别名: 7-bromo-1-benzothiophene-3-carboxylic acid
• CAS: 19075-62-8
• 化学式: C₉H₅BrO₂S
• mdl: MFCD18451782
• 分子量: 257.11
• InChiKey: LITREOVVQONLSU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  65.5
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• [EN] BENZOTHIOPHENECARBOXAMIDE DERIVATIVES AND PGD2 ANTAGONISTS COMPRISING THEM<br/>[FR] DERIVES DU BENZOTHIOPHENECARBOXAMIDE, ET ANTAGONISTES DE LA PGD2 LES COMPRENANT
  申请人：SHIONOGI & CO., LTD.

  公开号：WO1998025919A1

  公开（公告）日：1998-06-18

  (EN) A compound, a pharmaceutically acceptable salt thereof, or a hydrate thereof having PGD2-antagonistic activities, inhibitory activities against infiltration of eosinophils, and being useful as a drug for treating diseases, such as systemic mastocytosis and disorder of systemic mast cell activation, as well as tracheal contraction, asthma, allergic rhinitis, allergic conjunctivitis, urticaria, ischemic reperfusion injury, inflammation and atopic dermatitis , which is shown by formula (I), is provided.(FR) L'invention porte sur un composé, un de ses sels pharmacocompatibles, ou un de ses hydrates, présentant des activités antagonistes vis-à-vis de la PGD2, des activités inhibitrices vis-à-vis des infiltrations d'éosinophiles, et s'avérant utiles comme médicaments pour le traitement de maladies telles que: la mastocytose systémique; les troubles de l'activation systémique des mastocytes; la contraction de la trachée; l'asthme; la rhinite allergique; la conjonctivite allergique; l'urticaire; les lésions ischémiques de reperfusion; et les dermatites inflammatoires et atopiques. Ledit composé est représenté par la formule (I).

  一种化合物，其药学上可接受的盐或水合物具有PGD2-拮抗活性、抑制嗜酸性粒细胞浸润的活性，并且可用作治疗疾病的药物，例如系统性肥大细胞增生症和系统性肥大细胞活化障碍，以及气道收缩、哮喘、过敏性鼻炎、过敏性结膜炎、荨麻疹、缺血再灌注损伤、炎症和特应性皮炎。该化合物由公式(I)表示。
• Methods for the treatment of itching comprising administering PGD2 receptor antagonists
  申请人：Shionogi & Co., Ltd.

  公开号：US20030027854A1

  公开（公告）日：2003-02-06

  A PGD 2 receptor antagonist such as a compound of the formula (IA-a-5): 1 a pharmaceutical acceptable salt thereof or a hydrate thereof, has an efficacious activity for the prevention or treatment of itching and is useful as a medicament.

  一种PGD2受体拮抗剂，例如公式（IA-a-5）的化合物：1a其医药上可接受的盐或其水合物，具有预防或治疗瘙痒的有效活性，并可用作药物。
• REMEDIES FOR ITCHING CONTAINING PGD 2? ANTAGONISTS
  申请人：SHIONOGI & CO., LTD.

  公开号：EP1084711A1

  公开（公告）日：2001-03-21

  A PGD2 receptor antagonist such as a compound of the formula (IA-a-5): a pharmaceutical acceptable salt thereof or a hydrate thereof, has an efficacious activity for the prevention or treatment of itching and is useful as a medicament.

  PGD2 受体拮抗剂，如式（IA-a-5）化合物： 其药物可接受盐或其水合物，具有预防或治疗瘙痒的有效活性，可用作药物。
• DRUGS FOR IMPROVING THE PROGNOSIS OF BRAIN INJURY AND A METHOD OF SCREENING THE SAME
  申请人：Japan Science and Technology Agency

  公开号：EP1535629A1

  公开（公告）日：2005-06-01

  There are provided a compound for treatment or prevention of brain injury caused by diseases such as cerebrovascular disorder, brain degenerative disease and demyelinating disease and a method for screening the same. Brain injury in which prostaglandin D2 is participated is treated or prevented by inhibition of hematopoietic prostaglandin D synthase induced in microglia cell or macrophage of brain injury area by diseases such as cerebrovascular disorder, brain degenerative disease or demyelinating disease or by inhibition of activation of prostaglandin D receptor expressed in astroglia cell around the injured area. There is also provided a method of testing those pharmaceutical substances using a transgenic mouse in which human hematopoietic prostaglandin D synthase is expressed in large amounts.

  提供了一种用于治疗或预防脑血管疾病、脑变性疾病和脱髓鞘疾病等疾病引起的脑损伤的化合物及其筛选方法。 通过抑制脑血管疾病、脑变性疾病或脱髓鞘疾病等疾病在脑损伤区域的小胶质细胞或巨噬细胞中诱导的造血前列腺素 D 合成酶，或通过抑制损伤区域周围星形胶质细胞中表达的前列腺素 D 受体的活化，治疗或预防前列腺素 D2 参与的脑损伤。此外，还提供了一种利用大量表达人造血前列腺素 D 合酶的转基因小鼠检测这些药物的方法。
• Drugs for improving prognosis of brain injury
  申请人：Japan Science and Technology Agency

  公开号：EP1598065A2

  公开（公告）日：2005-11-23

  A compound for treatment or prevention of brain injury caused by diseases such as cerebrovascular disorder, brain degenerative disease and demyelinating disease. The compound comprises an antagonist for the prostaglandin D receptor as an effective ingredient. Brain injury in which prostaglandin D2 is a factor is treated or prevented by inhibition of hematopoietic prostaglandin D synthase induced in microglia cell or macrophage of brain area by diseases such as cerebrovascular disorder, brain degenerative disease or demyelinating disease or by inhibition of activation of prostaglandin D receptor expressed in astroglia cell around the injured area.

  一种化合物，用于治疗或预防由脑血管疾病、脑变性疾病和脱髓鞘疾病等疾病引起的脑损伤。该化合物的有效成分包括前列腺素 D 受体拮抗剂。 通过抑制脑血管疾病、脑变性疾病或脱髓鞘疾病等疾病在脑区小胶质细胞或巨噬细胞中诱导的造血前列腺素 D 合成酶，或通过抑制损伤区周围星形胶质细胞中表达的前列腺素 D 受体的活化，治疗或预防以前列腺素 D2 为因素的脑损伤。