1,1-Dioxo-3.3-dibutyl-5-phenyl-7-methoxy-8-carboxymethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine | 358375-99-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 1,1-Dioxo-3.3-dibutyl-5-phenyl-7-methoxy-8-carboxymethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine
• 英文别名: 1,1-Dioxo-3,3-dibutyl-5-phenyl-7-methoxy-8-carboxymethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine；2-[(3,3-dibutyl-7-methoxy-1,1-dioxo-5-phenyl-2,4-dihydro-1λ6,5-benzothiazepin-8-yl)oxy]acetic acid
• CAS: 358375-99-2
• 化学式: C₂₆H₃₅NO₆S
• 分子量: 489.633
• InChiKey: UCFQHQVPRFKZKP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  34
• 可旋转键数：
  11
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  102
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  1,1-dioxo-3,3-dibutyl-5-phenyl-7-methoxy-8-ethoxycarbonylmethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine 在 lithium hydroxide 、 溶剂黄146 作用下， 以 tetrahydrofuran-water 为溶剂， 以0.408 g (96%/O)的产率得到1,1-Dioxo-3.3-dibutyl-5-phenyl-7-methoxy-8-carboxymethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine
  参考文献：
  名称：

  1,5-Benzothiazepines and their use as hypolipidaemics

  摘要：

  本发明涉及式（I）的化合物，其中R1和R2分别选自C1-6烷基；R4和R5中的一个是式（IA）的基团：R3、R6、R7、R8、R9、R10和R11，另一个是如下定义的基团，其药学上可接受的盐、溶剂化合物、该类盐的溶剂化合物和它们的前药，以及它们作为远端胆酸转运（IBAT）抑制剂用于治疗高脂血症。还描述了它们的制备方法和含有它们的药物组合物。

  公开号：

  US20030166927A1

文献信息

• Chemical compounds
  申请人：——

  公开号：US20040067933A1

  公开（公告）日：2004-04-08

  The present invention relates to compounds of the formula (I): (wherein variable groups are as defined within) pharmaceutically acceptable salts, solvates, solvates of such salts and prodrugs thereof and their use as ileal bile acid transport (IBAT) inhibitors for the treatment of hyperlipidaemia. Processes for their manufacture and pharmaceutical compositions containing them are also described. 1

  本发明涉及式(I)的化合物：（其中变量团如所定义）药用可接受的盐、溶剂化物、这些盐的溶剂化物以及前药及其作为回肠胆酸转运(IBAT)抑制剂用于治疗高脂血症的用途。还描述了它们的制造过程和包含它们的药物组合物。
• Benzothiazepine compounds and their use as bile acid modulators
  申请人：Albireo AB

  公开号：US11014898B1

  公开（公告）日：2021-05-25

  The invention relates to 1,5-benzothiazepine derivatives of formula (I). These compounds are bile acid modulators having apical sodium-dependent bile acid transporter (ASBT) and/or liver bile acid transport (LBAT) inhibitory activity. The invention also relates to pharmaceutical compositions comprising these compounds and to the use of these compounds in the treatment of cardiovascular diseases, fatty acid metabolism and glucose utilization disorders, gastrointestinal diseases and liver diseases.

  这项发明涉及式(I)的1,5-苯并噻吩衍生物。这些化合物是胆酸调节剂，具有顶端钠依赖性胆酸转运蛋白（ASBT）和/或肝胆酸转运（LBAT）的抑制活性。该发明还涉及包含这些化合物的药物组合物，以及利用这些化合物治疗心血管疾病、脂肪酸代谢和葡萄糖利用障碍、胃肠道疾病和肝脏疾病的用途。
• [EN] BENZOTHIAZEPINE COMPOUNDS AND THEIR USE AS BILE ACID MODULATORS<br/>[FR] COMPOSÉS DE BENZOTHIAZÉPINE ET LEUR UTILISATION EN TANT QUE MODULATEURS DE L'ACIDE BILIAIRE
  申请人：ALBIREO AB

  公开号：WO2021110887A1

  公开（公告）日：2021-06-10

  The invention relates to 1,5-benzothiazepine derivatives of formula (I). These compounds are bile acid modulators having apical sodium-dependent bile acid transporter (ASBT) and/or liver bile acid transport (LBAT) inhibitory activity. The invention also relates to pharmaceutical compositions comprising these compounds and to the use of these compounds in the treatment of cardiovascular diseases, fatty acid metabolism and glucose utilization disorders, gastrointestinal diseases and liver diseases.

  这项发明涉及式(I)的1,5-苯并噻吩衍生物。这些化合物是胆酸调节剂，具有顶端钠依赖性胆酸转运蛋白（ASBT）和/或肝胆酸转运（LBAT）的抑制活性。该发明还涉及包含这些化合物的药物组合物，以及利用这些化合物治疗心血管疾病、脂肪酸代谢和葡萄糖利用障碍、胃肠道疾病和肝脏疾病。
• [EN] CHEMICAL COMPOUNDS<br/>[FR] 1,5-BENZOTHIAZEPINES ET LEUR UTILISATION EN TANT QU'AGENTS ANTIHYPERLIPIDEMIE
  申请人：ASTRAZENECA AB

  公开号：WO2002050051A1

  公开（公告）日：2002-06-27

  The present invention relates to compounds of the formula (I): (wherein variable groups are as defined within) pharmaceutically acceptable salts, solvates, solvates of such salts and prodrugs thereof and their use as ileal bile acid transport (IBAT) inhibitors for the treatment of hyperlipidaemia. Processes for their manufacture and pharmaceutical compositions containing them are also described.

  本发明涉及化合物的公式（I）（其中变量基团如定义），药学上可接受的盐，这些盐的溶剂，这些盐的溶剂和它们的前药，以及它们作为回肠胆汁酸转运（IBAT）抑制剂用于治疗高脂血症的用途。还描述了它们的制造过程和含有它们的制药组合物。
• Benzothiazepine derivatives
  申请人：AstraZeneca AB

  公开号：US07192945B2

  公开（公告）日：2007-03-20

  The present invention relates to compounds of the formula (I): (wherein variable groups are as defined within) pharmaceutically acceptable salts, solvates, solvates of such salts and prodrugs thereof and their use as ileal bile acid transport (IBAT) inhibitors for the treatment of hyperlipidaemia. Processes for their manufacture and pharmaceutical compositions containing them are also described

  本发明涉及式(I)的化合物：（其中变量基团的定义如下）药学上可接受的盐、溶剂、该类盐的溶剂和其前药，以及它们作为回肠胆汁酸转运（IBAT）抑制剂用于治疗高脂血症的用途。还描述了它们的制造过程和含有它们的药物组合物。