4-甲基-5-{[(2S)-2-甲基-1,4-二氮杂环庚-1-基]磺酰基}异喹啉二盐酸盐 | 451462-58-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异喹啉及其衍生物
• 中文名称: 4-甲基-5-{[(2S)-2-甲基-1,4-二氮杂环庚-1-基]磺酰基}异喹啉二盐酸盐
• 英文名称: (S)-2-Methyl-1-[(4-methyl-5-isoquinoline)sulfonyl]-homopiperazine
• 英文别名: 4-methyl-5-[[(2S)-2-methyl-1,4-diazepan-1-yl]sulfonyl]isoquinoline
• CAS: 451462-58-1
• 化学式: C₁₆H₂₁N₃O₂S
• 分子量: 319.4
• InChiKey: AWDORCFLUJZUQS-ZDUSSCGKSA-N

物化性质

• 沸点：
  519.6±60.0 °C(Predicted)
• 密度：
  1.218±0.06 g/cm3(Predicted)
• 溶解度：
  25℃：二甲基亚砜

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  70.7
• 氢给体数：
  1
• 氢受体数：
  5

文献信息

• [EN] BORON-CONTAINING RHO KINASE INHIBITORS<br/>[FR] INHIBITEURS DE LA RHO KINASE CONTENANT DU BORE
  申请人：PERCIPIAD INC

  公开号：WO2021011873A1

  公开（公告）日：2021-01-21

  The present invention provides boron-containing isoquinoline compounds as protein kinase-modulating compounds. These compounds are useful as neuroprotective and neuro-regenerative agents for the amelioration of glaucoma and other ocular neuropathies.

  本发明提供了含硼的异喹啉化合物作为蛋白激酶调节化合物。这些化合物可用作神经保护和神经再生剂，用于改善青光眼和其他眼神经病变。
• 4-haloisoquinoline derivative and drug containing the same
  申请人：Hidaka Hiroyoshi

  公开号：US20070088021A1

  公开（公告）日：2007-04-19

  The present invention relates to compounds which have a potent Rho-kinase inhibitory action and which are useful as therapeutic agents for treating diseases, such as hypertension, pulmonary hypertension, cerebral vasospasm, angina pectoris, cardiac failure, arteriosclerosis, glaucoma, dysuria, asthma, and erectile failure, and drugs containing the compounds. The present invention provides a 4-haloisoquinoline derivative represented by formula (1): an acid-added salt thereof, or a solvate of any of the foregoing, in which X is halogen, such as fluoro, chloro, bromo and iodo.

  本发明涉及具有强效Rho激酶抑制作用的化合物，可用作治疗疾病的治疗剂，如高血压、肺动脉高压、脑血管痉挛、心绞痛、心力衰竭、动脉硬化、青光眼、排尿困难、哮喘和勃起功能障碍，以及含有这些化合物的药物。本发明提供一种由式（1）表示的4-卤异喹啉衍生物：其酸盐加合物，或者上述任一化合物的溶剂化合物，其中X是卤素，如氟、氯、溴和碘。
• METHODS AND COMPOSITIONS FOR OCULAR CELL THERAPY
  申请人：Novartis AG

  公开号：US20200131474A1

  公开（公告）日：2020-04-30

  The present invention provides ocular cells, genetically modified by a CRISPR system targeting the expression of B2M for ocular cell therapy. The invention further provides methods of generating an expanded population of genetically modified ocular cells, for example limbal stem cells (LSCs) or corneal endothelial cells (CECs), wherein the cells are expanded involving the use of a LATS inhibitor and the expression of B2M in the cells has been reduced or eliminated. The present invention also provides a cell populations, preparations, uses and methods of therapy comprising said cells.

  本发明提供了通过CRISPR系统靶向B2M表达进行基因修饰的眼部细胞，用于眼部细胞治疗。该发明进一步提供了生成扩增的基因修饰眼部细胞群体的方法，例如角膜边缘干细胞（LSCs）或角膜内皮细胞（CECs），其中细胞的扩增涉及使用LATS抑制剂，并且细胞中的B2M表达已经降低或消除。本发明还提供了细胞群体、制剂、用途和包括所述细胞的治疗方法。
• [EN] METHODS AND COMPOSITIONS FOR OCULAR CELL THERAPY<br/>[FR] PROCÉDÉS ET COMPOSITIONS POUR UNE THÉRAPIE CELLULAIRE OCULAIRE
  申请人：NOVARTIS AG

  公开号：WO2021220132A1

  公开（公告）日：2021-11-04

  The present invention provides ocular cells, genetically modified by a CRISPR system targeting the expression of B2M for ocular cell therapy. The invention further provides methods of generating an expanded population of genetically modified ocular cells, for example limbal stem cells (LSCs) or corneal endothelial cells (CECs), wherein the cells are expanded involving the use of a LATS inhibitor and the expression of B2M in the cells has been reduced or eliminated. The present invention also provides cell populations, preparations, uses and methods of therapy comprising said cells.

  本发明提供了一种通过CRISPR系统靶向B2M表达进行基因修饰的眼部细胞，用于眼部细胞疗法。该发明进一步提供了一种生成扩增的基因修饰眼部细胞群体的方法，例如角膜缘干细胞（LSCs）或角膜内皮细胞（CECs），其中这些细胞在扩增过程中涉及使用LATS抑制剂，并且这些细胞中的B2M表达已经减少或消除。本发明还提供了细胞群体、制剂、用途和包括上述细胞的治疗方法。
• Therapeutic agent for treating glaucoma
  申请人：Hidaka Hiroyoshi

  公开号：US20080064681A1

  公开（公告）日：2008-03-13

  The present invention provides compounds useful as therapeutic agent for treating glaucoma and methods for treating glaucoma. That is, a therapeutic agent for treating glaucoma containing, as an active ingredient, a compound represented by formula (1) below is synthesized, and the therapeutic agent is administered in the form of eye drops to a glaucoma patient. Thus, the intraocular pressure is reduced. In the above formula, ring A represents a 5- to 11-membered cyclic amino group, which may have a substituted group, and X represents a halogen.

  本发明提供了作为治疗青光眼的治疗剂的化合物，以及治疗青光眼的方法。也就是说，合成了一种作为有效成分的化合物，其化学式如下所示，并且将这种治疗剂以眼药水的形式给青光眼患者使用。因此，眼内压得到了降低。在上述化学式中，环A代表一个5至11元环的氨基团，可能带有取代基，X代表一个卤素。