α,α-dimethylhomophthalic acid | 40484-15-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: α,α-dimethylhomophthalic acid
• 英文别名: 2-(2-carboxypropane-2-yl)benzoic acid；α.α-Dimethyl-homophthalsaeure；(2-Carboxyphenyl)dimethylessigsaeure；2-(2-Carboxyphenyl)-2-methylpropanoic acid；2-(2-carboxy-phenyl)-2-methyl-propionic acid；α-(2-Carboxy-phenyl)-isobuttersaeure；2-(2-Carboxy-phenyl)-2-methyl-propionsaeure；Phenylacetic acid, 2-hydroxycarbonyl-alpha,alpha-dimethyl-；2-(2-carboxypropan-2-yl)benzoic acid
• CAS: 40484-15-9
• 化学式: C₁₁H₁₂O₄
• 分子量: 208.214
• InChiKey: HRCUPVNYKOBRGP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  74.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  α,α-dimethylhomophthalic acid 以 乙酸酐 为溶剂， 反应 2.0h， 生成 4,4-二甲基-4H-异色烯-1,3-二酮
  参考文献：
  名称：

  通过 Pd(II)-催化芳基和乙烯基 C-H 键的羧化合成 1,2- 和 1,3-二羧酸

  摘要：

  已经开发了用于苯甲酸和苯乙酸衍生物直接羧化以形成二羧酸的 Pd(II) 催化反应方案。反应条件也适用于乙烯基 CH 键的羧化。来自羧酸的第一个 CH 插入 Pd-芳基配合物已通过 X 射线晶体学表征。

  DOI：

  10.1021/ja8063827
• 作为产物：
  描述：

  3-phenylpropyl-magnesium bromide 在 potassium permanganate 、 乙醚 、 硫酸 作用下， 生成 α,α-dimethylhomophthalic acid
  参考文献：
  名称：

  The Synthesis of Condensed Polynuclear Hydrocarbons by the Cyclodehydration of Aromatic Alcohols. II.¹ The Synthesis of Ionenes²

  摘要：

  DOI：

  10.1021/ja01319a064

文献信息

• Isoquinoline derivatives and methods of use thereof
  申请人：——

  公开号：US20040039009A1

  公开（公告）日：2004-02-26

  The invention provides novel classes of Isoquinoline Derivatives. Pharmaceutical compositions and methods of making and using the compounds, are also described.

  这项发明提供了新型的异喹啉衍生物。还描述了制备和使用这些化合物的药物组合物和方法。
• [EN] 1,3,4-OXADIAZOLE HOMOPHTHALIMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME<br/>[FR] COMPOSÉS DÉRIVÉS DE 1,3,4-OXADIAZOLE HOMOPHTALIMIDE UTILISÉS COMME INHIBITEUR DE L'HISTONE DÉSACÉTYLASE 6, ET COMPOSITION PHARMACEUTIQUE LES COMPRENANT
  申请人：CHONG KUN DANG PHARMACEUTICAL CORP

  公开号：WO2020240493A1

  公开（公告）日：2020-12-03

  The present invention relates to novel compounds having a histone deacetylase 6 (HDAC6) inhibitory activity, stereoisomers thereof or pharmaceutically acceptable salts thereof, a medicinal use thereof, and a method for preparing the same. The novel compounds according to the present invention, stereoisomers thereof or pharmaceutically acceptable salts thereof have the histone deacetylase 6 (HDAC6) inhibitory activity, and are effective in preventing or treating HDAC6-related diseases, comprising infectious diseases; neoplasm; endocrinopathy; nutritional and metabolic diseases; mental and behavioral disorders; neurological diseases; eye and ocular adnexal diseases; circulatory diseases; respiratory diseases; digestive diseases; skin and subcutaneous tissue diseases; musculoskeletal system and connective tissue diseases; and teratosis or deformities, or chromosomal aberration.

  本发明涉及具有组蛋白去乙酰化酶6（HDAC6）抑制活性的新化合物，其立体异构体或其药学上可接受的盐，其药用用途以及其制备方法。根据本发明的新化合物，其立体异构体或其药学上可接受的盐具有组蛋白去乙酰化酶6（HDAC6）抑制活性，并且在预防或治疗与HDAC6相关的疾病方面具有有效性，包括传染病；肿瘤；内分泌病；营养和代谢疾病；精神和行为障碍；神经系统疾病；眼部和眼附器疾病；循环系统疾病；呼吸系统疾病；消化系统疾病；皮肤和皮下组织疾病；肌肉骨骼系统和结缔组织疾病；以及畸形或变形，或染色体异常。
• [EN] ISOQUINOLINE DERIVATIVES AND METHODS OF USE THEREOF<br/>[FR] DERIVES D'ISOQUINOLINE ET METHODES D'UTILISATION
  申请人：INOTEK PHARMACEUTICALS CORP

  公开号：WO2005082368A1

  公开（公告）日：2005-09-09

  The present invention relates to Isoquinoline Derivatives, compositions comprising an effective amount of a Isoquinoline Derivative and methods for treating or preventing an inflammatory disease, a reperfusion injury, an ischemic condition, renal failure, diabetes, a diabetic complication, a vascular disease other than a cardiovascular disease, cardiovascular disease, reoxygenation injury resulting from organ transplantation, Parkinson's disease, or cancer, comprising administering to an animal in need thereof an effective amount of a Isoquinoline Derivative.

  本发明涉及异喹啉衍生物，包括含有有效量的异喹啉衍生物的组合物，以及用于治疗或预防炎症性疾病、再灌注损伤、缺血状况、肾衰竭、糖尿病、糖尿病并发症、心血管疾病以外的血管疾病、心血管疾病、器官移植导致的再氧化损伤、帕金森病或癌症的方法，包括向需要此的动物施用有效量的异喹啉衍生物。
• Methods for treating or preventing erectile dysfunction or urinary incontinence
  申请人：Szabo Csaba

  公开号：US20060019980A1

  公开（公告）日：2006-01-26

  The present invention relates to methods for treating or preventing erectile dysfunction or urinary incontinence, comprising administering to a subject in need thereof an effective amount of a compound of the invention.

  本发明涉及治疗或预防勃起功能障碍或尿失禁的方法，包括向需要的受试者施用本发明的化合物的有效量。
• Tetracyclic benzamide derivatives and methods of use thereof
  申请人：Inotek Pharmaceuticals Corporation

  公开号：US20040229895A1

  公开（公告）日：2004-11-18

  The invention relates to Tetracyclic Benzamide Derivatives; compositions comprising a Tetracyclic Benzamide Derivative; and methods for treating or preventing an inflammatory disease, a reperfusion disease, an ischemic condition, renal failure, diabetes, a diabetic complication, a vascular disease, or cancer, comprising administering to a subject in need thereof an effective amount of a Tetracyclic Benzamide Derivative.

  该发明涉及四环苯甲酰胺衍生物；包含四环苯甲酰胺衍生物的组合物；以及用于治疗或预防炎症性疾病、再灌注疾病、缺血症状、肾功能衰竭、糖尿病、糖尿病并发症、血管疾病或癌症的方法，包括向需要的受试者施用有效剂量的四环苯甲酰胺衍生物。