γ-aminobutyrylhistamine | 159329-71-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: γ-aminobutyrylhistamine
• 英文别名: GABA-HA；Aminobutyrylhistamine；4-amino-N-[2-(1H-imidazol-5-yl)ethyl]butanamide
• CAS: 159329-71-2
• 化学式: C₉H₁₆N₄O
• 分子量: 196.252
• InChiKey: HXYUWNUJDSMLIE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.1
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  83.8
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  γ-aminobutyrylhistamine 、 [(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-(3-methylimidazol-3-ium-1-yl)phosphinate 在 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以43%的产率得到2'-deoxythymidine-5'-N-(3-{N-[2-(1H-imidazol-4-yl)ethyl]carbamoyl}propyl)phosphamide lithium salt
  参考文献：
  名称：

  摘要：

  The reactions of histamine, the natural dipeptide carcinine (beta-Ala-HA), and its analogs with 5'-monodeoxyribonucleotides (dNMP) in the presence of triphenylphosphine, 2,2'-dipyridyl disulfide, and N-methylimidazole were studied. The yield of phosphamide derivatives decreases from 72% to 17% as the length of the linker group between the imidazole ring and the terminal aliphatic amino group is increased. Hydrolytic stability of the resulting conjugates was examined. The stability of the bonds in the -O-P(O)(2)-NH- group linking the nucleotide and peptide portions of the conjugate depends on the nature of the heterocyclic base of the nucleotide and decreases in the series dTMP > dCMP > dAMP.

  DOI：

  10.1023/a:1021329324527
• 作为产物：
  描述：

  组胺 在 盐酸 、 1-羟基苯并三唑 、 一水合肼 、 三乙胺 、 三氟乙酸 、 N,N'-二异丙基碳二亚胺 作用下， 以 1,4-二氧六环 、 乙醇 、 二氯甲烷 、 甲苯 、 乙腈 为溶剂， 反应 11.17h， 生成 γ-aminobutyrylhistamine
  参考文献：
  名称：

  碳酸酐酶激活剂：氨基酰基/二肽基组胺衍生物与同工酶I，II和IV具有高亲和力，可作为有效的激活剂。

  摘要：

  组胺（Hst）与四溴邻苯二甲酸酐反应，并用三苯甲基磺酰氯保护其咪唑部分，然后进行肼解反应，得到N-1-三苯甲基磺酰-组胺，这是一种关键中间体，在其氨基乙基部分被进一步衍生。在咪唑类和氨基部分脱保护后，在碳二亚胺存在下，关键中间体与N-Boc-氨基酸/二肽（Boc-AA）反应，得到了一系列通式为AA-Hst的化合物（AA =氨基酰基；二肽基）。分析了新衍生物作为三种碳酸酐酶（CA）同工酶的激活剂，它们分别是hCA I，hCA II（胞质形式）和bCA IV（膜结合形式）。观察到针对所有三种同工酶的有效活化，尤其是针对hCA I和bCA IV的活化，其最佳化合物的亲和力在纳摩尔范围内。另一方面，hCA II可以被约10-20 nM的亲和力激活。这类新型的CA激活剂可能导致针对CA缺乏综合症（一种骨骼，脑和肾脏的遗传性疾病）的药物/诊断剂的开发。

  DOI：

  10.1016/s0968-0896(99)00227-8

文献信息

• AMIDE COMPOUNDS, METHODS FOR PREPARATION, AND USE THEREOF AS AGENTS FOR THE TREATMENT AND PREVENTION OF DISEASES CAUSED BY RNA- AND/OR DNA-CONTAINING VIRUSES, AND CONCOMITANT DISEASES
  申请人：OBSCHESTVO S OGRANICHENNOI OTVETSTVENNOSTIYU "PHARMENTERPRISES"

  公开号：US20170183318A1

  公开（公告）日：2017-06-29

  The present invention relates to medicine and includes a method for preventing and treating diseases caused by RNA- and DNA-containing viruses, and concomitant diseases, wherein the method comprises the use of an effective amount of compounds of general formula I or pharmaceutically acceptable salts thereof. The invention also relates to methods for preparing said compounds, pharmaceutical compositions for the prevention or treatment of diseases caused by RNA- and DNA-containing viruses, said compositions comprising an effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof. The invention addresses the object of providing a novel agent effective in the treatment of diseases caused by an RNA-containing virus belonging to the Enterovirus, Metapneumovirus, Pneumovirus, Respirovirus, or Alfa-coronavirus genus, and/or by a DNA-containing virus belonging to the Adenoviridae and/or Herpesviridae family, and in the prevention and treatment of asthma exacerbation, chronic obstructive pulmonary disease, mucoviscidosis, conjunctivitis, gastroenteritis, hepatitis, myocarditis; in the prevention and treatment of rhinorrhea, acute and infectious rhinitis, pharyngitis, nasopharyngitis, tonsillitis, laryngitis, laryngotracheitis, laryngotracheobronchitis, bronchitis, bronchiolitis, pneumonia, or airway obstructive syndrome.

  本发明涉及医学，包括一种用于预防和治疗由RNA-和DNA-含病毒引起的疾病以及相关疾病的方法，其中该方法包括使用通式I的化合物或其药用可接受盐的有效量。该发明还涉及制备上述化合物的方法，用于预防或治疗由RNA-和DNA-含病毒引起的疾病的药物组合物，该组合物包括通式I的化合物或其药用可接受盐的有效量。该发明解决了提供一种新型药剂的目标，用于治疗属于肠病毒、副呼吸道病毒、呼吸道病毒、呼吸道病毒或阿尔法冠状病毒属的RNA-含病毒引起的疾病，和/或属于腺病毒科和/或疱疹病毒科的DNA-含病毒引起的疾病，并在预防和治疗哮喘急性发作、慢性阻塞性肺疾病、黏液囊病、结膜炎、胃肠炎、肝炎、心肌炎；在预防和治疗流涕、急性和感染性鼻炎、咽炎、鼻咽炎、扁桃体炎、喉炎、喉气管炎、喉气管支气管炎、支气管炎、支气管炎、肺炎或气道梗阻综合征方面具有有效性。
• COMBINED USE OF CARNOSINASE INHIBITOR WITH L-CARNOSINES AND COMPOSITION
  申请人：Innovative Vision Products, Inc.

  公开号：EP1586332A1

  公开（公告）日：2005-10-19

  The present invention provides combined use of a carnosinase inhibitor with L-carnosine and its related substance, and a composition containing the same, which are useful for treatment or prevention of various diseases, improvement of health conditions, improvement of exercise ability, improvement of skin health, prevention of the side effects of alcohol drinking and the like in mammals including human.

  本发明提供了肉毒碱酶抑制剂与左旋肉碱及其相关物质的联合使用方法，以及含有左旋肉碱及其相关物质的组合物，可用于治疗或预防包括人类在内的哺乳动物的各种疾病、改善健康状况、提高运动能力、改善皮肤健康、预防饮酒副作用等。
• Peptide derivatives or pharmaceutically acceptable salts thereof, method for producing the same, use of said derivatives and pharmaceutical composition
  申请人：Nebolsin, Vladimir Evgenievich

  公开号：EP2229935A1

  公开（公告）日：2010-09-22

  Derivatives of peptides of general formula or pharmaceutically acceptable salts thereof, their use as the agents possessing antioxidant, antiasthmatic, antihypoxic, antiinflammatory, antiviral, antibacterial, lipid-regulating, antitumor, antimetastatic, glucose lowering, adaptogenic and the other kinds of therapeutic effects, a method to produce them, a pharmaceutical composition or a cosmetic agent comprising as an active agent a peptide derivative of formula (I) or pharmaceutically or cosmetically acceptable salts thereof as well as a method of therapy or prevention of diseases.

  通式肽的衍生物 或其药学上可接受的盐，它们作为具有抗氧化、抗通气、抗缺氧、抗炎、抗病毒、抗菌、调节血脂、抗肿瘤、抗转移、降糖、适应性和其他各种治疗效果的制剂的用途，生产它们的方法，包含式 (I) 肽衍生物或其药学上或化妆品学上可接受的盐作为活性剂的药物组合物或化妆品制剂，以及治疗或预防疾病的方法。
• AMIDE COMPOUNDS AND METHODS FOR THE PRODUCTION AND USE THEREOF
  申请人：Obschestvo S Ogranichennoi Otvetstennostiyu "Pharmenterprises"

  公开号：EP3118211A1

  公开（公告）日：2017-01-18

  The present invention relates to medicine and includes a method for preventing and treating diseases caused by RNA- and DNA-containing viruses, and concomitant diseases, wherein the method comprises the use of an effective amount of compounds of general formula I or pharmaceutically acceptable salts thereof. The invention also relates to methods for preparing said compounds, pharmaceutical compositions for the prevention or treatment of diseases caused by RNA- and DNA-containing viruses, said compositions comprising an effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof. The invention addresses the object of providing a novel agent effective in the treatment of diseases caused by an RNA-containing virus belonging to the Enterovirus, Metapneumovirus, Pneumovirus, Respirovirus, or Alfa-coronavirus genus, and/or by a DNA-containing virus belonging to the Adenoviridae and/or Herpesviridae family, and in the prevention and treatment of asthma exacerbation, chronic obstructive pulmonary disease, mucoviscidosis, conjunctivitis, gastroenteritis, hepatitis, myocarditis; in the prevention and treatment of rhinorrhea, acute and infectious rhinitis, pharyngitis, nasopharyngitis, tonsillitis, laryngitis, laryngotracheitis, laryngotracheobronchitis, bronchitis, bronchiolitis, pneumonia, or airway obstructive syndrome.

  本发明涉及医药，包括一种预防和治疗由含RNA和DNA病毒引起的疾病以及伴随疾病的方法，其中该方法包括使用有效量的通式I化合物或其药学上可接受的盐。本发明还涉及制备所述化合物的方法、用于预防或治疗由含 RNA 和 DNA 病毒引起的疾病的药物组合物，所述组合物包含有效量的通式 I 化合物或其药学上可接受的盐。本发明的目的是提供一种新型制剂，有效治疗由肠病毒属、偏肺病毒属、肺炎病毒属、呼吸道病毒属或阿法-冠状病毒属的含 RNA 病毒引起的疾病、和/或属于腺病毒科和/或疱疹病毒科的含 DNA 病毒，以及预防和治疗哮喘加重、慢性阻塞性肺病、粘液粘稠病、结膜炎、肠胃炎、肝炎、心肌炎；预防和治疗鼻炎、急性和感染性鼻炎、咽炎、鼻咽炎、扁桃体炎、喉炎、喉气管炎、喉气管支气管炎、支气管炎、支气管炎、肺炎或气道阻塞综合征。
• Combined use of carnosinase inhibitor with l-carnosines and composition
  申请人：Babizhayev A. Mark

  公开号：US20060116328A1

  公开（公告）日：2006-06-01

  The present invention provides combined use of a carnosinase inhibitor with L-carnosine and its related substance, and a composition containing the same, which are useful for treatment or prevention of various diseases, improvement of health conditions, improvement of exercise ability, improvement of skin health, prevention of the side effects of alcohol drinking and the like in mammals including human.

  本发明提供了肉毒碱酶抑制剂与左旋肉碱及其相关物质的联合使用方法，以及含有左旋肉碱及其相关物质的组合物，可用于治疗或预防包括人类在内的哺乳动物的各种疾病、改善健康状况、提高运动能力、改善皮肤健康、预防饮酒副作用等。