3-吡啶丙硫醇 | 69603-49-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: 3-吡啶丙硫醇
• 英文名称: 3-(pyridin-3'-yl)propanethiol
• 英文别名: 3-pyridin-3-yl-propane-1-thiol；3-(3-Pyridyl)-1-propylmercaptan；3-(3-mercaptopropyl)pyridine；3-(3-pyridyl)propanethiol；3-(3-Pyridyl)-1-propanthiol；3-Pyridinepropanethiol；3-pyridin-3-ylpropane-1-thiol
• CAS: 69603-49-2
• 化学式: C₈H₁₁NS
• 分子量: 153.248
• InChiKey: MVLCWAAJDXMPMW-UHFFFAOYSA-N

物化性质

• 沸点：
  92-99 °C(Press: 0.15 Torr)
• 密度：
  1.049±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  10
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  13.9
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-吡啶丙硫醇 、 (2S)-1-(1,2-二氧代-3,3-二甲基戊基)-2-吡咯烷甲酸 在 4-二甲氨基吡啶 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 生成 3-(3-pyridyl)-1-propyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidinecarbothioate
  参考文献：
  名称：

  Synthesis of N-Glyoxyl Prolyl and Pipecolyl Amides and Thioesters and Evaluation of Their In Vitro and In Vivo Nerve Regenerative Effects

  摘要：

  The recent discovery that small molecule ligands for the peptidyl-prolyl isomerase (PPIase) FKBP12 possess powerful neuroprotective and neuroregenerative properties in vitro and in vivo suggests therapeutic utility for such compounds in neurodegenerative disease. The neurotrophic effects of these compounds are independent of the immunosuppressive pathways by which drugs such as FK506 and rapamycin operate. Previous work by ourselves and other groups exploring the structure-activity relationships (SAR) of small molecules that mimic only the FKBP binding domain portion of FK506 has focused on esters of proline and pipecolic acid. We have explored amide and thioester analogues of these earlier structures and found that they too are extremely potent in promoting recovery of lesioned dopaminergic pathways in a mouse model of Parkinson's disease. Several compounds were shown to be highly effective upon oral administration after lesioning of the dopaminergic pathway, providing further evidence of the potential clinical utility of a variety of structural classes of FKBP12 ligands.

  DOI：

  10.1021/jm010556c
• 作为产物：
  描述：

  3-(吡啶-3-基)-1-溴丙烷 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 26.0h， 生成 3-吡啶丙硫醇
  参考文献：
  名称：

  Synthesis of N-Glyoxyl Prolyl and Pipecolyl Amides and Thioesters and Evaluation of Their In Vitro and In Vivo Nerve Regenerative Effects

  摘要：

  The recent discovery that small molecule ligands for the peptidyl-prolyl isomerase (PPIase) FKBP12 possess powerful neuroprotective and neuroregenerative properties in vitro and in vivo suggests therapeutic utility for such compounds in neurodegenerative disease. The neurotrophic effects of these compounds are independent of the immunosuppressive pathways by which drugs such as FK506 and rapamycin operate. Previous work by ourselves and other groups exploring the structure-activity relationships (SAR) of small molecules that mimic only the FKBP binding domain portion of FK506 has focused on esters of proline and pipecolic acid. We have explored amide and thioester analogues of these earlier structures and found that they too are extremely potent in promoting recovery of lesioned dopaminergic pathways in a mouse model of Parkinson's disease. Several compounds were shown to be highly effective upon oral administration after lesioning of the dopaminergic pathway, providing further evidence of the potential clinical utility of a variety of structural classes of FKBP12 ligands.

  DOI：

  10.1021/jm010556c

文献信息

• Pyrrolidine derivative hair growth compositions and uses
  申请人：GPL NIL Holdings, Inc.,

  公开号：US20010049381A1

  公开（公告）日：2001-12-06

  This invention relates to pharmaceutical compositions and methods for treating alopecia and promoting hair growth using pyrrolidine derivatives.

  这项发明涉及使用吡咯烷衍生物治疗脱发并促进头发生长的药物组合物和方法。
• N-oxide of heterocyclic ester, amide, thioester, or ketone hair growth compositions and uses
  申请人：GPI NIL Holdings, Inc.

  公开号：US20020065297A1

  公开（公告）日：2002-05-30

  This invention relates to pharmaceutical compositions and methods for treating alopecia and promoting hair growth using an N-oxide of a heterocyclic ester, amide, thioester, or ketone.

  这项发明涉及使用杂环酯、酰胺、硫酯或酮的N-氧化物治疗脱发和促进头发生长的药物组合物和方法。
• Method for treating nerve injury caused as a result of surgery
  申请人：——

  公开号：US20030203890A1

  公开（公告）日：2003-10-30

  The present invention relates generally to methods for treating or preventing nerve injury in a warm-blooded animal caused as a consequence of surgery by administering neurotrophic compounds described below. The invention relates more specifically to methods for treating or preventing nerve injury caused as a consequence of prostate surgery as well as erectile dysfunction.

  本发明一般涉及通过给予下文描述的神经营养化合物来治疗或预防温血动物因手术而引起的神经损伤的方法。该发明更具体地涉及治疗或预防由前列腺手术以及勃起功能障碍引起的神经损伤的方法。
• Synthesis of N-heterocyclic ligands for use in affinity and mixed mode chromatography
  作者：Simon J. Mountford、Eva M. Campi、Andrea J. Robinson、Milton T.W. Hearn

  DOI：10.1016/j.tet.2010.11.003

  日期：2011.1

  designed to consist of a pyridinyl or related aza-heterocyclic nucleus bearing a pendant arm containing either an alkylamine, alkylthiol or hydroxyalkyl nucleophilic group to allow their facile immobilisation onto an activated support matrix. Ligand diversity was achieved by altering the length of the alkyl chain between the heterocyclic nucleus and nucleophilic group, varying the position of alkyl chain

  已合成了一组杂环配体，用于制备混合模式亲和色谱吸附剂，以用于纯化包括抗体在内的蛋白质。配体结构设计为由吡啶基或相关的氮杂杂环核组成，它们带有一个含烷基胺，烷硫醇或羟烷基亲核基团的侧链，以使其易于固定在活化的载体基质上。通过改变杂环核和亲核基团之间的烷基链的长度，改变烷基链与杂环的连接位置，以及将额外的取代基掺入吡啶基或相关的氮杂杂环中，可以实现配体多样性。配体结构的这种多样性旨在实现配体的关键结构特征，有效的蛋白质结合所需的待确定。与先前使用的用于制备类似的取代吡啶或氮杂杂环化合物的多步骤方法相反，本文所述配体的合成途径通常利用与容易获得的杂环前体的非常温和的一步反应。
• Penem derivatives and antimicrobial agents containing the same
  申请人：SUNTORY LIMITED

  公开号：EP0774465A1

  公开（公告）日：1997-05-21

  Penem derivatives represented by the following Formula (I): wherein Z represents a hydroxyl group or a fluorine atom, R1 represents a substituted or unsubstituted alkyl, alkenyl, aralkyl group, aryl group, heterocyclic, or acyl group, or a hydrogen atom, and R2 represents a hydrogen atom or a carboxyl-protecting group; and pharmacologically acceptable salts thereof are antibacterial agents effective against, inter alia, methicillin-resistant Staphylococcus aureus. The derivatives and salts are novel except when R1 is ethyl and Z is hydroxyl. The analogous compounds in which R2 is a carboxyl-protecting group and any hydroxyl group represented by Z is protected are novel process intermediates.

  Penem衍生物由以下公式（I）表示：其中Z代表一个羟基团或氟原子，R1代表一个取代或未取代的烷基，烯基，芳基甲基，芳基，杂环基或酰基，或氢原子，R2代表一个氢原子或羧基保护基；及其药理学上可接受的盐是有效的抗菌剂，可用于治疗耐甲氧西林金黄色葡萄球菌等感染。这些衍生物和盐是新颖的，除非R1是乙基且Z是羟基。其中R2是羧基保护基且Z代表的任何羟基被保护的类似化合物是新颖的工艺中间体。