Succinic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 2-hydroxy-ethyl ester | 204652-39-1

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: Succinic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 2-hydroxy-ethyl ester
• 英文别名: 4-O-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] 1-O-(2-hydroxyethyl) butanedioate
• CAS: 204652-39-1
• 化学式: C₃₃H₅₄O₅
• 分子量: 530.789
• InChiKey: RECHOGBDIQVFQG-ACBDEFBISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.2
• 重原子数：
  38
• 可旋转键数：
  13
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  72.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-马来酰亚胺基苯甲酸氯 、 Succinic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 2-hydroxy-ethyl ester 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  Synthesis of Novel Thiol-Reactive Amphiphilic Lipids Based on Cholesterol for Protein-Liposome Coupling

  摘要：

  The synthesis of a series of coupling lipids designed for covalently linking proteins to liposomes is described. The new compounds have in common a cholesterylsuccinyl unit as a lipid anchor and a thiol-reactive maleimidobenzoyl unit which are linked by alkyl or (poly)ethylene glycol spacers that differ in length and polarity.

  DOI：

  10.1007/pl00000090
• 作为产物：
  描述：

  胆固醇琥珀酸单酯 在 氯化亚砜 、 三乙胺 作用下， 以 甲苯 、 乙腈 为溶剂， 反应 5.0h， 生成 Succinic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 2-hydroxy-ethyl ester
  参考文献：
  名称：

  Synthesis of Novel Thiol-Reactive Amphiphilic Lipids Based on Cholesterol for Protein-Liposome Coupling

  摘要：

  The synthesis of a series of coupling lipids designed for covalently linking proteins to liposomes is described. The new compounds have in common a cholesterylsuccinyl unit as a lipid anchor and a thiol-reactive maleimidobenzoyl unit which are linked by alkyl or (poly)ethylene glycol spacers that differ in length and polarity.

  DOI：

  10.1007/pl00000090

文献信息

• 噻吩并吡啶类衍生物及其制备方法和用途
  申请人：陕西合成药业股份有限公司

  公开号：CN106554369A

  公开（公告）日：2017-04-05

  本发明涉及一种噻吩并吡啶类衍生物及其制备方法和用途，本发明所述的噻吩并吡啶类衍生物具有下式(I)所示的结构，其中R1、R2、R3、R4、R5、R6、L、m和n按权利要求书中定义，本发明还包括式(I)化合物的制备方法，其药用盐、溶剂化合物、多晶型体、对映体或外消旋混合物，含它们的药物组合物及其作为药物的用途，特别是用于预防或治疗动脉粥样硬化疾病、心肌梗死、中风、缺血性脑血栓、外周动脉疾病、急性冠脉综合征或冠脉介入术后的血栓形成。
• [EN] FOSFLUCONAZOLE DERIVATIVES, SYNTHESIS, AND USE IN LONG ACTING FORMULATIONS<br/>[FR] DÉRIVÉS DE FOSFLUCONAZOLE, SYNTHÈSE, ET UTILISATION DANS DES FORMULATIONS À LONGUE DURÉE D'ACTION
  申请人：SEPS PHARMA N V

  公开号：WO2010105910A1

  公开（公告）日：2010-09-23

  The invention relates to a compound of formula (I) and the salts, N-oxides, quaternary amines, and stereoisomers thereof, wherein R1 to R8 are as defined in the claims. The invention further relates to intermediates and methods for the preparation of the compounds of formula (I). The invention also relates to the compounds of formula (I) for use as a medicament, particularly for the prevention or treatment of fungal infections.

  该发明涉及公式(I)的化合物及其盐、N-氧化物、季铵盐和立体异构体，其中R1至R8如权利要求中所定义。该发明进一步涉及用于制备公式(I)化合物的前体和方法。该发明还涉及公式(I)的化合物，用于作为药物，特别是用于预防或治疗真菌感染。
• 泊沙康唑衍生物、合成和在长效制剂中的用途
  申请人：陕西合成药业股份有限公司

  公开号：CN106432338A

  公开（公告）日：2017-02-22

  本发明涉及泊沙康唑衍生物、合成和在长效制剂中的用途。本发明涉及式（）化合物及其盐、N-氧化物、季铵和立体异构体，其中R1—R8按权利要求书中定义。本发明还涉及制备式（）化合物的中间体和方法。本发明还涉及式（）化合物作为药物的用途，特别是用于预防或治疗真菌感染。
• Fosfluconazole Derivatives, Synthesis, and Use in Long Acting Formulations
  申请人：Gonnissen Yves

  公开号：US20120172336A2

  公开（公告）日：2012-07-05

  The invention relates to a compound of formula (1) and the salts, N-oxides, quaternary amines, and stereoisomers thereof, wherein R 1 to R 2 are as defined in the claims. The invention further relates to intermediates and methods for the preparation of the compounds of formula (I). The invention also relates to the compounds of formula (I) for use as a medicament, particularly for the prevention or treatment of fungal infections.

  本发明涉及一种式(1)的化合物及其盐、N-氧化物、季铵盐和立体异构体，其中R1到R2如权利要求中所定义。本发明还涉及制备式(I)化合物的中间体和方法。本发明还涉及用作药物的式(I)化合物，特别是用于预防或治疗真菌感染。
• Synthesis of Novel Thiol-Reactive Amphiphilic Lipids Based on Cholesterol for Protein-Liposome Coupling
  作者：Jörg T. Kley、Thomas Fichert、Ulrich Massing

  DOI：10.1007/pl00000090

  日期：1998.3

  The synthesis of a series of coupling lipids designed for covalently linking proteins to liposomes is described. The new compounds have in common a cholesterylsuccinyl unit as a lipid anchor and a thiol-reactive maleimidobenzoyl unit which are linked by alkyl or (poly)ethylene glycol spacers that differ in length and polarity.