1,1'-(3,4-dithia-hexane-1,6-diyl)-bis-piperidine | 4945-52-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 1,1'-(3,4-dithia-hexane-1,6-diyl)-bis-piperidine
• 英文别名: bis-(2-piperidino-ethyl)-disulfide；Bis-(2-piperidino-aethyl)-disulfid；Bis-<2-(N-piperidyl)aethyl>-disulfid；<2-Piperidino-aethyl>-disulfid；Piperidine, 1,1'-(dithiodiethylene)di-；1-[2-(2-piperidin-1-ylethyldisulfanyl)ethyl]piperidine
• CAS: 4945-52-2
• 化学式: C₁₄H₂₈N₂S₂
• 分子量: 288.522
• InChiKey: AYZBOBLAWWLWQI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  18
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  57.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1,1'-(3,4-dithia-hexane-1,6-diyl)-bis-piperidine 、 cyclosporin A 在 N,N-二甲基丙烯基脲 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 为溶剂， 反应 12.33h， 以9%的产率得到(3S,6S,9S,12R,15S,18S,21S,24S,27R,30S,33S)-30-ethyl-33-[(E,1R,2R)-1-hydroxy-2-methyl-hex-4-enyl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,25,28-nonamethyl-27-[2-(1-piperidyl)ethylsulfanyl]-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
  参考文献：
  名称：

  Synthesis of non-immunosuppressive cyclophilin-Binding cyclosporin A derivatives as potential anti-HIV-1 drugs

  摘要：

  Original cyclosporin A (CsA) derivatives bearing various alkylthio side chains at the sarcosine residue 3 (R configuration) and for the most potent and selective compounds a 4'-hydroxyl group at the Me-Leucine residue 4 were prepared in one or two steps from commercially available CsA. The [2-(dimethyl or diethylamino)-ethylthio-Sar](3)-[(4'-OH)MeLeu](4)-CsA derivatives 3k and 3l displayed potent in vitro anti-HIV-1 (IC50 similar to 46 nM) and low immunosuppressive activities (IC50 > 1500 nM). (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.09.042
• 作为产物：
  描述：

  N-(2-Mercaptoethyl)piperidine 在 盐酸 、 potassium hexacyanoferrate(III) 作用下， 以 水 为溶剂， 反应 0.5h， 生成 1,1'-(3,4-dithia-hexane-1,6-diyl)-bis-piperidine
  参考文献：
  名称：

  Structure-activity relationships among di- and tetramine disulfides related to benextramine

  摘要：

  The synthesis and irreversible alpha-blocking activity in the rat vas deferens of a series of tetra- and diamine disulfides 2-38, structural analogues of benextramine (BHC), are described. All compounds containing a central cystamine moiety displayed an irreversible alpha-adrenergic blockade at concentrations ranging from 10(-4) to 6 X 10(-6)M. Potency was increased in cystamines N,N'-disubstituted with 6-aminohexyl groups, especially when the outer nitrogen atoms bear arylalkyl substituents or are enclosed in a ring. However, N,N,N',N'-tetrasubstituted cystamines were poor blockers. Structural specificity in the outer portion of the tetramine disulfide is low, since many types of substituents gave rise to potent alpha-blockers. Even replacement of the outer amines with nonbasic ethers or amides was observed to maintain irreversible alpha-blockade.

  DOI：

  10.1021/jm00390a011

文献信息

• LEVINSTEIN MUSTARD GAS. IV. THE bis(2-CHLOROETHYL) POLYSULFIDES¹
  作者：REYNOLD C. FUSON、CHARLES C. PRICE、DONALD M. BURNESS、ROBERT E. FOSTER、WILLIAM R. HATCHARD、ROBERT D. LIPSCOMB

  DOI：10.1021/jo01175a010

  日期：1946.9
• ALVAREZ, M.;GRANADOS, R.;MAULEON, D.;ROSELL, G.;SALAS, M.;SALLES, J.;VALL+, J. MED. CHEM., 30,(1987) N 7, 1186-1193
  作者：ALVAREZ, M.、GRANADOS, R.、MAULEON, D.、ROSELL, G.、SALAS, M.、SALLES, J.、VALL+

  DOI：——

  日期：——
• US5965527A
  申请人：——

  公开号：US5965527A

  公开（公告）日：1999-10-12