3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-{[imino(thien-2-yl)methyl]amino}benzyl)propanamide | 515815-37-9

• 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: 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-{[imino(thien-2-yl)methyl]amino}benzyl)propanamide
• 英文别名: N-[[3-[[amino(thiophen-2-yl)methylidene]amino]phenyl]methyl]-3-(3,5-ditert-butyl-4-hydroxyphenyl)propanamide
• CAS: 515815-37-9
• 化学式: C₂₉H₃₇N₃O₂S
• 分子量: 491.698
• InChiKey: CCBIVXZIGJEZHF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  35
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  116
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-{[imino(thien-2-yl)methyl]amino}benzyl)propanamide 在 硼烷四氢呋喃络合物 作用下， 反应 1.5h， 生成 N-[3-({[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl]amino}methyl) phenyl]thiophene-2-carboximidamide
  参考文献：
  名称：

  Novel inhibitors of neuronal nitric oxide synthase with potent antioxidant properties

  摘要：

  A series of hybrid compounds possessing an nNOS pharmacophore linked to an antioxidant fragment has been synthesized. Among them, compound 8d, a propofol derivative, displayed the greatest dual potencies against nNOS (IC50 = 0.12 muM) and lipid peroxidation (IC50 = 0.4 muM) accompanied with e/nNOS selectivity (67.5). This shows that nNOS was able to accommodate very bulky groups such as di-tert-butyl or di-iso-propyl phenol in its active site. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00883-1
• 作为产物：
  描述：

  N-(3-硝基苯基甲基)氨基甲酸叔丁酯 在 palladium on activated charcoal 盐酸 、 氢碘酸 、 氢气 、 1-羟基苯并三唑 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 、 三乙胺 作用下， 以 1,4-二氧六环 、 乙醇 、 二氯甲烷 、 异丙醇 为溶剂， 20.0~60.0 ℃ 、151.99 kPa 条件下， 反应 15.0h， 生成 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-{[imino(thien-2-yl)methyl]amino}benzyl)propanamide
  参考文献：
  名称：

  Novel inhibitors of neuronal nitric oxide synthase with potent antioxidant properties

  摘要：

  A series of hybrid compounds possessing an nNOS pharmacophore linked to an antioxidant fragment has been synthesized. Among them, compound 8d, a propofol derivative, displayed the greatest dual potencies against nNOS (IC50 = 0.12 muM) and lipid peroxidation (IC50 = 0.4 muM) accompanied with e/nNOS selectivity (67.5). This shows that nNOS was able to accommodate very bulky groups such as di-tert-butyl or di-iso-propyl phenol in its active site. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00883-1

文献信息

• New derivatives of 2-(iminomethyl)amino-phenyl, their preparation, their use as medicaments and the pharmaceutical compositions containing them
  申请人：——

  公开号：US20030078420A1

  公开（公告）日：2003-04-24

  The invention relates to new derivatives of 2-(iminomethyl)amino-phenyl which are NO synthase inhibitors and can trap reactive oxygen species. These compounds can notably be used for the treatment of stroke, of neurodegenerative diseases and of ischemic or hemorragic cardiac or cerebral infarctions. These compounds include: N-{4-[({[4-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3-thiazol-2-yl]methyl}amino)methyl]phenyl}thiophene-2-carboximidamide; N-{3-[({[4-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3-thiazol-2-yl]methyl}amino)methyl]phenyl}thiophene-2-carboximidamide; N-(4-{[{[4-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3-thiazol-2-yl]methyl}(methyl)amino]methyl}phenyl)thiophene-2-carboximidamide; N-[3-({[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl]amino}methyl) phenyl]thiophene-2-carboximidamide; N-(3-{[(3,5-di-tert-butyl-4-hydroxybenzyl)amino]methyl}phenyl) thiophene-2-carboximidamide; N-[3-({[2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethyl]amino}methyl) phenyl]thiophene-2-carboximidamide; N-[3-({[3-(4-hydroxy-3,5-diisopropylphenyl)propyl]amino}methyl) phenyl]thiophene-2-carboximidamide; N-(3-{[(4-hydroxy-3,5-diisopropylbenzyl)amino]methyl}phenyl) thiophene-2-carboximidamide; N-[3-({[2-(4-hydroxy-3,5-diisopropylphenyl)ethyl]amino}methyl) phenyl]thiophene-2-carboximidamide; N-2-(3,5-di-tert-butyl-4-hydroxybenzoyl)-N-1-(4-{[imino(thien-2-yl)methyl]amino}phenyl)-L-leucinamide; and pharmaceutically acceptable salts thereof.

  这项发明涉及新的2-(亚甲基亚胺)氨基苯基衍生物，它们是一氧化氮合酶抑制剂，可以捕获活性氧物质。这些化合物可以显著用于中风、神经退行性疾病、缺血性或出血性心脏或脑梗死的治疗。 这些化合物包括： N-4-[(4-(3,5-二叔丁基-4-羟基苯基)-1,3-噻唑-2-基}甲基)氨基]苯基}噻吩-2-甲酰亚胺； N-3-[(4-(3,5-二叔丁基-4-羟基苯基)-1,3-噻唑-2-基}甲基)氨基]苯基}噻吩-2-甲酰亚胺； N-(4-[4-(3,5-二叔丁基-4-羟基苯基)-1,3-噻唑-2-基}甲基(甲基)氨基]甲基}苯基)噻吩-2-甲酰亚胺； N-[3-([3-(3,5-二叔丁基-4-羟基苯基)丙基]氨基}甲基)苯基]噻吩-2-甲酰亚胺； N-(3-[(3,5-二叔丁基-4-羟基苯基)甲基]氨基}苯基)噻吩-2-甲酰亚胺； N-[3-([2-(3,5-二叔丁基-4-羟基苯基)乙基]氨基}甲基)苯基]噻吩-2-甲酰亚胺； N-[3-([3-(4-羟基-3,5-二异丙基苯基)丙基]氨基}甲基)苯基]噻吩-2-甲酰亚胺； N-(3-[(4-羟基-3,5-二异丙基苯基)甲基]氨基}苯基)噻吩-2-甲酰亚胺； N-[3-([2-(4-羟基-3,5-二异丙基苯基)乙基]氨基}甲基)苯基]噻吩-2-甲酰亚胺； N-2-(3,5-二叔丁基-4-羟基苯甲酰)-N-1-4-[imino(噻唑-2-基)甲基]氨基}苯基-L-亮氨酰； 及其药学上可接受的盐。
• Derivatives of 2-(iminomethyl)amino-phenyl, their preparation, their use as medicaments and the pharmaceutical compositions containing them
  申请人：Chabrier de Lassauniere Etienne Pierre

  公开号：US20050043397A1

  公开（公告）日：2005-02-24

  A method of treating pain in a warm-blooded animal comprising administering to a warm-blooded animal in need thereof an amount of a compound of the formula wherein the substituents are defined in accordance with the disclosure.

  一种治疗温血动物疼痛的方法，包括向需要治疗的温血动物中投与一定量的化合物，该化合物的式如下：其中取代基根据公开说明定义。
• US6809088B2
  申请人：——

  公开号：US6809088B2

  公开（公告）日：2004-10-26
• US7122535B2
  申请人：——

  公开号：US7122535B2

  公开（公告）日：2006-10-17
• US7459558B2
  申请人：——

  公开号：US7459558B2

  公开（公告）日：2008-12-02