(±)-4-(1H-1,2,4-triazol-1-yl) methyl retinoate | 303731-02-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (±)-4-(1H-1,2,4-triazol-1-yl) methyl retinoate
• 英文别名: methyl (2E,4E,6E,8E)-3,7-dimethyl-9-[2,6,6-trimethyl-3-(1,2,4-triazol-1-yl)cyclohexen-1-yl]nona-2,4,6,8-tetraenoate
• CAS: 303731-02-4
• 化学式: C₂₃H₃₁N₃O₂
• 分子量: 381.518
• InChiKey: CMZQDIOWIOFCOW-GPLMESCTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  57
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (±)-4-(1H-1,2,4-triazol-1-yl) methyl retinoate 在 氢氧化钾 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以85%的产率得到(±)-4-(1H-1,2,4-triazol-1-yl)retinoic acid
  参考文献：
  名称：

  具有多种生物活性的新型视黄酸代谢阻断剂是人乳腺癌和前列腺癌细胞在体外的有效生长抑制剂，以及裸鼠中人乳腺癌的异种移植。

  摘要：

  新型视黄酸代谢阻断剂（RAMBAs）已经合成和表征。合成特征包括在全反式视黄酸（ATRA）和13-顺式视黄酸的C-4处引入亲核配体，以及修饰末端羧酸基团。我们的大多数化合物都是仓鼠肝微粒ATRA代谢酶的强效抑制剂。最有效的化合物是甲基（2E，4E，6E，8E）-9-（3-咪唑基-2,6,6-三甲基环己-1-烯基）-3,7-二甲基壬基-2，4,6,8-四烯酸酯（5）的IC（50）值为0.009 nM，比有名的RAMBA利拉唑（Liazal，IC（50）= 6000 nM）强666,667倍。出乎意料的是，化合物5的两种对映异构体的酶抑制活性之间基本没有差异。在MCF-7细胞增殖实验中，RAMBAs也以浓度依赖的方式增强ATRA介导的抗增殖活性。除了在微粒体制剂和完整的人类癌细胞（MCF-7，T47D和LNCaP）中作为ATRA代谢的高效抑制剂外，新型非典型RAMBAs还表现出多种生物学活性，

  DOI：

  10.1021/jm0401457
• 作为产物：
  描述：

  维A酸 在 manganese(IV) oxide 、 sodium tetrahydroborate 作用下， 以 甲醇 、 正己烷 、 二氯甲烷 、 乙腈 、 苯 为溶剂， 反应 25.75h， 生成 (±)-4-(1H-1,2,4-triazol-1-yl) methyl retinoate
  参考文献：
  名称：

  具有多种生物活性的新型视黄酸代谢阻断剂是人乳腺癌和前列腺癌细胞在体外的有效生长抑制剂，以及裸鼠中人乳腺癌的异种移植。

  摘要：

  新型视黄酸代谢阻断剂（RAMBAs）已经合成和表征。合成特征包括在全反式视黄酸（ATRA）和13-顺式视黄酸的C-4处引入亲核配体，以及修饰末端羧酸基团。我们的大多数化合物都是仓鼠肝微粒ATRA代谢酶的强效抑制剂。最有效的化合物是甲基（2E，4E，6E，8E）-9-（3-咪唑基-2,6,6-三甲基环己-1-烯基）-3,7-二甲基壬基-2，4,6,8-四烯酸酯（5）的IC（50）值为0.009 nM，比有名的RAMBA利拉唑（Liazal，IC（50）= 6000 nM）强666,667倍。出乎意料的是，化合物5的两种对映异构体的酶抑制活性之间基本没有差异。在MCF-7细胞增殖实验中，RAMBAs也以浓度依赖的方式增强ATRA介导的抗增殖活性。除了在微粒体制剂和完整的人类癌细胞（MCF-7，T47D和LNCaP）中作为ATRA代谢的高效抑制剂外，新型非典型RAMBAs还表现出多种生物学活性，

  DOI：

  10.1021/jm0401457

文献信息

• Potent inhibition of retinoic acid metabolism enzyme(s) by novel azolyl retinoids
  作者：Vincent C.O Njar、Ivo P Nnane、Angela M.H Brodie

  DOI：10.1016/s0960-894x(00)00391-7

  日期：2000.9

  Novel (+/-)-4-azolyl retinoic acid analogues 4, 5, 7 and 8 have been designed and synthesized and have been shown to be powerful inhibitors of hamster microsomal all-trans-retinoic acid 4-hydroxylase enzyme(s). (+/-)-4-(1H-Imidazol-1-yl)retinoic acid (4) is the most potent inhibitor of this enzyme reported to date. (C) 2000 Elsevier Science Ltd. All rights reserved.
• COMPOSITIONS AND METHODS FOR TREATING DISEASE
  申请人：OEHLEN Lambertus J.M.W.

  公开号：US20150164907A1

  公开（公告）日：2015-06-18

  Methods are provided for treating fibrotic diseases and conditions or cancer and other dysproliferative diseases by administering to a subject in need there of a therapeutically effective amount of a synergistic composition comprising a phosphatidylinositol 3-kinase inhibitor and a retinoid, optionally including a CYP26 inhibitor, wherein the therapeutically effective amount suppresses fibrosis or the growth of dysproliferative cells in vivo. Compositions comprising a combination of a phosphatidylinositol 3-kinase inhibitor and a retinoid, optionally in combination with a CYP26 inhibitor, are also described.
• COMPOSITIONS AND METHODS FOR TREATING DYSPROLIFERATIVE DISEASES
  申请人：ANGION BIOMEDICA CORP.

  公开号：US20160038490A1

  公开（公告）日：2016-02-11

  Methods are provided for treating cancer and other dysproliferative diseases by administering to a subject in need there of a therapeutically effective amount of a synergistic composition comprising an HER2 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; and a CYP26 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; wherein said therapeutically effective amount suppresses the growth of dysproliferative cells in vivo. Compositions comprising a combination of an HER2 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; and a CYP26 inhibitor a pharmaceutically acceptable salt or prodrug thereof are also described.
• [EN] METHODS AND USES OF CYTOCHROME P450 INHIBITORS<br/>[FR] PROCÉDÉS ET UTILISATIONS D'INHIBITEURS DU CYTOCHROME P450
  申请人：ANGION BIOMEDICA CORP

  公开号：WO2011016863A2

  公开（公告）日：2011-02-10

  Methods are provided for treating or preventing chronic obstructive pulmonary diseases such as emphysema, and fibrotic diseases including heart, liver, kidney and vascular diseases, by administering to a subject a pharmaceutical composition comprising a compound that inhibits cytochrome P450RA or CYP26.
• [EN] COMPOSITIONS AND METHODS FOR TREATING DYSPROLIFERATIVE DISEASES<br/>[FR] COMPOSITIONS ET MÉTHODES DE TRAITEMENT DE MALADIES DYSPROLIFÉRATIVES
  申请人：ANGION BIOMEDICA CORP

  公开号：WO2014015137A2

  公开（公告）日：2014-01-23

  Methods are provided for treating cancer and other dysproliferative diseases by administering to a subject in need there of a therapeutically effective amount of a synergistic composition comprising an HER2 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; and a CYP26 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; wherein said therapeutically effective amount suppresses the growth of dysproliferative cells in vivo. Compositions comprising a combination of an HER2 inhibitor, or a pharmaceutically acceptable salt or prodrug thereof; and a CYP26 inhibitor a pharmaceutically acceptable salt or prodrug thereof are also described.