3-{1-[(2-o-tolylamino-3H-benzimidazol-5-yl)-acetyl]-1,2,3,4-tetrahydro-quinolin-6-yl}-butyric acid | 261731-88-8

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: 3-{1-[(2-o-tolylamino-3H-benzimidazol-5-yl)-acetyl]-1,2,3,4-tetrahydro-quinolin-6-yl}-butyric acid
• 英文别名: (R/S) 3-{1-[(2-o-tolylamino-3H-benzimidazol-5-yl)-acetyl]-1,2,3,4-tetrahydro-quinolin-6-yl}-butyric acid；3-[1-[2-[2-(2-methylanilino)-3H-benzimidazol-5-yl]acetyl]-3,4-dihydro-2H-quinolin-6-yl]butanoic acid
• CAS: 261731-88-8
• 化学式: C₂₉H₃₀N₄O₃
• 分子量: 482.582
• InChiKey: VBIGQTBKSFLHII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  36
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  98.3
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  ethyl (R/S) 3-{1-[(2-o-tolylamino-3H-benzimidazol-5-yl)-acetyl]-1,2,3,4-tetrahydro-quinolin-6-yl}-butyrate 生成 3-{1-[(2-o-tolylamino-3H-benzimidazol-5-yl)-acetyl]-1,2,3,4-tetrahydro-quinolin-6-yl}-butyric acid
  参考文献：
  名称：

  Aza-bicycles which modulate the inhibition of cell adhesion

  摘要：

  该发明涉及式(I)的生理活性化合物，其中R1代表R3—Z3—，R3—L2—R4—Z3—，R3—L3—Ar1—L4—Z3—或R3—L3—Ar1—L2—R4—Z3—；R2代表氢，卤素，低烷基或低烷氧基；A1代表直链C1-3烷基链，可选择地被来自烷基、芳基、芳基烷基、杂芳基、杂芳基烷基、亚胺、氧代、硫代或被—ZR6、—NY1Y2、—CO2R6或—C(═O)—NY1Y2取代的一个或多个基团取代；L1代表直接键；一种烯烃亚烷基链、烷基链、炔烃亚烷基链、环烯烃亚烷基链、环烷基链、杂芳基二亚基链、杂环烷基链或芳基链，每种链可选择地被(a)酸性官能团、氰基、氧代、—S(O)mR9、R3、—C(═O)—R3、—C(═O)—OR3、—N(R8)—C(═O)R9、—N(R8)—SO2—R9、—NY4Y5或—[C(═O)—N(R10)—C(R5)(R11)]p—C(═O)—NY4Y5取代，或者被(b)酸性官能团取代的烷基，或S(O)mR9、—C(═O)—NY4Y5或—NY4Y5；一种—[C(═O)—N(R10)—C(R5)(R11)]p—链；一种—Z2—R12—链；一种—C(═O)—CH2—C(═O)—链；一种—R12—Z2—R12—链；一种—C(R4)(R13)—[C(═O)—N(R10)—C(R5)(R11)]p—链；或一种—L5—L6—L7—链；Z1为C(R7)(R7a)、C(═O)或CH(OH)；Y为羧基或酸生物同位素；以及相应的N-氧化物及其前药；以及这些化合物及其N-氧化物和前药的药学上可接受的盐和溶剂。这些化合物具有有价值的药理特性，特别是调节VCAM-1和纤维连接蛋白与整合素VLA-4(&agr;4&bgr;1)相互作用的能力。

  公开号：

  US06608084B1

文献信息

• AZA-BICYCLES WHICH MODULATE THE INHIBITION OF CELL ADHESION
  申请人：Aventis Pharma Limited

  公开号：EP1114028A1

  公开（公告）日：2001-07-11
• [EN] AZA-BICYCLES WHICH MODULATE THE INHIBITION OF CELL ADHESION<br/>[FR] BICYCLES AZA MODULANT L'INHIBITION DE L'ADHESION CELLULAIRE
  申请人：RHONE POULENC RORER LTD

  公开号：WO2000015612A1

  公开（公告）日：2000-03-23

  The invention is directed to physiologically active compounds of formula (I) wherein R1 represents R?3-Z3-, R3-L2-R4-Z3-, R3-L3-Ar1-L4-Z3- or R3-L3-Ar1-L2-R4-Z3-; R2¿ represents hydrogen, halogen, lower alkyl or lower alkoxy; A1 represents a straight chain C¿1-3?alkylene linkage optionally substituted by one or more groups chosen from alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, imino, oxo, thioxo, or alkyl substituted by -ZR?6, -NY1Y2, -CO¿2R6 or -C(=O)-NY1Y2; L1 represents a direct bond; an alkenylene, alkylene, alkynylene, cycloalkenylene, cycloalkylene, heteroaryldiyl, heterocycloalkylene or arylene linkage each optionally substituted by (a) an acidic functional group, cyano, oxo, -S(O)¿mR?9, R3, -C(=O)-R3, -C(=O)-OR?3, -N(R8¿)-C(=O)-R?9, -N(R8¿)-C(=O)-OR?9, -N(R8)-SO¿2-R?9, -NY4Y5¿ or -[C(=O)-N(R?10)-C(R5)(R11)]¿p-C(=O)-NY4Y5, or by (b) alkyl substituted by an acidic functional group, or by S(O)¿mR?9, -C(=O)-NY?4Y5 or -NY4Y5¿; a -[C(=O)-N(R?10)-C(R5)(R11)]¿p- linkage; a -Z2-R12- linkage; a -C(=O)-CH¿2?-C(=O)- linkage; a -R?12-Z2-R12¿- linkage; a -C(R4)(R13)-[C(=O)-N(R?10)-C(R5)(R11)]¿p- linkage; or a -L5-L6-L7- linkage; Z?1 is C(R7)(R7a¿), C(=O) or CH(OH); Y is carboxy or an acid bioisostere; and the corresponding N-oxides, and their prodrugs; and pharmaceutically acceptable salts and solvates of such compounds and their N-oxides and prodrugs. Such compounds have valuable pharmaceutical properties, in particular the ability to regulate the interaction of VCAM-1 and fibronectin with the integrin VLA-4 (α4β1).