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resin-bound (S)-2-(2-amino-5-bromo-benzoylamino)-3-biphenyl-4-yl-propionic acid

中文名称
——
中文别名
——
英文名称
resin-bound (S)-2-(2-amino-5-bromo-benzoylamino)-3-biphenyl-4-yl-propionic acid
英文别名
Ethyl 3-[4-(aminomethyl)phenyl]-2-propan-2-yloxypropanoate;hydrochloride
resin-bound (S)-2-(2-amino-5-bromo-benzoylamino)-3-biphenyl-4-yl-propionic acid化学式
CAS
——
化学式
C22H18BrN2O3Pol
mdl
——
分子量
301.81
InChiKey
QQSPEIKWFJYQMP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -1.67
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    63.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] ARYL AND HETEROARYL COMPOUNDS, COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSES ARYLE ET HETEROARYLE, COMPOSITIONS ET PROCEDES ASSOCIES
    申请人:TRANSTECH PHARMA INC
    公开号:WO2005014532A1
    公开(公告)日:2005-02-17
    This invention provides aryl and heteroaryl compounds of Formula (I) as described herein, and methods of their preparation. Also provided are pharmaceutical compositions made with the compounds of Formula (I) and methods for making such compositions. The compounds of Formula (I) may activate an erythropoietin receptor and thus, may be useful to induce red blood cell production. The compounds of Formula (I) and compositions including compounds of Formula (I) may be useful in a variety of applications including the management, treatment and/or control of diseases caused at least in part by deficient (or inefficient) EPO production relative to hemoglobin level.
    这项发明提供了如下所述的Formula (I)的芳基和杂环芳基化合物,以及它们的制备方法。还提供了使用Formula (I)化合物制备的药物组合物,以及制备这种组合物的方法。Formula (I)的化合物可能激活促红细胞生成素受体,因此可能有助于诱导红细胞的产生。包括Formula (I)化合物的化合物和组合物可能在各种应用中有用,包括管理、治疗和/或控制至少部分由于相对于血红蛋白水平缺乏(或效率低下)EPO产生而引起的疾病。
  • Carboxylic acid derivative and salt thereof
    申请人:——
    公开号:US20040102634A1
    公开(公告)日:2004-05-27
    The present invention provides a novel carboxylic acid compound, a salt thereof or a hydrate of them useful as an insulin sensitizer, and a medicament comprising the compound as an active ingredient. That is, the present invention provides a carboxylic acid compound represented by the following formula, a salt thereof, an ester thereof or a hydrate of them. 1 Wherein R 1 represents a hydrogen atom, hydroxyl group, halogen, carboxyl group, or a C 1-6 alkyl group etc., each of which may have one or more substituents; L represents a single bond, or a C 1-6 alkylene group, a C 2-6 alkenylene group or a C 2-6 alkynylene group, each of which may have one or more substituents; M represents a single bond, or a C 1-6 alkylene group, a C 2-6 alkenylene group or a C 2-6 alkynylene group, each of which may have one or more substituents; T represents a single bond, or a C 1-3 alkylene group, a C 2-3 alkenylene group or a C 2-3 alkynylene group, each of which may have one or more substituents; W represents a carboxyl group; 2 represents a single bond etc.; X represents a single bond, oxygen atom, a group represented by —NR X1 CQ 1 O— (wherein Q 1 represents an oxygen atom or sulfur atom; and R X1 represents a hydrogen atom, formyl group, or a C 1-6 alkyl group etc., each of which may have one or more substituents), —OCQ 1 NR X1 — (wherein Q 1 and R X1 are as defined above), —CQ 1 NR X1 O— (wherein Q 1 and R X1 are as defined above), ONR X1 CQ 1 — (wherein Q 1 and R X1 are as defined above), -Q 2 SO 2 — (wherein Q 2 is an oxygen atom or —NR X10 — (wherein R X10 represents a hydrogen atom, formyl group, or a C 1-6 alkyl group etc., each of which may have one or more substituents)) or —SO 2 Q 2 - (wherein Q 2 is as defined above), (wherein, provided that R X2 and R X3 , and/or R X4 and R X5 may together form a ring, Q 3 and Q 4 are the same as or different from each other and each represents an oxygen atom, (O)S(O) or NR X10 (wherein NR X10 is as defined above)); Y represents a 5- to 14-membered aromatic group etc., which may have one or more substituents and one or more hetero atoms; and the ring Z represents a 5- to 14-membered aromatic group which may have 0 to 4 substituents and one or more hetero atoms, and wherein part of the ring may be saturated.
    本发明提供了一种新型的羧酸化合物、其盐或水合物,作为胰岛素增敏剂,并且提供了一种包含该化合物作为活性成分的药物。即,本发明提供了由以下式表示的羧酸化合物、其盐、酯或水合物。其中,R1表示氢原子、羟基、卤素、羧基或C1-6烷基等,每个都可以有一个或多个取代基;L表示单键,或C1-6烷基、C2-6烯基或C2-6炔基等,每个都可以有一个或多个取代基;M表示单键,或C1-6烷基、C2-6烯基或C2-6炔基等,每个都可以有一个或多个取代基;T表示单键,或C1-3烷基、C2-3烯基或C2-3炔基等,每个都可以有一个或多个取代基;W表示羧基;2表示单键等;X表示单键、氧原子、由—NRX1CQ1O—表示的基团(其中,Q1表示氧原子或硫原子;RX1表示氢原子、甲酰基或C1-6烷基等,每个都可以有一个或多个取代基)、由—OCQ1NRX1—表示的基团(其中,Q1和RX1如上所定义)、由—CQ1NRX1O—表示的基团(其中,Q1和RX1如上所定义)、由ONRX1CQ1—表示的基团(其中,Q1和RX1如上所定义)、由-Q2SO2—表示的基团(其中,Q2是氧原子或—NRX10—(其中,RX10表示氢原子、甲酰基或C1-6烷基等,每个都可以有一个或多个取代基))或由—SO2Q2—表示的基团(其中,Q2如上所定义),(其中,假设RX2和RX3,以及RX4和RX5可以共同形成环,Q3和Q4相同或不同,每个表示氧原子、(O)S(O)或NRX10(其中,NRX10如上所定义));Y表示5-至14-成员芳香基等,可以有一个或多个取代基和一个或多个杂原子;环Z表示5-至14-成员芳香基,可以有0至4个取代基和一个或多个杂原子,其中环的一部分可以饱和。
  • CARBOXYLIC ACID DERIVATIVE AND SALT THEREOF
    申请人:Eisai Co., Ltd.
    公开号:EP1380562A1
    公开(公告)日:2004-01-14
    The present invention provides a novel carboxylic acid compound, a salt thereof or a hydrate of them useful as an insulin sensitizer, and a medicament comprising the compound as an active ingredient. That is, the present invention provides a carboxylic acid compound represented by the following formula, a salt thereof, an ester thereof or a hydrate of them. Wherein R1 represents a hydrogen atom, hydroxyl group, halogen, carboxyl group, or a C1-6 alkyl group etc., each of which may have one or more substituents; L represents a single bond, or a C1-6 alkylene group, a C2-6 alkenylene group or a C2-6 alkynylene group, each of which may have one or more substituents; M represents a single bond, or a C1-6 alkylene group, a C2-6 alkenylene group or a C2-6 alkynylene group, each of which may have one or more substituents; T represents a single bond, or a C1-3 alkylene group, a C2-3 alkenylene group or a C2-3 alkynylene group, each of which may have one or more substituents; W represents a carboxyl group; - - - represents a single bond etc. ; X represents a single bond, oxygen atom, a group represented by -NRX1CQ1O- (wherein Q1 represents an oxygen atom or sulfur atom; and RX1 represents a hydrogen atom, formyl group, or a C1-6 alkyl group etc., each of which may have one or more substituents), -OCQ1NRX1- (wherein Q1 and RX1 are as defined above), -CQ1NRx1O- (wherein Q1 and RX1 are as def ined above), ONRX1CQ1- (wherein Q1 and RX1 are as defined above), - Q2SO2- (wherein Q2 is an oxygen atom or -NRX10- (wherein RX10 represents a hydrogen atom, formyl group, or a C1-6 alkyl group etc., each of which may have one or more substituents)) or -SO2Q2- (wherein Q2 is as defined above), (wherein, provided that RX2 and RX3, and/or RX4 and RX5 may together form a ring, Q3 and Q4 are the same as or different from each other and each represents an oxygen atom, (O)S(O) or NRX10 (wherein NRX10 is as defined above)); Y represents a 5- to 14-membered aromatic group etc., which may have one or more substituents and one or more hetero atoms; and the ring Z represents a 5-to 14-membered aromatic group which may have 0 to 4 substituents and one or more hetero atoms, and wherein part of the ring may be saturated.
    本发明提供了一种可用作胰岛素增敏剂的新型羧酸化合物、其盐或其水合物,以及包含该化合物作为活性成分的药物。也就是说,本发明提供了由下式代表的羧酸化合物、其盐、其酯或它们的水合物。 其中 R1 代表氢原子、羟基、卤素、羧基或 C1-6 烷基等、L 代表单键,或 C1-6 亚烷基、C2-6 亚烯基或 C2-6 亚炔基,其中每个基团可带有一个或多个取代基;M 代表单键,或 C1-6 亚烷基、C2-6 亚烯基或 C2-6 亚炔基,其中每个基团可有一个或多个取代基; T 代表单键,或 C1-3 亚烷基、C2-3 亚烯基或 C2-3 亚炔基,其中每个基团可有一个或多个取代基; W 代表羧基; - - - 代表单键等;X 代表单键、氧原子、由 -NRX1CQ1O- 代表的基团(其中 Q1 代表氧原子或硫原子;RX1 代表氢原子、甲酰基或 C1-6 烷基等)、其中每个取代基可有一个或多个)、-OCQ1NRX1-(其中 Q1 和 RX1 如上定义)、-CQ1NRx1O-(其中 Q1 和 RX1 如上定义)、ONRX1CQ1-(其中 Q1 和 RX1 如上定义)、-Q2SO2-(其中 Q2 是氧原子或-NRX10-(其中 RX10 代表氢原子、甲酰基或 C1-6 烷基等、其中每个基团可具有一个或多个取代基))或-SO2Q2-(其中 Q2 如上定义)、 (其中,只要 RX2 和 RX3,和/或 RX4 和 RX5 可共同形成一个环,Q3 和 Q4 彼此相同或不同,且各自代表氧原子、(O)S(O)或 NRX10(其中 NRX10 如上定义));Y 代表 5 至 14 元芳香基团等、环 Z 代表 5 至 14 元芳香基团,可具有 0 至 4 个取代基和一个或多个杂原子,其中部分环可为饱和环。
  • US7544835B2
    申请人:——
    公开号:US7544835B2
    公开(公告)日:2009-06-09
  • [EN] ARYL AND HETEROARYL COMPOUNDS AND METHODS TO MODULATE COAGULATION<br/>[FR] COMPOSES ARYLE ET HETEROARYLE ET PROCEDES DE MODULATION DE LA COAGULATION
    申请人:TRANSTECH PHARMA INC
    公开号:WO2004014844A3
    公开(公告)日:2005-04-28
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