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Oxazole,4-(bromomethyl)-5-methyl-2-(4-methylphenyl)- | 1332766-86-5

中文名称
——
中文别名
——
英文名称
Oxazole,4-(bromomethyl)-5-methyl-2-(4-methylphenyl)-
英文别名
4-(bromomethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole
Oxazole,4-(bromomethyl)-5-methyl-2-(4-methylphenyl)-化学式
CAS
1332766-86-5
化学式
C12H12BrNO
mdl
——
分子量
266.13
InChiKey
KRBHSLQGIXVZTN-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):
    3.4
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    26
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • COMPOUND CONTAINING A NOVEL 4-ALKOXYPYRIMIDINE STRUCTURE AND MEDICINE CONTAINING SAME
    申请人:Miura Toru
    公开号:US20120322819A1
    公开(公告)日:2012-12-20
    Disclosed is novel compound and medicinal formulation containing same, possessing both angiotensin II receptor blocking and PPARγ activation effect, of use as a medicine for prevention and/or treatment of hypertension, heart disease, angina pectoris, cerebrovascular disorder, cerebral circulatory disturbances, post-ischemic peripheral circulatory damage, renal disease, arteriosclerosis, inflammatory disorder, type 2 diabetes, diabetic complications, insulin resistance syndrome, syndrome X, metabolic syndrome and hyperinsulinaemia. Further disclosed is the general formula I (where one or both of R 1 and R 2 represent a C 1-6 alkyl group, R 3 represents a C 1-6 alkyl group which may contain one or more substituent groups selected from group A, or a C 3-8 cycloalkyl group which may contain one or more substituent groups selected from group B.) which represents the compound, and salts thereof, solvates thereof, and medicinal compositions containing any of these.
    本文披露了一种新型化合物和含有该化合物的药物配方,具有同时具有抗血管紧张素II受体阻断和PPARγ激活作用的特性,可用作预防和/或治疗高血压、心脏病、心绞痛、脑血管疾病、脑循环障碍、缺血后周围循环损伤、肾脏疾病、动脉硬化、炎症性疾病、2型糖尿病、糖尿病并发症、胰岛素抵抗综合征、X综合征、代谢综合征和高胰岛素血症的药物。进一步披露了一般式I(其中R1和/或R2代表C1-6烷基基团,R3代表一个C1-6烷基基团,可以含有从A组中选择的一个或多个取代基,或者一个C3-8环烷基基团,可以含有从B组中选择的一个或多个取代基。)代表该化合物,以及其盐、溶剂化合物和含有这些化合物的药物组成物。
  • ANTIBACTERIAL AGENTS
    申请人:Brown David Ryall
    公开号:US20100173933A1
    公开(公告)日:2010-07-08
    Compounds of formula (I) have antibacterial activity: wherein R represents hydrogen or 1, 2 or 3 optional substituents; W is ═C(R 1 )— or ═N—; R 1 is hydrogen or an optional substituent and R 2 is hydrogen, methyl, or fluorine; or R 1 and R 2 taken together are —CH 2 —, —CH 2 CH 2 —, —O—, or, in either orientation, —O—CH 2 — or —OCH 2 CH 2 —; R 3 is a radical of formula -(Alk 1 ) m -(Z) p -(Alk 2 ) n -Q wherein m, p and n are independently 0 or 1, provided that at least one of m, p and n is 1, Z is —O—, —S—, —S(O)—, —S(O 2 )—, —NH—, —N(CH 3 )—, —N(CH 2 CH 3 )—, —C(═O)—, —O—(C═O)—, —C(═O)—O—, or an optionally substituted divalent monocyclic carbocyclic or heterocyclic radical having 3 to 6 ring atoms; or an optionally substituted divalent bicyclic heterocyclic radical having 5 to 10 ring atoms; Alk 1 and Alk 2 are optionally substituted C 1 -C 6 alkylene, C 2 -C 6 alkenylene, or C 2 -C 6 alkynylene radicals, which may optionally terminate with or be interrupted by —O—, —S—, —S(O)—, —S(O 2 )—, —NH—, —N(CH 3 )—, or —N(CH 2 CH 3 )—; and Q is hydrogen, halogen, nitrile, or hydroxyl or an optionally substituted monocyclic carbocyclic or heterocyclic radical having 3 to 6 ring atoms; or an optionally substituted bicyclic heterocyclic radical having 5 to 10 ring atoms.
    化学式为(I)的化合物具有抗菌活性:其中R代表氢或1、2或3个可选取代基;W是═C(R1)-或═N-;R1是氢或可选取代基,R2是氢、甲基或;或R1和R2一起取-CH2-、- -、-O-,或者,在任何方向上,取-O- -或-O -;R3是公式-(Alk1)m-(Z)p-(Alk2)n-Q的基团,其中m、p和n独立地为0或1,但至少有一个为1,Z是-O-、-S-、-S(O)-、-S(O2)-、-NH-、-N(CH3)-、-N( )-、-C(═O)-、-O-(C═O)-、-C(═O)-O-,或具有3至6个环原子的可选取代的单环碳环或杂环基团;或具有5至10个环原子的可选取代双环杂环基团;Alk1和Alk2是可选取代的C1-C6烷基、C2-C6烯基或C2-C6炔基基团,可以以-O-、-S-、-S(O)-、-S(O2)-、-NH-、-N( )-或-N( )-结尾或被中断;Q是氢、卤素、腈或羟基,或具有3至6个环原子的可选取代的单环碳环或杂环基团;或具有5至10个环原子的可选取代的双环杂环基团。
  • US8088791B2
    申请人:——
    公开号:US8088791B2
    公开(公告)日:2012-01-03
  • US8865736B2
    申请人:——
    公开号:US8865736B2
    公开(公告)日:2014-10-21
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