3-(三氟甲基)-4-氯苯甲酰胺 | 62584-23-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-(三氟甲基)-4-氯苯甲酰胺
• 英文名称: 3-Trifluormethyl-4-chlorbenzamid
• 英文别名: 4-Chloro-3-(trifluoromethyl)benzamide
• CAS: 62584-23-0
• 化学式: C₈H₅ClF₃NO
• 分子量: 223.582
• InChiKey: PIYDLRBTABXQSP-UHFFFAOYSA-N

物化性质

• 沸点：
  258℃
• 密度：
  1.455
• 闪点：
  110℃

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  43.1
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

反应信息

• 作为反应物：
  描述：

  3-(三氟甲基)-4-氯苯甲酰胺 以 二氯甲烷 、 乙腈 为溶剂， 生成 N-(2-oxoindolin-6-ylcarbamoyl)-4-chloro-3-(trifluoromethyl)benzamide
  参考文献：
  名称：

  Novel acylureidoindolin-2-one derivatives as dual Aurora B/FLT3 inhibitors for the treatment of acute myeloid leukemia

  摘要：

  A series of 6-acylureido derivatives containing a 3-(pyrrol-2-ylmethylidene)indolin-2-one scaffold were synthesized as potential dual Aurora B/FLT3 inhibitors by replacing the 6-arylureido moiety in 6-arylureidoindolin-2-one-based multi-kinase inhibitors. (Z)-N-(2-(pyrrolidin-l-yl)ethyl)-5-((6-(3-(2-fluoro-4-methoxybenzoyflureido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide (54) was identified as a dual Aurora B/FLT3 inhibitor (IC50 = 0.4 nM and 0.5 nM, respectively). Compound 54 also exhibited potent cytotoxicity with single-digit nanomolar IC50 values against the FLT3 mutant-associated human acute myeloid leukemia (AML) cell lines MV4-11 (FLT3-ITD) and MOLM-13 (FLT3-ITD). Compound 54 also specifically induced extrinsic apoptosis by inhibiting the phosphorylation of the Aurora B and FLT3 pathways in MOLM-13 cells. Compound 54 had a moderate pharmacokinetic profile. The mesylate salt of 54 efficiently inhibited tumor growth and reduced the mortality of BALB/c nude mice (subcutaneous xenograft model) that had been implanted with AML MOLM-13 cells. Compound 54 is more potent than sunitinib not only against FLT3-WT AML cells but also active against sunitinib-resistant FLT3-ITD AML cells. This study demonstrates the significance of dual Aurora B/FLT3 inhibitors for the development of potential agents to treat AML. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.07.108

文献信息

• Novel amides useful for treating pain
  申请人：Zheng Zhu Guo

  公开号：US20050080095A1

  公开（公告）日：2005-04-14

  The present invention relates to compounds of formula (I-VII) or a pharmaceutically acceptable salt or prodrug thereof, in which A, L, R 6 , R 7 and R 8 are defined herein. The present invention also relates to methods of trating pain using these compounds and pharmaceutical compositions including these compounds.

  本发明涉及式(I-VII)的化合物或其药用可接受的盐或前药，其中A、L、R6、R7和R8在此有所定义。本发明还涉及使用这些化合物治疗疼痛的方法以及包含这些化合物的药物组合物。
• COMPOUNDS FOR THE TREATMENT AND PREVENTION OF INFLUENZA
  申请人：Chen Li

  公开号：US20110195979A1

  公开（公告）日：2011-08-11

  A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R 1 to R 4 and Ar are as defined in description and in claims, can be used as a medicament.

  化合物的化学式（I）及其药用盐，其中R1至R4和Ar如描述和权利要求中所定义，可用作药物。
• [EN] 1H-BENZ IMIDAZOLE-5-CARBOXAMIDES AS ANTI-INFLAMMATORY AGENTS<br/>[FR] 1H-BENZIMIDAZOLE-5-CARBOXAMIDES COMME AGENTS ANTI-INFLAMMATOIRES
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2010034796A1

  公开（公告）日：2010-04-01

  There are provided compounds of formula (I), wherein R1, R6, R8, Q2, Q3, Q3a, Q4, L and A have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of the activity of a member of the MAPEG family is desired and/or required, and particularly in the treatment of inflammation and/or cancer.

  提供了具有式（I）的化合物，其中R1、R6、R8、Q2、Q3、Q3a、Q4、L和A的含义如描述中所给，并且其药学上可接受的盐，这些化合物在治疗需要或期望抑制MAPEG家族成员活性的疾病方面是有用的，特别是在炎症和/或癌症的治疗中。
• [EN] HETEROCYCLIC DIAMINE COMPOUNDS AS LIGANDS OF THE MELANIN CONCENTRATING HORMONE RECEPTOR USEFUL FOR THE TREATMENT OF OBESITY, DIABETES, EATING AND SEXUAL DISORDERS<br/>[FR] COMPOSÉS DE DIAMINE HÉTÉROCYCLIQUE COMME LIANTS DU RÉCEPTEUR D'HORMONE CONCENTRANT DE LA MÉLAMINE, UTILE POUR LE TRAITEMENT DE L'OBÉSITÉ, DU DIABÈTE ET DES TROUBLES SEXUELS ET DE L'ALIMENTATION
  申请人：NEUROGEN CORP

  公开号：WO2006015279A1

  公开（公告）日：2006-02-09

  Heterocyclic diamine compounds of formula (I) are provided. Such compounds may be used to modulate MCH receptor activity in vivo or in vitro, and are particularly useful in the treatment of a variety of metabolic, feeding and sexual disorders in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting MCH receptors (e.g., receptor localization studies). Formula: (I).

  提供了化学式（I）的杂环二胺化合物。这些化合物可用于调节体内或体外的MCH受体活性，并在治疗人类、驯养伴侣动物和家畜动物的各种代谢、进食和性功能障碍方面特别有用。提供了用于治疗此类障碍的药物组合物和方法，以及用于检测MCH受体（例如受体定位研究）的配体的方法。化学式：（I）。
• [EN] HISTONE ACETYLTRANSFERASE MODULATORS AND USESE THEREOF<br/>[FR] MODULATEURS DE L'HISTONE ACÉTYLTRANSFÉRASE ET LEURS UTILISATIONS
  申请人：UNIV COLUMBIA

  公开号：WO2012088420A1

  公开（公告）日：2012-06-28

  The invention provides compounds and compositions comprising compounds that modulate histone acyl transferase (HAT). The invention further provides methods for treating neurodegenerative disorders, conditions associated with accumulated amyloid-beta peptide deposits, Tau protein levels, and/or accumulations of alpha-synuclein as well as cancer by administering a compound that modulates HAT to a subject.

  这项发明提供了包含调节组蛋白酰基转移酶（HAT）的化合物和化合物组合物。该发明还提供了通过向受试者施用调节HAT的化合物来治疗神经退行性疾病、与累积的淀粉样蛋白β沉积、Tau蛋白水平和/或α-突触核蛋白积累相关的疾病以及癌症的方法。