N,3,4-trimethylbenzenesulfonamide | 7467-14-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N,3,4-trimethylbenzenesulfonamide
• CAS: 7467-14-3
• 化学式: C₉H₁₃NO₂S
• mdl: MFCD06042453
• 分子量: 199.27
• InChiKey: ZUFWTWNQQBBLDQ-UHFFFAOYSA-N

物化性质

• 沸点：
  325.2±52.0 °C(Predicted)
• 密度：
  1.154±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.333
• 拓扑面积：
  54.6
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• MODULATORS OF ATP-BINDING CASSETTE-TRANSPORTERS
  申请人：HADIDA RUAH SARA S.

  公开号：US20090143381A1

  公开（公告）日：2009-06-04

  Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator (“CFTR”). The present invention also relates to methods of treating ABC transporter mediated diseases using compounds of the present invention.

  本发明的化合物及其药用可接受的组合物可用作ATP结合盒（“ABC”）转运蛋白或其片段的调节剂，包括囊性纤维化跨膜传导调节蛋白（“CFTR”）。本发明还涉及使用本发明的化合物治疗ABC转运蛋白介导的疾病的方法。
• [EN] COMPOUNDS AND METHODS FOR THE TREATMENT OF NON‑ALCOHOLIC STEATOHEPATITIS<br/>[FR] COMPOSÉS ET PROCÉDÉS DESTINÉS AU TRAITEMENT DE LA STÉATOHÉPATITE NON ALCOOLIQUE
  申请人：AVALIV THERAPEUTICS

  公开号：WO2019111225A1

  公开（公告）日：2019-06-13

  Compounds and compositions are provided having the structure of Formula (I) or a pharmaceutically acceptable salt, tautomer, or stereoisomer thereof, wherein T, T', U, U', V, W, R1, R2, R3', n, o, o', o'', and o''' are as defined herein. Such compounds are useful for treating liver diseases and abnormal liver conditions, including non-alcoholic steatohepatitis via inhibition of the lysosomal enzyme cathepsin D. Accordingly, a variety of treatment methods are hereby disclosed, including treatment of underlying conditions such as hepatic inflammation, aberrant lipid metabolism, and irregular lysosomal function.

  提供具有Formula (I)结构或其药用可接受的盐、互变异构体或立体异构体的化合物和组合物，其中T、T'、U、U'、V、W、R1、R2、R3'、n、o、o'、o''和o'''如本文所定义。这些化合物可用于治疗肝病和异常肝脏状况，包括通过抑制溶酶体酶蛋白酶D来治疗非酒精性脂肪性肝炎。因此，这里公开了各种治疗方法，包括治疗基础疾病，如肝脏炎症、异常脂质代谢和溶酶体功能异常。
• [EN] ELECTRO-POLARIZABLE COMPOUND AND CAPACITOR<br/>[FR] COMPOSÉ ÉLECTRO-POLARISABLE ET CONDENSATEUR
  申请人：CAPACITOR SCIENCES INC

  公开号：WO2017176509A1

  公开（公告）日：2017-10-12

  An electro-polarizable compound has a general formula: _ _ | ____________ | | | | | | | [R1]m | | <-NLE | | | | | | | | [ Core1 ]-----|-[Core2]n |-[R4]k (I) | |___ |_______| | | | | | | | [R2]p [R3]s | |_ _| Core1 is an two-dimensional flat aromatic polycyclic conjugated molecule, R1 is a dopant group of which there are m=1, 2, 3 or 4. R2 is an ionic substituent, of which there are p=0, 1, 2, 3 or 4. Fragment NLE has a nonlinear polarization effect. Core2 is an electro-conductive oligomer, of which there are n=0, 2, or 4. R3 is an ionic substituent of which there are s=0, 1, 2, 3 or 4. R4 is a resistive substituent, of which there are k=0, 1, 2, 3, 4, 5, 6, 7 or 8.

  一个电极化合物的一般公式是： _ _ | ____________ | | | | | | | [R1]m | | <-NLE | | | | | | | | [ Core1 ]-----|-[Core2]n |-[R4]k (I) | |___ |_______| | | | | | | | [R2]p [R3]s | |_ _| Core1是一个二维平面芳香多环共轭分子，R1是一个掺杂基团，其数量为m=1, 2, 3或4。R2是一个离子取代基，其数量为p=0, 1, 2, 3或4。片段NLE具有非线性极化效应。Core2是一个电导性寡聚物，其数量为n=0, 2或4。R3是一个离子取代基，其数量为s=0, 1, 2, 3或4。R4是一个电阻性取代基，其数量为k=0, 1, 2, 3, 4, 5, 6, 7或8。
• HETERO RING DERIVATIVE
  申请人：Takahashi Fumie

  公开号：US20120165309A1

  公开（公告）日：2012-06-28

  [Object] A novel and excellent method for preventing or treating rejection in the transplantation of various organs, allergy diseases, autoimmune diseases, hematologic tumor, or the like, based on a PI3Kδ-selective inhibitory action and/or an IL-2 production inhibitory action, and/or a B cell proliferation inhibitory action (including an activation inhibitory action), is provided [Means for Solution] It was found that a 3-substituted triazine or 3-substituted pyrimidine derivative exhibits a PI3Kδ-selective inhibitory action, and/or an IL-2 production inhibitory action, and/or a B cell proliferation inhibitory action (including an activation inhibitory action), and can be an agent for preventing or treating rejection in the transplantation of various organs, allergy diseases (asthma, atopic dermatitis, etc.), autoimmune diseases (rheumatoid arthritis, psoriasis, ulcerative colitis, Crohn's disease, systemic lupus erythematosus, etc.), hematologic tumor (leukemia etc.), or the like, thereby completing the present invention.

  [目标]提供一种基于PI3Kδ选择性抑制作用和/或IL-2产生抑制作用和/或B细胞增殖抑制作用（包括激活抑制作用）的新颖优良方法，用于预防或治疗各种器官移植、过敏性疾病、自身免疫性疾病、血液肿瘤等的排斥反应。 [解决方案]发现3-取代-1,3,5-三嗪或3-取代嘧啶衍生物表现出PI3Kδ选择性抑制作用和/或IL-2产生抑制作用和/或B细胞增殖抑制作用（包括激活抑制作用），可以作为预防或治疗各种器官移植、过敏性疾病（哮喘、特应性皮炎等）、自身免疫性疾病（类风湿性关节炎、银屑病、溃疡性结肠炎、克罗恩病、系统性红斑狼疮等）、血液肿瘤（白血病等）等排斥反应的药物，从而完成了本发明。
• MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS
  申请人：Vertex Pharmaceuticals Incorporated

  公开号：US20140206689A1

  公开（公告）日：2014-07-24

  Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator (“CFTR”). The present invention also relates to methods of treating ABC transporter mediated diseases using compounds of the present invention.

  本发明的化合物及其药学上可接受的组成物，可用作ATP结合盒（“ABC”）转运蛋白或其片段的调节剂，包括囊性纤维化跨膜传导调节因子（“CFTR”）。本发明还涉及使用本发明的化合物治疗ABC转运蛋白介导的疾病的方法。