N-hexylnaphthalene-1-carboxamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: N-hexylnaphthalene-1-carboxamide
• 化学式: C₁₇H₂₁NO
• 分子量: 255.35
• InChiKey: UBOQXTIHTLXTEV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  19
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

文献信息

• Amine derivative compounds
  申请人：SANKYO COMPANY, LIMITED

  公开号：US20030078426A1

  公开（公告）日：2003-04-24

  An amine compound of the formula (I): 1 wherein R 1 represents an optionally substituted carbamoyl group, etc., R 2 represents a hydrogen atom, etc., R 3 represents a C 1 -C 10 alkyl group etc., W 1 , W 2 and W 3 are the same or different and each represent a single bond or a C 1 -C 8 alkylene group, X, Y and Q represent a sulfur atom, etc., Z represents a ═CH— group, etc., Ar represents a benzene ring, etc. and L represents a hydrogen atom, etc., or a pharmacologically acceptable salt thereof. These compounds are useful in the treatment and/or prophylaxis of diseases such as diabetes, hyperlipemia, arteriosclerosis, cancer, etc.

  化合物的结构式（I）如下：其中R1代表可选择取代的氨基甲酰基团，R2代表氢原子等，R3代表C1-C10烷基等，W1、W2和W3相同或不同，每个代表单键或C1-C8烷基链，X、Y和Q代表硫原子等，Z代表═CH—基团等，Ar代表苯环等，L代表氢原子等，或其药理学上可接受的盐。这些化合物在治疗和/或预防糖尿病、高脂血症、动脉硬化、癌症等疾病方面具有用处。
• Alpha-substituted carboxylic acid derivatives
  申请人：SANKYO COMPANY, LIMITED

  公开号：US20030069294A1

  公开（公告）日：2003-04-10

  The &agr;-substituted carboxylic acid derivatives having the formula (I): 1 wherein R 1 is an alkyl group, etc., R 2 is a hydrogen atom, etc., R 3 is a hydrogen atom, etc., A is ═CH-group, etc., B is an oxygen atom, etc., W 1 is a C 1 -C 8 alkylene group, W 2 is a single bond or a C 1 -C 8 alkylene group, X is a hydrogen atom, etc., Y is an oxygen atom, etc., and Z 1 is an alkoxy group, etc., and pharmacologically acceptable salts, esters and amides thereof are useful for treatment and/or prevention of diabetes mellitus, impaired glucose tolerance, gestational diabetes mellitus, or the like. Some of the derivatives of the formula (I) are novel compounds.

  具有如下式(I)的α-取代羧酸衍生物，其中R1是烷基基团，R2是氢原子，R3是氢原子，A是═CH-基团，B是氧原子，W1是C1-C8烷基基团，W2是单键或C1-C8烷基基团，X是氢原子，Y是氧原子，Z1是烷氧基团，其药理学上可接受的盐、酯和酰胺对于治疗和/或预防糖尿病、糖耐量受损、妊娠期糖尿病等疾病是有用的。其中一些具有如上式(I)的衍生物是新化合物。
• 5-DEUTERO-2,4-THIAZOLIDINEDIONE AND 5-DEUTERO-2,4-OXAZOLIDINEDIONE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME
  申请人：DeuteRx, LLC

  公开号：US20140221369A1

  公开（公告）日：2014-08-07

  The invention provides 5-deuterium enriched 2,4-thiazolidinediones and 2,4-oxazolidinediones, such as 5-(4-((6-(4-amino-3,5-dimethylphenoxy)-1-methyl-1H-benzo[d]imidazol-2-yl)methoxy)benzyl)-5-deutero-thiazolidine-2,4-dione, deuterated derivatives thereof, stereoisomers thereof, pharmaceutically acceptable salt forms thereof, and methods of treating medical disorders, such as cancer, using the same.

  该发明提供了5-氘富集的2,4-噻唑烷二酮和2,4-噁唑烷二酮，例如5-（4-（（6-（4-氨基-3,5-二甲基苯氧基）-1-甲基-1H-苯并[d]咪唑-2-基）甲氧基）苄基）-5-氘噻唑烷-2,4-二酮，其氘代衍生物，其立体异构体，其药学上可接受的盐形式，以及使用它们治疗医学疾病（例如癌症）的方法。
• Medicinal compositions containing diuretic and insulin resistance-improving agent
  申请人：Takaoka Masaya

  公开号：US20050288339A1

  公开（公告）日：2005-12-29

  The present invention relates to a pharmaceutical composition comprising an insulin sensitizer and a diuretic which can prevent or treat side effects such as edema, cardiac enlargement, body fluid retension or hydrothorax caused by administration of an insulin sensitizer.

  本发明涉及一种药物组合物，包括胰岛素增敏剂和利尿剂，可以预防或治疗由于胰岛素增敏剂的使用引起的水肿、心脏肥大、体液潴留或胸水等副作用。
• SUBSTITUTED FUSED HETEROCYCLIC COMPOUNDS
  申请人：Sankyo Company Limited

  公开号：EP1022272A1

  公开（公告）日：2000-07-26

  Described is a substituted fused heterocyclic compound which is represented by the following formula: [wherein R1 represents a group of the following formula: (in which R4: a substituted phenyl or a pyridyl which may have a substituent, R5: a hydrogen atom or the like, R6: a hydrogen atom, a C1-6 alkyl group or the like, D: an oxygen or sulfur atom, E: a CH group or a nitrogen atom, R2: a hydrogen atom or the like, R3: a 2,4-dioxothiazolidin-5-ylmethyl group or the like; A: a C1-6 alkylene group, and B: an oxygen or sulfur atom] or a pharmacologically acceptable salt thereof; and has excellent insulin-resistance improving action, lipid-peroxide-production inhibitory action, 5-lipoxygenase inhibitory action and the like.

  所述的是一种取代的融合杂环化合物，由下式表示： [其中 R1 代表下式的基团： (其中 R4：可具有取代基的取代苯基或吡啶基，R5：氢原子或类似物，R6：氢原子、C1-6 烷基或类似物，D：氧原子或硫原子，E：CH 基团或氮原子，R2：氢原子或类似物，R3：2，4-二氧代噻唑烷-5-基甲基或类似基团；A：C1-6 烷基；B：氧原子或硫原子]或其药理上可接受的盐；并具有优异的改善胰岛素抵抗作用、抑制脂质过氧化物生成作用、5-脂氧化酶抑制作用等。