美托碘铵 | 2424-71-7

• 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: 美托碘铵
• 中文别名: 美托兴碘铵
• 英文名称: Metocinium iodide
• 英文别名: 2-(2-hydroxy-2,2-diphenylacetyl)oxyethyl-trimethylazanium;iodide
• CAS: 2424-71-7
• 化学式: C19H24INO3
• 分子量: 441.3
• InChiKey: MGEPZVLQTPNDCU-UHFFFAOYSA-M

物化性质

• 熔点：
  195 °C

计算性质

• 辛醇/水分配系数(LogP)：
  -0.82
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  4

文献信息

• Diagnostic/therapeutic agents
  申请人：Klaveness Jo

  公开号：US20050002865A1

  公开（公告）日：2005-01-06

  Targetable diagnostic and/or therapeutically active agents, e.g. ultrasound contrast agents, comprising a suspension in an aqueous carrier liquid of a reporter comprising gas-containing or gas-generating material, said agent being capable of forming at least two types of binding pairs with a target.

  可定位的诊断和/或治疗活性剂，例如超声对比剂，包括悬浮在水载体液中的报告物，该报告物包含含气体或生成气体的材料，该剂能够与目标形成至少两种结合对。
• Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them
  申请人：WARNER-LAMBERT COMPANY

  公开号：EP0245825A1

  公开（公告）日：1987-11-19

  The present invention is 3,5-substituted, isoxazoles, pyrazoles, isothiazoles, and analogs thereof having 5- ipoxygenase or cyclooxygenase inhibiting activity or as a sunscreen.

  本发明是 3,5-取代的异噁唑、吡唑、异噻唑及其类似物，具有 5- ipoxygenase 或环氧合酶抑制活性或可用作防晒剂。
• Benzofuran derivatives
  申请人：MERCK FROSST CANADA INC.

  公开号：EP0338782A1

  公开（公告）日：1989-10-25

  Benzofuran derivatives are useful as inhibitors of mammalian leuktoriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation. The compounds are also useful as analgesics and as cytoprotective agents, and for these uses are made into pharmaceutical compositions. The compounds of the invention have the formula wherein: each R1 is independently hydrogen or C1 to C6 alkyl; R2 is hydrogen, C1 to C8 alkyl, -(CH2)n-het-Y, -(CH2)n-Q or - CH- Q, CH3 where Q is R3 is hydroxyl, , OCOCH2CH2COOH, OSO3H, or OPO3H2; each R4 is independently C1 to C6 alkyl; each R5 is independently H, C1 to C6 alkyl, or both R5s join to form a 5- or 6-membered ring with the N to which they are attached; Het is a heterocyclic group selected from pyridine, pyrazine, pyrimidine, oxazole, pyrazole, oxadiazole, tetrazole, quinoline, thiophene, furan, pyrrole, thiazole, thiadiazole, or imidazole; X is 0, S, SO, SO2; Y, Y1, Y2, Y3, Y4 and Z are each independently H, halogen, OH. C1 to C6 alkyl, C2 to C6 alkenyl, C1-6hydroxyalkyl, -COOR1, -COR1, nitro, carboxy (C1-6alkyl), C1 to C6 alkoxy, C1 to C6 alkylthio, -CH2SR1, OCH2CO2R1, and each n is independently 0 to 10; with the provisos that: (a) not all of R1, R2, Y, Y1, Y2, Y3, Y4, and Z are simultaneously H; (b) when up to 2 of R1, R2, Y, Y1, and Z are C1 to C2 alkyl, and the others of R1, R2, Y, Y1, and Z are H, then R3 is not OH; and (c) when n in is O and one of R3, Y, Y1 or Z is OH, then Ri is not H or Ci to C2 alkyl; or are acid-addition salts thereof.

  苯并呋喃衍生物可作为哺乳动物白细胞介素生物合成的抑制剂。因此，这些化合物是治疗过敏症、哮喘、心血管疾病和炎症的有效药物。这些化合物还可用作镇痛剂和细胞保护剂，并可用于制成药物组合物。本发明的化合物具有如下式子 其中 每个 R1 独立地为氢或 C1 至 C6 烷基； R2 是氢、C1 至 C8 烷基、-(CH2)n-het-Y、-( )n-Q 或-CH- Q, CH3 其中 Q 是 R3 是羟基、 OCO COOH、OSO3H 或 OPO3H2；每个 R4 独立地是 C1 至 C6 烷基； 每个 R5 独立地为 H、C1-C6 烷基，或两个 R5 与所连接的 N 连接形成 5 或 6 元环； Het 是杂环基团，选自吡啶、吡嗪、嘧啶、噁唑、吡唑、噁二唑、四唑、喹啉、噻吩、呋喃、吡咯、噻唑、噻二唑或咪唑； X 是 0、S、SO、SO2； Y、Y1、Y2、Y3、Y4 和 Z 各自独立地是 H、卤素、OH C1-C6烷基、C2-C6烯基、C1-6羟基烷基、-COOR1、-COR1、硝基、羧基（C1-6烷基）、C1-C6烷氧基、C1-C6烷硫基、- SR1、O CO2R1、 且每个 n 独立地为 0 至 10；但有以下条件： (a) 并非所有 R1、R2、Y、Y1、Y2、Y3、Y4 和 Z 同时都是 H； (b) 当 R1、R2、Y、Y1 和 Z 中最多有 2 个是 C1 至 C2 烷基，而 R1、R2、Y、Y1 和 Z 中的其它是 H 时，则 R3 不是 OH；以及 (c) 当 n 为 O 且 R3、Y、Y1 或 Z 中的一个为 OH 时，则 Ri 不是 H 或 Ci 至 C2 烷基；或为其酸加成盐。
• 3,5-ditertiarybutyl-4-hydroxyphenyl, 1,3,4-thiadiazoles and oxadiazoles linked by carbon, oxygen, and sulfur residues
  申请人：WARNER-LAMBERT COMPANY

  公开号：EP0449211A1

  公开（公告）日：1991-10-02

  The novel 3,5-ditertiarybutyl-4-hydroxyphenyl-thio-1,3,4-thiadiazoles and oxadiazoles and 3,5-ditertiarybutyl-4-hydroxyphenylmethanone-1,3,4-thiadiazoles and oxadiazoles of formula I and related compounds of the present invention are antiinflammatory agents having activity as inhibitors of 5- lipoxygenase, cyclooxygenase or both.

  式 I 的新型 3,5-二叔丁基-4-羟基苯硫基-1,3,4-噻二唑和噁二唑、3,5-二叔丁基-4-羟基苯甲酮-1,3,4-噻二唑和噁二唑以及相关化合物是抗炎剂，具有 5-脂氧合酶或环氧合酶抑制剂的活性。 及本发明的相关化合物是抗炎剂，具有作为 5-脂氧合酶、环氧化酶或两者的抑制剂的活性。
• (Bicyclic-azaarylmethoxy)indoles as inhibitors of leukotriene biosynthesis
  申请人：MERCK FROSST CANADA INC.

  公开号：EP0535924A1

  公开（公告）日：1993-04-07

  Compounds having the formula I : are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating diarrhea, hypertension, angina, platelet aggregation, cerebral spasm, premature labor, spontaneous abortion, dysmenorrhea, and migraine.

  具有式 I ： 是白三烯生物合成的抑制剂。这些化合物可用作抗哮喘、抗过敏、抗炎和细胞保护剂。它们还可用于治疗腹泻、高血压、心绞痛、血小板聚集、脑痉挛、早产、自然流产、痛经和偏头痛。