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1-[(3S,4R)-3-([1,1′-联苯基]-4-基甲基)-3,4-二氢-4-羟基-2H-1-苯并吡喃-7-基]-环戊烷羧酸 | 158081-99-3

中文名称
1-[(3S,4R)-3-([1,1′-联苯基]-4-基甲基)-3,4-二氢-4-羟基-2H-1-苯并吡喃-7-基]-环戊烷羧酸
中文别名
(+)-1-(3S,4R)-[3-(4-苯基苄基)-4-羟基色烷-7-基]环戊烷羧酸
英文名称
1-(3-(4-Phenylbenzyl)-4-hydroxychroman-7-yl)cyclopentane-1-carboxylic acid
英文别名
1-[(3S,4R)-4-hydroxy-3-[(4-phenylphenyl)methyl]-3,4-dihydro-2H-chromen-7-yl]cyclopentane-1-carboxylic acid
1-[(3S,4R)-3-([1,1′-联苯基]-4-基甲基)-3,4-二氢-4-羟基-2H-1-苯并吡喃-7-基]-环戊烷羧酸化学式
CAS
158081-99-3
化学式
C28H28O4
mdl
——
分子量
428.5
InChiKey
KMNLXCBYBKHKSK-BKMJKUGQSA-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):
    5.5
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • BIARYL SUBSTITUTED HETEROCYCLE INHIBITORS OF LTA4H FOR TREATING INFLAMMATION
    申请人:Sandanayaka Vincent
    公开号:US20070066820A1
    公开(公告)日:2007-03-22
    The present invention relates to a chemical genus of biaryl substituted heterocycle inhibitors of LTA4H (leukotriene A4 hydrolase) useful for the treatment and prevention and prophylaxis of inflammatory diseases and disorders. The compounds have general formula Ψ: An example is
    这项发明涉及一种化学类别的双芳基取代杂环抑制剂,用于治疗、预防和预防炎症性疾病和紊乱。这些化合物具有一般公式Ψ:一个例子是
  • Novel Methods for Bone Treatment by Modulating an Arachidonic Acid Metabolic or Signaling Pathway
    申请人:O'Connor James Patrick
    公开号:US20110105959A1
    公开(公告)日:2011-05-05
    Methods for promoting osteogenesis to accelerate or enhance bone fracture healing, treat bone defects, and enhance bone formation are disclosed. The methods rely on in vivo or ex vivo modulation of an arachidonic acid metabolic or signaling pathway in general, and, in particular, utilize 5-lipoxygenase inhibitors, leukotriene A4 hydrolase inhibitors, and/or leukotriene B4 receptor antagonists. These molecules can be delivered alone or in combination with one or more agents that inhibit bone resorption, regulate calcium resorption from bone, enhance bone accumulation, enhance bone formation, induce bone formation, impair growth of microorganisms, reduce inflammation, and/or reduce pain.
    公开了促进成骨作用以加速或增强骨折愈合、治疗骨缺陷和增强骨形成的方法。这些方法依赖于体内或体外调节花生四烯酸代谢或信号通路的总体,特别是利用5-脂氧合酶抑制剂白三烯A4解酶抑制剂和/或白三烯B4受体拮抗剂。这些分子可以单独或与一个或多个抑制骨吸收、调节从骨中吸收、增强骨积累、增强骨形成、诱导骨形成、抑制微生物生长、减少炎症和/或减轻疼痛的剂量联合使用。
  • Preventive or therapeutic agent for age-related macular degeneration
    申请人:JUNTENDO EDUCATIONAL FOUNDATION
    公开号:US10849954B2
    公开(公告)日:2020-12-01
    To provide a new preventive or therapeutic agent for age-related macular degeneration. The present invention relates to a preventive or therapeutic agent for age-related macular degeneration containing a BLT1 antagonist or a LTB4 biosynthesis inhibitor as an active ingredient. The administration form of the preventive or therapeutic agent for age-related macular degeneration of the present invention includes eye drops, injections, oral agents (tablets, granules, dispersions, capsules), ointments, and creams. The form of these pharmaceutical compositions can be formulated by combining with a pharmaceutically acceptable carrier.
    为老年性黄斑变性提供一种新的预防或治疗剂。 本发明涉及一种老年性黄斑变性的预防或治疗剂,其活性成分含有 BLT1 拮抗剂或 LTB4 生物合成抑制剂。本发明的老年性黄斑变性预防剂或治疗剂的给药形式包括滴眼剂、注射剂、口服剂(片剂、颗粒剂、分散剂、胶囊剂)、软膏和霜剂。这些药物组合物的形式可以通过与药学上可接受的载体结合来配制。
  • PREVENTIVE OR THERAPEUTIC AGENT FOR AGE-RELATED MACULAR DEGENERATION
    申请人:JUNTENDO EDUCATIONAL FOUNDATION
    公开号:US20170333516A1
    公开(公告)日:2017-11-23
    To provide a new preventive or therapeutic agent for age-related macular degeneration. The present invention relates to a preventive or therapeutic agent for age-related macular degeneration containing a BLT1 antagonist or a LTB 4 biosynthesis inhibitor as an active ingredient. The administration form of the preventive or therapeutic agent for age-related macular degeneration of the present invention includes eye drops, injections, oral agents (tablets, granules, dispersions, capsules), ointments, and creams. The form of these pharmaceutical compositions can be formulated by combining with a pharmaceutically acceptable carrier.
  • US7402684B2
    申请人:——
    公开号:US7402684B2
    公开(公告)日:2008-07-22
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同类化合物

麦冬高异黄酮A 麦冬二氢高异黄酮A 顺式-3,4-二氢-3-(苯基甲基)-2H-1-苯并吡喃-4-醇 表苏木醇 苏木酮A 苏木酚 甲磺酸,三氟-,3,4-二氢-4-羰基-3-(苯基亚甲基)-2H-1-苯并吡喃-7-基酯 甲基麦冬黄酮B 甲基麦冬黄烷酮B SB743921抑制剂 Isobonducellin; (3Z)-2,3-二氢-7-羟基-3-[(4-甲氧基苯基)亚甲基]-4H-1-苯并吡喃-4-酮 9H-占吨-1-羧酸,5-乙酰基-7-[(5-羧基-6,7-二羟基-4-羰基-2H-1-苯并吡喃-3(4H)-亚基)羟甲基]-2,3-二羟基-6-甲基-9-羰基- 8-醛基麦冬高黄酮B 7,3',4'-三羟基-3-苄基-2H-苯并吡喃 4-O-甲基表苏木酚 4-O-甲基蘇木黃素 4'-Demethyl-3,9-dihydroeucomin; 5,7-二羟基-3-(4-羟基苄基)色满-4-酮 3¢-O-甲基苏木醇 3-苯甲酰基-6-硝基-2-苯基-4H-1-苯并吡喃 3-苯甲酰-色酮 3-苄基-4H-1-苯并吡喃-4-酮 3-苄基-2H-色烯 3-p-茴香酰刺槐黄素 3-[1-(3-羟基-4-甲氧基苯基)甲基]-6-氯色满-4-酮 3-[(4-羟基苯基)甲基]-2,3-二氢色烯-4-酮 3-(4-羟基苄基)-4H-色烯-4-酮 3-(1,3-苯并二氧戊环-5-基甲基)-5-羟基-7-甲氧基-8-甲基-4-氧代苯并吡喃-6-甲醛 3,4-二氢-4-羟基-3-(苯基甲基)- 2H-1-苯并吡喃-2-酮 3,4-二氢-3-苄基-6-氯甲基香豆素 3'-去氧-4-甲氧基苏木醇 3'-去氧-4-O-甲基表苏木酚 2-甲基-3-(4-硝基苯甲酰基)色酮 2,3-二氢-7-羟基-3-[(4-甲氧基苯基)甲基]-4H-1-苯并吡喃-4-酮 2,3-二氢-5,8-二羟基-3-[(4-羟基苯基)甲基]-7-甲氧基-4H-1-苯并吡喃-4-酮 2,3-二氢-5,7-二羟基-3-[(3-羟基-4-甲氧基苯基)甲基]-4H-1-苯并吡喃-4-酮 1-[(3S,4R)-3-([1,1′-联苯基]-4-基甲基)-3,4-二氢-4-羟基-2H-1-苯并吡喃-7-基]-环戊烷羧酸 (E)-7-羟基-8-甲氧基-3-(4-甲氧基苯亚甲基)色满-4-酮 (6,8-二溴-2-吗啉-4-基-2H-色烯-3-基)(苯基)甲酮 (3E)-8-羟基-7-甲氧基-3-[(4-甲氧基苯基)亚甲基]色满-4-酮 (3E)-7,8-二羟基-3-[(4-甲氧基苯基)亚甲基]色满-4-酮 (3E)-3-[(3,4-二甲氧基苯基)亚甲基]-6-甲氧基色满-4-酮 (3E)-3-(3,4-二甲氧苯亚甲基)-2,3-二氢-4H-色烯-4-酮 Tri-O-acetyl-3,9-dihydro-autumnalin 4--3-(p-chlorobenzyl)chroman (S)-3-((R)-hydroxy(naphthalen-1-yl)methyl)chroman-4-one 3-benzoyl-chroman-4-one 8-methoxy-3-(2-oxo-2-o-tolyl-ethyl)-chroman-4-one 3-(2-Hydroxy-benzyl)-7-methyl-chroman-4-one 8-methoxy-3-(2-(3-methoxy-2-(prop-2-yn-1-yloxy)phenyl)-2-oxoethyl)chroman-4-one Isoponolid-hexamethylether