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7-Fluoro-3-(4-methoxy-phenyl)-1H-isothiochromen-4-ol

中文名称
——
中文别名
——
英文名称
7-Fluoro-3-(4-methoxy-phenyl)-1H-isothiochromen-4-ol
英文别名
7-fluoro-3-(4-methoxyphenyl)-1H-isothiochromen-4-ol
7-Fluoro-3-(4-methoxy-phenyl)-1H-isothiochromen-4-ol化学式
CAS
——
化学式
C16H13FO2S
mdl
——
分子量
288.342
InChiKey
NADOBIHJAGRWSV-UHFFFAOYSA-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):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    54.8
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Tricyclic compounds and uses thereof
    申请人:——
    公开号:US20020077333A1
    公开(公告)日:2002-06-20
    Substituted isoquinolines, isochromanones and isothiochromanones that inhibit the pro-inflammatory cytokines tumor necrosis factor-alpha (TNF-alpha) and/or interleukin-6 (IL-6) and/or the enzyme cyclooxygenase-2 (COX-2) and/or interleukin-10 (IL-10). Compositions containing such compounds and methods of using such compounds for treatment and/or prevention of inflammation, inflammatory diseases, immunologic diseases and other diseases mediated by TNF-alpha, IL-6, COX-2 and/or IL-10 are also disclosed.
    抑制促炎细胞因子肿瘤坏死因子-α(TNF-α)和/或白细胞介素-6(IL-6)和/或环氧合酶-2(COX-2)和/或白细胞介素-10(IL-10)的取代异喹啉酮、异色酮和异硫色酮。还公开了含有此类化合物的组合物和使用此类化合物治疗和/或预防炎症、炎症性疾病、免疫性疾病和 TNF-α、IL-6、COX-2 和/或 IL-10 介导的其他疾病的方法。
  • TRICYCLIC COMPOUNDS AND USES THEREOF
    申请人:Calyx Therapeutics, Inc.
    公开号:EP1324994A2
    公开(公告)日:2003-07-09
  • EP1324994A4
    申请人:——
    公开号:EP1324994A4
    公开(公告)日:2004-06-16
  • [EN] TRICYCLIC COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSES TRICYCLIQUES ET LEURS UTILISATIONS
    申请人:CALYX THERAPEUTICS INC
    公开号:WO2002030888A2
    公开(公告)日:2002-04-18
    Substituted isoquinolines, isochromanones and isothiochromanones that inhibit the pro-inflammatory cytokines tumor necrosis factor-alpha (TNF-alpha) and/or interleukin-6 (IL-6) and/or the enzyme cyclooxygenase-2 (COX-2) and/or interleukin-10 (IL-10). Compositions containing such compounds and methods of using such compounds for treatment and/or prevention of inflammation, inflammatory diseases, immunologic diseases and other diseases mediated by TNF-alpha, IL-6, COX-2 and/or IL-10 are also disclosed.
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同类化合物

2-溴乙酰氧基黄体酮 3-(4-propylphenyl)-1H-isothiochromene 3-(4-pentylphenyl)-1H-isothiochromene 1-(3,5-di-tert-butyl-4-hydroxyphenyl)-3-(3,4-dimethoxyphenyl)-6,7-dimethoxy-1,2-dihydro-2-thianaphthalene 2-oxide 1H-3-bromo-4-benzylthiobenzothiopyran 1-Phenyl-2-benzothiopyran-2-ium perchlorate 7-Methoxy-3-phenyl-2-benzothiopyran-2-ium perchlorate 1-(4-Chlorophenyl)-2-methyl-1H-2-benzothiopyran-2-ium perchlorate 1,2-Diphenyl-2-thiochromenium Naphtho[2,1-c]thiopyran-3-ium perchlorate Isothiochromeno[4,3-b]indol-11-ium;perchlorate (Z)-1-benzylidene-6-methoxy-3-(trifluoromethyl)-1H-isothiochromene 8,10-Dithiahexacyclo[10.6.2.13,6.02,7.09,19.016,20]henicosa-9(19),12,14,16(20),17-pentaen-11-one (Z)-1-benzylidene-7-fluoro-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-benzylidene-7-methyl-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-(4-methoxybenzylidene)-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-(4-methylbenzylidene)-3-(trifluoromethyl)-1H-isothiochromene 4-(4-chlorophenyl)-6-methoxy-1H-2-benzothiopyran-1-thione 4-(4-chlorophenyl)-1H-2-benzothiopyran-1-thione 7-Methoxy-3-phenyl-2-thio-3-chromen 1-(p-Chlorphenyl)-2-thio-3-chromen 1-Phenyl-2-thio-3-chromen 1,3-Diphenyl-7-methoxy-2-thio-3-chromen 6-methoxy-4-phenyl-1H-2-benzothiopyran-1-thione 6-methoxy-4-(4-methoxyphenyl)-1H-2-benzothiopyran-1-thione 4-phenyl-1H-2-benzothiopyran-1-thione 3-(Azepane-1-carbonyl)isothiochromen-1-one 4-phenyl-1H-2-benzothiopyran 2-thianaphthylium perchlorate 4-methyl-1-oxo-1H-isothiochromene-3-carboxylic acid 3-benzoyl-2'-isopropenyl-2'-methylspiro<1H-2-benzothiopyran-1,1'-cyclopropane> 3-Phenyl-1,2-dithio-isocumarin 7,8-Dimethoxy-1-oxoisothiochromene-3-carbonyl chloride (Z)-1-benzylidene-3-(trifluoromethyl)-1H-isothiochromene 5-trifluoromethyl-1H-2-benzothiopyran-1-one Dimethyl 1-hydroxy-1-phenylisothiochromene-3,4-dicarboxylate 1-oxo-1H-isothiochromene-3-carboxylic acid (4-phenylthiazol-2-yl)amide 4-methyl-1H-benzo[h]isothiochromene 2,2-dioxide 1-formylmethylene-3-phenyl-2-benzothiopyran 4-(4-methylphenyl)-1H-2-benzothiopyran-1-thione 1,2-bis(1H-isothiochromen-3-yl)ethane benzo[c]thiopyran S,S-dioxide 3-Methoxy-1,2-dithio-isocumarin 3-iodo-4-(naphthalen-1-ylmethylsulfanyl)-1H-benzo[h]isothiochromene 1H-3-iodo-4-(4-methylbenzylthio)-6-methylbenzothiopyran 7-chloro-1-oxo-1H-isothiochromene-3-carboxylic acid 7-bromo-1-oxo-1H-isothiochromene-3-carboxylic acid 3-phenyl-1H-isothiochromen-1-one 3-(p-tolyl)-1H-isothiochromen-1-one 3-(4-chlorophenyl)-1H-isothiochromen-1-one