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(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol;(2R,3R)-3,5,7-trihydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-2,3-dihydrochromen-4-one

中文名称
——
中文别名
——
英文名称
(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol;(2R,3R)-3,5,7-trihydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-2,3-dihydrochromen-4-one
英文别名
——
(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentol;(2R,3R)-3,5,7-trihydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-2,3-dihydrochromen-4-one化学式
CAS
——
化学式
C32H39NO15
mdl
——
分子量
677.6
InChiKey
XJCLWAHIAAEFAT-FUVGLPQDSA-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):
    -1.0
  • 重原子数:
    48
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    268
  • 氢给体数:
    11
  • 氢受体数:
    16

文献信息

  • CHOROIDAL NEOVASCULARIZATION SUPPRESSOR OR DRUSEN FORMATION SUPPRESSOR, AND METHOD FOR ASSESSING OR SCREENING FOR SAME
    申请人:Link Genomics, Inc.
    公开号:EP3391883A1
    公开(公告)日:2018-10-24
    The existent therapeutic drugs for CNV are merely pharmaceuticals for a symptomatic therapy, and therapeutic drugs for radical cure are strongly demanded. Also, a therapeutic drug for Dry AMD does not exist, and therapeutic drugs for radical cure are strongly demanded. The present invention provides a prophylactic and/or therapeutic agent for choroidal neovascularization, containing a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient. Also, the present invention provides a drusen suppressor comprising a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient.
    现有的 CNV 治疗药物仅仅是对症治疗的药物,人们强烈需要根治性的治疗药物。同样,干性老年黄斑变性的治疗药物也不存在,人们对根治性治疗药物的需求非常强烈。本发明提供了一种脉络膜新生血管的预防和/或治疗药物,其活性成分含有一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。此外,本发明还提供了一种色素沉着抑制剂,其活性成分是一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。
  • CHOROIDAL NEOVASCULARIZATION SUPPRESSOR OR DRUSEN FORMATION SUPPRESSOR
    申请人:Link Genomics, Inc.
    公开号:EP3750540A1
    公开(公告)日:2020-12-16
    The existent therapeutic drugs for CNV are merely pharmaceuticals for a symptomatic therapy, and therapeutic drugs for radical cure are strongly demanded. Also, a therapeutic drug for Dry AMD does not exist, and therapeutic drugs for radical cure are strongly demanded. The present invention provides a prophylactic and/or therapeutic agent for choroidal neovascularization, containing a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient. Also, the present invention provides a drusen suppressor comprising a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient.
    现有的 CNV 治疗药物仅仅是对症治疗的药物,人们强烈需要根治性的治疗药物。同样,干性老年黄斑变性的治疗药物也不存在,人们对根治性治疗药物的需求非常强烈。本发明提供了一种脉络膜新生血管的预防和/或治疗药物,其活性成分含有一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。此外,本发明还提供了一种色素沉着抑制剂,其活性成分是一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。
  • Silybin injection and preparation method therefor
    申请人:TASLY PHARMACEUTICAL GROUP CO., LTD.
    公开号:US10314923B2
    公开(公告)日:2019-06-11
    A silybin injection contains silybin, sulfobutyl ether-β-cyclodextrin, an organic solvent for injection, a pH regulator, and may further contain a co-solvent, a lyophilization bulking agent, and water for injection.
    水飞蓟宾注射液含有水飞蓟宾、磺丁基醚-β-环糊精、注射用有机溶剂、pH 值调节剂,还可能含有助溶剂、冻干膨松剂和注射用
  • Choroidal neovascularization suppressor or drusen formation suppressor, and method for assessing or screening for same
    申请人:Link Genomics, Inc.
    公开号:US10761087B2
    公开(公告)日:2020-09-01
    The existent therapeutic drugs for CNV are merely pharmaceuticals for a symptomatic therapy, and therapeutic drugs for radical cure are strongly demanded. Also, a therapeutic drug for Dry AMD does not exist, and therapeutic drugs for radical cure are strongly demanded. The present invention provides a prophylactic and/or therapeutic agent for choroidal neovascularization, containing a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient. Also, the present invention provides a drusen suppressor comprising a compound having an activity of suppressing epithelial-mesenchymal transition in retinal pigment epithelial cells, as an active ingredient.
    现有的 CNV 治疗药物仅仅是对症治疗的药物,人们强烈需要根治性的治疗药物。同样,干性老年黄斑变性的治疗药物也不存在,人们对根治性治疗药物的需求非常强烈。本发明提供了一种脉络膜新生血管的预防和/或治疗药物,其活性成分含有一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。此外,本发明还提供了一种色素沉着抑制剂,其活性成分是一种具有抑制视网膜色素上皮细胞上皮-间质转化活性的化合物。
  • SILYBIN INJECTION AND PREPARATION METHOD THEREFOR
    申请人:Tasly Pharmaceutical Group Co., Ltd.
    公开号:EP3243512B1
    公开(公告)日:2021-09-15
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同类化合物

红景天灵 水飞蓟素B2 水飞蓟素A,B 水飞蓟宾磷脂酰胆碱(SPC) 水飞蓟宾 水飞蓟宾 水飞木质灵 次大风子素 异水飞蓟宾B 异水飞蓟宾 亚聚丙基二醇,甲苯二异氰酸酯,羟基丙基甲丙烯酰酸酯聚合物 4-[(2R)-5,7-二羟基-2-[(2R)-2-(4-羟基-3-甲氧基苯基)-3-[(4-羟基-4-氧代丁酰基)氧基甲基]-2,3-二氢-1,4-苯并二氧杂环己-7-基]-4-氧代色满-3-基]氧基-4-氧代丁酸 3,7-二羟基-2-(1,4-苯并二恶烷-6-基)色满-4-酮 3,7-二羟基-2-((2,3-二苯基)-1,4-苯并二恶烷-6-基)色满-4-酮 2,3-脱氢水飞蓟宾B 2,3-脱氢水飞蓟宾A Dehydrosilybinpentaacetat 2-[2-(3,4-dimethoxy-phenyl)-3-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxin-6-yl]-3,5,7-trimethoxy-chromen-4-one 2-[3-(3,4-dimethoxy-phenyl)-2-hydroxymethyl-2,3-dihydro-benzo[1,4]dioxin-6-yl]-3,5,7-trimethoxy-chromen-4-one Hydrocarpin-tetramethylether-acetat 2-[2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5-dihydroxy-7-dodecanoyloxy-4H-1-benzopyran-4-one 2-[2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5-dihydroxy-7-octanoyloxy-4H-1-benzopyran-4-one 3-Hydroxy-2-[2-hydroxy-5-(5-hydroxy-3,7-dimethoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-3-(4-hydroxy-3-methoxy-phenyl)-propionic acid ethyl ester Dehydrosilybin-tetramethylether 2-[2,3-dihydro-2-((cis-11-eicosenoyl)-oxymethyl)-3-(4-hydroxy-3-methoxyphenyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one 2-[2,3-dihydro-2-(dodecanoyloxymethyl)-3-(4-hydroxy-3-methoxyphenyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one N-(4-chlorophenyl)-2-[2-(3-{4-[(4-chlorophenylcarbamoyl)methoxy]-3-methoxyphenyl}-2-hydroxymethyl-2,3-dihydrobenzo[1,4]dioxin-6-yl)-3,5-dihydroxy-4-oxo-4H-chromen-7-yloxy]acetamide 2-[2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5-dihydroxy-7-(cis-11-eicosenoyl)-oxy-4H-1-benzopyran-4-one 2,3-Dehydrosilybin-tetramethylether-acetat 2-[2,3-dihydro-2-(hexadecanoyloxymethyl)-3-(4-hydroxy-3-methoxyphenyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one N-(4-methoxyphenyl)-2-[3,5-dihydroxy-2-(2-hydroxymethyl-3-{3-methoxy-4-[(4-methoxy-phenylcarbamoyl)methoxy]phenyl}-2,3-dihydro-benzo[1,4]dioxin-6-yl)-4-oxo-4H-chromen-7-yloxy]acetamide 2-[2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-yl]-2,3-dihydro-7-butanoyloxy-3,5-dihydroxy-4H-1-benzopyran-4-one bis((3-(4-hydroxy-3-methoxyphenyl)-6-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)-2,3-dihydrobenzo-[b][1,4]dioxin-2-yl)methyl) dodecanedioate N-p-tolyl-2-(3,5-dihydroxy-2-{2-hydroxymethyl-3-[3-methoxy-4-(p-tolylcarbamoylmethoxy)-phenyl]-2,3-dihydrobenzo-[1,4]dioxin-6-yl}-4-oxo-4H-chromen-7-yloxy)acetamide 3,5,20,23-silybin tetraacetate 8-amino-2-benzo[1,3]dioxol-5-yl-6-methoxy-chroman-4-one 3,5,7,20-tetra-O-acetylsilybin Disilybin N-(2,4-dichlorophenyl)-2-[2-(3-{4-[(2,4-dichlorophenylcarbamoyl)methoxy]-3-methoxyphenyl}-2-hydroxymethyl-2,3-dihydrobenzo[1,4]dioxin-6-yl)-3,5-dihydroxy-4-oxo-4H-chromen-7-yloxy]acetamide Hydnocarpin-tetraacetat 5,7,20-tri-O-benzylsilybin (-)-hydnocarpin 5,7,4'',9''-tetraacetate O7-brombutyl-O3',O4'-ethylidene luteolin 3,5,7,20-O-tetra-acetyl-23-O-methansulfonyl-silybin 2-bromoethyl 2-((2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-5-hydroxy-4-oxo-4H-chromen-7-yl)oxy)acetate 23-azide-silybin 3,5,7,20-O-tetra-acetyl-23-O-sulphate silybin 2-(2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(4-hydroxy-3-methoxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl)-3,5,7-trihydroxychroman-4-one