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1-methoxy-3-methoxy carbonyl-5,10-dioxo-5,10-dihydro-1H-naphtho-[2,3-c]-pyran | 169322-70-7

中文名称
——
中文别名
——
英文名称
1-methoxy-3-methoxy carbonyl-5,10-dioxo-5,10-dihydro-1H-naphtho-[2,3-c]-pyran
英文别名
methyl 1-methoxy-5,10-dioxo-1H-benzo[g]isochromene-3-carboxylate
1-methoxy-3-methoxy carbonyl-5,10-dioxo-5,10-dihydro-1H-naphtho-[2,3-c]-pyran化学式
CAS
169322-70-7
化学式
C16H12O6
mdl
——
分子量
300.268
InChiKey
QPKKYFJSLSZICG-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):
    1.6
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    78.9
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-methoxy-3-methoxy carbonyl-5,10-dioxo-5,10-dihydro-1H-naphtho-[2,3-c]-pyran三乙基硅烷三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 生成 3-methoxy carbonyl-5,10-dioxo-5,10-dihydro-1H-naphtho-[2,3-c]-pyran
    参考文献:
    名称:
    Novel 1,3-disubstituted-5,10-dihydro-5,10-dioxo-1H-mbenzo[g]isochromene-3-carboxamides as potent antitumor agents
    摘要:
    Novel antitumor 5,10-dihydro-5,10-dioxo-1H-benzo[g]isochromene-3-carboxamides were discovered. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(98)00274-1
  • 作为产物:
    描述:
    参考文献:
    名称:
    Dehydrogenation by air: Preparation of 1,3-disubstituted-5,1-dioxo-5,10-dihydro-1H-benzo[g] isochromene scaffold
    摘要:
    Naphthaquinopyrans 5a-d, 10 and 12 have been converted to benzoisochromene IIb via base-promoted air oxidation. A mechanism is proposed to account for the observed results. Use of peroxide scavenger was found necessary for consistent yields. IIb proved to be a versatile scaffold for diversity expansion. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)00287-1
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文献信息

  • Antineoplastic heteronapthoquinones
    申请人:Biochem Pharma Inc.
    公开号:US05736523A1
    公开(公告)日:1998-04-07
    This invention relates to a naphthoquinone derivatives, to processes and to intermediates for preparing these derivatives, to pharmaceutical composition and to the use of these derivatives as antitumor agents in mammals.
    这项发明涉及萘醌衍生物,涉及制备这些衍生物的过程和中间体,涉及制药组合物以及将这些衍生物作为抗肿瘤药物在哺乳动物中使用的方法。
  • Processes antineoplastic heteronaphthoquinones
    申请人:BioChem Pharma Inc.
    公开号:US05606037A1
    公开(公告)日:1997-02-25
    This invention relates to a naphthoquinone derivatives, to processes and to intermediates for preparing these derivatives, to pharmaceutical composition and to the use of these derivatives as antitumor agents in mammals.
    这项发明涉及萘醌衍生物,涉及制备这些衍生物的过程和中间体,涉及制药组合物以及将这些衍生物作为抗肿瘤药物在哺乳动物中使用的方法。
  • US5606037A
    申请人:——
    公开号:US5606037A
    公开(公告)日:1997-02-25
  • US5736523A
    申请人:——
    公开号:US5736523A
    公开(公告)日:1998-04-07
  • [EN] ANTINEOPLASTIC HETERONAPHTHOQUINONES<br/>[FR] HETERONAPHTOQUINONES ANTINEOPLASIQUES
    申请人:BIOCHEM PHARMA INC.
    公开号:WO1995012588A1
    公开(公告)日:1995-05-11
    (EN) Tricyclic heteronaphthoquinone derivatives, that have antineoplastic activity, are disclosed, together with processes for their synthesis. Some of these antineoplastic compounds have a saccharide moiety. Some members of this structurally distinct group exhibit activity against multiple drug resistant cancer cells.(FR) La présente invention concerne d'une part des dérivés tricycliques d'hétéronaphtoquinone à activité antinéoplasique et d'autre part les procédés de synthèse correspondants. Certains de ces composés antinéoplasiques comportent une fraction saccharide. Certains membres de ce groupe structurellement distinct font preuve d'une activité contre les cellules cancéreuses résistant à plusieurs médicaments.
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同类化合物

黄麦格霉素 镰刀菌素甲醚 芦替菌素 脱氢胆碱 红葱醌 紫黄素 灰色菌素B 异红葱乙素 富仑菌素 B 乳醌霉素A 七尾霉素C 七尾霉素 O-乙基镰红菌素 N-(乙酰氧基)-N-((4-甲基苯基)甲氧基)苯酰胺 N-(4,5-二氢-1,3-噻唑-2-基)-2,4-二甲氧基苯酰胺 9-羟基-7-甲氧基-3-甲基-1H-苯并[g]异苯并吡喃-5,10-二酮 7,9-二羟基-3-甲基-1H-苯并[g]异苯并吡喃-5,10-二酮 3-羟基-3,4-二氢-1H-苯并[g]异苯并吡喃-5,10-二酮 3-溴噻吩 3,9-二羟基-7-甲氧基-3-甲基-1,4-二氢苯并[g]异苯并吡喃-5,10-二酮 3,7,9-三羟基-3-甲基-1,4-二氢苯并[g]异苯并吡喃-5,10-二酮 3,4-二氢-3-羟基-7,9-二甲氧基-3-甲基-1H-萘并[2,3-c]吡喃-5,10-二酮 2-甲基溴丁烷 2-[((1S,3R)-9-hydroxy-1-methyl-5,10-dioxo-3,4-dihydro-1H-benzo[g]isochromen-3-yl]acetate甲基] 1H-萘并[2,3-c]吡喃-6,9-二酮,3,4-二氢-8,10-二羟基-7-甲氧基-1,3-二甲基-,(1R,3S)- 1H-萘并[2,3-c]吡喃-6,9-二酮,3,4-二氢-5,10-二羟基-7-甲氧基-1,3-二甲基-,(1R,3S)- 1H-氮杂卓,2-[(4-乙氧苯基)甲基]六氢- 10-羟基-8-[(2R,4S,5R)-5-羟基-4-(羟基甲基)-1,3-二恶烷-2-基]-3-甲基-7-(2-氧代丙基)-1-丙基-1H-苯并[g]异苯并吡喃-6,9-二酮 1,5,10-三羟基-7-甲氧基-3-甲基-1H-苯并[g]异苯并吡喃-6,9-二酮 (5R,3aR,11bR)-4'alpha-乙酰氧基-3',3a,4',5',6',11b-六氢-3'alpha,7-二羟基-6'beta-甲基螺[5H-呋喃并[3,2-b]萘并[2,3-d]吡喃-5,2'-[2H]吡喃]-2,6,11(3H)-三酮 (3aR-(3aalpha,5alpha,11balpha))-3,3a,5,11b-四氢-8-羟基-7-甲氧基-5-甲基-2H-呋喃并(3,2-b)萘并(2,3-d)吡喃-2,6,11-三酮 cis-3,4-dihydro-4-hydroxy-3-methyl-1H-naphtho<2,3-c>pyran-5,10-dione 10-hydroxy-7-methoxy-3-methylbenzo[g]isochromene-1,6,9-trione (1S,3R,4R)-3,4-dihydro-4,7,9-trihydroxy-1,3-dimethylnaphtho[2,3-c]pyran-5,10-quinone (1S,3R,4S)-3,4-dihydro-4,7,9-trihydroxy-1,3-dimethylnaphtho[2,3-c]pyran-5,10-quinone (1R,3S,4R)-3,4-dihydro-4,7,9-trihydroxy-1,3-dimethylnaphtho[2,3-c]pyran-5,10-quinone (1R,3S,4S)-3,4-dihydro-4,7,9-trihydroxy-1,3-dimethylnaphtho[2,3-c]pyran-5,10-quinone 2,4-dihydro-1-(hydroxymethyl)-1H-naphtho<2,3-c>pyran-3,5,10-trione (+/-)-3,4-dihydro-1-hydroxy-7,9-dimethoxy-1-methyl-3-(1-propyl)-1H-naphtho<2,3-c>pyran-5,10-quinone fusarubin 8-O-methylfusarubin (1'R*,3'R*)-methyl [1'-hydroxy-5',10'-dioxo-3',4',5',10'-tetrahydro-1'H-naphtho[2,3-c]pyran-3'-yl]acetate 3-methyl-1H-naphtho<2,3-c>pyran-5,10-dione Bromomethyl (5,10-dioxo-5,10-dihydronaphtho[2,3-C]pyran-3-yl) Ketone (3aR,5S,11bR)-5-Methyl-3,3a,5,11b-tetrahydro-1,4-dioxa-cyclopenta[a]anthracene-2,6,11-trione 5-epi-frenolicin B (3aS,5S,11bS)-7-hydroxy-5-propyl-3,3a,5,11b-tetrahydro-2H-benzo[g]thro[3,2-c]isochromene-2,6,11-trione (1R,3R)-3-((4-benzyl-1H-1,2,3-triazol-1-yl)methyl)-9-methoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromene-5,10-dione (1R,3R)-3-((4-(2-hydroxyphenyl)-1H-1,2,3-triazol-1-yl)methyl)-9-methoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromene-5,10-dione (1R,3R)-3-((4-hexyl-1H-1,2,3-triazol-1-yl)methyl)-9-methoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromene-5,10-dione