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4,9-dihydroxyperylene-3,10-quinone | 10190-97-3

中文名称
——
中文别名
——
英文名称
4,9-dihydroxyperylene-3,10-quinone
英文别名
4,9-Dihydroxy-3,10-perylenchinon;4,9-Dihydroperylen-3,10-chinon;4,9-dihydroxy-perylene-3,10-dione;4,9-Dihydroxy-perylen-3,10-dion;4,9-Dihydroxy-3,10-perylenedione;4,9-dihydroxyperylene-3,10-dione
4,9-dihydroxyperylene-3,10-quinone化学式
CAS
10190-97-3
化学式
C20H10O4
mdl
——
分子量
314.297
InChiKey
LLWVFANUCOSMDH-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):
    4.8
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

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:
    4,9-dihydroxyperylene-3,10-quinone盐酸 、 titanium(III) chloride 、 硝酸溶剂黄146 作用下, 生成 2,11-Diamino-4,9-dihydroxy-perylene-3,10-dione
    参考文献:
    名称:
    抗肿瘤药。134.新的与shiraiachrome-A-和钙磷蛋白-C有关的derivatives衍生物作为细胞毒和抗病毒剂以及蛋白激酶C的抑制剂。
    摘要:
    作为细胞毒原理,已经从中国竹真菌Shimia bambusicola的菌丝体中分离出Shiraiachrome-A和-B。合成了一系列与Shiraiachrome-A和-B以及Calphostin-C有关的新per衍生物(7-27),并对其细胞毒性,抗病毒活性和对蛋白激酶C的抑制活性进行了评估。结果表明11 12和12是有效的针对HCT-8,RPMI-7951和TE-671实体肿瘤细胞的细胞毒剂,而24和26显示出对HSV-1和HSV-2的强抗病毒活性。化合物10是蛋白激酶C的抑制剂。
    DOI:
    10.1021/jm00093a001
  • 作为产物:
    描述:
    5-羟基对萘醌三氯化铝 、 sodium chloride 作用下, 反应 3.0h, 生成 4,9-dihydroxyperylene-3,10-quinone
    参考文献:
    名称:
    抗肿瘤药。134.新的与shiraiachrome-A-和钙磷蛋白-C有关的derivatives衍生物作为细胞毒和抗病毒剂以及蛋白激酶C的抑制剂。
    摘要:
    作为细胞毒原理,已经从中国竹真菌Shimia bambusicola的菌丝体中分离出Shiraiachrome-A和-B。合成了一系列与Shiraiachrome-A和-B以及Calphostin-C有关的新per衍生物(7-27),并对其细胞毒性,抗病毒活性和对蛋白激酶C的抑制活性进行了评估。结果表明11 12和12是有效的针对HCT-8,RPMI-7951和TE-671实体肿瘤细胞的细胞毒剂,而24和26显示出对HSV-1和HSV-2的强抗病毒活性。化合物10是蛋白激酶C的抑制剂。
    DOI:
    10.1021/jm00093a001
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文献信息

  • Synthesis and Properties of BF<sub>2</sub> Complexes to Dihydroxydiones of Tetracene and Perylene: Novel Electron Acceptors Showing n-Type Semiconducting Behavior
    作者:Katsuhiko Ono、Hiroyuki Yamaguchi、Keijiro Taga、Katsuhiro Saito、Jun-ichi Nishida、Yoshiro Yamashita
    DOI:10.1021/ol802470k
    日期:2009.1.1
    BF2 complexes containing tetracene and perylene moieties were synthesized as new types of electron-deficient arene compounds. These compounds exhibit long wavelength absorption and high electron affinities, as revealed through spectral and electrochemical studies, due to their quadrupolar structures represented by resonance contributors. The BF2 complex containing tetracene exhibits an n-type semiconducting
    合成了含有并四苯和per部分的BF 2配合物,作为新型的缺电子芳烃化合物。这些化合物表现出长波吸收和高电子亲和力,这是通过光谱和电化学研究揭示出来的,这归因于它们的四极结构以共振贡献者为代表。含有并四苯的BF 2配合物表现出n型半导体行为。这些化合物是通过BF 2螯合功能化的新型电子受体。
  • Untersuchungen �ber Perylen und seine Derivate
    作者:Konrad Funke
    DOI:10.1007/bf01518467
    日期:1933.2
  • Colouring matters of the aphididœ. Part X. Preparation and properties of 4 : 9-dihydroxyperylene-3 : 10-quinone
    作者:A. Calderbank、A. W. Johnson、A. R. Todd
    DOI:10.1039/jr9540001285
    日期:——
  • Allport; Bu'Lock, Journal of the Chemical Society, 4090,4093
    作者:Allport、Bu'Lock
    DOI:——
    日期:——
  • US5095099A
    申请人:——
    公开号:US5095099A
    公开(公告)日:1992-03-10
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同类化合物

苝-3,10-二酮 竹红菌乙素 痂囊腔菌素A 格孢毒素II 格孢毒素I 抑制剂C 卡弗他丁A 4,9-二羟基-6,7-二(2-羟基丙基)-1,5,8,12-四甲氧基苝-3,10-二酮 1-[3,10-二羟基-12-[2-(4-羟基苯甲酰基)氧基丙基]-2,6,7,11-四甲氧基-4,9-二氧代二萘嵌苯-1-基]丙-2-基4-羟基苯甲酸酯 1-[3,10-二羟基-12-(2-羟基丙基)-2,6,7,11-四甲氧基-4,9-二氧代二萘嵌苯-1-基]丙-2-基苯甲酸酯 (1S,12aR,12bS)-1,2,12a,12b-四氢-1,4,9,12a-四羟基-3,10-苝二酮 Dimethyl 3,10-Dihydro-2,4,6,7,9,11-hexamethoxy-3,10-dioxo-1,12-perylenediacetate Elsinochrome A Alterlosin I 4,10-dihydroxy-5,9-dihydrodinaphtho<2,1-b:1',2'-d>furan-5,9-dione Stemphyltoxin I Acetic acid 6,7,12-triacetoxy-3,10-dihydroxy-4,9-dioxo-4,9-dihydro-perylen-1-yl ester 4,9-Dihydroxy-1,6,7,12-tetramethoxy-perylene-3,10-dione 1,3,4,6,8,15-Hexahydroxy-10,13-bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxymethyl)-dibenzo[a,o]perylene-7,16-dione 1,3,4,6,8,15-Hexahydroxy-10-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxymethyl)-13-methyl-dibenzo[a,o]perylene-7,16-dione Acetic acid 4,9,12-triacetoxy-3,10-dioxo-3,10-dihydro-perylen-1-yl ester Cercosporin, pure 2,11-dihydroxy-4,6,7,9-tetramethoxy-1,12-bis-n-propyl-3,10-perylenequinone 7,19-dihydroxy-5-(2-hydroxypropyl)-21-[(2R)-2-hydroxypropyl]-6,20-dimethoxy-12,14-dioxahexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1,3(8),4,6,10,15,18(23),19,21-nonaene-9,17-dione 2,11-Diamino-perylene-3,10-dione Stemphyltoxin III (3aS)-7,13-dihydroxy-1t,3c,8t,10c-tetramethyl-(3ar,10ac)-1,3,3a,8,10,10a-hexahydro-2,4,9,11-tetraoxa-dibenzo[bc,kl]coronene-6,14-dione [(2S)-1-[3,10-dihydroxy-12-[(2S)-2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxoperylen-1-yl]propan-2-yl] benzoate 2,4,6,7,9,11-hexamethoxy-1,12-bis-propyl-3,10-perylenequinone 6-[1-(9,17-Dihydroxy-5,10,16,21-tetramethoxy-13-methyl-7,19-dioxo-12-hexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1(15),2(11),3(8),4(22),5,9,12,16,18(23),20-decaenyl)ethylideneamino]hexane-1-sulfonic acid 1,2,5,6-tetrahydroxy-dibenzo[a,o]perylene-7,16-dione calphostin D Phleichrome calphostin A [6-acetyl-8-(3-acetyl-5,7-diacetyloxy-2-methyl-4-oxo-1H-naphthalen-1-yl)-4-acetyloxy-7-methyl-5-oxo-8H-naphthalen-2-yl] acetate (13S)-12-acetyl-9,13,17-trihydroxy-5,10,16,21-tetramethoxy-13-methylhexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaene-7,19-dione 4,9-Dihydroxy-1,5,6,7,8,12-hexamethylperylene-3,10-dione Carbonic acid, 2-(12-(2-(benzoyloxy)propyl)-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl)-1-methylethyl 4-hydroxyphenyl ester (-)-Phleichrome 1,3,4,6,8,15-Hexahydroxy-9,14-diisopropyl-10,13-dimethoxy-dibenzo[a,o]perylene-7,16-dione 1,6-dihydroxydibenzoperylene-7,16-dione 5-[1-(9,17-Dihydroxy-5,10,16,21-tetramethoxy-13-methyl-7,19-dioxo-12-hexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1(15),2(11),3(8),4(22),5,9,12,16,18(23),20-decaenyl)ethylideneamino]pentane-1-sulfonic acid 4-[1-(9,17-Dihydroxy-5,10,16,21-tetramethoxy-13-methyl-7,19-dioxo-12-hexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1(15),2(11),3(8),4(22),5,9,12,16,18(23),20-decaenyl)ethylideneamino]butane-1-sulfonic acid Cercosporin (12R,13S)-12-acetyl-9,16-dihydroxy-13-[(1S)-1-hydroxyethyl]-5,10,15,20-tetramethoxyhexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4(21),5,9,15,17(22),19-nonaene-7,18-dione 10,13-dimethyl-1,3,4,6-tetrahydroxy-helianthrone 12-Acetyl-16-(butylamino)-9,17-dihydroxy-5,10,21-trimethoxy-13-methylhexacyclo[13.8.0.02,11.03,8.04,22.018,23]tricosa-1(15),2(11),3(8),4(22),5,9,12,16,18(23),20-decaene-7,19-dione 5,7,11,13,16,18,22,24-Octahydroxy-6,12,17,23-tetramethyloctacyclo[13.11.1.12,10.03,8.04,25.019,27.021,26.014,28]octacosa-3,5,7,10,12,14(28),15(27),16,18,21,23,25-dodecaene-9,20-dione [(2R)-1-[3,10-dihydroxy-12-[(2S)-2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxoperylen-1-yl]propan-2-yl] benzoate [(2S)-1-[3,10-dihydroxy-12-[(2R)-2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxoperylen-1-yl]propan-2-yl] benzoate