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picrasidine O | 101219-63-0

中文名称
——
中文别名
——
英文名称
picrasidine O
英文别名
4-methoxy-6-methyl-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-4,7,9(16),10,12,14-hexaene-2,3-dione
picrasidine O化学式
CAS
101219-63-0
化学式
C16H12N2O3
mdl
——
分子量
280.283
InChiKey
HPAUUBGCMSMJQK-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):
    2.2
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    51.5
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    DL-色氨酸 反应 0.33h, 生成 picrasidine O
    参考文献:
    名称:
    Koike, Kazuo; Yoshino, Hiroshi; Nikaido, Tamotsu, Heterocycles, 1999, vol. 51, # 2, p. 315 - 323
    摘要:
    DOI:
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文献信息

  • Studies on the alkaloids from Picrasma quassioides Bennet. VI. Structures of picrasidines N, O, and Q.
    作者:TAICHI OHMOTO、KAZUO KOIKE
    DOI:10.1248/cpb.33.4901
    日期:——
    Three new alkaloids, picrasidines N (I), O (II), and Q (III), have been isolated from the root wood of Picrasma quassioides BENNET (Simaroubaceae). The structures were determined on the basis of spectral analysis and chemical evidence.
    从 Picrasma quassioides BENNET(樗树科)的根木中分离出了三种新生物碱,即苦木碱 N (I)、O (II) 和 Q (III)。根据光谱分析和化学证据确定了它们的结构。
  • Novel Nature-Inspired Anticancer and Antibacterial Motifs and Pharmaceutical Composition Thereof
    申请人:University of Sharjah
    公开号:US20210317121A1
    公开(公告)日:2021-10-14
    There is provided novel anticancer and antibacterial compounds, pharmaceutically acceptable salts thereof, and processes for their preparation. The compounds have anticancer activity, which results in the reduction of tumour cell proliferation, enhances cancers cells apoptosis and regulation of iron signalling. The compounds are also particularly active against various Gram-negative and Gram-positive multidrug-resistant bacteria, such as extended-spectrum beta-lactamase (ESBL) producing and colistin-resistant Escherichia coli , carbapenem-resistant E. coli , carbapenem-resistant Acinetobacter baumannii , and methicillin-resistant Staphylococcus aureus (MRSA) including those with reduced susceptibility to many control antibiotics.
  • Koike, Kazuo; Yoshino, Hiroshi; Nikaido, Tamotsu, Heterocycles, 1999, vol. 51, # 2, p. 315 - 323
    作者:Koike, Kazuo、Yoshino, Hiroshi、Nikaido, Tamotsu
    DOI:——
    日期:——
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同类化合物

长春考酯 长春曲尔 铁屎米酮N氧化物 铁屎米酮 苦木西碱Q 温可纳特 9-羟基铁屎米酮 9-甲氧基铁屎米酮N氧化物 9-甲氧基-6H-吲哚并[3,2,1-De][1,5]萘啶-6-酮 9,10-二甲氧基铁屎米酮 7,14-二苯基二吲哚并[3,2,1-去:3',2',1'-ij][1,5]萘啶-6,13-二酮 5-羟基-6-铁屎米酮 5-羟基-4-甲氧基铁屎米酮 5-甲氧基铁屎米酮 4,5-二甲氧基铁屎米酮 11-羟基-6H-吲哚并[3,2,1-de][1,5]萘啶-6-酮 11-甲基-20,21-二去甲埃那美宁 10-羟基-6H-吲哚并[3,2,1-de][1,5]萘啶-6-酮 1-羟基-6-铁屎米酮 1,2,3,3a,4,5-六氢铁屎米酮 1,2,3,3a,4,5-六氢-3-甲基-6H-吲哚并(3,2,1-de)(1,5)萘啶-6-酮单甲烷磺酸盐 1,2,3,3a,4,5-六氢-3-乙基-6H-吲哚并(3,2,1-de)(1,5)萘啶-6-酮 (3S,16S)-17alpha,21-环氧-14,15-二氢-14alpha-羟基-12-甲氧基埃那美宁-14-羧酸甲酯 4-[2-[[(15S,17R,19R)-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-yl]oxy]ethyl]morpholine (+/-)-deethyleburnamine (+/-)-16-epideethyleburnamine 3-butyl-4-methoxycanthin-5,6-dione 3-butyl-9-methoxycanthin-5,6-dione 4-methoxy-5-propoxycanthinone 4-methoxy-5-sec-butoxycanthinone 4-methoxy-5-butoxycanthinone 4-ethyl-3-methylcanthin-5,6-dione 10-bromo-4-methoxy-3-methylcanthin-5,6-dione 8,10-dibromo-3-methylcanthin-5,6-dione 4-methoxy-5-(2-bromoethoxy)canthinone 7,14-bis(5'-bromo-3'-dodecyl-[2,2'-bithiophen]-5-yl)diindolo[3,2,1-de:3',2',1'-ij][1,5]naphthyridine-6,13-dione 7,14-bis(5'-hexyl-[2,2'-bithiophen]-5-yl)diindolo[3,2,1-de:3',2',1'-ij][1,5]naphthyridine-6,13-dione 7,14-bis(3'-dodecyl-[2,2'-bithiophen]-5-yl)diindolo[3,2,1-de:3',2',1'-ij][1,5]naphthyridine-6,13-dione ethyl (2S,3aS,6S)-6-(3,3-dimethyl-2-oxobutyl)-2,3,3a,4,5,6-hexahydro-1H-indolo<3,2,1-de><1,5>naphthyridine-2-carboxylate ethyl (2S,3aS,6S)-6-(2-methyl-2-propenyl)-2,3,3a,4,5,6-hexahydro-1H-indolo<3,2,1-de><1,5>naphthyridine-2-carboxylate trans-11-methoxydeethyleburnamonine 3-benzyl-10-methoxy-1,2,3,3a,4,5-hexahydro-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one 10-methoxy-6-oxo-6H-indolo[3,2,1-de][1,5]naphthyridine-3-oxide 4-methoxy-5-isobutoxycanthinone 3-methylcanthin-6-on-3-ium p-toluenesulfonate 6-methyl-5-phenyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one (3aα,6β)-3-Benzyl-2,3,3a,4,5,6-hexahydro-1H-indolo<3.2.1-de><1.5>naphthyridin-6-ol 5-acetoxycanthin-6-one 3,4-diethyl-2,3,3a,4,5,6-hexahydro-6-oxo-1H-indolo(3,2,1-de)(1,5)-naphthyridine N-oxide-benzo[e]canthin-6-one