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3-硝基-1-芘基l | 86674-49-9

中文名称
3-硝基-1-芘基l
中文别名
——
英文名称
1-hydroxy-3-nitropyrene
英文别名
3-hydroxy-1-nitropyrene;1-nitropyrene-3-ol;1-Nitropyren-3-ol;3-nitropyren-1-ol
3-硝基-1-芘基l化学式
CAS
86674-49-9
化学式
C16H9NO3
mdl
——
分子量
263.252
InChiKey
BOQCPFGCIYLAGN-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

物化性质

  • 溶解度:
    可溶于氯仿(少许)、DMSO(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    66
  • 氢给体数:
    1
  • 氢受体数:
    3

ADMET

代谢
3-羟基-1-硝基芘是1-硝基芘的人类已知代谢物。
3-hydroxy-1-nitropyrene is a known human metabolite of 1-nitropyrene.
来源:NORMAN Suspect List Exchange

安全信息

  • 海关编码:
    2907199090

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    3-硝基-1-芘基l氯化铵 作用下, 以 乙醇 为溶剂, 生成 3-hydroxy-1-aminopyrene
    参考文献:
    名称:
    Role of O-acetyltransferase in activation of oxidised metabolites of the genotoxic environmental pollutant 1-nitropyrene
    摘要:
    The genotoxic environmental contaminant l-nitropyrene is metabolised in mammalian systems by pathways more complex than the straightforward nitroreduction which accounts for most of its biological activity in bacteria. In order to evaluate the role of O-acetyltransferase (OAT) activity in generation of genotoxic intermediates from 1-nitropyrene, the mutagenicity of the major primary oxidised metabolites of 1-nitropyrene was characterised in the Ames Salmonella typhimurium plate incorporation assay with strain TA98, and with variants of TA98 deficient (TA98/1,8-DNP6) or enhanced (YG1024) in O-acetyltransferase. 1-Nitropyren-3-ol was more mutagenic in the absence than in the presence of S9, while 1-nitropyren-4-ol, 1-nitropyren-6-ol and 1-nitropyren-8-ol required S9 for maximum expression of mutagenicity. 1-Nitropyren-4-ol (176 rev/nmol without S9, 467 rev/nmol with S9 in TA98) and 1-nitropyren-6-ol (13 rev/nmol without S9, 266 rev/nmol with S9 in TA98) were overall the most potent nitropyrenol isomers assayed. 1-Acetamidopyren-8-ol and 2-acetamidopyrene 4,5-quinone were only minimally active. 1-Acetamidopyren-3-ol exhibited direct-acting mutagenicity. 1-Acetamidopyren-6-ol, previously shown to be a major contributor to mutagenicity in the urines of rats dosed with l-nitropyrene (Ball et al., 1984b), was confirmed as a potent (359 rev/nmol) S9-dependent mutagen. Both the direct-acting and the S9-dependent mutagenicity of all the compounds studied was enhanced in the OAT-overproducing strain and much diminished (though not always entirely lost) in the OAT-deficient strain, showing that OAT amplifies expression of the genotoxicity of these compounds. 1-Acetamidopyren-6-ol required both 89 and OAT activity in order to exhibit any mutagenicity; this finding strongly implicates N-hydroxylation followed by O-esterification, as opposed to further S9-catalyzed ring oxidation, as a major route of activation for urinary metabolites of 1-nitropyrene.
    DOI:
    10.1016/s0165-1218(96)90026-9
  • 作为产物:
    描述:
    1,3-二硝基芘二环己烷并-18-冠醚-6 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.17h, 以98%的产率得到3-硝基-1-芘基l
    参考文献:
    名称:
    硝化多环芳烃的化学氧化:与超氧阴离子自由基羟基化。
    摘要:
    硝化的多环芳烃(nitroPAH)是一种强力的诱变剂,可以通过还原和/或氧化方式代谢。硝基PAH的生物氧化(例如羟基化和环氧化)是已知的,但是仅在几篇论文中报道了化学氧化。由于具有硝基取代基的芳环的电子不足特性,NitroPAH几乎不会被各种化学氧化剂氧化。超氧阴离子自由基的亲核反应性是已知的,因此本研究中进行了硝基PAH与化学生成的超氧阴离子自由基的氧化。当1-硝基py与KO2 / 18-crown-6在二甲基甲酰胺中反应时,可以制备产率得到5-,6-,8-和9-羟基-1-硝基py和1-羟基py。三个异构体二硝基nitro,3-硝基荧蒽,6-硝基苯并[a] py,和6-硝基铬被氧化为羟基衍生物,其中一些对应于硝基PAH的氧化代谢产物。用三氟过氧乙酸将二硝基吡啶氧化,得到K区氧化产物。
    DOI:
    10.1021/tx00043a003
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文献信息

  • Photodegradation Mechanisms of 1-Nitropyrene, an Environmental Pollutant: The Effect of Organic Solvents, Water, Oxygen, Phenols, and Polycyclic Aromatics on the Destruction and Product Yields
    作者:Zulma I. García-Berríos、Rafael Arce
    DOI:10.1021/jp2126416
    日期:2012.4.12
    ϕ(-1-NO2Py), was larger in toluene, benzene, and polar protic solvents (10–3) in comparison with nonpolar and polar aprotic solvents, where the yield is on the order of 10–4. In solvents with an abstractable hydrogen atom, the products formed in higher yields were 1-OHPy and 1-OH-x-NO2Py. These represent 60–80% of the photodestruction yield and result from abstraction and recombination reactions of the pyrenoxy
    这项工作描述了在由有机溶剂和气溶胶颗粒的已知成分组成的化学模型系统中对 1-硝基芘 (1-NO 2 Py) 的光降解机制的研究。光产物如 1-羟基芘 (1-OHPy)、1-羟基- x -硝基芘 (1-OH- x -NO 2 Py)、1-亚硝基芘以及 1,6- 和 1,8-芘二酮通过高-高效液相色谱(HPLC)和高效液相色谱/质谱(HPLC/MS)技术,其量子产率显示出对溶剂类型的显着依赖性。与非极性和极性非质子溶剂相比,1-NO 2 Py 的光降解量子产率在甲苯、苯和极性质子溶剂 (10 –3 ) 中更大,其中产率在10 – 4的顺序。在具有可提取氢原子的溶剂中,以较高收率形成的产物是1-OHPy和1-OH- x -NO 2 Py。这些代表了 60-80% 的光破坏产率,是芘氧基自由基的提取和重组反应的结果,芘氧基自由基是硝基芳族化合物中硝基-亚硝酸盐重排的中间产物。 O 2对光降解产率的
  • Enzymatic nucleic acid synthesis: compositions and methods for altering monomer incorporation fidelity
    申请人:——
    公开号:US20030134807A1
    公开(公告)日:2003-07-17
    Nucleotide triphosphate probes containing a molecular and/or atomic tag on a a &ggr; and/or &bgr; phosphate group and/or a base moiety having a detectable property are disclosed, and kits and method for using the tagged nucleotides in sequencing reactions and various assay. Also, phosphate and polyphosphate molecular fidelity altering agents are disclosed.
    本发明公开了含有分子和/或原子标记的三磷酸核苷酸探针(标记在一个&ggr;和/或&bgr;磷酸基团和/或具有可检测特性的碱基上),以及在测序反应和各种检测中使用标记核苷酸的试剂盒和方法。此外,还公开了磷酸和多磷酸分子保真度改变剂。
  • Determination of nitrated polynuclear aromatic hydrocarbons in particulate extracts by using capillary column gas chromatography with nitrogen selective detection
    作者:M. C. Paputa-Peck、R. S. Marano、Dennis. Schuetzle、T. L. Riley、C. V. Hampton、T. J. Prater、L. M. Skewes、T. E. Jensen、P. H. Ruehle、. et al.
    DOI:10.1021/ac00262a027
    日期:1983.10.1
  • ENZYMATIC NUCLEIC ACID SYNTHESIS: COMPOSITIONS AND METHODS FOR ALTERING MONOMER INCORPORATION FIDELITY
    申请人:Visigen Biotechnologies, Inc.
    公开号:EP1354064A2
    公开(公告)日:2003-10-22
  • Enzymatic nucleic acid synthesis: methods for direct detection of tagged monomers
    申请人:Hardin H. Susan
    公开号:US20070172859A1
    公开(公告)日:2007-07-26
    Nucleotide triphosphate probes containing a molecular and/or atomic tag on a a γ and/or β phosphate group and/or a base moiety having a detectable property are disclosed, and kits and method for using the tagged nucleotides in sequencing reactions and various assay. Also, phosphate and polyphosphate molecular fidelity altering agents are disclosed.
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