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3-[2-[[3-(3-hydroxypropyl)-4-methyl-1H-pyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-3-yl]propan-1-ol | 202583-55-9

中文名称
——
中文别名
——
英文名称
3-[2-[[3-(3-hydroxypropyl)-4-methyl-1H-pyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-3-yl]propan-1-ol
英文别名
——
3-[2-[[3-(3-hydroxypropyl)-4-methyl-1H-pyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-3-yl]propan-1-ol化学式
CAS
202583-55-9
化学式
C17H26N2O2
mdl
——
分子量
290.406
InChiKey
PWEXEHYTCPLVBZ-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):
    2.1
  • 重原子数:
    21
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    72
  • 氢给体数:
    4
  • 氢受体数:
    2

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

反应信息

  • 作为反应物:
    描述:
    3-[2-[[3-(3-hydroxypropyl)-4-methyl-1H-pyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-3-yl]propan-1-ol4-二甲氨基吡啶四氯苯醌对甲苯磺酸三乙胺 作用下, 以 吡啶 为溶剂, 反应 21.0h, 生成 3-((4Z,10Z,15Z,19Z)-18-{3-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-propyl}-8,12-diethyl-3,7,13,17-tetramethyl-22,24-dihydro-porphin-2-yl)-propan-1-ol
    参考文献:
    名称:
    A Porphyrin Embedded in DNA
    摘要:
    Oligodeoxynucleotides containing an alkylporphyrin linked to the phosphate groups of DNA via oxypropyl chains have been synthesized. To our knowledge, these are the first porphyrin-nucleic acid conjugates bearing the porphyrin embedded in the backbone of DNA. Chain assembly was achieved by automated solid-phase synthesis using a dimethoxytrityl-protected porphyrin phosphoramidite and standard DNA building blocks. The thermal stability of duplexes involving the octadecamer 5'-CGCGCCTTC-P-CATTGCGG-3', where -P- denotes the porphyrin, was found to depend on the sequence of the complementary strand., A duplex where a thymidine residue in the complementary strand faces the porphyrin gives a higher melting point than duplexes bearing an abasic site or a dT(3) loop at this position. Duplex formation is accompanied by 180% hypochromicity at 501 nm, and other spectral changes unprecedented in porphyrinoids interacting with nucleic acids. Footprinting with nuclease S1, together with CD spectropolarimetry, indicates that the alkylporphyrin is embedded in a B-type duplex, with highly nuclease-sensitive phosphates only in the local environment of the porphyrin. Peak shifts in the NMR spectrum of the porphyrin-containing duplex, together with. fluorescence data, point toward an interaction between the porphyrin and the stacked nucleobases. Porphyrin-containing DNA-and RNA-duplexes, conveniently prepared with the porphyrin phosphoramidite described here, are expected to be valuable for photochemical and electron-transfer studies, as well as potential cofactor-using nucleic acid-based enzymes which could have had a role in prebiotic evolution.
    DOI:
    10.1021/jo9718051
  • 作为产物:
    参考文献:
    名称:
    A Porphyrin Embedded in DNA
    摘要:
    Oligodeoxynucleotides containing an alkylporphyrin linked to the phosphate groups of DNA via oxypropyl chains have been synthesized. To our knowledge, these are the first porphyrin-nucleic acid conjugates bearing the porphyrin embedded in the backbone of DNA. Chain assembly was achieved by automated solid-phase synthesis using a dimethoxytrityl-protected porphyrin phosphoramidite and standard DNA building blocks. The thermal stability of duplexes involving the octadecamer 5'-CGCGCCTTC-P-CATTGCGG-3', where -P- denotes the porphyrin, was found to depend on the sequence of the complementary strand., A duplex where a thymidine residue in the complementary strand faces the porphyrin gives a higher melting point than duplexes bearing an abasic site or a dT(3) loop at this position. Duplex formation is accompanied by 180% hypochromicity at 501 nm, and other spectral changes unprecedented in porphyrinoids interacting with nucleic acids. Footprinting with nuclease S1, together with CD spectropolarimetry, indicates that the alkylporphyrin is embedded in a B-type duplex, with highly nuclease-sensitive phosphates only in the local environment of the porphyrin. Peak shifts in the NMR spectrum of the porphyrin-containing duplex, together with. fluorescence data, point toward an interaction between the porphyrin and the stacked nucleobases. Porphyrin-containing DNA-and RNA-duplexes, conveniently prepared with the porphyrin phosphoramidite described here, are expected to be valuable for photochemical and electron-transfer studies, as well as potential cofactor-using nucleic acid-based enzymes which could have had a role in prebiotic evolution.
    DOI:
    10.1021/jo9718051
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文献信息

  • A Porphyrin Embedded in DNA
    作者:Kurt Berlin、Rishi K. Jain、Matthew D. Simon、Clemens Richert
    DOI:10.1021/jo9718051
    日期:1998.3.1
    Oligodeoxynucleotides containing an alkylporphyrin linked to the phosphate groups of DNA via oxypropyl chains have been synthesized. To our knowledge, these are the first porphyrin-nucleic acid conjugates bearing the porphyrin embedded in the backbone of DNA. Chain assembly was achieved by automated solid-phase synthesis using a dimethoxytrityl-protected porphyrin phosphoramidite and standard DNA building blocks. The thermal stability of duplexes involving the octadecamer 5'-CGCGCCTTC-P-CATTGCGG-3', where -P- denotes the porphyrin, was found to depend on the sequence of the complementary strand., A duplex where a thymidine residue in the complementary strand faces the porphyrin gives a higher melting point than duplexes bearing an abasic site or a dT(3) loop at this position. Duplex formation is accompanied by 180% hypochromicity at 501 nm, and other spectral changes unprecedented in porphyrinoids interacting with nucleic acids. Footprinting with nuclease S1, together with CD spectropolarimetry, indicates that the alkylporphyrin is embedded in a B-type duplex, with highly nuclease-sensitive phosphates only in the local environment of the porphyrin. Peak shifts in the NMR spectrum of the porphyrin-containing duplex, together with. fluorescence data, point toward an interaction between the porphyrin and the stacked nucleobases. Porphyrin-containing DNA-and RNA-duplexes, conveniently prepared with the porphyrin phosphoramidite described here, are expected to be valuable for photochemical and electron-transfer studies, as well as potential cofactor-using nucleic acid-based enzymes which could have had a role in prebiotic evolution.
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