摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3,3'-(3,7,12,17-tetramethyl-1,19-dioxo-8,13-divinyl-1,19,22,24-tetrahydro-21H-biline-2,18-diyl)-bis-propionic acid dimethyl ester | 26280-00-2

中文名称
——
中文别名
——
英文名称
3,3'-(3,7,12,17-tetramethyl-1,19-dioxo-8,13-divinyl-1,19,22,24-tetrahydro-21H-biline-2,18-diyl)-bis-propionic acid dimethyl ester
英文别名
biliverdin IXγ dimethyl ester;γ-biliverdin-IX dimethyl ester;biliverdin IX γ dimethyl ester
3,3'-(3,7,12,17-tetramethyl-1,19-dioxo-8,13-divinyl-1,19,22,24-tetrahydro-21H-biline-2,18-diyl)-bis-propionic acid dimethyl ester化学式
CAS
26280-00-2
化学式
C35H38N4O6
mdl
——
分子量
610.71
InChiKey
BKJQAYAVJLILPL-RUXNVCPMSA-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

  • 沸点:
    862.2±65.0 °C(Predicted)
  • 密度:
    1.23±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.29
  • 重原子数:
    45.0
  • 可旋转键数:
    11.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    138.95
  • 氢给体数:
    3.0
  • 氢受体数:
    7.0

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis of γ-oxyprotoporphyrin IX and pterobiline (biliverdin IX<sub>γ</sub>)
    作者:Anthony H. Jackson、Rhiannydd M. Jenkins、D. Michael Jones、Stephen A. Matlin
    DOI:10.1039/c39810000763
    日期:——
    The γ-meso-hydroxy-derivative of protopor-phyrin IX has been synthesised by condensation of a bis(formylpyrroly) ketone and a dispyrrolylmethane; the iron complex underwent oxidative ring-opening to give biliverdin IXγ(ptrobiline), the blue -green butterfly pigment, thus providing a modle for its biosynthesis.
    的γ -内消旋-羟基衍生物protopor-卟啉IX的已经由双(formylpyrroly)酮和dispyrrolylmethane的缩合合成; 络合物后行氧化开环,得到胆绿素IX γ(ptrobiline),蓝-绿色颜料蝴蝶,从而提供了其生物合成的模型。。
  • Heme-iron utilization by Leptospira interrogans requires a heme oxygenase and a plastidic-type ferredoxin-NADP+ reductase
    作者:Anabel Soldano、Huili Yao、Mario Rivera、Eduardo A. Ceccarelli、Daniela L. Catalano-Dupuy
    DOI:10.1016/j.bbagen.2014.07.021
    日期:2014.11
    Background: Heme oxygenase catalyzes the conversion of heme to iron, carbon monoxide and biliverdin employing oxygen and reducing equivalents. This enzyme is essential for heme-iron utilization and contributes to virulence in Leptospira interrogans. Methods: A phylogenetic analysis was performed using heme oxygenases sequences from different organisms including saprophytic and pathogenic Leptospira species. L. interrogans heme oxygenase (LepHO) was cloned, overexpressed and purified. The structural and enzymatic properties of LepHO were analyzed by UV-vis spectrophotometry and (1)H NMR. Heme-degrading activity, ferrous iron release and biliverdin production were studied with different redox partners. Results: A plastidic type, high efficiently ferredoxin-NADP(+) reductase (LepFNR) provides the electrons for heme turnover by heme oxygenase in L. interrogans. This catalytic reaction does not require a ferredoxin. Moreover, LepFNR drives the heme degradation to completeness producing free iron and α-biliverdin as the final products. The phylogenetic divergence between heme oxygenases from saprophytic and pathogenic species supports the functional role of this enzyme in L. interrogans pathogenesis. Conclusions: Heme-iron scavenging by LepHO in L. interrogans requires only LepFNR as redox partner. Thus, we report a new substrate of ferredoxin-NADP(+) reductases different to ferredoxin and flavodoxin, the only recognized protein substrates of this flavoenzyme to date. The results presented here uncover a fundamental step of heme degradation in L. interrogans. General significance: Our findings contribute to understand the heme-iron utilization pathway in Leptospira. Since iron is required for pathogen survival and infectivity, heme degradation pathway may be relevant for therapeutic applications.
  • Synthesis of biliverdin IXγ (pterobilin)
    作者:Anthony H. Jackson、Rhianydd M. Jenkins、D.Michael Jones、Stephen A. Matlin
    DOI:10.1016/s0040-4020(01)88698-1
    日期:1983.1
查看更多