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pavoninin-1 | 89936-15-2

中文名称
——
中文别名
——
英文名称
pavoninin-1
英文别名
[(2R,6R)-6-[(7R,8S,9S,10R,13R,14S,17R)-7-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-methylheptyl] acetate
pavoninin-1化学式
CAS
89936-15-2;94426-01-4
化学式
C37H59NO9
mdl
——
分子量
661.877
InChiKey
BRNQQEJYQPMDNG-CIALHVAPSA-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

  • 比旋光度:
    D20 +19° (c = 1.1 in chloroform)
  • 沸点:
    803.5±65.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    47
  • 可旋转键数:
    12
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    152
  • 氢给体数:
    4
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    pavoninin-1吡啶盐酸甲醇 作用下, 以 四氯化碳 为溶剂, 反应 2.0h, 生成 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (2R,6R)-6-((8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methyl-heptyl ester
    参考文献:
    名称:
    Pavoninins, shark-repelling and ichthyotoxic steroid n-acetylglucosaminides from the defense secretion of the sole pardachirus pavoninus (soleidae)
    摘要:
    DOI:
    10.1016/s0040-4020(01)96470-1
  • 作为产物:
    描述:
    鹅去氧胆酸palladium dihydroxide 吡啶2,4,6-三甲基吡啶lead(IV) acetate4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 重铬酸吡啶2,6-二叔丁基-4-甲基吡啶三氟甲磺酸酐 、 4 A molecular sieve 、 camphor-10-sulfonic acid 、 氢氟酸氢气双氧水sodium hexamethyldisilazane二甲基亚砜 作用下, 以 四氢呋喃甲醇乙醇二氯甲烷乙酸乙酯N,N-二甲基甲酰胺乙腈 为溶剂, 反应 170.78h, 生成 pavoninin-1
    参考文献:
    名称:
    Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
    摘要:
    Pavoninin-1 (1), which was isolated from a defense secretion of the sole Pardachirus spp. as an ichthyotoxic and a shark repellent principle, and its structural analogue 2 were synthesized, where glycosylation using an 2-azidoglycosyl sulfoxide (10) afforded the corresponding beta-glycoside exclusively in high yield. Introduction of the alpha,beta-unsaturated ketone system in the ring A of 1 was achieved by phenylselenenylation of dihydropavoninin-1 (3) and subsequent oxidative elimination without protection of the hydroxyl groups in the sugar portion. The mode of action of these glycosides was evaluated for their perturbation on phosphatidylcholine liposomal membrane, using the fluorescent dye leakage method. The results revealed that membrane affinity does not parallel membrane perturbation but rather compensates it, and the spatial arrangement of hydrophobic and hydrophilic regions within a molecule is likely to reflect on the difference in potency of action among them. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(97)00170-3
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文献信息

  • Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
    作者:Yuki Ohnishi、Kazuo Tachibana
    DOI:10.1016/s0968-0896(97)00170-3
    日期:1997.12
    Pavoninin-1 (1), which was isolated from a defense secretion of the sole Pardachirus spp. as an ichthyotoxic and a shark repellent principle, and its structural analogue 2 were synthesized, where glycosylation using an 2-azidoglycosyl sulfoxide (10) afforded the corresponding beta-glycoside exclusively in high yield. Introduction of the alpha,beta-unsaturated ketone system in the ring A of 1 was achieved by phenylselenenylation of dihydropavoninin-1 (3) and subsequent oxidative elimination without protection of the hydroxyl groups in the sugar portion. The mode of action of these glycosides was evaluated for their perturbation on phosphatidylcholine liposomal membrane, using the fluorescent dye leakage method. The results revealed that membrane affinity does not parallel membrane perturbation but rather compensates it, and the spatial arrangement of hydrophobic and hydrophilic regions within a molecule is likely to reflect on the difference in potency of action among them. (C) 1997 Elsevier Science Ltd.
  • Pavoninins, shark-repelling and ichthyotoxic steroid n-acetylglucosaminides from the defense secretion of the sole pardachirus pavoninus (soleidae)
    作者:Kazuo Tachibana、Masahiro Sakaitani、Koji Nakanishi
    DOI:10.1016/s0040-4020(01)96470-1
    日期:1985.1
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