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雷藤二萜醌 B | 142937-50-6

中文名称
雷藤二萜醌 B
中文别名
雷藤二萜醌B
英文名称
19-hydroxy-3,11,14-trioxoabieta-8,12-diene
英文别名
triptoquinone B;(4bS,8S,8aR)-8-(hydroxymethyl)-4b,8-dimethyl-2-propan-2-yl-6,8a,9,10-tetrahydro-5H-phenanthrene-1,4,7-trione
雷藤二萜醌 B化学式
CAS
142937-50-6
化学式
C20H26O4
mdl
——
分子量
330.424
InChiKey
RYYRZMIBKOKIRO-UIAACRFSSA-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:
    475.4±45.0 °C(Predicted)
  • 密度:
    1.19±0.1 g/cm3(Predicted)
  • 溶解度:
    溶于氯仿、二氯甲烷、乙酸乙酯、DMSO、丙酮等。

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    71.4
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 储存条件:
    储存条件:2-8℃,干燥,密闭。

SDS

SDS:a5b8403a5d69c579da4a6c4f255340b3
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制备方法与用途

三托醌B(+)-三托醌B是一种倍半萜生物碱,也是一种白细胞介素-1抑制剂。研究显示,Triptoquinone B能显著抑制人外周血单个核细胞释放白细胞介素1α和β。

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:
    参考文献:
    名称:
    Synthetic studies on diterpenoid quinones with interleukin-1 inhibitory activity. Total synthesis of (.+-.)- and (+)-triptoquinone A
    摘要:
    An efficient first total synthesis of (+/-)- and (+)-triptoquinone A (1), a novel diterpenoid quinone with significant inhibitory activity against interleukin-1 releases, has been completed. Birch reduction of tricyclic enone (+/-)-7, prepared from known 6-methoxy-2-isopropyl-1-naphthol (22), which is readily available in large quantities, was followed by immediate enolate trapping to provide silyl enol ether (+/-)-30. Compound 30 was converted into carboxylic acid (+/-)-4 via the corresponding enol triflate (+/-)-31 either by sequential palladium-catalyzed carbonylation and oxidation or by direct carboxylation. The total synthesis of (+/-)-1 was completed by oxidation of (+/-)-4 with CAN in 12 steps from 22 in 19% overall yield at best. A second, enantioselective total synthesis of (+)-1 was accomplished via (+/-)-7, which was prepared by (-)-N- [4-(trifluoromethyl)benzyl]cinchonidinium bromide (33) catalyzed asymmetric Michael reaction of 6 with ethyl vinyl ketone and a subsequent aldol condensation. The absolute structures of triptoquinone B (2) and C (3), which were isolated concomitantly with triptoquinone A from the same plant sources, were established by a series of chemical reactions based on (+)-7.
    DOI:
    10.1021/jo00081a021
  • 作为产物:
    描述:
    Bromomethyl-((2S,4aR)-7-isopropyl-8-methoxy-1,4a-dimethyl-2,3,4,4a,9,10-hexahydro-phenanthren-2-yloxy)-dimethyl-silane 在 sodium hypochloritepotassium dihydrogenphosphate三氯化铝 、 potassium nitrososulfonate 、 偶氮二异丁腈三丁基氯化锡双氧水 、 sodium cyanoborohydride 、 potassium hydrogencarbonate乙硫醇 作用下, 以 四氢呋喃甲醇乙醇溶剂黄146叔丁醇 为溶剂, 生成 雷藤二萜醌 B
    参考文献:
    名称:
    Enantiocontrolled total synthesis of the diterpenoids, triptoquinone B, C and triptocallol
    摘要:
    An efficient and enantiocontrolled synthesis of triptoquinone B and C, which possess interleukin-1 inhibitory activity, has been accomplished employing the lipase-catalyzed kinetic resolution and a highly diastereoselective radical cyclization as key synthetic steps. In addition, the first total synthesis of triptocallol has been achieved utilizing the same strategy. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)00841-1
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文献信息

  • Glucosyltransferase Capable of Catalyzing the Last Step in Neoandrographolide Biosynthesis
    作者:Yuan Li、Hui-Xin Lin、Jian Wang、Jian Yang、Chang-Jiang-Sheng Lai、Xing Wang、Bao-Wei Ma、Jin-Fu Tang、Yong Li、Xin-Lin Li、Juan Guo、Wei Gao、Lu-Qi Huang
    DOI:10.1021/acs.orglett.8b02146
    日期:2018.10.5
    ApUGT, a diterpene glycosyltransferase from Andrographis paniculata, could transfer a glucose to the C-19 hydroxyl moiety of andrograpanin to form neoandrographolide. This glycosyltransferase has a broad substrate scope, and it can glycosylate 26 natural and unnatural compounds of different structural types. This study provides a basis for exploring the glycosylation mechanism of ent-labdane-type diterpenes and plays an important role in diversifying the structures used in drug discovery.
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同类化合物

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