anhydroepipicropodophyllol | 78391-86-3

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物 - 芳基四氢萘木脂素
• 英文名称: anhydroepipicropodophyllol
• 英文别名: neoanhydropicropodophyllol；Anhydropikropodophyllol；5,6,7,8-Tetrahydro-8alpha-(3,4,5-trimethoxyphenyl)-5beta,7beta-(epoxymethano)naphtho[2,3-d]-1,3-dioxole-6beta-methanol；[(1S,11R,12S,15R)-11-(3,4,5-trimethoxyphenyl)-5,7,14-trioxatetracyclo[10.2.1.02,10.04,8]pentadeca-2,4(8),9-trien-15-yl]methanol
• CAS: 78391-86-3
• 化学式: C₂₂H₂₄O₇
• 分子量: 400.428
• InChiKey: GAPFRQMOPFLDIS-REABXYAWSA-N

物化性质

• 沸点：
  533.3±50.0 °C(Predicted)
• 密度：
  1.292±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  75.6
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  anhydroepipicropodophyllol 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 以79%的产率得到(1S,11R,12S,15S)-11-(3,4,5-trimethoxyphenyl)-5,7,14-trioxatetracyclo[10.2.1.02,10.04,8]pentadeca-2,4(8),9-triene-15-carbaldehyde
  参考文献：
  名称：

  环木脂醛的合成及其抗肿瘤活性。

  摘要：

  已经制备了几种与HT-29结肠癌的选择性抗肿瘤药9-脱氧-9-氧代-α-阿朴二十碳五烯酸甲酯有关的醛，并评估了它们对四种肿瘤细胞系的细胞毒活性（P-388，A- 549，HT-29和MEL-28）。他们所有人都没有内酯环，但将细胞毒性维持在microM水平或以下。

  DOI：

  10.1016/s0223-5234(00)00176-8
• 作为产物：
  描述：

  鬼臼毒素 在 盐酸 、 氢氧化钾 、 lithium aluminium tetrahydride 作用下， 以 甲醇 、 乙醚 、 氯仿 为溶剂， 反应 2.0h， 生成 anhydroepipicropodophyllol
  参考文献：
  名称：

  Castro, M. A.; Gordaliza, M.; Corral, J. M. Miguel del, Organic Preparations and Procedures International, 1994, vol. 26, # 5, p. 539 - 548

  摘要：

  DOI：

文献信息

• Cytotoxic cyclolignans related to podophyllotoxin
  作者：Marina Gordaliza、José M Miguel del Corral、M Angeles Castro、Pablo A Garcı́a-Garcı́a、Arturo San Feliciano

  DOI：10.1016/s0014-827x(01)01030-8

  日期：2001.4

  The cyclolignan family of natural products includes compounds with important antineoplastic and antiviral properties such as podophyllotoxin and two of their semisynthetic derivatives, etoposide and teniposide. The latter are included in a wide variety of cancer chemotherapy protocols. Due to these biological activities, cyclolignans have been the objective of numerous studies focused to prepare better and safer anticancer drugs. Several cyclolignans related to podophyllotoxin have, been prepared and evaluated for their cytotoxic activities on four neoplastic cell lines (P-388, A-549, HT-29 and MEL-28); some of them have antiviral and immunosuppressive activities. (C) 2001 Elsevier Science S.A. All rights reserved.
• Modes of Methyleneoxy Bridging and Their Effect on Tetrahydronaphthalene Lignan Cytotoxicity
  作者：Robert T. LaLonde、Frank Ramdayal、Anatole Sarko、Koichi Yanai、Mianji Zhang

  DOI：10.1021/jm020158p

  日期：2003.3.1

  Dioxatricyclodecane, oxabicyclooctane, and benzodihydropyran derivatives of alpha-conidendrin (ACON), podophyllotoxin (PT), and sikkimotoxin (SK) were prepared to learn which methyleneoxy bridging modes and arene and aryl substituents coincided with high cytotoxicity. PT-derived dioxatricyclodecane 14 showed in vitro activity at 10(-8) M. SK analogue 12 was less active, and ACON analogue 11 was inactive at 10(-4) M. In vivo intraperitoneal and subcutaneous activities of 14 were observed. In vitro cytotoxicities were higher for oxabicyclooctanes when hydroxymethyl group and methyleneoxy bridge were cis, as in deoxypicropodophyllin analog 20, rather than trans, as in PT analogue 5. Acetylation of the hydroxymethyl group of 20 lowered activities, whereas acetylation of 5 increased or lowered activities. Reduction of the hydroxymethyl group of 5 to a methyl group increased cytotoxicities. Molecular dynamics indicated the THN scaffold of benzodihydropyrans was conformationally mobile, but scaffolds of oxabicyclooctanes and dioxatricyclodecanes were immobile. Each of three PT-benzodihydropyrans was less active than its oxabicyclooctane counterpart.
• Castro, M. A.; Gordaliza, M.; Corral, J. M. Miguel del, Organic Preparations and Procedures International, 1994, vol. 26, # 5, p. 539 - 548
  作者：Castro, M. A.、Gordaliza, M.、Corral, J. M. Miguel del、Feliciano, A. San

  DOI：——

  日期：——
• Synthesis and antineoplastic activity of cyclolignan aldehydes
  作者：Marina Gordaliza、M Angeles Castro、José M Miguel del Corral、M Luisa López-Vázquez、Pablo A. García、M Dolores García-Grávalos、Arturo San Feliciano

  DOI：10.1016/s0223-5234(00)00176-8

  日期：2000.8

  Several aldehydes related to methyl 9-deoxy-9-oxo-alpha-apopicropodophyllate, a selective antitumour agent against the HT-29 colon carcinoma, have been prepared and evaluated for their cytotoxic activities on four neoplastic cell lines (P-388, A-549, HT-29 and MEL-28). All of them lacked the lactone ring but maintained their cytotoxicity at, or under, the microM level.

  已经制备了几种与HT-29结肠癌的选择性抗肿瘤药9-脱氧-9-氧代-α-阿朴二十碳五烯酸甲酯有关的醛，并评估了它们对四种肿瘤细胞系的细胞毒活性（P-388，A- 549，HT-29和MEL-28）。他们所有人都没有内酯环，但将细胞毒性维持在microM水平或以下。