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来自滇桂崖爬藤的抗血管生成聚酮

Antiangiogenic polyketides from Peperomia dindygulensis Miq.

机构信息

Department of Traditional Chinese Medicine, Shanghai Institute of Pharmaceutical Industry, Shanghai 200040, China.

出版信息

Molecules. 2012 Apr 13;17(4):4474-83. doi: 10.3390/molecules17044474.

DOI:10.3390/molecules17044474
PMID:22504832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6268633/
Abstract

Two new polyketides: 2Z-(heptadec-12-enyl)-4-hydroxy-3,4,7,8-tetrahydro-2H-chromen-5(6H)-one (1) and 2-(heptadec-12-enyl)-5-hydroxy-5,6,7,8-tetrahydrochromen- 4-one (2), together with eleven known compounds: 4-hydroxy-2-[(3,4-methylenedioxy- phenyl)tridecanoyl] cyclohexane-1,3-dione (3), oleiferinone (4), 4-hydroxy-2-[(3,4- methylenedioxyphenyl)undecanoyl]cyclohexane-1,3-dione (5), 4-hydroxy-2-[(11-phenyl- undecanoyl)cyclohexane-1,3-dione (6), proctorione C (7), surinone C (8), 5-hydroxy- 7,8,4'-trimethoxyflavone (9), 5-hydroxy-7,8,3',4'-tetramethoxyflavone (10), 5-hydroxy- 7,3',4'-trimethoxyflavone (11), 5,8-dihydroxy-7,3',4'-trimethoxyflavone (12) and cepharanone B (13) were isolated from the whole plant of Peperomia dindygulensis Miq. Their structures were elucidated by spectroscopic methods, including 2D-NMR techniques. Compounds 2, 3, 5 and 8 inhibited human umbilical vein endothelial cell (HUVEC) proliferation and compounds 5 and 8 sharply suppressed HUVEC tube formation.

摘要

两种新的聚酮类化合物

2Z-(十七-12-烯基)-4-羟基-3,4,7,8-四氢-2H-色满-5(6H)-酮(1)和 2-(十七-12-烯基)-5-羟基-5,6,7,8-四氢色满-4-酮(2),以及 11 种已知化合物:4-羟基-2-[(3,4-亚甲二氧基-苯基)十三烷酰基]环己烷-1,3-二酮(3)、油烯酮(4)、4-羟基-2-[(3,4-亚甲二氧基苯基)十一烷酰基]环己烷-1,3-二酮(5)、4-羟基-2-[(11-苯基-十一烷酰基)环己烷-1,3-二酮(6)、普罗科酮 C(7)、苏林酮 C(8)、5-羟基-7,8,4'-三甲氧基黄酮(9)、5-羟基-7,8,3',4'-四甲氧基黄酮(10)、5-羟基-7,3',4'-三甲氧基黄酮(11)、5,8-二羟基-7,3',4'-三甲氧基黄酮(12)和头孢酮 B(13),从 Peperomia dindygulensis Miq 的全植物中分离得到。它们的结构通过包括 2D-NMR 技术在内的光谱方法阐明。化合物 2、3、5 和 8 抑制人脐静脉内皮细胞(HUVEC)增殖,化合物 5 和 8 显著抑制 HUVEC 管形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/65420517321c/molecules-17-04474-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/d02d206ce801/molecules-17-04474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/b26f8b61def4/molecules-17-04474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/3ea7e8971301/molecules-17-04474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/1cdd5623172f/molecules-17-04474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/52e83dc0f1de/molecules-17-04474-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/65420517321c/molecules-17-04474-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/d02d206ce801/molecules-17-04474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/b26f8b61def4/molecules-17-04474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/3ea7e8971301/molecules-17-04474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/1cdd5623172f/molecules-17-04474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/52e83dc0f1de/molecules-17-04474-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3924/6268633/65420517321c/molecules-17-04474-g006.jpg

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