Stereochemistry and NMR Data Assignment of Cyclopeptide Alkaloids from Zizyphus oxyphylla

被引：0

作者：

Nisar, Muhammad ^{[1
]}

Kaleem, Waqar Ahmad ^{[2
]}

Adhikari, Achyut ^{[3
]}

Ali, Zulfiqar ^{[3
]}

Hussain, Nusrat ^{[3
]}

Khan, Inamullah ^{[2
]}

Qayum, Mughal ^{[2
]}

Choudhary, M. Iqbal ^{[3
]}

机构：

[1] Univ Peshawar, Inst Chem Sci, Peshawar 25120, Pakistan

[2] Univ Peshawar, Dept Pharm, Peshawar 25120, Pakistan

[3] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan

来源：

NATURAL PRODUCT COMMUNICATIONS | 2010年 / 5卷 / 08期

关键词：

Zizyphus oxyphylla; cyclopeptide alkaloids; NMR data assignment; PEPTIDE ALKALOIDS;

D O I：

暂无

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

The structures of (3S,7R,13S)-6-[2-(dimethylamino)-3-phenylpropanoyl]-19-methoxy-2-oxa-6,9,15-triazatetracyclo[16.3.1.0(3,7).0(9,13)]docosa-1-(22),16,18,20-tetraene-8,14-dione (1), nummularin-C (2) and nummularin-R (3) have been previously determined mainly based on mass spectrometric data. Stereochemistry and complete H-1 and C-13 NMR spectroscopic data assignments of these compounds are now described. Compounds 1 and 2 are reported for the first time from Zizyphus oxyphylla.

引用

页码：1205 / 1208

页数：4

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