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新型海洋海绵氨基酸,10. 来自Xestospongia属海绵的xestoaminols

Novel marine sponge amino acids, 10. Xestoaminols from Xestospongia sp.

作者信息

Jiménez C, Crews P

机构信息

Department of Chemistry, University of California, Santa Cruz 95064.

出版信息

J Nat Prod. 1990 Jul-Aug;53(4):978-82. doi: 10.1021/np50070a033.

Abstract

The study of the anthelminthic components from a Fiji sponge Xestospongia sp. has yielded new amino alcohols, xestoaminols A-C. Xestoaminol B, (2S*)-aminotetradeca-11, 13-dien-(3R*)-ol [2], is isomeric to known Xestospongia products, (2S)-aminotetradeca-5,7-dien-(3R)-ol [6] and (2S)-aminotetradeca-5,7-dien-(3S)-ol [7], recently reported by Gulavita and Scheuer. Xestoaminols A [1] and C [3] are, respectively, the dihydro and tetrahydro derivatives of xestoaminol B. A combined nmr and molecular mechanics study on the oxazolidinone of xestoaminol A provided the basis for the relative stereochemistry assigned at C-2 and C-3 in xestoaminol A. This compound was extremely active in assays testing for action against parasites, microbes, and reverse transcriptase.

摘要

对斐济海绵Xestospongia sp.的驱虫成分研究已产生了新的氨基醇类化合物,即xestoaminols A - C。Xestoaminol B,(2S*)-氨基十四碳-11,13-二烯-(3R*)-醇[2],与Gulavita和Scheuer最近报道的已知Xestospongia产物(2S)-氨基十四碳-5,7-二烯-(3R)-醇[6]和(2S)-氨基十四碳-5,7-二烯-(3S)-醇[7]是同分异构体。Xestoaminols A [1]和C [3]分别是xestoaminol B的二氢和四氢衍生物。对xestoaminol A的恶唑烷酮进行的核磁共振和分子力学联合研究为xestoaminol A中C-2和C-3处的相对立体化学归属提供了依据。该化合物在针对寄生虫、微生物和逆转录酶作用的检测中表现出极高的活性。

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