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独眼环肽A,一种从长柄九节中分离出的具有生物活性的31个残基的环肽。

Cyclopsychotride A, a biologically active, 31-residue cyclic peptide isolated from Psychotria longipes.

作者信息

Witherup K M, Bogusky M J, Anderson P S, Ramjit H, Ransom R W, Wood T, Sardana M

机构信息

Department of Medicinal Chemistry, Merck Research Laboratories, West Point, Pennsylvania 19486.

出版信息

J Nat Prod. 1994 Dec;57(12):1619-25. doi: 10.1021/np50114a002.

Abstract

A preliminary characterization is provided of a naturally occurring cyclic peptide with interesting and potent biological activity. A 31-residue cyclic peptide, designated cyclopsychotride A [1], was obtained from the organic extract of the tropical plant, Psychotria longipes. Compound 1 inhibited [125I] neurotensin (NT) binding to HT-29 cell membranes (IC50 3 microM) and also stimulated increased levels of cytosolic Ca2+ in two unrelated cell lines that do not express NT receptors. The peptide was found to dose-dependently increase intracellular Ca2+ at concentrations ranging from 3 to 30 microM, and this response was not blocked by a known NT antagonist. Cyclopsychotride A [1] possesses three disulfide linkages and is thought to be the largest cyclic peptide isolated from a natural source. Both 1H-nmr and cd spectroscopy showed 1 to be highly structured.

摘要

对一种具有有趣且强大生物活性的天然存在的环肽进行了初步表征。从热带植物长柄九节木的有机提取物中获得了一种由31个残基组成的环肽,命名为环九节肽A [1]。化合物1抑制[125I]神经降压素(NT)与HT - 29细胞膜的结合(IC50为3 microM),并且还在两种不表达NT受体的无关细胞系中刺激胞质Ca2+水平升高。发现该肽在3至30 microM的浓度范围内剂量依赖性地增加细胞内Ca2+,并且这种反应不受已知NT拮抗剂的阻断。环九节肽A [1]具有三个二硫键,被认为是从天然来源分离出的最大环肽。1H - NMR和圆二色光谱均表明1具有高度结构化。

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