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博特罗霍丁 K 和 L,两种新型真菌来源的细胞毒环缩酚酸酮。

Botryorhodines K and L, two new cytotoxic depsidones from a fungus of the genus Arcopilus.

机构信息

Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama, 939-0398, Japan.

Department of Physical Chemistry, Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, 4-20-1 Nasahara, Takatsuki City, Osaka, 569-1094, Japan.

出版信息

J Antibiot (Tokyo). 2023 Nov;76(11):673-677. doi: 10.1038/s41429-023-00652-9. Epub 2023 Sep 5.

DOI:10.1038/s41429-023-00652-9
PMID:37670100
Abstract

Botryorhodines K (1) and L (2), two new depsidone derivatives, along with one known metabolite, 4-O-demethylbarbatic acid (3), were isolated from the culture extract of a fungus of the genus Arcopilus. The structures of 1‒3 were determined by the analysis of NMR and MS spectral data and the absolute configuration of 1 was established by single-crystal X-ray diffraction analysis. Compounds 1 and 2 showed antimicrobial activity against Gram-positive bacteria and cytotoxicity against murine leukemia P388 cells.

摘要

博特罗红菌素 K(1)和 L(2),两种新的去甲鞣花酸衍生物,以及一种已知的代谢产物 4-O-去甲巴马丁酸(3),从真菌属 Arcopilus 的培养提取物中分离得到。通过分析 NMR 和 MS 光谱数据确定了 1-3 的结构,通过单晶 X 射线衍射分析确定了 1 的绝对构型。化合物 1 和 2 对革兰氏阳性菌表现出抗菌活性,对小鼠白血病 P388 细胞表现出细胞毒性。

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本文引用的文献

1
Catellatolactams A-C, Plant Growth-Promoting Ansamacrolactams from a Rare Actinomycete of the Genus .卡特拉托拉他姆 A-C,植物生长促进的链霉菌属中罕见放线菌的活性安莎大环内酯。
J Nat Prod. 2022 Aug 26;85(8):1993-1999. doi: 10.1021/acs.jnatprod.2c00331. Epub 2022 Aug 10.
2
Kumemicinones A-G, Cytotoxic Angucyclinones from a Deep Sea-Derived Actinomycete of the Genus .库米霉素 A-G,来自深海放线菌属的细胞毒 Angucyclinones
J Nat Prod. 2022 Apr 22;85(4):1098-1108. doi: 10.1021/acs.jnatprod.1c01205. Epub 2022 Mar 28.
3
β-lactam antibiotics: An overview from a medicinal chemistry perspective.
β-内酰胺类抗生素:从药物化学角度综述。
Eur J Med Chem. 2020 Dec 15;208:112829. doi: 10.1016/j.ejmech.2020.112829. Epub 2020 Sep 16.
4
Bulbimidazoles A-C, Antimicrobial and Cytotoxic Alkanoyl Imidazoles from a Marine Gammaproteobacterium Species.灯泡咪唑 A-C,海洋γ-变形菌来源的抗微生物和细胞毒性烷酰咪唑。
J Nat Prod. 2020 Apr 24;83(4):1295-1299. doi: 10.1021/acs.jnatprod.0c00082. Epub 2020 Mar 19.
5
Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009.从海洋海绵来源真菌 Setosphaeria sp. SCSIO41009 中分离得到的螺环苯酞和异香豆素。
J Nat Prod. 2018 Aug 24;81(8):1860-1868. doi: 10.1021/acs.jnatprod.8b00345. Epub 2018 Aug 9.
6
Diversity and taxonomy of and chaetomium-like fungi from indoor environments.室内环境中曲霉属和类毛壳菌的多样性与分类学
Stud Mycol. 2016 Jun;84:145-224. doi: 10.1016/j.simyco.2016.11.005. Epub 2016 Dec 8.
7
Roseopurpurins: Chemical Diversity Enhanced by Convergent Biosynthesis and Forward and Reverse Michael Additions.玫瑰红紫素:通过会聚生物合成和正向与逆向迈克尔加成增强的化学多样性。
Org Lett. 2016 Sep 2;18(17):4340-3. doi: 10.1021/acs.orglett.6b02099. Epub 2016 Aug 18.
8
Chaetoglobosin O and Other Phytotoxic Metabolites from Cylindrocladium floridanum, a Causal Fungus of Alfalfa Black Rot Disease.佛罗里达柱枝双孢,一种苜蓿黑腐病致病真菌产生的球毛壳菌素O及其他植物毒性代谢产物。
Biosci Biotechnol Biochem. 1996 Jan;60(2):360-1. doi: 10.1271/bbb.60.360.
9
New depsidones and isoindolinones from the mangrove endophytic fungus Meyerozyma guilliermondii (HZ-Y2) isolated from the South China Sea.从中国南海分离的红树林内生真菌季也蒙毕赤酵母(HZ-Y2)中提取的新型缩酚酸肽和异吲哚啉酮。
Beilstein J Org Chem. 2015 Jul 16;11:1187-93. doi: 10.3762/bjoc.11.133. eCollection 2015.
10
Chemical and bioactive diversities of the genus Chaetomium secondary metabolites.该属真菌次生代谢产物的化学和生物多样性。
Mini Rev Med Chem. 2012 Feb;12(2):127-48. doi: 10.2174/138955712798995066.