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Secondary metabolites from the fungus Emericella nidulans.来自构巢曲霉的次生代谢产物。
Nat Prod Commun. 2013 Sep;8(9):1285-8.
2
Neocosmospora sp.-derived resorcylic acid lactones with in vitro binding affinity for human opioid and cannabinoid receptors.新型拟青霉来源的具有体外结合人阿片类和大麻素受体亲和力的瑞香素内酯。
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Antifungal metabolites from the roots of Diospyros virginiana by overpressure layer chromatography.过压层离析法从柿树根中分离到的抗真菌代谢产物。
Chem Biodivers. 2011 Dec;8(12):2331-40. doi: 10.1002/cbdv.201000310.
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Benzyl derivatives with in vitro binding affinity for human opioid and cannabinoid receptors from the fungus Eurotium repens.真菌扩展青霉来源的具有体外人阿片类和大麻素受体结合亲和力的苄基衍生物。
J Nat Prod. 2011 Jul 22;74(7):1636-9. doi: 10.1021/np200147c. Epub 2011 Jun 13.
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Antileishmanial activity of the hydroalcoholic extract of Miconia langsdorffii, isolated compounds, and semi-synthetic derivatives.麦科尼亚·朗斯多夫提取物、分离化合物和半合成衍生物的抗利什曼原虫活性。
Molecules. 2011 Feb 22;16(2):1825-33. doi: 10.3390/molecules16021825.
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In vivo assessment of DNA damage and protective effects of extracts from Miconia species using the comet assay and micronucleus test.使用彗星试验和微核试验对红果仔属植物提取物的DNA损伤及保护作用进行体内评估。
Mutagenesis. 2008 Nov;23(6):501-7. doi: 10.1093/mutage/gen043. Epub 2008 Sep 2.
7
Flavanone glycosides from Miconia trailii.来自毛萼紫金牛的黄酮苷。
J Nat Prod. 2003 Jan;66(1):39-41. doi: 10.1021/np020429z.
8
Phenolic compounds from Miconia myriantha inhibiting Candida aspartic proteases.来自多花红果薄柱草的酚类化合物对念珠菌天冬氨酸蛋白酶的抑制作用
J Nat Prod. 2001 Oct;64(10):1282-5. doi: 10.1021/np010172p.
9
Triterpene and flavanone glycoside from Rhododendron simsii.映山红中的三萜和黄烷酮糖苷。
Phytochemistry. 2001 Apr;56(8):875-9. doi: 10.1016/s0031-9422(00)00493-3.
10
C-methyl-flavonoids from the leaf waxes of some Myrtaceae.一些桃金娘科植物叶蜡中的C-甲基黄酮类化合物。
Phytochemistry. 2000 Dec;55(8):965-70. doi: 10.1016/s0031-9422(00)00348-4.

来自于……的黄烷酮

Flavanones from .

作者信息

Tarawneh Amer H, León Francisco, Ibrahim Mohammed A, Pettaway Sara, McCurdy Christopher R, Cutler Stephen J

机构信息

Department of Medicinal Chemistry, The University of Mississippi, University, MS 38677, USA.

National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.

出版信息

Phytochem Lett. 2014 Feb;7:130-132. doi: 10.1016/j.phytol.2013.11.001.

DOI:10.1016/j.phytol.2013.11.001
PMID:24976876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4070512/
Abstract

A glycosidic flavanone miconioside C () has been isolated from the methanolic extract of the stems of , together with 7--β-D-apiofuranosyl-(1→6)-β-D-glucopyranosylmatteucinol (), miconioside B (), matteucinol (), farrerol () and desmethoxymatteucinol (). Their structures were mainly established by extensive NMR studies (H NMR, C NMR, DEPT, H-H COSY, HSQC, HMBC) and mass spectrometry. The compounds - were evaluated for binding assays using cannabinoid receptors (CB1 and CB2).

摘要

一种糖苷类黄烷酮米可尼苷C()已从[植物名称]茎的甲醇提取物中分离出来,同时还分离出了7--β-D-阿朴呋喃糖基-(1→6)-β-D-吡喃葡萄糖基马特乌西诺醇()、米可尼苷B()、马特乌西诺醇()、杜鹃素()和去甲氧基马特乌西诺醇()。它们的结构主要通过广泛的核磁共振研究(氢核磁共振、碳核磁共振、DEPT、氢-氢化学位移相关谱、异核单量子相干谱、异核多键相关谱)和质谱来确定。对化合物-进行了使用大麻素受体(CB1和CB2)的结合试验评估。