Um alle Funktionen dieser Seite zu nutzen, aktivieren Sie bitte die Cookies in Ihrem Browser.
Mit einem my.bionity.com-Account haben Sie immer alles im Überblick - und können sich Ihre eigene Website und Ihren individuellen Newsletter konfigurieren.
- Meine Merkliste
- Meine gespeicherte Suche
- Meine gespeicherten Themen
- Meine Newsletter
1.947 Aktuelle Fachpublikationen in Journal of Natural Productsrss
20.11.2015 | Mehrdad Iranshahi; Maria Giovanna Chini; Milena Masullo; Amirhossein Sahebkar; Azita Javidnia; Mahsa Chitsazian Yazd ..., Journal of Natural Products, 2015
Curcumin, or diferuloylmethane, a polyphenolic molecule isolated from the rhizome of Curcuma longa, is reported to modulate multiple molecular targets involved in cancer and inflammatory processes. On the basis of its pan-inhibitory characteristics, here we show that simple chemical modifications ...
19.11.2015 | Jing-Jing Zhang; Xing-Wei Yang; Xia Liu; Jun-Zeng Ma; Yang Liao; Gang Xu, Journal of Natural Products, 2015
Hyperuralones C–H (1–6), six new 1,9-seco-bicyclic polyprenylated acylphloroglucinols (1,9-seco-BPAPs) derived from the normal polyprenylated acylphloroglucinols with a bicyclo[3.3.1]nonane-2,4,9-trione core, together with six known analogues, were isolated from the aerial parts of Hypericum ...
17.11.2015 | Christina Nord; Audrius Menkis; Anders Broberg, Journal of Natural Products, 2015
Eight illudane sesquiterpenes were obtained from the wood-decomposing fungus Granulobasidium vellereum (Ellis and Cragin) Jülich; among them were the enantiomers of the known compounds illudin M (1) and dihydroilludin M (4) and the diastereomers of illudin M (2) and illudin S (3), as well as two ...
17.11.2015 | Tran Dinh Thang; Ping-Chung Kuo; Nguyen Thi Bich Ngoc; Tsong-Long Hwang; Mei-Lin Yang; Shih-Huang Ta; E-Jian Lee; Da ..., Journal of Natural Products, 2015
Journal of Natural Products DOI: 10.1021/acs.jnatprod.5b00449
17.11.2015 | Yasuhiro Igarashi; Kazuki Yamamoto; Takao Fukuda; Akane Shojima; Jiro Nakayama; Lorena Carro; Martha E. Trujillo, Journal of Natural Products, 2015
Journal of Natural Products DOI: 10.1021/acs.jnatprod.5b00540
13.11.2015 | Tian-Xiao Li; Ming-Hua Yang; Xiao-Bing Wang; Ying Wang; Ling-Yi Kong, Journal of Natural Products, 2015
Nine new meroterpenes (1–9) and one new dioxolanone derivative (10), along with seven known compounds (11–17), were isolated from solid cultures of the endophytic fungus Guignardia sp., obtained from Euphorbia sieboldiana. Their structures were elucidated by analysis of UV, IR, 1D and 2D NMR, and ...
13.11.2015 | Verónica Egas; Rubén A. Toscano; Edelmira Linares; Robert Bye; Francisco J. Espinosa-García; Guillermo Delgado, Journal of Natural Products, 2015
Eight cadinane-type sesquiterpenoids (1–8) together with some triterpenoids, flavonoids, and sterols were isolated from the aerial parts of Heterotheca inuloides. The structures of the new compounds (1–4) were elucidated on the basis of extensive 1D and 2D NMR spectroscopic data analysis. The ...
13.11.2015 | Fernando M. S. Junior; Cody L. Covington; Ana Carolina F. de Albuquerque; Jonathas F. R. Lobo; Ricardo M. Borges; Ma ..., Journal of Natural Products, 2015
(−)-Centratherin is a bioactive sesquiterpenoid lactone, whose absolute configuration (AC) was not established, but has been proposed based on those of germacrane precursors. To verify this proposal, the experimental electronic circular dichroism (ECD), electronic dissymmetry factor (EDF), ...
12.11.2015 | Ze-Zhao Jiao; Su Yue; Hong-Xiang Sun; Tian-Yun Jin; Hai-Na Wang; Rong-Xiu Zhu; Lan Xiang, Journal of Natural Products, 2015
A polyamide column chromatography method using an aqueous ammonia mobile phase was developed for large-scale accumulation of water-soluble indoline amide glucosides from a medicinal plant, Portulaca oleracea. Ten new [oleraceins H, I, K, L, N, O, P, Q, R, S (1–10)] and four known [oleraceins A–D ...
12.11.2015 | Priscila de M. Cândido-Bacani; Patrícia de O. Figueiredo; Maria de F. C. Matos; Fernanda R. Garcez; Walmir S. Garcez, Journal of Natural Products, 2015
The bioactive ethyl acetate phase obtained from the latex of Croton urucurana Baillon afforded a novel orbitide (1), [1–9-NαC]-crourorb A1, that proved active against NCI-ADR/RES (ovary, multidrug-resistance phenotype) cells with the same potency as doxorubicin (positive control) and inactive up ...