Literature DB >> 24219809

Enmein-type 6,7-seco-ent-kauranoids from Isodon sculponeatus.

Hua-Yi Jiang1, Wei-Guang Wang, Min Zhou, Hai-Yan Wu, Rui Zhan, Xiao-Nian Li, Xue Du, Yan Li, Jian-Xin Pu, Han-Dong Sun.   

Abstract

Fourteen enmein-type 6,7-seco-ent-kaurane diterpenoids, seven new ones (sculponins M-S, 1-7) and seven known compounds (8-14), were isolated from the aerial parts of Isodon sculponeatus . Compound 1 is the first example of an ent-kauranoid, possessing a 11,12-epoxy group, and compounds 6 and 7 have a rare 3,6-epoxy group. The structures were established primarily by NMR and MS methods, and the absolute configurations of 1, 3, and 6 were determined by single-crystal X-ray diffraction. Compound 14 showed significant cytotoxic activity against five human tumor lines, with IC50 values ranging from 1.0 to 3.5 μM, and it also inhibited NO production in LPS-stimulated RAW264.7 cells, with an IC50 value of 2.2 μM.

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Year:  2013        PMID: 24219809     DOI: 10.1021/np400669t

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  Ent-kaurane-type diterpenoids from Isodonis Herba activate human hair follicle dermal papilla cells proliferation via the Akt/GSK-3β/β-catenin transduction pathway.

Authors:  Yoshiaki Manse; Fenglin Luo; Kazuhiro Kato; Akane Okazaki; Eriko Okada-Nishida; Mitsuhiro Yanagida; Sho Nakamura; Toshio Morikawa
Journal:  J Nat Med       Date:  2021-01-08       Impact factor: 2.343

  1 in total

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