| Literature DB >> 25499882 |
Nguyen Xuan Nhiem1, Nguyen Thi Thu Hien1, Bui Huu Tai2, Hoang Le Tuan Anh1, Dan Thi Thuy Hang1, Tran Hong Quang1, Phan Van Kiem1, Chau Van Minh1, Wonmin Ko3, Seungjun Lee3, Hyuncheol Oh3, Seung Hyun Kim4, Young Ho Kim5.
Abstract
Three new ent-kaurane diterpenoids, 7β,16α,17-trihydroxy-ent-kauran-19-oic acid (1), 7β,17-dihydroxy-16α-ent-kauran-19-oic acid 19-O-β-d-glucopyranoside ester (2), 7β,17-dihydroxy-ent-kaur-15-en-19-oic acid 19-O-β-d-glucopyranoside ester (3) along with five known compounds, paniculoside IV (4), 16α,17-dihydroxy-ent-kaurane (5), 16β,17-dihydroxy-ent-kaurane (6), 16β,17-dihydroxy-ent-kauran-19-al (7), and 16β,17-dihydroxy-ent-kauran-19-oic acid (8) were isolated from the fruits of Annona glabra. Their chemical structures were elucidated by physical and chemical methods. All compounds were evaluated for inhibitory activity against nitric oxide (NO) production in LPS-stimulated RAW 264.7 macrophages. As the results, compound 3 showed potent inhibitory LPS-stimulated NO production in RAW 264.7 macrophages with the IC50 value of 0.01±0.01μM; compounds 1 and 7 showed significant inhibitory NO production with the IC50 values of 0.39±0.12μM and 0.32±0.04μM, respectively.Entities:
Keywords: Annona glabra; Annonaceae; Anti-inflammation; ent-Kaurane diterpene
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Year: 2014 PMID: 25499882 DOI: 10.1016/j.bmcl.2014.11.059
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823