Next Article in Journal
Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
Next Article in Special Issue
N-(4-bromophenethyl) Caffeamide Protects Skin from UVB-Induced Inflammation Through MAPK/IL-6/NF-κB-Dependent Signaling in Human Skin Fibroblasts and Hairless Mouse Skin
Previous Article in Journal
Astragalus Polysaccharide Protect against Cadmium-Induced Cytotoxicity through the MDA5/NF-κB Pathway in Chicken Peripheral Blood Lymphocytes
Previous Article in Special Issue
COX Inhibition Profile and Molecular Docking Studies of Some 2-(Trimethoxyphenyl)-Thiazoles
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Acyclic Triterpenoids from Alpinia katsumadai Inhibit IL-6-Induced STAT3 Activation

Immunoregulatory Material Research Center, Korea Research Institute of Bioscience and Biotechnology, 181 Ipsin-gil, Jeongeup-si, Jeonbuk 56212, Korea
*
Authors to whom correspondence should be addressed.
Molecules 2017, 22(10), 1611; https://doi.org/10.3390/molecules22101611
Submission received: 25 August 2017 / Accepted: 21 September 2017 / Published: 25 September 2017
(This article belongs to the Special Issue Anti-inflammatory Agents)

Abstract

The seeds of Alpinia katsumadai yielded two new acyclic triterpenoids, 2,3,6,22,23-pentahydroxy-2,6,11,15,19,23-hexamethyl-tetracosa-7,10,14,18-tetraene (3) and 2,3,6,22,23-pentahydroxy-2,10,15,19,23-hexamethyl-7-methylenetetracosa-10,14,18-triene (4), as well as two known compounds, 2,3,22,23-tertrahydroxy-2,6,10,15,19,23-hexamethyl-tetracosa-6,10,14,18-tetraene (1) and 2,3,5,22,23-pentahydroxy-2,6,10,15,19,23-hexamethyl-tetracosa-6,10,14,18-tetraene (2). The absolute configurations of 2 and 3, which were determined by means of a modified Mosher’s method, are suggested as (3R; 5S; 22R) and (3R; 22R), respectively. Compounds 14 inhibited IL-6-induced JAK2/STAT3 activity in a dose-dependent fashion, with IC50 values of 0.67, 0.71, 2.18, and 2.99 μM. Moreover, IL-6-stimulated phosphorylation of STAT3 was significantly suppressed in U266 cells by the administration of A. katsumadai EtOH extract and Compounds 1 and 2. These results suggest that major phytochemicals, Compounds 1 and 2, obtained from A. katsumadai may be useful candidates for designing new IL-6 inhibitors as anti-inflammatory agents.
Keywords: Alpinia katsumadai; acyclic triterpenoids; IL-6; STAT3; inflammation Alpinia katsumadai; acyclic triterpenoids; IL-6; STAT3; inflammation
Graphical Abstract

Share and Cite

MDPI and ACS Style

Jang, H.-J.; Lee, S.-J.; Lee, S.; Jung, K.; Lee, S.W.; Rho, M.-C. Acyclic Triterpenoids from Alpinia katsumadai Inhibit IL-6-Induced STAT3 Activation. Molecules 2017, 22, 1611. https://doi.org/10.3390/molecules22101611

AMA Style

Jang H-J, Lee S-J, Lee S, Jung K, Lee SW, Rho M-C. Acyclic Triterpenoids from Alpinia katsumadai Inhibit IL-6-Induced STAT3 Activation. Molecules. 2017; 22(10):1611. https://doi.org/10.3390/molecules22101611

Chicago/Turabian Style

Jang, Hyun-Jae, Seung-Jae Lee, Soyoung Lee, Kyungsook Jung, Seung Woong Lee, and Mun-Chual Rho. 2017. "Acyclic Triterpenoids from Alpinia katsumadai Inhibit IL-6-Induced STAT3 Activation" Molecules 22, no. 10: 1611. https://doi.org/10.3390/molecules22101611

APA Style

Jang, H.-J., Lee, S.-J., Lee, S., Jung, K., Lee, S. W., & Rho, M.-C. (2017). Acyclic Triterpenoids from Alpinia katsumadai Inhibit IL-6-Induced STAT3 Activation. Molecules, 22(10), 1611. https://doi.org/10.3390/molecules22101611

Article Metrics

Back to TopTop