(±)-Homocrepidine A, a Pair of Anti-inflammatory Enantiomeric Octahydroindolizine Alkaloid Dimers from Dendrobium crepidatum

Y Hu, C Zhang, X Zhao, Y Wang, D Feng… - Journal of Natural …, 2016 - ACS Publications
A pair of racemic indolizidine enantiomers,(±)-homocrepidine A (1), and a piperidine
derivative, homocrepidine B (2), were isolated from Dendrobium crepidatum along with the …

Anti-inflammatory activity of licochalcone A isolated from Glycyrrhiza inflata

Y Cui, M Ao, J Hu, L Yu - Zeitschrift für Naturforschung C, 2008 - degruyter.com
Licochalcone A was isolated from the roots of Glycyrrhiza inflata and evaluated for its anti-
inflammatory activity in xylene-induced mice ear edema and carrageenan-induced paw …

Efficient synthesis of the immunomodulating compound KRP-203

M Hamada, M Kiuchi, K Adachi - Synthesis, 2007 - thieme-connect.com
A practical and concise synthesis of KRP-203 (1) was achieved by utilizing a palladium
coupling reaction mediated by XantPhos and Pd 2 (dba) 3 as the key step. The coupling …

[HTML][HTML] Dieckol attenuates the nociception and inflammatory responses in different nociceptive and inflammatory induced mice model

Z Li, Y Wang, J Zhao, H Zhang - Saudi Journal of Biological Sciences, 2021 - Elsevier
Pain is the common indicator of inflammatory ailments and traumatic tissue injuries. The
dieckol is an important therapeutic compound, which present in many seaweeds. The …

New synthetic anti-inflammatory chrysin analog, 5, 7-dihydroxy-8-(pyridine-4yl) flavone

H Lim, JH Jin, H Park, HP Kim - European journal of pharmacology, 2011 - Elsevier
To identify anti-inflammatory flavonoid derivatives with optimal chemical structures, various 8-
heterocyclic-substituted chrysin derivatives were previously synthesized and their effects on …

Total synthesis and anti-inflammatory evaluation of penchinone A and its structural analogues

Y Oh, YJ Jang, M Jeon, HS Kim, JH Kwak… - The Journal of …, 2017 - ACS Publications
The first total synthesis and biological evaluation of penchinone A and its structural
analogues are described. The key steps for the preparation of penchinone A derivatives …

Inhibition of IL-8 secretion on BxPC-3 and MIA PaCa-2 cells and induction of cytotoxicity in pancreatic cancer cells with marine natural products

EA Guzmán, D Harmody, TP Pitts, B Vera-Diaz… - Anti-cancer …, 2017 - journals.lww.com
Pancreatic cancer presents one of the most negative prognosis of all cancers as it has
usually metastasized by the time a patient is diagnosed. The American Cancer Society …

Licochalcone A Derivatives as Selective Dipeptidyl Peptidase 4 Inhibitors with Anti-Inflammatory Effects

CQ Li, JH Shi, J Mu, AQ Wang, LW Zou… - Journal of Natural …, 2023 - ACS Publications
A set of 22 analogs of licochalcone A was designed and synthesized to explore their
potentials as dipeptidyl peptidase 4 (DPP4) inhibitors with anti-inflammatory effects. The anti …

Synthesis of licochalcone analogues with increased anti-inflammatory activity

SJ Kim, CG Kim, SR Yun, JK Kim, JG Jun - Bioorganic & medicinal …, 2014 - Elsevier
Licohalcones have been reported to have various biological activities. However, most of
licochalcones also showed cytotoxicity even though their versitile utilities. Licochalcones B …

Aryl benzofuran derivatives from the stem bark of Calpocalyx dinklagei attenuate inflammation

DWFG Kapche, NM Lekane, SS Kulabas, H Ipek… - Phytochemistry, 2017 - Elsevier
Abstract Calpocalyx dinklagei Harms (Fabaceae) is a tropical medicinal tree, which is
indigenous to Western Africa. A phytochemical study of this local plant species from its stem …