scispace - formally typeset
D

Deepa Alex

Researcher at University of Macau

Publications -  12
Citations -  591

Deepa Alex is an academic researcher from University of Macau. The author has contributed to research in topics: Angiogenesis & Zebrafish. The author has an hindex of 9, co-authored 9 publications receiving 545 citations. Previous affiliations of Deepa Alex include Hong Kong University of Science and Technology & University of Hong Kong.

Papers
More filters
Journal ArticleDOI

In vitro and in vivo structure and activity relationship analysis of polymethoxylated flavonoids: identifying sinensetin as a novel antiangiogenesis agent.

TL;DR: In vivo structure-activity relationship (SAR) analysis indicated that a flavonoid with a methoxylated group at the C3' position offers a stronger antiangiogenesis activity, whereas the absence of a meth Oxylated Group at theC8 position offers lower lethal toxicity in addition to enhancing the antiang iogenesis activity.
Journal ArticleDOI

Expression of Brassica juncea 3-hydroxy-3-methylglutaryl CoA synthase is developmentally regulated and stress-responsive.

TL;DR: HMGS assays confirmed that Escherichia coli-expressed recombinant BjHMGS1 shows HMGS activity that is inhibited by F244, a specific inhibitor of HMGS, suggesting that, like HMGR, HMGS is involved in defence.
Journal ArticleDOI

Inhibition of TNF-α-mediated endothelial cell-monocyte cell adhesion and adhesion molecules expression by the resveratrol derivative, trans-3,5,4'-trimethoxystilbene.

TL;DR: It is shown, for the first time, that its derivative trans‐3,5,4′‐trimethoxystilbene (TMS) may be a more potent anti‐inflammatory agent than resveratrol.
Journal ArticleDOI

Nobiletin, a polymethoxylated flavonoid from citrus, shows anti‐angiogenic activity in a zebrafish in vivo model and HUVEC in vitro model

TL;DR: Nobiletin, a polymethoxylated flavonoid from citrus fruits, showed anti‐angiogenic activity in both in vivo and in vitro in human umbilical vein endothelial cells (HUVECs), and nobiletin has a great potential for future research and development as a cytostatic anti‐proliferative agent.