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Susan L. Morris-Natschke

Researcher at University of North Carolina at Chapel Hill

Publications -  287
Citations -  9762

Susan L. Morris-Natschke is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Cytotoxicity & Camptothecin. The author has an hindex of 48, co-authored 284 publications receiving 8331 citations. Previous affiliations of Susan L. Morris-Natschke include China Medical University (Taiwan) & Shandong University.

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Anti-aids agents. Part 58: synthesis and anti-HIV activity of 1-thia-di-O-(-)-camphanoyl-(+)-cis-khellactone(1-thia-DCK) analogues

Peng Xia, +10 more
- 21 Jun 2004 - 
TL;DR: The bioassay results indicated that thia-DCK analogues merit attention as potential HIV-1 inhibitors.
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Chemical Structures and Biological Activities of Limonoids from the Genus Swietenia (Meliaceae).

Yun Peng Sun, +9 more
- 29 Jun 2018 - 
TL;DR: This paper will give a comprehensive overview of the recent phytochemical and pharmacological research on the terpenes from Swietenia plants and encourage further drug discovery research.
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Secondary metabolites from the Chinese liverwort Cephaloziella kiaeri.

Rui Juan Li, +10 more
- 13 Sep 2013 - 
TL;DR: Sixteen new clerodane diterpenoids, cephaloziellins A-P (1-16), and two known analogues (17 and 18) were isolated from an EtOH extract of the Chinese liverwort, and the structures of 5, 9, and 15 were confirmed by single-crystal X-ray diffraction analyses.
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Membrane-Interactive Phospholipids Inhibit HIV Type 1-Induced Cell Fusion and Surface gp160/gp120 Binding to Monoclonal Antibody

Lisa Krugner-Higby, +9 more
- 01 Jun 1995 - 
TL;DR: Results suggest that anti-HIV-1 activity of PL compounds involves alteration of cell surface membranes and viral envelopes.
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Synthesis, antitumor activity, and mechanism of action of 6-acrylic phenethyl ester-2-pyranone derivatives

Sai Fang, +10 more
- 08 Apr 2015 - 
TL;DR: Compound is a promising compound as an antitumor agent that showed good ADMET properties with good absorption, low hepatotoxicity, and good solubility, and thus, could easily be bound to carrier proteins, without inhibition of CYP2D6.