Novel Cytotoxic, Alkylated Hydroquinones from Lannea welwitschii

Author:

Groweiss Amiram1,Cardellina John H.1,Pannell Lewis K.1,Uyakul Duangchan1,Kashman Yoel1,Boyd Michael R.1

Affiliation:

1. Laboratory of Drug Discovery Research and Development, Developmental Therapeutics Program, Division of Cancer Treatment, Diagnosis, and Centers, National Cancer Institute−Frederick Cancer Research and Development Center, P.O. Box B, Building 1052, Room 121, Frederick, Maryland 21702-1201, and Laboratory of Analytical Chemistry, National Institute of Diabetes and Digestive Kidney Disease, 9000 Rockville Pike, Building 8, Room B2A23, Bethesda, Maryland 20892

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Reference10 articles.

1. Boyd, M. R.; Paull, K. D.; Rubinstein, L. R. InCytotoxic AnticancerDrugs:  Models and Concepts for Drug Discovery and Development.Developments in Oncology; Valeriote, F. A., Corbett, T. H., Baker, L. H., Eds. Kluwer Academic Publishers:  Amsterdam, 1992; pp 11−34.

2. Analogs of poison ivy urushiol. Synthesis and biological activity of disubstituted n-alkylbenzenes

3. Sex Pheromones in Snakes

4. Quaternary ammonium salts for butylation and mass spectral identification of volatile organic acids

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