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- Publications
- Influence
Structural identification of the major DNA adduct formed by aflatoxin B1 in vitro.
- J. Essigmann, R. Croy, +4 authors G. Wogan
- Medicine, Chemistry
- Proceedings of the National Academy of Sciences…
- 1 May 1977
The covalent binding of the hepatocarcinogen aflatoxin B1 by rat liver microsomes to calf thymus DNA resulted in a binding level equal to one aflatoxin residue per 60 DNA nucleotides. An aflatoxin… Expand
Activation of specific RXR heterodimers by an antagonist of RXR homodimers
- D. Lala, R. Mukherjee, +6 authors R. A. Heyman
- Biology, Medicine
- Nature
- 3 October 1996
RETINOID X receptor (RXR) plays a central role in the regulation of many intracellular receptor signalling pathways1 and can mediate ligand-dependent transcription, acting as a homodimer or as a… Expand
Malonyl Coenzyme A Decarboxylase Inhibition Protects the Ischemic Heart by Inhibiting Fatty Acid Oxidation and Stimulating Glucose Oxidation
- J. Dyck, J. Cheng, +9 authors G. Lopaschuk
- Chemistry, Medicine
- Circulation research
- 14 May 2004
Abnormally high rates of fatty acid oxidation and low rates of glucose oxidation are important contributors to the severity of ischemic heart disease. Malonyl coenzyme A (CoA) regulates fatty acid… Expand
Matrix metalloproteinase inhibitors: a structure-activity study.
- D. Levy, F. Lapierre, +9 authors R. E. Galardy
- Chemistry, Medicine
- Journal of medicinal chemistry
- 15 January 1998
Modifications around the dipeptide-mimetic core of a hydroxamic acid based matrix metalloproteinase inhibitor were studied. These variations incorporated a variety of natural, unnatural, and… Expand
Synthesis and structure-activity relationship of small-molecule malonyl coenzyme A decarboxylase inhibitors.
- J. Cheng, M. Chen, +13 authors A. Nadzan
- Chemistry, Medicine
- Journal of medicinal chemistry
- 11 February 2006
The discovery and structure-activity relationship of first-generation small-molecule malonyl-CoA decarboxylase (MCD; CoA = coenzyme A) inhibitors are reported. We demonstrated that MCD inhibitors… Expand
Novel nonsecosteroidal vitamin D mimics exert VDR-modulating activities with less calcium mobilization than 1,25-dihydroxyvitamin D3.
- M. Boehm, P. Fitzgerald, +9 authors E. Allegretto
- Chemistry, Medicine
- Chemistry & biology
- 1 May 1999
BACKGROUND
The secosteroid 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) acts through the vitamin D receptor (VDR) to elicit many activities that make it a promising drug candidate for the treatment of a… Expand
Identification of the first retinoid X, receptor homodimer antagonist.
- S. S. Canan Koch, L. J. Dardashti, +5 authors A. Nadzan
- Chemistry, Medicine
- Journal of medicinal chemistry
- 16 August 1996
Synthesis of retinoid X receptor-specific ligands that are potent inducers of adipogenesis in 3T3-L1 cells.
- S. S. Canan Koch, L. J. Dardashti, +4 authors A. Nadzan
- Chemistry, Medicine
- Journal of medicinal chemistry
- 5 February 1999
A novel series of oxime ligands has been synthesized that displays potent, specific activation of the retinoid X receptors (RXRs). The oximes of 3-substituted… Expand