Neal Castagnoli
Affiliations: | 1987 | University of California, San Francisco, San Francisco, CA | |
| 1987- | Virginia Polytechnic Institute and State University, Blacksburg, VA, United States |
Area:
Organic Chemistry, Pharmaceutical Chemistry, BiochemistryWebsite:
https://chem.vt.edu/people/faculty/ncastagnoli.htmlGoogle:
"Neal Castagnoli"Bio:
https://pharm.ucsf.edu/history-bts/benet
DOI: 10.1021/jo01027a029
Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Henry Rapoport | grad student | 1964 | UC Berkeley | |
| (Synthesis of pyrrole and polypyrrole systems.) | ||||
Children
Sign in to add trainee| Mark S. Cushman | grad student | 1969-1973 | UCSF |
| Wolfgang Sadee | post-doc | 1970 | UCSF (Neurotree) |
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Publications
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| Bergström MA, Isin EM, Castagnoli N, et al. (2011) Bioactivation pathways of the cannabinoid receptor 1 antagonist rimonabant Drug Metabolism and Disposition. 39: 1823-1832 |
| Pretorius A, Ogunrombi MO, Fourie H, et al. (2010) Interactions of 1-methyl-3-phenylpyrrolidine and 3-methyl-1-phenyl-3-azabicyclo[3.1.0]hexane with monoamine oxidase B. Bioorganic & Medicinal Chemistry. 18: 4111-8 |
| Mali'n TJ, Weidolf L, Castagnoli N, et al. (2010) P450-catalyzed vs. electrochemical oxidation of haloperidol studied by ultra-performance liquid chromatography/electrospray ionization mass spectrometry. Rapid Communications in Mass Spectrometry : Rcm. 24: 1231-40 |
| Strydom B, Malan SF, Castagnoli N, et al. (2010) Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues Bioorganic and Medicinal Chemistry. 18: 1018-1028 |
| Manley-King CI, Terre'Blanche G, Castagnoli N, et al. (2009) Inhibition of monoamine oxidase B by N-methyl-2-phenylmaleimides Bioorganic and Medicinal Chemistry. 17: 3104-3110 |
| Pretorius A, Ogunrombi MO, Terre'blanche G, et al. (2008) Deuterium isotope effects for the oxidation of 1-methyl-3-phenyl-3-pyrrolinyl analogues by monoamine oxidase B. Bioorganic & Medicinal Chemistry. 16: 8813-7 |
| Frédérick R, Dumont W, Ooms F, et al. (2006) Synthesis, structural reassignment, and biological activity of type B MAO inhibitors based on the 5H-indeno[1,2-c]pyridazin-5-one core. Journal of Medicinal Chemistry. 49: 3743-7 |
| Jurva U, Bissel P, Isin EM, et al. (2005) Model electrochemical-mass spectrometric studies of the cytochrome P450-catalyzed oxidations of cyclic tertiary allylamines Journal of the American Chemical Society. 127: 12368-12377 |
| Liu X, Zang L, Van der Schyf CJ, et al. (1999) Studies on the pyrrolinone metabolites derived from the tobacco alkaloid 1-methyl-2-(3-pyridinyl)pyrrole (beta-nicotyrine). Chemical Research in Toxicology. 12: 508-12 |
| Palmer SL, Mabic S, Castagnoli N. (1997) Probing the active sites of monoamine oxidase A and B with 1,4-disubstituted tetrahydropyridine substrates and inactivators. Journal of Medicinal Chemistry. 40: 1982-9 |