John W. Daly
Affiliations: | Laboratory of Bioorganic Chemistry | NIDDK, Bethesda, MD, United States |
Area:
amphibian-derived alkaloidsWebsite:
https://pubs.acs.org/cen/news/86/i10/8610notw11.htmlGoogle:
"John William Daly"Bio:
(1933 - 2008)
http://www.nasonline.org/member-directory/deceased-members/3003893.html
http://searchworks.stanford.edu/view/2041331
http://www.pharmacognosy.us/wordpress/wp-content/uploads/ASPNL44_2_08.pdf
Mean distance: 17.19 (cluster 7) | S | N | B | C | P |
Cross-listing: Chemistry Tree
Parents
Sign in to add mentor| Richard Hallenbeck Eastman | grad student | 1958 | Stanford (Chemistry Tree) | |
| (The synthesis and properties of sabinene hydrate; a constituent of American peppermint oil) | ||||
| Bernhard Witkop | post-doc | 1958-1960 | NIH (Chemistry Tree) | |
Children
Sign in to add trainee| Patrick Maurice Dansette | post-doc | (Chemistry Tree) | |
| Phil Skolnick | post-doc | 1972-1977 | NIH - NIDDK |
| Christa E. Müller | post-doc | 1989-1990 | |
| Robert T. Mason | post-doc | 1987-1991 | National Institutes of Health - NIDDK |
Collaborators
Sign in to add collaborator| Julius Axelrod | collaborator | NIH | |
| Kenneth A. Jacobson | collaborator | 1985-2003 | NIDDK, National Institutes of Health |
BETA: Related publications
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Publications
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| Nikodijević O, Jacobson KA, Daly JW. (2024) Effects of Combinations of Methylxanthines and Adenosine Analogs on Locomotor Activity in Control and Chronic Caffeine-Treated Mice. Drug Development Research. 30: 104-110 |
| Fitch RW, Spande TF, Garraffo HM, et al. (2010) Phantasmidine: an epibatidine congener from the ecuadorian poison frog Epipedobates anthonyi. Journal of Natural Products. 73: 331-7 |
| Fitch RW, Sturgeon GD, Patel SR, et al. (2009) Epiquinamide: a poison that wasn't from a frog that was. Journal of Natural Products. 72: 243-7 |
| Fitch RW, Spande TF, Garraffo HM, et al. (2009) Dioicine: A novel prenylated purine alkaloid from Gymnocladus dioicus Heterocycles. 79: 583-598 |
| Kobayashi S, Toyooka N, Zhou D, et al. (2007) Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptors. Beilstein Journal of Organic Chemistry. 3: 30 |
| Toyooka N, Kobayashi S, Zhou D, et al. (2007) Synthesis of poison-frog alkaloids 233A, 235U, and 251AA and their inhibitory effects on neuronal nicotinic acetylcholine receptors. Bioorganic & Medicinal Chemistry Letters. 17: 5872-5 |
| Dismukes K, Rogers M, Daly JW. (2006) CYCLIC ADENOSINE 3′,5′-MONOPHOSPHATE FORMATION IN GUINEA-PIG BRAIN SLICES: EFFECT OF H1- AND H2-HISTAMINERGIC AGONISTS Journal of Neurochemistry. 26: 785-790 |
| Fitch RW, Kaneko Y, Klaperski P, et al. (2005) Halogenated and isosteric cytisine derivatives with increased affinity and functional activity at nicotinic acetylcholine receptors. Bioorganic & Medicinal Chemistry Letters. 15: 1221-4 |
| Fitch RW, Pei XF, Kaneko Y, et al. (2004) Homoepiboxidines: further potent agonists for nicotinic receptors. Bioorganic & Medicinal Chemistry. 12: 179-90 |
| Shi D, Padgett WL, Daly JW. (2003) Caffeine analogs: effects on ryanodine-sensitive calcium-release channels and GABAA receptors. Cellular and Molecular Neurobiology. 23: 331-47 |