John W. Daly

Affiliations: 
Laboratory of Bioorganic Chemistry NIDDK, Bethesda, MD, United States 
Area:
amphibian-derived alkaloids
Website:
https://pubs.acs.org/cen/news/86/i10/8610notw11.html
Google:
"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)
 
SNBCP
Cross-listing: Chemistry Tree

Parents

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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

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Phil Skolnick post-doc 1972-1977 NIH - NIDDK
BETA: Related publications

Publications

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Andriamaharavo NR, Garraffo HM, Saporito RA, et al. (2010) Roughing it: a mantellid poison frog shows greater alkaloid diversity in some disturbed habitats. Journal of Natural Products. 73: 322-30
Ohtani M, Daly JW, Oka T. (2009) Co-existence of muscarinic and nicotinic receptors and their functional interaction in mouse Beta-TC6 cells. European Journal of Pharmacology. 604: 150-7
Kem WR, Rocca J, Garraffo HM, et al. (2009) Synthesis and spectroscopic comparison of the eight methyl-2,3′-bipyridyls and identification of a hoplonemertine alkaloid as 3-methyl-2,3′-bipyridyl Heterocycles. 79: 1025-1041
Fitch RW, Spande TF, Garraffo HM, et al. (2009) Dioicine: A novel prenylated purine alkaloid from Gymnocladus dioicus Heterocycles. 79: 583-598
Zhou D, Toyooka N, Nemoto H, et al. (2009) Synthesis, determination of the absolute stereochemistry, and evaluations at the nicotinic acetylcholine receptors of a hydroxyindolizidine alkaloid from the ant Myrmicaria melanogaster Heterocycles. 79: 565-571
Dumbacher JP, Menon GK, Daly JW. (2009) Skin as a toxin storage organ in the endemic new Guinean genus Pitohui Auk. 126: 520-530
Nelson A, Garraffo HM, Spande TF, et al. (2008) Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus). Beilstein Journal of Organic Chemistry. 4: 6
Daly JW, Garraffo HM, Spande TF, et al. (2008) Individual and geographic variation of skin alkaloids in three species of Madagascan poison frogs (Mantella). Journal of Chemical Ecology. 34: 252-79
Saporito RA, Donnelly MA, Norton RA, et al. (2008) Oribatid mites as a major dietary source for alkaloids in poison frogs (Proceedings of the National Academy of Sciences of the United States of America (2007) 104, 21, (8885-8890) DOI: 10.1073/pnas.0702851104) Proceedings of the National Academy of Sciences of the United States of America. 105: 17587
Toyooka N, Zhou D, Nemoto H, et al. (2007) Flexible synthetic routes to poison-frog alkaloids of the 5,8-disubstituted indolizidine-class I: synthesis of common lactam chiral building blocks and application to the synthesis of (-)-203A, (-)-205A, and (-)-219F. Beilstein Journal of Organic Chemistry. 3: 29
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