Zobrazeno 1 - 10
of 12
pro vyhledávání: '"C W, Hutchins"'
The reaction of N-arylhydroxamic acids and N-aryl-N-alkylhydroxylamines with ynamines, α-chloroenamines, β-chloro-α,β-ethylenic esters, α,β-acetylenic esters, and α-allenic esters was investigated. N-Aryl-O-vinylhydroxylamines were presumably
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b02fda43adb4fbf9b2a526170f6da168
https://doi.org/10.1159/000430625
https://doi.org/10.1159/000430625
Autor:
Y. C. Martin, Chun Wel Lin, B. R. Bianchi, I. Lico, M. J. Bennett, L. Bednarz, M. W. Holladay, K. E. Asin, Thomas R. Miller, A. M. Nadzan, C. W. Hutchins, A. L. Nikkel, D. G. Witte
Publikováno v:
Peptides 1992 ISBN: 9789401046466
Peptides 1992
Peptides 1992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f183f5352fd3a51549482be37a108db3
https://doi.org/10.1007/978-94-011-1470-7_279
https://doi.org/10.1007/978-94-011-1470-7_279
Publikováno v:
The Journal of biological chemistry. 267(25)
Several serines present in transmembrane domain V are conserved among members of the G-protein-coupled receptor family that bind catecholamines. Two of these serines that are present in the beta-adrenergic receptor were previously shown by site-direc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32694046c92c380ebb84886d95781486
https://pubmed.ncbi.nlm.nih.gov/1355478
https://pubmed.ncbi.nlm.nih.gov/1355478
Autor:
A. M. Nadzan, D. S. Garvey, M. W. Holladay, K. Shiosaki, M. D. Tufano, Y. K. Shue, J. Y. L. Chung, P. D. May, C. S. May, C. W. Lin, T. R. Miller, D. G. Witte, B. R. Bianchi, C. A. W. Wolfram, S. Burt, C. W. Hutchins
Publikováno v:
Peptides ISBN: 9789401050050
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::155b34b97db623f207510ca55addc372
https://doi.org/10.1007/978-94-011-2264-1_31
https://doi.org/10.1007/978-94-011-2264-1_31
Autor:
S H, Rosenberg, J F, Dellaria, D J, Kempf, C W, Hutchins, K W, Woods, R G, Maki, E, de Lara, K P, Spina, H H, Stein, J, Cohen
Publikováno v:
Journal of medicinal chemistry. 33(6)
A series of low-nanomolar renin inhibitors containing novel C-terminal heterocycles has been designed by formally cyclizing the C-terminus of a glycol-based inhibitor to the second hydroxyl. Molecular modeling suggests that the heterocyclic oxygen hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b964f44ceb442bf5d1e0eb515a5590
https://pubmed.ncbi.nlm.nih.gov/2187994
https://pubmed.ncbi.nlm.nih.gov/2187994
Publikováno v:
Journal of medicinal chemistry. 24(7)
The 6-demethoxy analogue of thebaine has been easily prepared from codeine via isocodeine and its sulfenate ester. This diene, 7, readily undergoes reaction with vinyl ketones to afford Diels-Alder adducts of the 6,14-ethenomorphinan type. Further re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75599bc2c2c192b6e7c149bd4433000c
https://pubmed.ncbi.nlm.nih.gov/7277381
https://pubmed.ncbi.nlm.nih.gov/7277381
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0074f6c58014ed6106d30e6b6f77dd30
https://doi.org/10.1002/chin.198147294
https://doi.org/10.1002/chin.198147294
Autor:
R. M. COATES, C. W. HUTCHINS
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58cb02ce2f47e3a49d4a491d810cbac8
https://doi.org/10.1002/chin.198014239
https://doi.org/10.1002/chin.198014239
Autor:
R S, Kennedy, C W, Hutchins
Publikováno v:
The Journal of sports medicine and physical fitness. 16(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30856e3f6cafe8051b85fe1392c0f605
https://pubmed.ncbi.nlm.nih.gov/979227
https://pubmed.ncbi.nlm.nih.gov/979227
Autor:
P R, Jeanneret, C W, Hutchins
Publikováno v:
Aerospace medicine. 37(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7f804af729969e1eaca4fc2c4dde656
https://pubmed.ncbi.nlm.nih.gov/5954444
https://pubmed.ncbi.nlm.nih.gov/5954444