Zobrazeno 1 - 10
of 880
pro vyhledávání: '"W. L. Duax"'
Autor:
W. Klyne
Publikováno v:
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 33:3273-3274
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b151d492c947fa6b2b15b793f16e17f
https://doi.org/10.1107/s0567740877010826
https://doi.org/10.1107/s0567740877010826
Autor:
W. L. Duax, J. F. Griffin
Publikováno v:
Steric Aspects of Biomolecular Interactions ISBN: 9781351076890
Steric Aspects of Biomolecular Interactions
Steric Aspects of Biomolecular Interactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27bf9c25565faef17d9343f6dc5d2916
https://doi.org/10.1201/9781351076890-4
https://doi.org/10.1201/9781351076890-4
Publikováno v:
Journal of Molecular Endocrinology. 33:253-261
Human 3beta-hydroxysteroid dehydrogenase/isomerase (3beta-HSD) is a key steroidogenic enzyme that catalyzes the first step in the conversion of circulating dehydroepiandrosterone (DHEA), pregnenolone or 17alpha-hydroxypregenolone to produce the appro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6643e66e13087e037121642f2f4ae2
https://doi.org/10.1677/jme.0.0330253
https://doi.org/10.1677/jme.0.0330253
Publikováno v:
Chemistry of Natural Compounds. 31:570-574
The structure of the product of condensation of gossypol with (−)-α-phenylethylamine has been determined. It has been shown that a possible cause of the difficulty in separating racemic gossypol into optically active components is not a racemizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0de1ca645b7300a2924b246827b9d0ed
https://doi.org/10.1007/bf01164882
https://doi.org/10.1007/bf01164882
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::958f96951441f2ee432ddcd9a1fc7841
https://doi.org/10.1002/chin.199547237
https://doi.org/10.1002/chin.199547237
Autor:
W. L. Duax, Ž. Ružić-Toroš, Biljana Nigović, D. Horvatić, N. Bresciani-Pahor, J. J. Stezowski, Volker Magnus, Biserka Kojić-Prodić
Publikováno v:
Acta Crystallographica Section B Structural Science. 47:107-115
The crystal structures of six biologically active cnojugates of the plant growth hormone (auxin), indole-3-acetic acid (IAA), with the amino acids L-alanine (1), alpha-amino-L-butyric acid (2), L-norvaline (3), DL-aspartic acid (4), L-isoleucine (5),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18624fc51f8cba2163b6e59f69341305
https://doi.org/10.1107/s0108768190009077
https://doi.org/10.1107/s0108768190009077
Publikováno v:
Topics in Stereochemistry, Volume 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38d5116d0822dbd139da3cc24b905cd2
https://doi.org/10.1002/9780470147184.ch5
https://doi.org/10.1002/9780470147184.ch5
Autor:
W. L. Duax, B. B. Maji, Suvankar Ganguly, Asok Banerjee, S. Pain, G. Biswas, Biswajit Das, K. L. Ghatak
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:2386-2388
The title tropinyl ester, 8-methyl-8-azabicydo[3.2.1]oct-3-yl 2-isopropylbenzo[b]thiophene-3-carboxylate, is an analogue of the parasympathomimetic neurotransmitter acetyl choline. The molecule is stabilized in the observed conformation by an intramo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b50700ab115a4e09166d2f2326d34e4
https://doi.org/10.1107/s0108270195004872
https://doi.org/10.1107/s0108270195004872
Autor:
Dao-Wei Zhu, V. Pletnev, Sheng-Xiang Lin, W. Pangborn, D. Ghosh, Fernand Labrie, W. L. Duax, Zdzislaw Wawrzak, M. Erman
Publikováno v:
Annals of the New York Academy of Sciences. 761:341-343
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12095afb5c8a341d114df6535606436
https://doi.org/10.1111/j.1749-6632.1995.tb31388.x
https://doi.org/10.1111/j.1749-6632.1995.tb31388.x
Publikováno v:
The Journal of biological chemistry. 276(21)
Porcine testicular carbonyl reductase (PTCR) belongs to the short chain dehydrogenases/reductases (SDR) superfamily and catalyzes the NADPH-dependent reduction of ketones on steroids and prostaglandins. The enzyme shares nearly 85% sequence identity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2a3ff3010c7a5174613d66872f654e3
https://pubmed.ncbi.nlm.nih.gov/11279087
https://pubmed.ncbi.nlm.nih.gov/11279087