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Metabolism of xilobam in laboratory animals and man

Autor: R. S. Egan, W. N. Wu, J. F. Hills

Publikováno v: Xenobiotica; the fate of foreign compounds in biological systems. 24(7)

1. Biotransformation and excretion of xilobam (Xm) were studied after single oral doses of Xm-14C in mouse, rat, dog and man. 2. Following oral administration of Xm-14C, recoveries of total 14C (0-24 h) in urine wereor = 78% of the dose in all specie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5f8281eb0fc315f216d22d8b746c024
https://pubmed.ncbi.nlm.nih.gov/7975729

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Studies on the Genus Speerschneidera

Autor: Josef Hafellner, R. S. Egan

Publikováno v: The Lichenologist. 13:11-26

Both light and scanning electron microscopy have been used to investigate the morphology and development of Speerschneidera euploca (Tuck.) Trevisan. This monotypic genus produces lecanoralean apothecia and Lecanora-type asci; the latter negates the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b3abfea252f8232462f82d0555db5aa4
https://doi.org/10.1017/s0024282981000042

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Fenoctimine Sulfate Hydration

Autor: F. A. Chrzanowski, J. E. Mills, C. Y. Ko, V. Paragamian, Walkling Wd, J. N. Plampin, R. S. Egan

Publikováno v: Drug Development and Industrial Pharmacy. 10:241-258

Fenoctimine sulfate was demonstrated to exist in two distinct crystalline forms, i.e., form A (low melting, 0.5 mole water of hydration), and form B (high melting, anhydrous). These forms can exist separately, in crystalline mixtures with each other,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e274f6b82abcb1f0e53665aca48299d4
https://doi.org/10.3109/03639048409064648

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Oxidation and Reduction of 8,9-Anhydroerythronolide B 6,9-Hemiacetal

Autor: P. Kurath, R. S. Egan

Publikováno v: Helvetica Chimica Acta. 54:523-532

Die Reaktion von Erythronolid B mit Saure lieferte das bisher unbekannte 8, 9-Anhydroerythronolid-B-6, 9-hemiacetal. Diese Verbindung wurde oxydativ in (8S, 9S)-8, 9-Anhydroerythronolid-B-6, 9-hemiacetal 8,9-epoxid und (8S)-8-Hydroxyerythronolid B um

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aaeb64209e1cd3d415e7bef9e24de28b
https://doi.org/10.1002/hlca.19710540211

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The contrasting behavior of cyclic and acyclic 2-amidomethyleneresorcinols towards cyclization with acetaldehyde

Autor: H. E. Zaugg, R. S. Egan, D. L. Arendsen

Publikováno v: Journal of Heterocyclic Chemistry. 16:21-23

The two cyclic amidomethylene resorcinols, 3a and 3b, readily undergo cyclization with acetaldehyde to the azacannabinoids 4 and 6, respectively. However, the acyclic amidomethylene resorcinol 10, under the same conditions, gives the benzodioxan 11.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b702e2c4cb19d8eca88c0af7b477e727
https://doi.org/10.1002/jhet.5570160105

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