Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Anthony H. Olavesen"'
Publikováno v:
Carbohydrate Research. 208:306-311
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db0fcf4128a13fa59abe389af4f80dcf
https://doi.org/10.1016/0008-6215(90)80117-l
https://doi.org/10.1016/0008-6215(90)80117-l
Publikováno v:
Biochemical pharmacology. 41(9)
In this paper we report on the use of biotin-labelled hyaluronidase for the analysis of the serum kinetics, tissue distribution and sub-cellular localization of normal and deglycosylated enzyme in the rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2cff88f8af8814d6eba2567f4162b73
https://pubmed.ncbi.nlm.nih.gov/2018571
https://pubmed.ncbi.nlm.nih.gov/2018571
Publikováno v:
Biochemical Society transactions. 18(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::307f73b972af28e431f6c65609cb2771
https://pubmed.ncbi.nlm.nih.gov/2373245
https://pubmed.ncbi.nlm.nih.gov/2373245
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 17:793-800
DL-[2-14C]Octan-2-sulPhate was prepared by sulphating DL-[2-14C]octan-2-ol with pyridine-SO3 adduct. Synthesis of the DL-[2-14C]alkanol started with carboxylation of hexyl magnesium bromide with 14CO2. Subsequent methylation with diazomethane and red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1004b50ddf36375386357e99be62a71
https://doi.org/10.1002/jlcr.2580170606
https://doi.org/10.1002/jlcr.2580170606
Publikováno v:
Xenobiotica. 6:667-678
1. The metabolism of the odd-numbered carbon chain surfactant, potassium undecyl [35S]sulphate in the rat was investigated. 2. The major route for elimination of radioactivity was the urine, regardless of the route of administration. 3. The surfactan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e305bfaefdc6859fb2d7a0dbead6fae0
https://doi.org/10.3109/00498257609151679
https://doi.org/10.3109/00498257609151679
Publikováno v:
Toxicology and Applied Pharmacology. 45:105-117
When [1-14C]dodecyl sulfonate and [1-14C]hexadecyl sulfonate were administered orally and ip to free-ranging rats and iv to anesthetized rats, the major route of excretion of radioactivity was urinary. Small amounts only of parent surfactant appeared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e6b0bd5921ba7f1a0f35f85ff699c64
https://doi.org/10.1016/0041-008x(78)90032-7
https://doi.org/10.1016/0041-008x(78)90032-7
Autor:
Peter Gacesa, Kenneth S. Dodgson, C. G. Curtis, Anthony H. Olavesen, Julia S. Earnshaw, Gillian M. Powell
Publikováno v:
Biochemical Pharmacology. 34:2199-2203
A highly purified commercial preparation of bovine testicular hyaluronidase (GL enzyme, Hyalosidase) was labelled with 125 iodine without measurable loss of enzyme activity. The labelled preparation was administered intravenously into rats and the se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd60054d16d0f25513022a83d90b6b7
https://doi.org/10.1016/0006-2952(85)90418-6
https://doi.org/10.1016/0006-2952(85)90418-6
Publikováno v:
Biochemical Journal. 168:373-377
The metabolic fates and modes of excretion of diethylstilboestrol mono[35S]sulphate and diethylstilboestrol di[35S]sulphate were studied in the guinea pig. Comparative studies were also made with [G-3H]diethylstilboestrol and phenolphthalein di[35S]s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f21e27ad296d51a43dc75089e3e3501f
https://doi.org/10.1042/bj1680373
https://doi.org/10.1042/bj1680373
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Enzymology. 661:205-212
Purified bovine testicular hyaluronidase (hyaluronate 4-glycanohydrolase, EC 3.2.1.35) was inactivated by butane-2,3-dione in either borate or Hepes buffer, pH 8.3. The presence of borate enhanced the inactivation process which followed pseudo-first-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67bfb139e978073dc2383d7a594d2281
https://doi.org/10.1016/0005-2744(81)90005-x
https://doi.org/10.1016/0005-2744(81)90005-x
Publikováno v:
Journal of Labelled Compounds. 10:151-160
The preparation of 2, 6-dimethoxy [U-14C]phenol was carried out in five steps from [U-14C]phenol. [U-14C]Phenol was converted to 2-[U-14C]phenoxy-5-nitrobenzophenone which was sequentially hydroxylated with hydrogen peroxide-acetic acid to give the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b138a15f0b75a05b21d434a02850017d
https://doi.org/10.1002/jlcr.2590100117
https://doi.org/10.1002/jlcr.2590100117