Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Andrew R. Knaggs"'
Autor:
Andrew R. Knaggs
Publikováno v:
Natural Product Reports. 17:269-292
Autor:
Andrew R. Knaggs
Publikováno v:
Natural Product Reports. 16:525-560
Autor:
T. Rashid, P. J. Sidebottom, P. S. Marshall, Andrew R. Knaggs, R. J. P. Cannell, I. M. Ismail
Publikováno v:
Xenobiotica. 27:147-157
1. Biotransformation of warfarin by the fungus Beauveria bassiana (ATCC 7159) yielded the first reported phase II warfarin metabolite, 3'4'-dihydroxywarfarin-3'-[4-methoxyglucoside], another previously unreported metabolite, 3',4'-dihydroxywarfarin a
Autor:
Derek R. Sutherland, Karl M. Cable, Philip J. Sidebottom, Andrew R. Knaggs, Guy N. Wells, Richard J. P. Cannell
Publikováno v:
Tetrahedron Letters. 36:477-480
The formation of the hydantoin biotransformation product (3) of Alosetron (1) has been shown to proceed via migration of the tricyclic lactam moiety and occurs with complete retention of both hydrogens in the C-7′ methylene group.
Autor:
Paul E. Fleming, Kevin Walker, Andrew R. Knaggs, M. Haertel, Heinz G. Floss, Ursula Mocek, A. Lansing
Publikováno v:
Pure and Applied Chemistry. 66:2045-2048
The biosynthesis of the plant antitumor agent, taxol, was studied by feeding radioactive or stable isotope-labeled precursors to cut stems or to inner bark tissue of Taxus brevifolia. The labeled taxol was purified to radiochemical purity and subject
Publikováno v:
Journal of the American Chemical Society. 115:7557-7568
The biosynthesis of the highly modified thiopeptide antibiotic, nosiheptide (1), was studied by feeding radioactive and stable-isotope-labeled precursors to cultures of the producing organism, Streptomyces actuosus. The stable isotope enrichments and
Publikováno v:
ChemInform. 22
Precursor feeding experiments establish that the isocyanide groups in xanthocillin-X monomethyl ether (XME)1 do not originate from (i) compounds associated with C1-tetrahydrofolate metabolism; (ii) the ureido group of citrulline, carbamoyl phosphate,
Autor:
Andrew R. Knaggs, Richard B. Herbert
Publikováno v:
ChemInform. 23
Results of experiments using ‘resting’ cells of Pseudomonas fluorescens with [2-13C]-, [1-13C]- and [2-2H2]-glycine as precursors show that glyoxylic acid is specifically the source of C-1 and C-2 of the antibiotic obafluorin 1. The 13C labelling
Autor:
Andrew R. Knaggs, Richard B. Herbert
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 24
The biosynthesis of the highly modified thiopeptide antibiotic, nosiheptide (1), was studied by feeding radioactive and stable-isotope-labeled precursors to cultures of the producing organism, Streptomyces actuosus. The stable isotope enrichments and