Zobrazeno 1 - 10
of 12
pro vyhledávání: '"D. P. Mcadam"'
Autor:
D. P. Mcadam, J. H. Skerritt
Publikováno v:
ChemInform. 24
By use of t-butyl 3-[ chloro ( methoxy ) phosphorothioylamino ] propanoate (1), a general method was developed that allowed the preparation of analogues of specific organothiophosphates ; these analogues are suitable for use as haptens in the develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06a530f2810d44aa01fadaa1bd573bfc
https://doi.org/10.1002/chin.199343179
https://doi.org/10.1002/chin.199343179
Autor:
Gary P. Jamieson, Alan R. P. Paterson, D. P. Mcadam, Marie B. Snook, Morris J. Robins, James D. Craik, Carol E. Cass, Anne M. Brocklebank, James S. Wiley, William H. Sawyer
Publikováno v:
Biochemical Journal. 273:667-672
The N6-(4-nitrobenzyl) derivative of adenosine is a tight-binding inhibitor of the equilibrative inhibitor-sensitive nucleoside transporter of mammalian cells. A fluorescent ligand for this transporter has been synthesized by allowing an adenosine an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b06344623439a2cfdb4aee7c3b5788ee
https://doi.org/10.1042/bj2730667
https://doi.org/10.1042/bj2730667
Autor:
Carol E. Cass, D. P. Mcadam, F. R. Agbanyo, Morris J. Robins, J.-I. Asakura, Wendy P. Gati, James D. Craik, Alan R. P. Paterson, Damaraju Vijayalakshmi
Publikováno v:
Biochemical Journal. 270:605-614
Derivatives of N6-(4-aminobenzyl)adenosine (substituted at the aminobenzyl group) and 5′-linked derivatives of N6-(4-nitrobenzyl)adenosine (NBAdo) were evaluated as inhibitors of site-specific binding of [3H]nitrobenzylthioinosine (NBMPR) to pig er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3f4ffb599c7e6070b09e353d7b348f
https://doi.org/10.1042/bj2700605
https://doi.org/10.1042/bj2700605
Autor:
Bruce S. Ferguson, Rodney J. Bushway, H. L. Beasely, D. P. McAdam, K. A. Larkin, John H. Skerritt
Publikováno v:
Bulletin of environmental contamination and toxicology. 59(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::542eb2a278d2e1b67c5d1ca815914aa8
https://pubmed.ncbi.nlm.nih.gov/9256389
https://pubmed.ncbi.nlm.nih.gov/9256389
Autor:
J. H. Skerritt, D. P. Mcadam
Publikováno v:
Australian Journal of Chemistry. 46:959
By use of t-butyl 3-[ chloro ( methoxy ) phosphorothioylamino ] propanoate (1), a general method was developed that allowed the preparation of analogues of specific organothiophosphates ; these analogues are suitable for use as haptens in the develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02cf7b8b899fb71fb54df0217585ac98
https://doi.org/10.1071/ch9930959
https://doi.org/10.1071/ch9930959
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ad0b34f59c8a74a1140a14650db4ecf
https://doi.org/10.1002/chin.198811333
https://doi.org/10.1002/chin.198811333
Publikováno v:
Chemischer Informationsdienst. 14
The treatment of aldose derivatives that are protected at all but the anomeric hydroxy groups with N-dichloromethylene-N,N-dialkylammonium chlorides (alkyl = Me, Et) provides an improved method of preparing the corresponding glycosyl chlorides. Analo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec7c69777be8891767118c56dca4b535
https://doi.org/10.1002/chin.198348296
https://doi.org/10.1002/chin.198348296
Autor:
D. P. MCADAM, R. V. STICK
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb68aa49fbebd89da89fce75dce02cd
https://doi.org/10.1002/chin.198624306
https://doi.org/10.1002/chin.198624306
Autor:
R. V. Stick, D. P. Mcadam
Publikováno v:
ChemInform. 20
Two analogues of Viehe's salt (Me2N+=CCl2Cl-), namely Me2N+=CBr2 Br- and Et2N+=CBr2 Br-, were prepared and treated with various carbohydrate alcohols and diols. With the diols, the products formed corresponded to those previously obtained with Viehe'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4fd778ab3ad94ffb14144fddabab3f3
https://doi.org/10.1002/chin.198906301
https://doi.org/10.1002/chin.198906301
Publikováno v:
Australian Journal of Chemistry. 36:1239
The treatment of aldose derivatives that are protected at all but the anomeric hydroxy groups with N-dichloromethylene-N,N-dialkylammonium chlorides (alkyl = Me, Et) provides an improved method of preparing the corresponding glycosyl chlorides. Analo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7189039feaf40a01434c51f9f1da228b
https://doi.org/10.1071/ch9831239
https://doi.org/10.1071/ch9831239