Zobrazeno 1 - 10
of 147
pro vyhledávání: '"William O. Foye"'
Autor:
William O. Foye
Publikováno v:
Radioprotectors ISBN: 9781003068181
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bc9f6c9eb3ec1a81a0341de65caff84
https://doi.org/10.4324/9781003068181-3
https://doi.org/10.4324/9781003068181-3
Publikováno v:
Burger's Medicinal Chemistry and Drug Discovery
Various approaches have been developed for diminishing the effects of radiation on normal tissues or enhancing tumor cell killing by ionizing radiation. An important potential use for these agents is to modify the outcome of radiation therapy. Potent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::351499a883799f94a5ac58e6267cde1a
https://doi.org/10.1002/0471266949.bmc077
https://doi.org/10.1002/0471266949.bmc077
Autor:
Suparna Chatterji, William O. Foye
Publikováno v:
Journal of Pharmaceutical Sciences. 85:810-814
The radiation-protective bis(methylthio) and methylthio amino derivatives of 1-methylpyridinium- and 1-methylquinolinium-2-dithioacetic acids, a series of non-thiol sulfur-containing compounds, have been examined for their ability to complex Cu(II) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ff057250f48a2cdf7bae2fac3128b4c
https://doi.org/10.1021/js960090z
https://doi.org/10.1021/js960090z
Publikováno v:
Bioelectrochemistry and Bioenergetics. 36:171-174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::484d15b1347cdd260b6c997aac7c9c31
https://doi.org/10.1016/0302-4598(94)01766-t
https://doi.org/10.1016/0302-4598(94)01766-t
Autor:
William O. Foye
Publikováno v:
Annals of Pharmacotherapy. 26:1144-1147
OBJECTIVE: Sulfur-containing compounds have been used in the search for whole-body radiation-protective compounds, in the design of amphetamine derivatives that retain appetite-suppressive effects but lack most behavioral effects characteristic of am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8de04bb7684905ab4773c623388d3456
https://doi.org/10.1177/106002809202600918
https://doi.org/10.1177/106002809202600918
Publikováno v:
Journal of Ethnopharmacology. 34:215-219
High doses of 60Co radiation (4.0-8.0 Gy) in mice, rats and rabbits caused increases in rate of platelet aggregation during the first 5 days after irradiation. The inhibitory effects of the extracts of five Chinese drug plants and acetylsalicylic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad8f39260c24d97ea478a93093a0b66
https://doi.org/10.1016/0378-8741(91)90040-k
https://doi.org/10.1016/0378-8741(91)90040-k
Autor:
William O. Foye
Publikováno v:
Kirk-Othmer Encyclopedia of Chemical Technology
Sulfonamides derived from sulfanilamide (p-aminobenzenesulfonamide) are commonly referred to as sulfa drugs. The sulfa drugs are still important as antimicrobials, although they have been replaced in many systemic infections by the natural and semisy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e01422be48cd12e0f1d1d6fd5a90012d
https://doi.org/10.1002/0471238961.1921120606152505.a01
https://doi.org/10.1002/0471238961.1921120606152505.a01
Synthesis and antihypertensive activity of N-(alkyl/alkenyl/aryl)-N-heterocyclic ureas and thioureas
Autor:
Chutima Matayatsuk, William O. Foye, Opa Vajragupta, Lek Ruangreangyingyod, Yuvadee Wongkrajang, Aungkana Pathomsakul
Publikováno v:
Scopus-Elsevier
A variety of N-(alkyl/alkenyl/aryl-N-heterocyclic ureas and thioureas were synthesized as potential antihypertensives. The selected heterocyclic nuclei were the 6-substituted quinoline and the pyridine. Eleven synthesized compounds and seven related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bec106be082838628b54b24329f81135
https://pubmed.ncbi.nlm.nih.gov/8699324
https://pubmed.ncbi.nlm.nih.gov/8699324
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59b0f1c5fd35351e81ee05749f892e83
https://doi.org/10.1002/chin.199046212
https://doi.org/10.1002/chin.199046212
Publikováno v:
Journal of pharmaceutical sciences. 79(6)
A series of guanylhydrazones derived from 2- and 4-pyridine and 4-quinoline carboxyaldehydes was synthesized from S-methylisothio-semicarbazide hydroiodide using known procedures. The compounds are analogous to anticancer and antiviral thiosemicarbaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e65e9ccf527f96de6a82aacaf166bdf
https://pubmed.ncbi.nlm.nih.gov/2395098
https://pubmed.ncbi.nlm.nih.gov/2395098