Zobrazeno 1 - 10
of 20
pro vyhledávání: '"R. Bukownik"'
Publikováno v:
Journal of the American Chemical Society. 110(18)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5842b5abec323bfebe9e0b96432924b
https://pubmed.ncbi.nlm.nih.gov/22148800
https://pubmed.ncbi.nlm.nih.gov/22148800
Autor:
T. Kallimopoulos, Koji Nakanishi, R. Bukownik, R. Goodnow, M. Niwa, Deborah Lenares, K. Konno
Publikováno v:
Tetrahedron. 46:3267-3286
The synthesis of the non-competative glutamate receptor inhibitor, philanthotoxin 433 (PhTX-433) is described. Furthermore, two synthetic routes are described for the preparation of a variety of structural analogs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::812c10ff08e6b5fbe679aadd1585cfea
https://doi.org/10.1016/s0040-4020(01)85463-6
https://doi.org/10.1016/s0040-4020(01)85463-6
Autor:
Peter N.R. Usherwood, N. A. Anis, A. T. Eldefrawi, Mohyee E. Eldefrawi, R. Goodnow, R. Bukownik, Koji Nakanishi
Publikováno v:
Journal of medicinal chemistry. 34(8)
125I2-iodinated philanthotoxin-343 (PhTX-343), [125I2]PhTX-343-arginine, and [125I2]PhTX-343-lysine were synthesized and evaluated as probes for glutamate receptors in rat brain synaptic membranes. It was found that these probes were not specific for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0eccf19e957267b8ede2b90b55c16a8
https://pubmed.ncbi.nlm.nih.gov/1652018
https://pubmed.ncbi.nlm.nih.gov/1652018
Autor:
T. Kallimopoulos, D. Lenares, R. Bukownik, K. Konno, M. Niwa, R. Jun. Goodnow, Koji Nakanishi
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::310b533c4976a4969070771942bd1bf1
https://doi.org/10.1002/chin.199039297
https://doi.org/10.1002/chin.199039297
Autor:
N, Anis, S, Sherby, R, Goodnow, M, Niwa, K, Konno, T, Kallimopoulos, R, Bukownik, K, Nakanishi, P, Usherwood, A, Eldefrawi
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 254(3)
The effects of varying the structure of philanthotoxin (PhTX) were investigated on binding of the channel blockers: [3H]perhydrohistrionicotoxin (H12-HTX) to the nicotinic acetylcholine receptor (nACh-R) of Torpedo electric organ and [3H]MK-801 [( 3H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::249548fae73e9726ca90fbe758166987
https://pubmed.ncbi.nlm.nih.gov/2168484
https://pubmed.ncbi.nlm.nih.gov/2168484
Autor:
K. Konno, R. Bukownik, Mohyee E. Eldefrawi, P.N.R. Usherwood, Koji Nakanishi, R. Goodnow, Amira T. Eldefrawi, M. Niwa, T. Kallimopoulos, Mary Bruce
Publikováno v:
Toxicon : official journal of the International Society on Toxinology. 28(11)
M. Bruce , R. Bukownik , A. T. Eldefrawi , M. E. Eldefrawi , R. Goodnow , Jr, T. Kallimopoulos , K. Konno , K. Nakanishi , M. Niwa and P. N. R. Usherwood . Structure-activity relationships of analogues of the wasp toxin philanthotoxin: non-competitiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8e574b927064b8f553c49876b89437a
https://pubmed.ncbi.nlm.nih.gov/1965063
https://pubmed.ncbi.nlm.nih.gov/1965063
Publikováno v:
Inclusion Phenomena and Molecular Recognition ISBN: 9781461278870
It is now well established that some water soluble cyclophanes can bind to neutral organic molecules in aqueous solutions. Benzenoid, naphthalenoid, and larger aromatic molecules will form inclusion complexes with properly constructed cyclophanes [3]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b986651f16f391efda664b3378e1ca98
https://doi.org/10.1007/978-1-4613-0603-0_3
https://doi.org/10.1007/978-1-4613-0603-0_3
Autor:
Craig S. Wilcox, Rudolph R. Bukownik
Publikováno v:
The Journal of Organic Chemistry. 53:463-471
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c6a8ba979bbab33c8fafe03622df67b
https://doi.org/10.1021/jo00238a001
https://doi.org/10.1021/jo00238a001
Publikováno v:
Synthetic Communications. 11:599-603
A couple of years ago, Fujita and co-workers1 reported the reduction of 2-thiazoline-2-thiol esters to alcohols with sodium borohydride in aqueous tetrahydrofuran. In connection with an ongoing synthetic project which requires the selective reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c4944ef2f91031df3c818a72a983809
https://doi.org/10.1080/00397918108063631
https://doi.org/10.1080/00397918108063631
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8c5ec2eff55e176b6e37257e1ad4d5b
https://doi.org/10.1002/chin.198213122
https://doi.org/10.1002/chin.198213122