Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Vassil I. Ognyanov"'
Autor:
Vassil I. Ognyanov, M. A. Klitenick, J. Jia, D. Ashton, L. R. Kowalski, Stanley Charles Bell, M. De Vivo, C. Tsai, S. M. Lechner, B. N. Atkinson, C.-S. Tham
Publikováno v:
Molecular Pharmacology. 60:1414-1420
High-affinity glycine transport in neurons and glial cells is a primary means of inactivating synaptic glycine. We have synthesized a potent selective inhibitor of glycine transporter 1 (GlyT1), and characterized its activity using a quail fibroblast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5879cd7c7e271d970dc91b3c6713d5
https://doi.org/10.1124/mol.60.6.1414
https://doi.org/10.1124/mol.60.6.1414
Publikováno v:
Tetrahedron. 52:4363-4376
A base promoted ring expansion reaction of 2-oxocyclododecane-1-carbonitrile ( 6 ) with several diarylcarbodiimides gives 14-membered α-enaminolactams ( 12–17 ), whereas N -alkyl- N ′-aryl- and N , N ′-dialkylcarbodiimides do not react at all.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973fc962a5ca407b88f701e75088055c
https://doi.org/10.1016/0040-4020(96)00090-7
https://doi.org/10.1016/0040-4020(96)00090-7
Publikováno v:
Journal of the American Chemical Society. 115:4429-4434
Syntheses of three optically pure, deoxygenated myo-inositol 1,4,5-trisphosphate analogues from quebrachitol are reported together with their binding affinities and 45 Ca 2+ release activity. The ligand-binding affinities of the analogues were determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13c2e7e6fb5e98f71fbd78eccd7ac679
https://doi.org/10.1021/ja00064a002
https://doi.org/10.1021/ja00064a002
Publikováno v:
Tetrahedron Letters. 34:219-222
The synthesis of the (−)-sodium salt of the hexadeoxy-1, 4, 5-tris(methylenesulfonic acid) analogue of IP3 by use of an asymmetric Diels-Alder reaction is described together with the effects of this compound in binding to the IP3 receptor.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70f05b5981dba49a89604499ccde32ee
https://doi.org/10.1016/s0040-4039(00)60551-8
https://doi.org/10.1016/s0040-4039(00)60551-8
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5833620b9a3e57477c1e5621c26a16fa
https://doi.org/10.1002/chin.199149067
https://doi.org/10.1002/chin.199149067
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4d046f4b928a3f1b9a846e41a0cc1c1
https://doi.org/10.1002/chin.199217213
https://doi.org/10.1002/chin.199217213
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0ee875ff9f63694541ccc20f3373b3c
https://doi.org/10.1002/chin.199427245
https://doi.org/10.1002/chin.199427245
Publikováno v:
ChemInform. 27
A base promoted ring expansion reaction of 2-oxocyclododecane-1-carbonitrile ( 6 ) with several diarylcarbodiimides gives 14-membered α-enaminolactams ( 12–17 ), whereas N -alkyl- N ′-aryl- and N , N ′-dialkylcarbodiimides do not react at all.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0efa6bc7ea1d3a7d19f0db1e56e33d3
https://doi.org/10.1002/chin.199628200
https://doi.org/10.1002/chin.199628200
Publikováno v:
Helvetica Chimica Acta. 75:62-68
Synthesis of Macrocyles by Ring Enlargement of 14-Membered Cyclic Imides In the presence of a base, cyclododecanone derivative 2, activated in α-position by an allyloxycarbonyl group, underwent ring enlargement with isocyanates to give 14-membered i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36174d06e43e74da0b02f3aae9670a02
https://doi.org/10.1002/hlca.19920750104
https://doi.org/10.1002/hlca.19920750104
Publikováno v:
Journal of the American Chemical Society. 113:6992-6996
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a90e972c5e8f6fb781f5d8ad360bfb8d
https://doi.org/10.1021/ja00018a042
https://doi.org/10.1021/ja00018a042