Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nand Baindur"'
Autor:
Carl L. Manthey, Nand Baindur, Ioanna Petrounia, Celine Schalk-Hihi, Naresh Chadha, Christian Andrew Baumann, Heidi Ott, Benjamin M. Brandt, Raymond J. Patch, Mark R. Player, Davoud Asgari, Barry A. Springer, Theodore E. Carver
Publikováno v:
Journal of Medicinal Chemistry. 48:1717-1720
2-Hydroxy-4,6-diamino-[1,3,5]triazines are described which are a novel class of potent inhibitors of the VEGF-R2 (flk-1/KDR) tyrosine kinase. 4-(Benzothiazol-6-ylamino)-6-(benzyl-isopropyl-amino)-[1,3,5]triazin-2-ol (14d) exhibited low nanomolar pote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b94f50d28b146febb8ae2b013be4b1ff
https://doi.org/10.1021/jm049372z
https://doi.org/10.1021/jm049372z
Publikováno v:
Journal of Combinatorial Chemistry. 5:653-659
An efficient solution-phase parallel synthesis of a library of 3,5,7-trisubstituted [1,2,3]triazolo[4,5-d]pyrimidines is described. Monosubstituted amidines may be converted to 2-substituted 5-amino-4,6-dihydroxypyrimidines in four steps. Treatment w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7bdecf1440329252017c2f34f4ae2a8
https://doi.org/10.1021/cc020110x
https://doi.org/10.1021/cc020110x
Autor:
Nand Baindur, Margery A. Chaikin, Davoud Asgari, Wing S. Cheung, Ioanna Petrounia, Robert R. Donatelli, Taxiarchis Georgiadis, Naresh Chadha, Raymond J. Patch, Mark R. Player, Benjamin M. Brandt
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(22)
A series of 2′-aminoanilides have been identified which exhibit potent and selective inhibitory activity against the cFMS tyrosine kinase. Initial SAR studies within this series are described which examine aroyl and amino group substitutions, as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b254ce72dd5d6d9327f28dd38d984ba2
https://pubmed.ncbi.nlm.nih.gov/17904845
https://pubmed.ncbi.nlm.nih.gov/17904845
Publikováno v:
Journal of combinatorial chemistry. 6(2)
Monoamides of oxalic acid are of interest as bioisosteric replacements for phosphate groups in the design of new enzyme inhibitors. Here, we have demonstrated the use of oxalic acid as a linker to the Wang resin to synthesize individual or libraries
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::441c8b19780c1505c5f2763378d4e59a
https://pubmed.ncbi.nlm.nih.gov/15002971
https://pubmed.ncbi.nlm.nih.gov/15002971
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::117bcf8c365b7d8fa40be11068ba55f6
https://doi.org/10.1002/chin.200403157
https://doi.org/10.1002/chin.200403157
Autor:
Nand Baindur, Celine Schalk-Hihi, Matthew Wayne Olson, Keli C. Dzordzorme, Ruth Steele, Jennifer Kirkpatrick, Kenneth R. Singleton, Marina I. Nelen, Min Xiang, Lawrence Kuo, James Lenhard, Mike Gaul, Gee Hong Kuo, Christian Andrew Baumann, Todd J. Matthew, Wenfeng Sun, Erica L Nulton
Publikováno v:
The FASEB Journal. 22:332-332
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa89010ccc3d040dc634cce0fa3ae3fb
https://doi.org/10.1096/fasebj.22.2_supplement.332
https://doi.org/10.1096/fasebj.22.2_supplement.332