Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Endre Kasztreiner"'
Autor:
Kosary Judit, A. Jednakovits, L Jaszlits, K. Czako, E. Diesler, Endre Kasztreiner, György Rabloczky
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da2d1be1d2b6f5be8f4d56ccd65c0a4
https://doi.org/10.1002/chin.199206202
https://doi.org/10.1002/chin.199206202
Autor:
György Rabloczky, Péter Mátyus, Ágnes Behr, Kosary Judit, Varga Ildiko, Endre Kasztreiner, L. Jaszlits, E. Diesler
Publikováno v:
ChemInform. 26
[1,4]Benzodioxanylmethyl-, [1,4]benzodioxanylmethylaminopropyl- and phenoxyethylaminoethyl-substituted lactams were synthesised and their hypotensive activity was investigated. Some of these compounds show moderate to high hypotensive effect, but the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80a116b47cd6f0d64c1bdb17e22c6395
https://doi.org/10.1002/chin.199506159
https://doi.org/10.1002/chin.199506159
Autor:
K. Czako, L Jaszlits, A. Jednakovits, György Rabloczky, Endre Kasztreiner, Kosary Judit, E. Diesler
Publikováno v:
European Journal of Medicinal Chemistry. 26:739-742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6e083c83af79133bc3e120b3dbebc1a
https://doi.org/10.1016/0223-5234(91)90125-7
https://doi.org/10.1016/0223-5234(91)90125-7
Autor:
Aniko Tegdes, Benjamin Podányi, Mária Kiirthy, Endre Kasztreiner, Kosary Judit, György Rabloczky, Péter Mátyus, Makk Nandor
Publikováno v:
Scopus-Elsevier
The new pyrimido[5,4-b][1,4]oxazinones 4a-c and 6a,b, 7a,c were obtained from 6-amino-2,3-dimethyl-4(3H)-pyrimidone (1) and 4-substituted pyrimido[5,4–6][1,4]oxazinones 5, 7a, respectively, while derivatives 8a-e of the novel ring system 1,4-dioxin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b37a838bec743c6e031d5e9718862d5
https://doi.org/10.1002/jhet.5570270207
https://doi.org/10.1002/jhet.5570270207
Autor:
Kosary Judit, Ágnes Behr, Varga Ildiko, L. Jaszlits, Endre Kasztreiner, Péter Mátyus, E. Diesler, György Rabloczky
Publikováno v:
Scopus-Elsevier
[1,4]Benzodioxanylmethyl-, [1,4]benzodioxanylmethylaminopropyl- and phenoxyethylaminoethyl-substituted lactams were synthesised and their hypotensive activity was investigated. Some of these compounds show moderate to high hypotensive effect, but the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7329af8025d04977d61e5c6fad0190e5
https://pubmed.ncbi.nlm.nih.gov/7979923
https://pubmed.ncbi.nlm.nih.gov/7979923
Publikováno v:
Monatshefte f�r Chemie Chemical Monthly. 117:867-874
The novel ring system, 6H-1,2,4-triazino[4,3—b]1,2,4-triazolo[3,4—f]-pyridazine was prepared either by ring closure of1-(1-ethoxycarbonylethylene)-2-(1,2,4-triazolo[4,3—b]pyridazinyl-6)-hydrazine derivatives (4, 5, 7) in polyphosphoric acid or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83a29c1f97985f79365ad09f325b463e
https://doi.org/10.1007/bf00810078
https://doi.org/10.1007/bf00810078
Publikováno v:
European Journal of Medicinal Chemistry. 24:97-99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1435407a4730374ba09e052aac6f1f9f
https://doi.org/10.1016/0223-5234(89)90171-2
https://doi.org/10.1016/0223-5234(89)90171-2
Publikováno v:
ChemInform. 20
Synthesis of derivatives 4 and 6 of two novel tricyclic ring systems, 1, 2, 4-triazolo[3, 4-c]pyrimido[5, 4-b]-[1, 4]oxazine and imidazo[1, 2-c]pyrimido[5, 4-b][1, 4]oxazine, respectively is described. Although the parent pyrimido[5, 4-b]oxazines pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bf6846231e33e6bebebc19b1154237d
https://doi.org/10.1002/chin.198942207
https://doi.org/10.1002/chin.198942207
The biochemical function of DA and the role of DA-NA conversion in the NA formation were reinvestigated in rat hypothalamic slices. Studies were performed with a new DBH inhibitor, GYKI 11 473, which affected both DA-NA transformation and the uptake
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53b4d49b466e745551b1a6f6f01ba436
https://doi.org/10.1016/b978-1-4832-8363-0.50047-1
https://doi.org/10.1016/b978-1-4832-8363-0.50047-1
