Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Paul Levitan"'
Publikováno v:
Journal of Medicinal Chemistry. 26:1638-1642
Members of a series of basic amide and ester derivatives of 2-substituted pyrido[2,1-b]quinazoline-8-carboxylic acids were prepared and evaluated for their ability to prevent slow-reacting substance of anaphylaxis (SRS-A) induced contractions of guin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38688dc0ab5b4c2f0f0f1db9d291a514
https://doi.org/10.1021/jm00365a016
https://doi.org/10.1021/jm00365a016
Publikováno v:
Helvetica Chimica Acta. 63:832-840
The 5-amino-3-arylamino-1,2,4-oxadiazoles 2 are conveniently prepared by oxidative cyclization of the arylamidinoureas 10. The process is also capable of producing a variety of the 5-substituted-amino analogs 32 when the appropriately substituted gua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c49e1a73fcc5e64671c26a58138b4520
https://doi.org/10.1002/hlca.19800630411
https://doi.org/10.1002/hlca.19800630411
Publikováno v:
Journal of Heterocyclic Chemistry. 16:333-337
The condensation of various halomethyl heterocycles with the potassium salt of the alanine derivative 3, followed by hydrolysis, gave a series of novel 3-heterocyclic-2-methylalanines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b3339ba806a153d7f0530ef90a3238b
https://doi.org/10.1002/jhet.5570160226
https://doi.org/10.1002/jhet.5570160226
Publikováno v:
Journal of Medicinal Chemistry. 23:1387-1392
Structure-activity studies were carried out on a series of antihypertensive 1-(2-aminoethyl)-3-(substituted phenyl)thioureas. From this class of compounds, the 2,6-dichlorophenyl analogue 2 was found to have potent oral antihypertensive activity in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::035899ff718a55a1e081b2c7a5c4e225
https://doi.org/10.1021/jm00186a019
https://doi.org/10.1021/jm00186a019
Publikováno v:
Helvetica Chimica Acta. 63:841-859
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0020ecf95e09726b022e14f98b767d1
https://doi.org/10.1002/hlca.19800630412
https://doi.org/10.1002/hlca.19800630412
Publikováno v:
Tetrahedron Letters. 11:4121-4124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd79b10546e8ba80cfc244ece19f0ee6
https://doi.org/10.1016/s0040-4039(01)98682-4
https://doi.org/10.1016/s0040-4039(01)98682-4
Publikováno v:
The Journal of Organic Chemistry. 38:373-377
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1259b879487db24a28c9da6c20896e9e
https://doi.org/10.1021/jo00942a035
https://doi.org/10.1021/jo00942a035
Publikováno v:
Chemischer Informationsdienst. 15
Members of a series of basic amide and ester derivatives of 2-substituted pyrido[2,1-b]quinazoline-8-carboxylic acids were prepared and evaluated for their ability to prevent slow-reacting substance of anaphylaxis (SRS-A) induced contractions of guin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::444674c3a812dea73640225d3e3f2eb1
https://doi.org/10.1002/chin.198415239
https://doi.org/10.1002/chin.198415239
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceafc8d1d803c6a62c5dffc19a33d3ca
https://doi.org/10.1002/chin.198035224
https://doi.org/10.1002/chin.198035224
Autor:
Margaret O'Donnell, Jefferson Wright Tilley, A. F. Welton, L. D. Tobias, Joan M. Lind, Paul Levitan, Herman J. Crowley
Publikováno v:
Journal of medicinal chemistry. 30(1)
A series of N-(heterocyclic alkyl)pyrido[2,1-b]quinazoline-8-carboxamides were evaluated for their ability to antagonize slow-reacting substance of anaphylaxis (SRS-A) induced contractions of guinea pig ilea and to inhibit thromboxane synthase in vit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653cac799a431309a371198bbc2a7ce7
https://pubmed.ncbi.nlm.nih.gov/2879917
https://pubmed.ncbi.nlm.nih.gov/2879917