Zobrazeno 1 - 9
of 9
pro vyhledávání: '"J M, Couquelet"'
Publikováno v:
Pharmaceutica acta Helvetiae. 66(5-6)
It has been possible to prepare from 8-(2-phenylethyl)-1,3,8-triaza [4, 5] spirodecane-2,4-dione a new series of derivatives substituted on the nitrogen atom in the 3-position of the hydantoïn ring. Several compounds exhibited sedative, anticonvulsa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55f576131a65b2a3c859c0125af398ef
https://pubmed.ncbi.nlm.nih.gov/1686098
https://pubmed.ncbi.nlm.nih.gov/1686098
Publikováno v:
Journal of Heterocyclic Chemistry. 21:305-310
Reaction of hydrazine hydrate with 4,5-dihydro-3H-4-acetyl furan-2-ones I led to ring opening and rearrangement into 6-methyl-4,5-dihydro-2H-pyridazin-3-ones II (1–20), the structure of which was determined by spectroscopic methods (ir, 1H and 13C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7a493414a1ae3907bb87372529eb64e
https://doi.org/10.1002/jhet.5570210207
https://doi.org/10.1002/jhet.5570210207
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65f692af722eb36ba30e4bafbbd28d0
https://doi.org/10.1002/chin.197843199
https://doi.org/10.1002/chin.197843199
Publikováno v:
Annales pharmaceutiques francaises. 36(1-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee9c5aa3cdc431cfd1abe14349207a88
https://pubmed.ncbi.nlm.nih.gov/677731
https://pubmed.ncbi.nlm.nih.gov/677731
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4b1c80a030b41d8eda88cc800846678
https://doi.org/10.1002/chin.198448225
https://doi.org/10.1002/chin.198448225
Publikováno v:
Arzneimittel-Forschung. 26(11)
A series of pyrazoline derivatives was synthetised and evaluated for toxicological and pharmacological effects; analgesic, hypnotic, anti-inflammatory, antipyretic and cardiovascular properties were screened. Tested compounds were found to have a low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d068183512f372691d8eb63fde51fff1
https://pubmed.ncbi.nlm.nih.gov/1037245
https://pubmed.ncbi.nlm.nih.gov/1037245
Publikováno v:
Il Farmaco; edizione scientifica. 43(10)
The reaction of 3-chloro pyridazines with various amines led to a series of minaprine analogues. Most of them exhibited significant antidepressant activity. The influence of the substituents attached to the pyridazine ring was discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::398463d9c460112a72f88aa5da9982ce
https://pubmed.ncbi.nlm.nih.gov/3240830
https://pubmed.ncbi.nlm.nih.gov/3240830
Publikováno v:
Annales pharmaceutiques francaises. 46(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abc81e87be70acef592c2072e793cd80
https://pubmed.ncbi.nlm.nih.gov/2905592
https://pubmed.ncbi.nlm.nih.gov/2905592
Publikováno v:
Annales pharmaceutiques francaises. 39(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::789e4c7cca74fdc0be5104f713f8c7e7
https://pubmed.ncbi.nlm.nih.gov/7294650
https://pubmed.ncbi.nlm.nih.gov/7294650