Zobrazeno 1 - 10
of 30
pro vyhledávání: '"G, Bethegnies"'
Publikováno v:
Synthetic Communications. 34:1041-1048
The synthesis of a new series of phenylsulfonylsemicarbazide which was substituted in ortho position by a methoxy group is described. The protection of the phenyl ring by a bromine, in order to eliminate the obtention of undesired regioisomers, is ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16512896aacb15caa91d79f54f88e443
https://doi.org/10.1081/scc-120028635
https://doi.org/10.1081/scc-120028635
Autor:
P. Depreux, G. Bethegnies
Publikováno v:
Synthetic Communications. 23:1189-1193
This communication describes a convenient procedure for the preparation of alkylated derivatives of phenobarbital using phase-transfer catalysis without solvent conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4819cc19568c11926b46e80f7168d7c2
https://doi.org/10.1080/00397919308018596
https://doi.org/10.1080/00397919308018596
Autor:
G. Bethegnies, P. Depreux
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4704453676cb0e9883daa1882a2b532a
https://doi.org/10.1002/chin.199336199
https://doi.org/10.1002/chin.199336199
Publikováno v:
ChemInform. 35
The synthesis of a new series of phenylsulfonylsemicarbazide which was substituted in ortho position by a methoxy group is described. The protection of the phenyl ring by a bromine, in order to eliminate the obtention of undesired regioisomers, is ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dacb46050b97dfc05a3ceafed6e5f70
https://doi.org/10.1002/chin.200432158
https://doi.org/10.1002/chin.200432158
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 48(6)
Derivatives with epoxypropyloxy, allyloxy and allyl hydroxychromone structures were synthesized and tested against protoscoleces of Echinococcus multilocularis. Compounds IV-IX were tested in vitro and compound VII proved the most active of them with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8afa241f95818cf19d7cb6f202dfdb7
https://pubmed.ncbi.nlm.nih.gov/8373504
https://pubmed.ncbi.nlm.nih.gov/8373504
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2733558971263119fdc7b75940da4a92
https://doi.org/10.1002/chin.198101219
https://doi.org/10.1002/chin.198101219
Publikováno v:
Comptes rendus des seances de la Societe de biologie et de ses filiales. 176(4)
In the rat, (phenylthio-4 phenylamino)-2 nicotinic and [(chloro-4 phenylthio)-4 phenylamino]-2 nicotinic acids inhibit the hypotensive prostaglandin-mediated action of arachidonic acid. They inhibit also the formation from arachidonic acid, of prosta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4d9b54d23f1fcd88707d0ff4f87c46e
https://pubmed.ncbi.nlm.nih.gov/6217877
https://pubmed.ncbi.nlm.nih.gov/6217877
Publikováno v:
Annales pharmaceutiques francaises. 38(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7558bb84ccedc812a2ce7c345eafb2d1
https://pubmed.ncbi.nlm.nih.gov/7425476
https://pubmed.ncbi.nlm.nih.gov/7425476
Publikováno v:
Il Farmaco; edizione scientifica. 41(6)
Some 7-chloro(phenylthio)-4-phenylaminoquinolines substituted in the benzene rings were prepared and subject to the Winter test for potential antiinflammatory activity and the acetic acid test for analgesic activity. Derivative (I) was devoid of anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1931cdf8e7d9f4f6391d61910b29e4ee
https://pubmed.ncbi.nlm.nih.gov/3488919
https://pubmed.ncbi.nlm.nih.gov/3488919
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 44(7-8)
Several acid and closely related non acid derivatives of 2-phenylthio- and 4-phenylthio-N-acyl phenylamines have been synthesized and tested in vivo, on the carrageenan RFE assay, and in vitro, on prostaglandin synthesis inhibition assay. Compound (X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f2a6eaf79db250f077635cd64075bdb
https://pubmed.ncbi.nlm.nih.gov/2590366
https://pubmed.ncbi.nlm.nih.gov/2590366