Zobrazeno 1 - 10
of 51
pro vyhledávání: '"A. Marcincal-Lefebvre"'
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:
Farmaco (Societa chimica italiana : 1989). 47(9)
Twelve derivatives with alkylaminoalkyloxy chromone structures were synthesized and tested upon protoscoleces of Echinococcus multilocularis metacestode kept alive in vitro. Assays were performed with protoscoleces attached to the germinal layer in o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a7d3405d1658695a6d90c8e1565ebfe
https://pubmed.ncbi.nlm.nih.gov/1300123
https://pubmed.ncbi.nlm.nih.gov/1300123
Autor:
Depreux, P., Marcincal-Lefebvre, A.
Publikováno v:
Canadian Journal of Chemistry; 1986, Vol. 64 Issue 3, p626-632, 7p
Publikováno v:
Journal of Medicinal Chemistry. 24:889-893
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1795a4a8fed9ddf5831bc8386568908
https://doi.org/10.1021/jm00139a025
https://doi.org/10.1021/jm00139a025
Publikováno v:
European Journal of Medicinal Chemistry. 22:75-78
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a07b2d153aa5530240dff5cdcc87914
https://doi.org/10.1016/0223-5234(87)90176-0
https://doi.org/10.1016/0223-5234(87)90176-0
Autor:
Depreux, P., Marcincal-Lefebvre, A.
Publikováno v:
Canadian Journal of Chemistry; March 1986, Vol. 64 Issue: 3 p626-632, 7p
Autor:
D. Bar, A. Marcincal-Lefebvre
Publikováno v:
Chemischer Informationsdienst. 8
Die Chlorcarbonsaurehydrazide (I) (Ausbeuten bei der Darstellung aus Diphenylhydrazin 95 bzw. 77%) reagieren mit den entsprechenden sek. Aminen unter Bildung der α- bzw. β- Aminosaurehydrazide (II), die durch LiAlH4 zu den Alkylhydrazinen (III) red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c8b93db0420f792a5cb8372ba4d8a36
https://doi.org/10.1002/chin.197704146
https://doi.org/10.1002/chin.197704146
Publikováno v:
Annales pharmaceutiques francaises. 38(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::009b52c7f6b802f50562fb8eecc6f7ed
https://pubmed.ncbi.nlm.nih.gov/7416698
https://pubmed.ncbi.nlm.nih.gov/7416698
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:
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