Synthesis and opioid activities of some naltrexone oxime ethers
- Author
- MAVUNKEL, B. J; RZESOTARSKI, W. J; KAPLITA, P. V; DEHAVEN-HUDKINS, D. L
Sciocs Nova Inc., Baltimore MD 21224, United States - Source
European journal of medicinal chemistry. 1994, Vol 29, Num 9, pp 659-666 ; ref : 26 ref
- CODEN
- EJMCA5
- ISSN
- 0223-5234
- Scientific domain
- Organic chemistry; Pharmacology drugs
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité biologique Analgésique narcotique Analogue In vivo Morphinane dérivé Naltrexone Oxime Phénols Récepteur opiacé κ Souris 4,5-Epoxymorphinan-6-one(17-cyclopropylméthyl-3,14-dihydroxy) alkyloxime 4,5-Epoxymorphinan-6-one(17-cyclopropylméthyl-3,14-dihydroxy) aryloxime 4,5-Epoxymorphinan-6-one(17-cyclopropylméthyl-3,14-dihydroxy) cyclanyloxime Epoxy-10,4a-(iminoéthano)phénanthrène dérivé Mammalia Rodentia Vertebrata
- Keyword (en)
- Biological activity Narcotic analgesic Analog In vivo Morphinan derivatives Oxime Phenols Opiate receptor κ Mouse Mammalia Rodentia Vertebrata
- Keyword (es)
- Actividad biológica Analgésico narcotico Análogo In vivo Oxima Fenoles Receptor opiáceo κ Ratón Mammalia Rodentia Vertebrata
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4240580
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/0223-5234(94)90027-2 
https://dx.doi.org/10.1016/0223-5234(94)90027-2
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