Structure-activity study of 5-substituted 1-carbobenzoxy-2-iminohydantoins as potential anticonvulsant agents
- Author
- ZHONG-YUE SUN; CHUL-HOON KNOW; WURPEL, J. N. D
St. John's univ., coll. pharmacy allied health professions, dep. pharmaceutical sci., Jamaica NY 11439, United States - Source
Journal of medicinal chemistry (Print). 1994, Vol 37, Num 18, pp 2841-2845 ; ref : 10 ref
- CODEN
- JMCMAR
- ISSN
- 0022-2623
- Scientific domain
- Pharmacology drugs
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Animal Anticonvulsivant Carbamate organique Cycle 5 chaînons Guanidines Hétérocycle azote In vivo Relation structure activité Souris Hydantoïne dérivé Imidazolidine-1-carboxylique acide(5-alkyl-2-imino-4-oxo) ester benzyle Mammalia Rodentia Vertebrata
- Keyword (en)
- Animal Anticonvulsant Organic carbamate Five membered ring Guanidines Nitrogen heterocycle In vivo Structure activity relation Mouse Mammalia Rodentia Vertebrata
- Keyword (es)
- Animal Anticonvulsivante Carbamato orgánico Ciclo 5 eslabones Guanidinas Heterociclo nitrógeno In vivo Relación estructura actividad Ratón Mammalia Rodentia Vertebrata
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4219193
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
10.1021/jm00044a003 
https://dx.doi.org/10.1021/jm00044a003
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