Amide, urea, and carbamate analogues of the muscarinic agent [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chloride
- Author
- NILSSON, B. M; VARGAS, H. M; HACKSELL, U
Univ. Uppsala, Uppsala biomedical cent., dep. organic pharmaceutical chemistry, 751 23 Uppsala, Sweden - Source
Journal of medicinal chemistry (Print). 1992, Vol 35, Num 15, pp 2787-2798 ; ref : 69 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)
- Activité biologique Amine tertiaire Carbamate organique Carboxamide Chlore Composé organique Composé acétylénique In vitro Récepteur muscarinique Voie intraveineuse Ammonium(4-[(3-chlorophényl) carbamoyloxy] pent-2-ynyl triméthyl) Benzèneacétique acide(3-chloro) [4-(diméthylamino) but-2-ynyl méthyl] amide Urée(1-[3-chlorophényl]-3-[4-(diméthylamino) but-2-ynyl]-3 méthyl)
- Keyword (en)
- Biological activity Tertiary amine Organic carbamate Carboxamide Chlorine Organic compounds Acetylenic compound In vitro Muscarinic receptor Intravenous administration
- Keyword (es)
- Actividad biológica Amina terciaria Carbamato orgánico Carboxamida Cloro Compuesto orgánico Compuesto acetilénico In vitro Receptor muscarínico Vía intravenosa
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5431720
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/jm00093a011 
https://dx.doi.org/10.1021/jm00093a011
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