Synthesis and evaluation of 2-(5-methoxythiophen-3-yl)ethylamines as potential dopamine agonists
- Author
- CARDELLINI, M1 ; CINGOLANI, G. M1 ; CLAUDI, F1 ; DI STEFANO, A1 ; GIORGIONI, G1 ; CANTALAMESSA, F; CAGNOTTO, A; SKORUPSKA, M
[1] Univ. Camerino, dep. chemical sci., 62032 Camerino, Italy - Source
European journal of medicinal chemistry. 1994, Vol 29, Num 6, pp 423-429 ; ref : 27 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 Affinité Agoniste Aminoéther Cycle 5 chaînons Hétérocycle soufre Récepteur dopaminergique D1 Récepteur dopaminergique D2 Thiophène(2-méthoxy-5-[2-([phénéthyl propyl]amino)éthyl]) Thiophène(2-méthoxy-5-[2-(phénéthylamino)éthyl])
- Keyword (en)
- Biological activity Affinity Agonist Aminoether Five membered ring Sulfur heterocycle D1 Dopamine receptor D2 Dopamine receptor
- Keyword (es)
- Actividad biológica Afinidad Agonista Aminoeter Ciclo 5 eslabones Heterociclo azufre Receptor dopaminérgico D1 Receptor dopaminérgico D2
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4131785
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)90069-8 
https://dx.doi.org/10.1016/0223-5234(94)90069-8
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