Structure characteristics of histamine H2 receptor antagonists that scavenge hypochlorous acid
- Author
- TJONG-LIE CHING1 ; JANG DE JONG; AALT BAST1
[1] Vrije univ. Amsterdam, Leiden/Amsterdam cent. drug res., div. molecular pharmacology, 1081 HV Amsterdam, Netherlands - Source
European journal of pharmacology. Molecular pharmacology section. 1994, Vol 268, Num 1, pp 89-93 ; ref : 24 ref
- ISSN
- 0922-4106
- Scientific domain
- Pharmacology drugs
- Publisher
- Elsevier, Amsterdam
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Keyword (fr)
- Antihistaminique Antiulcéreux Cimétidine Famotidine Hypochloreux acide In vitro Intercepteur radical Mécanisme action Radical libre Ranitidine Relation structure activité Récepteur histaminergique H2
- Keyword (en)
- Antihistaminic Antiulcer agent Hypochlorous acid In vitro Radical scavenger Mechanism of action Free radical Structure activity relation H2 receptor
- Keyword (es)
- Antihistamínico Antiulceroso Hipocloroso ácido In vitro Interceptor radical Mecanismo acción Radical libre Relación estructura actividad Receptor histaminérgico H2
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02H Digestive system
- Discipline
- Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4124686
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
10.1016/0922-4106(94)90123-6 
https://dx.doi.org/10.1016/0922-4106(94)90123-6
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