N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium

Preferred Label : N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium;

MeSH note : a neurotoxic quaternary haloperidol metabolite in rat liver; structure in first source;

MeSH synonym : 4-CFOBP; HPP( ); 4-(4-chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxobutyl)pyridinium; BCPP( );

MeSH Related Number : N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium iodide; N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium perchlorate; N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium chloride; 131437-00-8 (perchlorate); 143305-09-3 (iodide); 150214-90-7 (chloride);

Registry Number MeSH : 125785-69-5;

Related CAS MeSH : 143305-09-3 (N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium iodide); 131437-00-8 (N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium perchlorate); 150214-90-7 (N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium chloride);

related registry number list (CISMeF) : 131437-00-8 (perchlorate); 143305-09-3 (iodide); 150214-90-7 (chloride);

Is substance : O;

Details

Origin ID

C085216;

UMLS CUI

C0250626;

Automatic exact mappings (from CISMeF team)
- Allopurinol [NCIt concept]
- HPP1 Gene [NCIt concept]
- Hereditary pyropoikilocytosis (disorder) [SNOMED CT concept]
- Hyperpigmentation with or without hypopigmentation, familial progressive [OMIM Phenotype]
- Hypophosphatasia [ORDO Disease]
- Pyropoikilocytosis, hereditary [OMIM Phenotype]
- succinimido 3-(4-hydroxyphenyl)propionate [Substance BNPC]
MeSH term(s) associated for indexing
- haloperidol [MeSH Descriptor]
- pyridinium compounds [MeSH Descriptor]
Record concept(s)
- N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium [MeSH concept]
- N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium chloride [MeSH concept]
- N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium iodide [MeSH concept]
- N-(4'-fluorobutyrophenone)-4-(4-chlorophenyl)pyridinium perchlorate [MeSH concept]
Semantic type(s)
- Organic Chemical [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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