Record Information
Version1.0
Creation date2015-10-09 22:31:18 UTC
Update date2017-01-19 02:36:27 UTC
FoodComEx IDPC000555
FoodDB RecordFDB022740
Chemical Information
NameClotrimazole
DescriptionClotrimazole is an imidazole derivative with a broad spectrum of antimycotic activity. It inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. -- Pubchem; There is the potential for drug interactions with Clotrimazole if taken orally, as it is a potent, specific inhibitor of cytochrome P450 oxidase enzymes and so may alter the metabolism of other drugs.; Clotrimazole is an antifungal medication commonly used in the treatment of fungal infections of both humans and animals such as vaginal yeast infections and ringworm. -- Wikipedia; An imidazole derivative with a broad spectrum of antimycotic activity. It inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane.; Clotrimazole is a potent, specific inhibitor of cytochrome P450 oxidase enzymes. Hence, it may alter the metabolism of other drugs particularly if taken orally. -- Wikipedia; Clotrimazole is an antifungal medication commonly used in the treatment of fungal infections of both humans and animals such as vaginal yeast infections and ringworm. It also used to treat athlete's foot and jock itch. [HMDB]
CAS Number23593-75-1
Structure
Thumb
Synonyms
SynonymSource
(Chlorotrityl)imidazolehmdb
1-((2-Chlorophenyl)diphenylmethyl)-1H-imidazoleChEBI
1-(a-(2-Chlorophenyl)benzhydryl)imidazoleGenerator
1-(alpha-(2-Chlorophenyl)benzhydryl)imidazoleChEBI
1-(O-chloro-a,a-Diphenylbenzyl)imidazoleGenerator
1-(O-chloro-alpha,alpha-Diphenylbenzyl)imidazoleChEBI
1-(O-chloro-α,α-diphenylbenzyl)imidazoleGenerator
1-(o-Chlorotrityl)imidazolehmdb
1-(α-(2-chlorophenyl)benzhydryl)imidazoleGenerator
Canestenhmdb
Canesten 1-Day Cream Combi-Pakhmdb
Canesten 1-Day Therapyhmdb
Canesten 3-Day Therapyhmdb
Canesten 6-Day Therapyhmdb
Canesten Combi-Pak 1-Day Therapyhmdb
Canesten Combi-Pak 3-Day Therapyhmdb
Canesten Creamhmdb
Canesten Solutionhmdb
Canestinehmdb
Chlotrimazolehmdb
Clotrimadermhmdb
Clotrimaderm Creamhmdb
Clotrimazolhmdb
Clotrimazolehmdb
Clotrimazolumhmdb
Desamix Fhmdb
Empecidhmdb
Fem Carehmdb
FemCarehmdb
Gyne lotriminhmdb
Gyne-lotriminhmdb
Gyne-Lotrimin 3hmdb
Gyne-Lotrimin 3 Combination Packhmdb
Gyne-Lotrimin Combination Packhmdb
Gyne-Lotrimin3hmdb
Gyne-Lotrimin3 Combination Packhmdb
Gynixhmdb
Lopac-C-6019hmdb
Lotrimaxhmdb
Lotriminhmdb
Lotrimin AFhmdb
Lotrimin AF Creamhmdb
Lotrimin AF Jock-Itch Creamhmdb
Lotrimin AF Lotionhmdb
Lotrimin AF Solutionhmdb
Lotrimin Creamhmdb
Lotrimin Lotionhmdb
Lotrimin Solutionhmdb
Lotrisonehmdb
Mono-baycutenhmdb
Monobaycutenhmdb
Mycelaxhmdb
Mycelexhmdb
Mycelex 7hmdb
Mycelex Creamhmdb
Mycelex Ghmdb
Mycelex OTChmdb
Mycelex Solutionhmdb
Mycelex Trocheshmdb
Mycelex Twin Packhmdb
Mycelex-7hmdb
Mycelex-7 Combination Packhmdb
Mycelex-Ghmdb
Mycelex: MycosporinRimazolehmdb
Myclo Creamhmdb
Myclo Solutionhmdb
Myclo Spray Solutionhmdb
Myclo-Gynehmdb
Mycosporinhmdb
Mykosporinhmdb
Neo-Zol Creamhmdb
Otomaxhmdb
Pedisafehmdb
Prestwick_120hmdb
Rimazolehmdb
Tibatinhmdb
Trimystenhmdb
Trivagizole 3hmdb
Veltrimhmdb
Chemical FormulaC22H17ClN2
IUPAC name1-[(2-chlorophenyl)diphenylmethyl]-1H-imidazole
InChI IdentifierInChI=1S/C22H17ClN2/c23-21-14-8-7-13-20(21)22(25-16-15-24-17-25,18-9-3-1-4-10-18)19-11-5-2-6-12-19/h1-17H
InChI KeyVNFPBHJOKIVQEB-UHFFFAOYSA-N
Isomeric SMILESClC1=CC=CC=C1C(N1C=CN=C1)(C1=CC=CC=C1)C1=CC=CC=C1
Average Molecular Weight344.837
Monoisotopic Molecular Weight344.108026261
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
KingdomOrganic compounds
Super ClassBenzenoids
ClassTriphenyl compounds
Sub ClassNot Available
Direct ParentTriphenyl compounds
Alternative Parents
Substituents
  • Triphenyl compound
  • Chlorobenzene
  • Halobenzene
  • Aryl chloride
  • Aryl halide
  • Monocyclic benzene moiety
  • N-substituted imidazole
  • Azole
  • Heteroaromatic compound
  • Imidazole
  • Azacycle
  • Organoheterocyclic compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Organochloride
  • Organohalogen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointNot Available
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 1 g
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci J10369
AKSci N713
Cayman Chemical 15278
Glentham GA8137
Toronto Research Chemicals C587400