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Details

Stereochemistry RACEMIC
Molecular Formula C15H17ClN2O2
Molecular Weight 292.761
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLIMBAZOLE

SMILES

CC(C)(C)C(=O)C(OC1=CC=C(Cl)C=C1)N2C=CN=C2

InChI

InChIKey=OWEGWHBOCFMBLP-UHFFFAOYSA-N
InChI=1S/C15H17ClN2O2/c1-15(2,3)13(19)14(18-9-8-17-10-18)20-12-6-4-11(16)5-7-12/h4-10,14H,1-3H3

HIDE SMILES / InChI

Molecular Formula C15H17ClN2O2
Molecular Weight 292.761
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, includ https://en.wikipedia.org/wiki/Climbazole

Climbazole is a topical antifungal agent commonly used in the treatment of human fungal skin infections such as dandruff[2] and eczema. Climbazole is an antimycotic agent with a high in vitro and in vivo efficacy against P. ovale. After a 1-week washout and a 4-week treatment the clinical evaluation showed a successful reduction of dandruff under the climbazole 0.65% shampoo, skin redness and itching in 80% of the volunteers and a mild improvement in 20% of the volunteers. The cosmetic acceptability was very good by the majority. It is concluded that the formulation tested is effective in the treatment of moderate to severe dandruff. It is most commonly found as an active ingredient in OTC anti-dandruff and anti-fungal products, including shampoos, lotions and conditioners. May cause localized irritation of the skin with symptoms including redness, rashes and itching

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Induction and inhibition of cytochrome P450 and drug-metabolizing enzymes by climbazole.
2002 Jan

Sample Use Guides

shampoo
Route of Administration: Topical
In Vitro Use Guide
climbazole (CLIM) showed good in vitro activity against M. pachydermatis with the the range of MICs (Minimal Inhibitory Concentration ) was between < 0.06 and 1 ug/ml with an empirical median mean of 0.06 ug/ml;
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:25:28 GMT 2023
Edited
by admin
on Fri Dec 15 16:25:28 GMT 2023
Record UNII
9N42CW7I54
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLIMBAZOLE
INCI   INN   MART.   USP-RS   WHO-DD  
INN   INCI  
Official Name English
climbazole [INN]
Common Name English
2-BUTANONE, 1-(4-CHLOROPHENOXY)-1-(1H-IMIDAZOL-1-YL)-3,3-DIMETHYL-
Systematic Name English
CLIMBAZOLE [MART.]
Common Name English
Climbazole [WHO-DD]
Common Name English
NSC-759808
Code English
(RS)-1-(4-CHLOROPHENOXY)-1-IMIDAZOL-1-YL-3,3-DIMETHYLBUTAN-2-ONE
Systematic Name English
CRINIPAN AD
Brand Name English
CLIMBAZOLE [USP-RS]
Common Name English
BAY-E 6975
Code English
1-(4-CHLOROPHENOXY)-1-(1H-IMIDAZOL-1-YL)-3,3-DIMETHYL-2-BUTANONE
Systematic Name English
CLIMBAZOLE [INCI]
Common Name English
BAYPIVAL
Brand Name English
1-(P-CHLOROPHENOXY)-1-IMIDAZOL-1-YL-3,3-DIMETHYL-2-BUTANONE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
Code System Code Type Description
EVMPD
SUB06662MIG
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
RS_ITEM_NUM
1135600
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
INN
4374
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
SMS_ID
100000084294
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
WIKIPEDIA
CLIMBAZOLE
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
DAILYMED
9N42CW7I54
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
CHEBI
83499
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
MESH
C108286
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
NCI_THESAURUS
C78033
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
ECHA (EC/EINECS)
253-775-4
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL1437764
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
NSC
759808
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
DRUG CENTRAL
5064
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID6046555
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
ALANWOOD
climbazole
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
RXCUI
191566
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY RxNorm
CAS
38083-17-9
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
FDA UNII
9N42CW7I54
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
PUBCHEM
37907
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
DRUG BANK
DB15580
Created by admin on Fri Dec 15 16:25:28 GMT 2023 , Edited by admin on Fri Dec 15 16:25:28 GMT 2023
PRIMARY
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