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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

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
Climbazole is a new potent inducer of rat hepatic cytochrome P450.
2001 Aug
[Clinical effectiveness and tolerance of climbazole containing dandruff shampoo in patients with seborrheic scalp eczema].
2001 Aug 16
Induction and inhibition of cytochrome P450 and drug-metabolizing enzymes by climbazole.
2002 Jan
Efficacy of a piroctone olamine/climbazol shampoo in comparison with a zinc pyrithione shampoo in subjects with moderate to severe dandruff.
2011 Jun

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;
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
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PRIMARY
INN
4374
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PRIMARY
SMS_ID
100000084294
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PRIMARY
WIKIPEDIA
CLIMBAZOLE
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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
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MESH
C108286
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NCI_THESAURUS
C78033
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PRIMARY
ECHA (EC/EINECS)
253-775-4
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PRIMARY
ChEMBL
CHEMBL1437764
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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
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DRUG CENTRAL
5064
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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
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PRIMARY RxNorm
CAS
38083-17-9
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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