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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H38ClFO5
Molecular Weight 509.05
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOCORTOLONE CAPROATE

SMILES

[H][C@@]12C[C@@H](C)[C@H](C(=O)COC(=O)CCCCC)[C@@]1(C)C[C@H](O)[C@@]3(Cl)[C@@]2([H])C[C@H](F)C4=CC(=O)C=C[C@]34C

InChI

InChIKey=MMTRTBFDFNRBQO-ANHDKODLSA-N
InChI=1S/C28H38ClFO5/c1-5-6-7-8-24(34)35-15-22(32)25-16(2)11-18-19-13-21(30)20-12-17(31)9-10-27(20,4)28(19,29)23(33)14-26(18,25)3/h9-10,12,16,18-19,21,23,25,33H,5-8,11,13-15H2,1-4H3/t16-,18+,19+,21+,23+,25-,26+,27+,28+/m1/s1

HIDE SMILES / InChI

Molecular Formula C28H38ClFO5
Molecular Weight 509.05
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: https://www.ncbi.nlm.nih.gov/pubmed/22798972

Clocortolone (used in form of pivalate prodrug) is a topical glucocorticoid that was approved by FDA for the treatment of corticosteroid-responsive skin disorders. The drug exerts its anti-inflammatory action by binding to glucocorticoid receptor which results in regulation of the expression of proinflammatory cytokines and further antiproliferative, immunosuppressive, and initial vasoconstrictive effects.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CLODERM

Approved Use

Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Launch Date

1977
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
likely
PubMed

PubMed

TitleDatePubMed
[Experiences with clocortolone in treating of skin diseases in hospital and ambulatory care].
1969 Sep 27
[Clocortolone (Cl 68) versus fluocinolone, a double-blind, randomized lateral comparison].
1973 Jul
Clocortolone, a new topical steroid in dermatoses.
1973 Mar 24
[Human-pharmacokinetic Studies on Penetration Kinetics of a 6 alpha-Fluoro-9 alpha-chloro-16 alpha-methyl-delta 1,4-pregnadiene-11 beta-dihydroxy-3,20-dione-21-trimethyl-acetic acid (Clocortolone Trimethyl-acetic acid) after e picutaneous application].
1978
Clocortolone pivalate: a paired comparison clinical trial of a new topical steroid in eczema/atopic dermatitis.
1980 Jan
Safety and efficacy of clocortolone pivalate 0.1 percent cream in the treatment of atopic dermatitis, contact dermatitis, and seborrheic dermatitis.
1981 Jun
Clocortolone pivalate cream 0.1% used concomitantly with tacrolimus ointment 0.1% in atopic dermatitis.
2003 Aug
Clocortolone Pivalate.
2006
Adherence to clocortolone pivalate cream 0.1% in a pediatric population with atopic dermatitis.
2008 May
Clinical utility of clocortolone pivalate for the treatment of corticosteroid-responsive skin disorders: a systematic review.
2012
A Comprehensive Review of Clocortolone Pivalate 0.1% Cream: Structural Development, Formulation Characteristics, and Studies Supporting Treatment of Corticosteroid-responsive Dermatoses.
2012 Jul
Identification and characterization of three impurities in clocortolone pivalate.
2012 Mar 25
Clocortolone pivalate: a topical corticosteroid with a unique structure.
2013 Feb
The role of a midpotency topical corticosteroid and the clinical relevance of formulation characteristics in the management of commonly encountered eczematous and inflammatory dermatoses in adults and children: focus on the pharmacologic properties of clocortolone pivalate 0.1% cream.
2013 Feb
Patents

Sample Use Guides

Apply Cloderm (clocortolone pivalate) 1% cream to the affected areas 3 times/day.
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:53:19 GMT 2023
Edited
by admin
on Fri Dec 15 16:53:19 GMT 2023
Record UNII
871M9PSU7T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOCORTOLONE CAPROATE
Common Name English
PREGNA-1,4-DIENE-3,20-DIONE, 9-CHLORO-6-FLUORO-11-HYDROXY-16-METHYL-21-((1-OXOHEXYL)OXY)-, (6.ALPHA.,11.BETA.,16.ALPHA.)-
Common Name English
CLOCORTOLONE HEXANOATE
WHO-DD  
Common Name English
Clocortolone hexanoate [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C521
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
Code System Code Type Description
FDA UNII
871M9PSU7T
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
ECHA (EC/EINECS)
225-513-9
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID30964141
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
NCI_THESAURUS
C98251
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
SMS_ID
100000090230
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
DRUG BANK
DB14653
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
CAS
4891-71-8
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
EVMPD
SUB01351MIG
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
PUBCHEM
107603
Created by admin on Fri Dec 15 16:53:19 GMT 2023 , Edited by admin on Fri Dec 15 16:53:19 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY