U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C22H27ClF2O5
Molecular Weight 444.897
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOMETASONE

SMILES

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

InChI

InChIKey=GGXMRPUKBWXVHE-MIHLVHIWSA-N
InChI=1S/C22H27ClF2O5/c1-10-4-11-12-5-15(24)13-6-16(27)14(23)7-19(13,2)21(12,25)17(28)8-20(11,3)22(10,30)18(29)9-26/h6-7,10-12,15,17,26,28,30H,4-5,8-9H2,1-3H3/t10-,11+,12+,15+,17+,19+,20+,21+,22+/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H27ClF2O5
Molecular Weight 444.897
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Halometasone, a high-potency topical glucocorticoid that inhibits inflammation, epidermal hyperplasia, and allergic reactions, constrict blood vessels and relieve pruritus. Halometasone as the cream is used for the treatment of patients with chronic psoriasis vulgaris, eczematous dermatoses, and occupational contact dermatitis. Besides, this drug can reduce acute adverse effects induced by pulsed dye laser for the treatment of port wine stain (PWS) birthmarks. Halometasone acts via the binding to steroid receptors to modulate the protein synthesis and to regulate the function of inflammatory cells and lysosomes and ultimately to reduce inflammatory responses.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P04150
Gene ID: 2908.0
Gene Symbol: NR3C1
Target Organism: Homo sapiens (Human)
Patents

Sample Use Guides

1.41% of halometasone cream used for consecutive 7 days on a lesion area of 400 cm2 can be absorbed via the skin
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:33 GMT 2023
Edited
by admin
on Fri Dec 15 15:01:33 GMT 2023
Record UNII
J69Z9UU41Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOMETASONE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
Halometasone [WHO-DD]
Common Name English
halometasone [INN]
Common Name English
HALOMETASONE [MI]
Common Name English
HALOMETASONE [MART.]
Common Name English
2-CHLORO-6.ALPHA.,9-DIFLUORO-11.BETA.,17,21-TRIHYDROXY-16.ALPHA.-METHYLPREGNA-1,4-DIENE-3,20-DIONE
Systematic Name English
Classification Tree Code System Code
WHO-ATC D07AC12
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
WHO-VATC QD07AC12
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
Code System Code Type Description
RXCUI
26416
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY RxNorm
INN
4647
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
DRUG BANK
DB13728
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
PUBCHEM
9846332
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
DRUG CENTRAL
1352
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
MESH
C036518
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
ChEMBL
CHEMBL1587228
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
NCI_THESAURUS
C170038
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID1048382
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
CAS
50629-82-8
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
ECHA (EC/EINECS)
256-664-9
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
SMS_ID
100000083923
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
EVMPD
SUB08001MIG
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
MERCK INDEX
m5903
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY Merck Index
FDA UNII
J69Z9UU41Z
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
WIKIPEDIA
HALOMETASONE
Created by admin on Fri Dec 15 15:01:34 GMT 2023 , Edited by admin on Fri Dec 15 15:01:34 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY