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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H27ClF2O5.H2O
Molecular Weight 462.912
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOMETASONE MONOHYDRATE

SMILES

O.[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=LIVSBYNMLPEZHQ-DNGJBDHLSA-N
InChI=1S/C22H27ClF2O5.H2O/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;1H2/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

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 Sat Dec 16 01:33:22 GMT 2023
Edited
by admin
on Sat Dec 16 01:33:22 GMT 2023
Record UNII
0PJ4SNG9CS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOMETASONE MONOHYDRATE
WHO-DD  
Common Name English
SICORTEN
Brand Name English
PREGNA-1,4-DIENE-3,20-DIONE, 2-CHLORO-6,9-DIFLUORO-11,17,21-TRIHYDROXY-16-METHYL-, HYDRATE (1:1), (6.ALPHA.,11.BETA.,16.ALPHA.)-
Common Name English
Halometasone monohydrate [WHO-DD]
Common Name English
Code System Code Type Description
FDA UNII
0PJ4SNG9CS
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
CAS
1310709-74-0
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
EVMPD
SUB72874
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID2046460
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
RXCUI
237025
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY RxNorm
PUBCHEM
56649463
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
SMS_ID
100000135992
Created by admin on Sat Dec 16 01:33:22 GMT 2023 , Edited by admin on Sat Dec 16 01:33:22 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE