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
SMILES
O.C[C@@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C(Cl)=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO
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
| 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 |
| 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
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P04150 Gene ID: 2908.0 Gene Symbol: NR3C1 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/29250537 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/29250537
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
Edited
Mon Mar 31 20:54:01 GMT 2025
by
admin
on
Mon Mar 31 20:54:01 GMT 2025
|
| Record UNII |
0PJ4SNG9CS
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
0PJ4SNG9CS
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | |||
|
1310709-74-0
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | |||
|
SUB72874
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | |||
|
DTXSID2046460
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | |||
|
237025
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | RxNorm | ||
|
56649463
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY | |||
|
100000135992
Created by
admin on Mon Mar 31 20:54:01 GMT 2025 , Edited by admin on Mon Mar 31 20:54:01 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ANHYDROUS->SOLVATE |