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

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H31ClF2O5
Molecular Weight 484.96
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOBETASOL PROPIONATE

SMILES

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

InChI

InChIKey=BDSYKGHYMJNPAB-LICBFIPMSA-N
InChI=1S/C25H31ClF2O5/c1-5-21(32)33-25(20(31)12-26)13(2)8-15-16-10-18(27)17-9-14(29)6-7-22(17,3)24(16,28)19(30)11-23(15,25)4/h6-7,9,13,15-16,18-19,30H,5,8,10-12H2,1-4H3/t13-,15-,16-,18-,19-,22-,23-,24-,25-/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H31ClF2O5
Molecular Weight 484.96
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:33:49 UTC 2023
Edited
by admin
on Fri Dec 15 15:33:49 UTC 2023
Record UNII
91A0K1TY3Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOBETASOL PROPIONATE
MI   ORANGE BOOK   USAN   USP-RS   VANDF  
USAN  
Official Name English
DUOBRII COMPONENT HALOBETASOL PROPIONATE
Brand Name English
ULTRAVATE
Brand Name English
ULOBETASOL PROPIONATE [MART.]
Common Name English
CGP-14458
Code English
ULOBETASOL PROPIONATE
MART.   WHO-DD  
Common Name English
HALOBETASOL PROPIONATE [USAN]
Common Name English
HALOBETASOL PROPIONATE [USP MONOGRAPH]
Common Name English
Ulobetasol propionate [WHO-DD]
Common Name English
CGP-14,458
Code English
IDP-118 COMPONENT HALOBETASOL PROPIONATE
Common Name English
HALOBETASOL PROPIONATE COMPONENT OF DUOBRII
Brand Name English
JEMDEL
Brand Name English
PREGNA-1,4-DIENE-3,20-DIONE, 21-CHLORO-6,9-DIFLUORO-11-HYDROXY-16-METHYL-17-(1-OXOPROPOXY)-, (6.ALPHA.,11.BETA.,16.BETA.)-
Systematic Name English
HALOBETASOL PROPIONATE [USP-RS]
Common Name English
HALOBETASOL PROPIONATE [ORANGE BOOK]
Common Name English
HALOBETASOL PROPIONATE [VANDF]
Common Name English
BMY-30056
Code English
BRYHALI
Brand Name English
HALOBETASOL PROPIONATE [MI]
Common Name English
21-Chloro-6α,9-difluoro-11β,17-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione 17-propionate
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C521
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
Code System Code Type Description
MERCK INDEX
m5899
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY Merck Index
DRUG CENTRAL
1349
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
WIKIPEDIA
Ulobetasol propionate
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
RS_ITEM_NUM
1302906
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
SMS_ID
100000084781
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
DAILYMED
91A0K1TY3Z
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
CAS
66852-54-8
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
DRUG BANK
DB00596
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
ChEMBL
CHEMBL1200908
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
USAN
BB-2
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
EVMPD
SUB05030MIG
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
PUBCHEM
6918178
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID6046636
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
FDA UNII
91A0K1TY3Z
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
NCI_THESAURUS
C47553
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY
RXCUI
45318
Created by admin on Fri Dec 15 15:33:49 UTC 2023 , Edited by admin on Fri Dec 15 15:33:49 UTC 2023
PRIMARY RxNorm
Related Record Type Details
TARGET -> AGONIST
Halobetasol propionate is thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins.The initial interaction, however, is due to the drug binding to the cytosolic glucocorticoid receptor. After binding the receptor the newly formed receptor-ligand complex translocates itself into the cell nucleus, where it binds to many glucocorticoid response elements (GRE) in the promoter region of the target genes.
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
USP
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY