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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H29BrF2O7
Molecular Weight 559.394
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOPREDONE ACETATE

SMILES

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

InChI

InChIKey=YCISZOVUHXIOFY-HKXOFBAYSA-N
InChI=1S/C25H29BrF2O7/c1-12(29)34-11-21(33)24(35-13(2)30)6-5-14-15-7-18(27)16-8-19(31)17(26)9-23(16,4)25(15,28)20(32)10-22(14,24)3/h8-9,14-15,18,20,32H,5-7,10-11H2,1-4H3/t14-,15-,18+,20-,22-,23-,24-,25-/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H29BrF2O7
Molecular Weight 559.394
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/341904

Halopredone (THS-201; (17,21-bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione; halopredone acetate; Topicon) is a highly topical corticosteroid. When it is used for intraarticular injections, the effects last longer than any other steroids which have been used, and it has less general effects. Halopredone acetate is used for arthritis and osteoarthritis (OA) patients. For RA patients, mean dose for a wrist is 12.5 mg and that for a knee is 25 mg. About 90% cases showed effectiveness and in about 45% cases the duration of effect is longer than 4 weeks. More than half cases of OA showed also improvements. It also possesses positive anti-inflammatory properties in dermatologic patients.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Clinical study of the relationship between dose and response to halopredone acetate in dermatoses.
1977
Patents

Patents

Sample Use Guides

In Vivo Use Guide
for rats: locally: 80 micrograms/pellet s.c.: 100 mg/kg
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:08:49 GMT 2023
Edited
by admin
on Fri Dec 15 19:08:49 GMT 2023
Record UNII
24NUL39JY1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOPREDONE ACETATE
JAN   MI   USAN   WHO-DD  
USAN  
Official Name English
Halopredone acetate [WHO-DD]
Common Name English
TOPICON
Brand Name English
HALOPREDONE ACETATE [JAN]
Common Name English
HALOPREDONE ACETATE [MI]
Common Name English
HALOPREDONE ACETATE [USAN]
Common Name English
THS-201
Code English
PREGNA-1,4-DIENE-3,20-DIONE, 17,21-BIS(ACETYLOXY)-2-BROMO-6,9-DIFLUORO-11-HYDROXY-, (6.BETA.,11.BETA.)-
Common Name English
HALOART
Brand Name English
THS 201
Code English
Code System Code Type Description
FDA UNII
24NUL39JY1
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
MERCK INDEX
m1183
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C166537
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
CAS
57781-14-3
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106520
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID30206477
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
PUBCHEM
91667
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
ECHA (EC/EINECS)
260-951-4
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
MESH
C015912
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
DRUG CENTRAL
1354
Created by admin on Fri Dec 15 19:08:49 GMT 2023 , Edited by admin on Fri Dec 15 19:08:49 GMT 2023
PRIMARY
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ACTIVE MOIETY