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

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H29FO6
Molecular Weight 420.4712
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOFLUPREDONE ACETATE

SMILES

[H][C@@]12CC[C@](O)(C(=O)COC(C)=O)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)C=C[C@]34C

InChI

InChIKey=ZOCUOMKMBMEYQV-GSLJADNHSA-N
InChI=1S/C23H29FO6/c1-13(25)30-12-19(28)22(29)9-7-16-17-5-4-14-10-15(26)6-8-20(14,2)23(17,24)18(27)11-21(16,22)3/h6,8,10,16-18,27,29H,4-5,7,9,11-12H2,1-3H3/t16-,17-,18-,20-,21-,22-,23-/m0/s1

HIDE SMILES / InChI
Isoflupredone is a veterinary drug used in cows, pigs and horses for the treatment of wide range of conditions: ketosis, musculoskeletal disorders, hypersensitivity, infections, inflammatory diseases, etc. The drug belongs to the class of corticosteroids and exerts its therapeutic effect by binding to glucocorticoid and mineralocorticoid receptors of animals.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
Palliative
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
Primary
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
Curative
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
Palliative
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
Palliative
PREDEF

Approved Use

Bovine Ketosis, Musculoskeletal Conditions, Allergic Reactions, Overwhelming Infections with Severe Toxicity, Shock, etc.

Launch Date

1959
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

The usual intramuscular dose for cattle is 10 to 20 mg, according to the size of the animal and severity of the condition. This dose may be repeated in 12 to 24 hours if indicated. The usual intramuscular dose for horses is 5 to 20 mg repeated as necessary. The usual intramuscular dose for swine is 5 mg for a 300 pound animal.
Route of Administration: Intramuscular
In Vitro Use Guide
Unknown
Name Type Language
ISOFLUPREDONE ACETATE
GREEN BOOK   MART.   USAN   USP   USP-RS   WHO-DD  
USAN  
Official Name English
NSC-12600
Code English
ISOFLUPREDONE ACETATE [MART.]
Common Name English
Isoflupredone acetate [WHO-DD]
Common Name English
9-Fluoro-11β,17,21-trihydroxypregna-1,4-diene-3,20-dione 21-acetate
Systematic Name English
NSC-37977
Code English
ISOFLUPREDONE ACETATE [GREEN BOOK]
Common Name English
ISOFLUPREDONE ACETATE [USP-RS]
Common Name English
ISOFLUPREDONE 21-ACETATE
MI  
Common Name English
ISOFLUPREDONE ACETATE [USP MONOGRAPH]
Common Name English
ISOFLUPREDONE ACETATE [USAN]
Common Name English
PREGNA-1,4-DIENE-3,20-DIONE, 21-(ACETYLOXY)-9-FLUORO-11,17-DIHYDROXY-, (11.BETA.)-
Systematic Name English
U-6013
Code English
ISOFLUPREDONE 21-ACETATE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C521
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C77005
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-423-9
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
DRUG BANK
DB14640
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
NSC
37977
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
FDA UNII
55P9TUL75S
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
RXCUI
1364586
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY RxNorm
DRUG CENTRAL
4962
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL1608183
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PRIMARY
CAS
338-98-7
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PRIMARY
RS_ITEM_NUM
1348907
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
NSC
12600
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
MESH
C065592
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
DAILYMED
55P9TUL75S
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
SMS_ID
100000142026
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EPA CompTox
DTXSID3045306
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
MERCK INDEX
m6490
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY Merck Index
EVMPD
SUB107857
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
PUBCHEM
224246
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY