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

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H30O3
Molecular Weight 354.4825
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MELENGESTROL

SMILES

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

InChI

InChIKey=OKHAOBQKCCIRLO-IBVJIVQJSA-N
InChI=1S/C23H30O3/c1-13-10-17-18(21(4)8-6-16(25)12-19(13)21)7-9-22(5)20(17)11-14(2)23(22,26)15(3)24/h10,12,17-18,20,26H,2,6-9,11H2,1,3-5H3/t17-,18+,20+,21-,22+,23+/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H30O3
Molecular Weight 354.4825
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/2676933 and http://www.fda.gov/AnimalVeterinary/Products/ApprovedAnimalDrugProducts/FOIADrugSummaries/ucm064715.htm

Melengestrol is a steroidal progestin and antineoplastic agent which was never marketed. An acylated derivative, melengestrol acetate, is used as a growth promoter in animals. Melengestrol acetate (MGA) is one of six steroidal hormone growth promoters approved for use in Canada and USA. These products are used to improve growth rate and feed efficiency, as well as to suppress estrus in beef heifers (CFIA 2008). They are not approved for use in any species other than beef cattle meant for slaughter. MGA is the only drug of its kind that is administered in animal feed, and its labelled dose in Canada is 0.4mg per heifer per day (CFIA 2008). A mandatory withdrawal of 2 days before slaughter is applied to any animal that is administered MGA.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.418 nM [IC50]
Target ID: Rat prostatic tumor growth
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
HEIFERMAX 500

Approved Use

For increased rate of weight gain, improved feed efficiency, suppression of estrus in Heifers.

Launch Date

2004
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

Melengestrol (HEIFERMAX® 500) should be thoroughly mixed in liquid Type C medicated feed which must be fed at 0.5 to 2.0 pounds per head daily to provide 0.25 to 0.5 mg of melengestrol acetate per head per day. Average daily intakes approximating the middle of this range provide the most optimal and economical improvements in rate of weight gain and feed utilization. Constant daily intakes of 0.35 to 0.50 mg per head per day give a high degree of estrus suppression. Levels of 0.25 to 0.35 mg provide a lower but still effective degree of estrus suppression.
Route of Administration: Oral
Total body mass and snout-vent length of X. laevis larvae were significantly reduced by the 100 ng/L melengestrol
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:07:07 GMT 2023
Edited
by admin
on Fri Dec 15 19:07:07 GMT 2023
Record UNII
BX98J4T6JU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MELENGESTROL
INN  
INN  
Official Name English
PREGNA-4,6-DIENE-3,20-DIONE, 17-HYDROXY-6-METHYL-16-METHYLENE-
Systematic Name English
melengestrol [INN]
Common Name English
BDH-1921
Code English
17-HYDROXY-6-METHYL-16-METHYLENEPREGNA-4,6-DIENE-3,20-DIONE
Systematic Name English
MELENGESTREL
Common Name English
MELENGESTEROL
Common Name English
Classification Tree Code System Code
CFR 21 CFR 558.342
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
NCI_THESAURUS C776
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
227-073-3
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
EVMPD
SUB08722MIG
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
NCI_THESAURUS
C1659
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID00204869
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
CAS
5633-18-1
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
SMS_ID
100000081466
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
DRUG BANK
DB11529
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
WIKIPEDIA
MELENGESTROL
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
FDA UNII
BX98J4T6JU
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
RXCUI
1537799
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY RxNorm
DAILYMED
BX98J4T6JU
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
INN
1528
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
PUBCHEM
9906614
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
ChEMBL
CHEMBL1328968
Created by admin on Fri Dec 15 19:07:07 GMT 2023 , Edited by admin on Fri Dec 15 19:07:07 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY