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Details

Stereochemistry ABSOLUTE
Molecular Formula C64H83N17O12.C2H4O2
Molecular Weight 1342.5025
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DESLORELIN ACETATE

SMILES

CC(O)=O.[H][C@]1(CCC(=O)N1)C(=O)N[C@@H](CC2=CNC=N2)C(=O)N[C@@H](CC3=CNC4=C3C=CC=C4)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC5=CC=C(O)C=C5)C(=O)N[C@H](CC6=CNC7=CC=CC=C67)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N8CCC[C@H]8C(=O)NCC

InChI

InChIKey=LYCYLGFSIXIXAB-NUZRHMIVSA-N
InChI=1S/C64H83N17O12.C2H4O2/c1-4-68-62(92)53-16-10-24-81(53)63(93)46(15-9-23-69-64(65)66)74-56(86)47(25-35(2)3)75-58(88)49(27-37-30-70-43-13-7-5-11-41(37)43)77-57(87)48(26-36-17-19-40(83)20-18-36)76-61(91)52(33-82)80-59(89)50(28-38-31-71-44-14-8-6-12-42(38)44)78-60(90)51(29-39-32-67-34-72-39)79-55(85)45-21-22-54(84)73-45;1-2(3)4/h5-8,11-14,17-20,30-32,34-35,45-53,70-71,82-83H,4,9-10,15-16,21-29,33H2,1-3H3,(H,67,72)(H,68,92)(H,73,84)(H,74,86)(H,75,88)(H,76,91)(H,77,87)(H,78,90)(H,79,85)(H,80,89)(H4,65,66,69);1H3,(H,3,4)/t45-,46-,47-,48-,49+,50-,51-,52-,53-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C64H83N17O12
Molecular Weight 1282.4505
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 3
Optical Activity UNSPECIFIED

Molecular Formula C2H4O2
Molecular Weight 60.052
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Deslorelin is an GnRH agonist used in veterinary. It effects contraception by temporarily suppressing the reproductive endocrine system and preventing production of pituitary (FSH and LH) and gonadal hormones (estradiol and progesterone in females and testosterone in males). The observed effects are similar to those following ovariectomy or castration, but are reversed after the hormone content of the implant is depleted or the implant is removed. As an agonist, deslorelin first stimulates the reproductive system, which can result in estrus and ovulation in females or temporary enhancement of testosterone and semen production in males. Then, down-regulation follows the initial period of stimulation. Although deslorelin can also be an effective contraceptive in males of some species, manufacturer recommends its use primarily in females, since monitoring efficacy in females by suppression of estrous behavior or of gonadal steroids in feces is more straightforward than ensuring continued absence of sperm in males, since most institutions cannot perform regular semen collections. It can, however, be used to ameliorate aggression in males of some species, but higher dosages are usually needed. While the major application of deslorelin was initially male contraception, due to its two differing actions, either the stimulation of oestrus or the sterilization of fertility, its use has been increasing in the bitch as well. SUPRELORIN® F (deslorelin acetate) Implant is a once-yearly, subcutaneous implant that assists in the management of adrenal disease in ferrets.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:32:30 GMT 2023
Edited
by admin
on Fri Dec 15 15:32:30 GMT 2023
Record UNII
679007NR5C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DESLORELIN ACETATE
GREEN BOOK   MI   WHO-DD  
Common Name English
DESLORELIN ACETATE [EMA EPAR VETERINARY]
Common Name English
5-OXO-L-PROLYL-L-HISTIDYL-L-TRYPTOPHYL-L-SERYL-L-TYROSYL-D-TRYPTOPHYL-L-LEUCYL-L-ARGINYL-N-ETHYL-L-PROLINAMIDE ACETATE
Common Name English
DESLORELIN ACETATE [MI]
Common Name English
6-D-TRYPTOPHAN-9-(N-ETHYL-L-PROLINAMIDE)-1-9-LUTEINIZING HORMONE-RELEASING FACTOR (SWINE) ACETATE
Common Name English
SUPRELORIN
Brand Name English
(D-TRP(SUP 6),DES-GLY(SUP 10))-LH-RH ETHYLAMIDE ACETATE
Common Name English
Deslorelin acetate [WHO-DD]
Common Name English
DESLORELIN ACETATE [GREEN BOOK]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1910
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
EMA VETERINARY ASSESSMENT REPORTS SUPRELORIN [AUTHORIZED]
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
EMA VETERINARY ASSESSMENT REPORTS SUPRELORIN [AUTHORIZED]
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
Code System Code Type Description
CAS
82318-06-7
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
MESH
C066438
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
DRUG BANK
DBSALT001674
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID1046683
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
SMS_ID
300000023687
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
MERCK INDEX
m4194
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C82600
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
PUBCHEM
25077533
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
FDA UNII
679007NR5C
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
DAILYMED
679007NR5C
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY
RXCUI
1311743
Created by admin on Fri Dec 15 15:32:30 GMT 2023 , Edited by admin on Fri Dec 15 15:32:30 GMT 2023
PRIMARY RxNorm
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ACTIVE MOIETY