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Details

Stereochemistry ABSOLUTE
Molecular Formula C59H84N16O12
Molecular Weight 1209.3983
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEUPROLIDE

SMILES

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC2=CC=C(O)C=C2)NC(=O)[C@H](CO)NC(=O)[C@H](CC3=CNC4=C3C=CC=C4)NC(=O)[C@H](CC5=CNC=N5)NC(=O)[C@@H]6CCC(=O)N6

InChI

InChIKey=GFIJNRVAKGFPGQ-LIJARHBVSA-N
InChI=1S/C59H84N16O12/c1-6-63-57(86)48-14-10-22-75(48)58(87)41(13-9-21-64-59(60)61)68-51(80)42(23-32(2)3)69-52(81)43(24-33(4)5)70-53(82)44(25-34-15-17-37(77)18-16-34)71-56(85)47(30-76)74-54(83)45(26-35-28-65-39-12-8-7-11-38(35)39)72-55(84)46(27-36-29-62-31-66-36)73-50(79)40-19-20-49(78)67-40/h7-8,11-12,15-18,28-29,31-33,40-48,65,76-77H,6,9-10,13-14,19-27,30H2,1-5H3,(H,62,66)(H,63,86)(H,67,78)(H,68,80)(H,69,81)(H,70,82)(H,71,85)(H,72,84)(H,73,79)(H,74,83)(H4,60,61,64)/t40-,41-,42-,43+,44-,45-,46-,47-,48-/m0/s1

HIDE SMILES / InChI

Molecular Formula C59H84N16O12
Molecular Weight 1209.3983
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 3
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:53:43 UTC 2023
Edited
by admin
on Sat Dec 16 16:53:43 UTC 2023
Record UNII
EFY6W0M8TG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEUPROLIDE
HSDB   MI   VANDF  
Common Name English
LEUPRORELIN SLOW RELEASE
Common Name English
leuprorelin [INN]
Common Name English
LEUPROLIDE [HSDB]
Common Name English
LEUPRORELIN
EP   INN   MART.   WHO-DD  
INN  
Official Name English
TAP-144 FREE BASE
Code English
Leuprorelin [WHO-DD]
Common Name English
LEUPORELIN
Common Name English
NSC-377526
Code English
LEUPROLIDE [MI]
Common Name English
LEUPROLIDE [VANDF]
Common Name English
CKD-841
Code English
ABBOTT-43818 FREE BASE
Code English
(-)-LEUPROLIDE
Common Name English
LEUPRORELIN [MART.]
Common Name English
LEUPRORELIN [EP MONOGRAPH]
Common Name English
5-OXO-L-PROLYL-L-HISTIDYL-L-TRYPTOPHYL-L-SERYL-L-TRYOSYL-D-LEUCYL-L-LEUCYL-L-ARGINYL-N-ETHYL-L-PROLINAMIDE
Common Name English
PGLU-HIS-TRP-SER-TYR-D-LEU-LEU-ARG-PRO-NHC2H5
Common Name English
Classification Tree Code System Code
WHO-ATC L02AE51
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
NDF-RT N0000175654
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
NDF-RT N0000009332
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
WHO-VATC QL02AE02
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
NDF-RT N0000175655
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
NCI_THESAURUS C1910
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
WHO-ATC L02AE02
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
LIVERTOX NBK548676
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
Code System Code Type Description
INN
5025
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
WIKIPEDIA
Leuprorelin
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
EVMPD
SUB08449MIG
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
DAILYMED
EFY6W0M8TG
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
NCI_THESAURUS
C62042
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
RXCUI
42375
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY RxNorm
MERCK INDEX
m6779
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY Merck Index
FDA UNII
EFY6W0M8TG
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
DRUG BANK
DB00007
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
CAS
53714-56-0
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
SMS_ID
100000088225
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
IUPHAR
1175
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
DRUG CENTRAL
1559
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID50872411
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
PUBCHEM
657181
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
ChEMBL
CHEMBL1201199
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
NSC
377526
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
CHEBI
6427
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
HSDB
6518
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
MESH
D016729
Created by admin on Sat Dec 16 16:53:43 UTC 2023 , Edited by admin on Sat Dec 16 16:53:43 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE INACTIVE -> PARENT
MAJOR
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC Males
PHARMACOKINETIC