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Details

Stereochemistry ABSOLUTE
Molecular Formula C80H113ClN18O13
Molecular Weight 1570.319
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GANIRELIX

SMILES

CCNC(NCC)=NCCCC[C@@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@H](CO)NC(=O)[C@@H](CC2=CN=CC=C2)NC(=O)[C@@H](CC3=CC=C(Cl)C=C3)NC(=O)[C@@H](CC4=CC5=CC=CC=C5C=C4)NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN=C(NCC)NCC)C(=O)N6CCC[C@H]6C(=O)N[C@H](C)C(N)=O

InChI

InChIKey=GJNXBNATEDXMAK-PFLSVRRQSA-N
InChI=1S/C80H113ClN18O13/c1-9-84-79(85-10-2)88-38-17-15-24-60(70(104)94-62(41-49(5)6)71(105)93-61(25-16-18-39-89-80(86-11-3)87-12-4)78(112)99-40-20-26-68(99)77(111)90-50(7)69(82)103)92-73(107)64(44-53-30-35-59(102)36-31-53)97-76(110)67(48-100)98-75(109)66(46-55-21-19-37-83-47-55)96-74(108)65(43-52-28-33-58(81)34-29-52)95-72(106)63(91-51(8)101)45-54-27-32-56-22-13-14-23-57(56)42-54/h13-14,19,21-23,27-37,42,47,49-50,60-68,100,102H,9-12,15-18,20,24-26,38-41,43-46,48H2,1-8H3,(H2,82,103)(H,90,111)(H,91,101)(H,92,107)(H,93,105)(H,94,104)(H,95,106)(H,96,108)(H,97,110)(H,98,109)(H2,84,85,88)(H2,86,87,89)/t50-,60-,61+,62+,63-,64+,65-,66-,67+,68+/m1/s1

HIDE SMILES / InChI

Molecular Formula C80H113ClN18O13
Molecular Weight 1570.319
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 10
E/Z Centers 5
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:34:25 UTC 2023
Edited
by admin
on Sat Dec 16 17:34:25 UTC 2023
Record UNII
IX503L9WN0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GANIRELIX
EMA EPAR   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
GANIRELIX [VANDF]
Common Name English
Ganirelix [WHO-DD]
Common Name English
GANIRELIX [MI]
Common Name English
GANIRELIX [EMA EPAR]
Common Name English
ORGALUTRAN
Brand Name English
ganirelix [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QH01CC01
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
NDF-RT N0000008638
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
NDF-RT N0000175084
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
NDF-RT N0000175839
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
EMA ASSESSMENT REPORTS ORGALUTRAN (AUTHORIZED: REPRODUCTIVE TECHNIQUES, ASSISTED)
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
NCI_THESAURUS C2092
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
WHO-ATC H01CC01
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
EMA ASSESSMENT REPORTS ORGALUTRAN (AUTHORIZED: OVULATION INDUCTION)
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID401027283
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
PUBCHEM
16130957
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
MESH
C061018
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
SMS_ID
100000085437
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
RXCUI
35825
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY RxNorm
DAILYMED
IX503L9WN0
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
WIKIPEDIA
GANIRELIX
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
ChEMBL
CHEMBL1251
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
DRUG BANK
DB06785
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
DRUG CENTRAL
1279
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
CAS
124904-93-4
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
MERCK INDEX
m5665
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY Merck Index
INN
6830
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
CAS
123246-29-7
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
SUPERSEDED
FDA UNII
IX503L9WN0
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
EVMPD
SUB07883MIG
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
NCI_THESAURUS
C77423
Created by admin on Sat Dec 16 17:34:26 UTC 2023 , Edited by admin on Sat Dec 16 17:34:26 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE -> PARENT
MAJOR
FECAL
Related Record Type Details
ACTIVE MOIETY