Ganirelix
This medication is a synthetic hormone that blocks the action of gonadotropin-releasing hormone to prevent premature ovulation during fertility treatments. By suppressing the LH surge, it allows controlled timing of egg retrieval in women undergoing assisted reproduction.
Masse moléculaire
1570,3000 g/mol
LogP
5,40
TPSA
451,00 Ų
Règle des 5 de Lipinski
Non conforme
Aires thérapeutiques
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Structure 2D
Cite this structure
Embed this structure
SMILES
CC/N=C(\NCC)NCCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCN/C(=N/CC)NCC)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1cccnc1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(C)=O)C(=O)N1CCC[C@H]1C(=O)N[C@H](C)C(N)=O
InChI
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
Molecular Formula
C80H113ClN18O13
HBD / HBA
16 / 16
Liaisons Rotatives
48
Atomes Lourds
112
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Foire aux questions
This medication is a synthetic hormone that blocks the action of gonadotropin-releasing hormone to prevent premature ovulation during fertility treatments. By suppressing the LH surge, it allows controlled timing of egg retrieval in women undergoing assisted reproduction.
Yes, Ganirelix is an approved drug. It has reached clinical phase 4. It is classified as a Protein.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1251. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 16130957. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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