leuprolide [4680]



leuprolide


SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H]1CCC(=O)N1
InChIKey GFIJNRVAKGFPGQ-LIJARHBVSA-N
Sequence XHWSYLLRP

Chemical Properties

Hydrogen bond acceptors 14
Hydrogen bond donors 15
Rotatable bonds 32
Log P -1.438
Molecular weight (Da) 1208.6
Stereochemistry info unspecified

Database connections

Model (AF2) GnRH1
Model (Boltz2) GnRH1

Bioactivities

Receptor Activity Source
Protein Gene Species Family Class Type Min Avg Max Database
Receptor Activity Source
Protein Gene Species Family Class Type Min Avg Max Database

leuprolide


Drug properties

Molecular type Peptide
Physiological/Surrogate Surrogate
Approved drug Yes

Distribution across phases (no. indications)

Phase I 0
Phase II 4
Phase III 3
Phase IV 7

Database connections

Model (AF2) GnRH1
Model (Boltz2) GnRH1

Sankey plot

Drug Information

Target Disease
Gene Protein Receptor family Ligand type Class Name Phase ICD11 ATC Association score