Linzagolix Choline

CHEMBL4298171 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
611.6 g/mol
LogP
Phase
4

A choline salt form of linzagolix, a gonadotropin-releasing hormone receptor antagonist used to manage heavy menstrual bleeding caused by uterine fibroids. It reduces estrogen levels by blocking GnRH signaling in the pituitary gland.

Molecular Weight

611.6000 g/mol

TPSA

166.00 Ų

Mechanism of Action

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

2D Structure

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SMILES

COc1cc(F)c(-n2c(=O)[nH]c3csc(C(=O)[O-])c3c2=O)cc1OCc1c(OC)ccc(F)c1F.C[N+](C)(C)CCO

InChI

InChI=1S/C22H15F3N2O7S.C5H14NO/c1-32-14-4-3-10(23)18(25)9(14)7-34-16-6-13(11(24)5-15(16)33-2)27-20(28)17-12(26-22(27)31)8-35-19(17)21(29)30;1-6(2,3)4-5-7/h3-6,8H,7H2,1-2H3,(H,26,31)(H,29,30);7H,4-5H2,1-3H3/q;+1/p-1

Molecular Formula

C27H28F3N3O8S

HBD / HBA

2 / 12

Rotatable Bonds

8

Heavy Atoms

42

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.

Frequently Asked Questions

A choline salt form of linzagolix, a gonadotropin-releasing hormone receptor antagonist used to manage heavy menstrual bleeding caused by uterine fibroids. It reduces estrogen levels by blocking GnRH signaling in the pituitary gland.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Linzagolix Choline is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4298171. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 53357800. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Medical Disclaimer

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.