Relugolix

CHEMBL1800159 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
623.6 g/mol
LogP
3.2
Phase
4

A GnRH receptor antagonist used to treat advanced prostate cancer in men and uterine fibroids and endometriosis pain in women, by rapidly reducing sex hormone levels. Unlike GnRH agonists, it begins working quickly without causing an initial hormone surge.

الوزن الجزيئي

623,6000 g/mol

LogP

3,20

TPSA

157,00 Ų

قاعدة ليبينسكي للخمسة

راسب

المجالات العلاجية

آلية العمل

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

الآلية

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

البنية ثنائية الأبعاد

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SMILES

CONC(=O)Nc1ccc(-c2sc3c(c2CN(C)C)c(=O)n(-c2ccc(OC)nn2)c(=O)n3Cc2c(F)cccc2F)cc1

InChI

InChI=1S/C29H27F2N7O5S/c1-36(2)14-19-24-26(39)38(22-12-13-23(42-3)34-33-22)29(41)37(15-18-20(30)6-5-7-21(18)31)27(24)44-25(19)16-8-10-17(11-9-16)32-28(40)35-43-4/h5-13H,14-15H2,1-4H3,(H2,32,35,40)

Molecular Formula

C29H27F2N7O5S

HBD / HBA

2 / 11

الروابط القابلة للدوران

9

الذرات الثقيلة

44

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.

الأسئلة الشائعة

A GnRH receptor antagonist used to treat advanced prostate cancer in men and uterine fibroids and endometriosis pain in women, by rapidly reducing sex hormone levels. Unlike GnRH agonists, it begins working quickly without causing an initial hormone surge.

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

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

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1800159. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 10348973. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

إخلاء المسؤولية الطبية

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.