Selinexor

CHEMBL3545185 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
443.3 g/mol
LogP
3.0
Phase
4

Selinexor is a first-in-class selective inhibitor of nuclear export (SINE) compound that blocks exportin 1 (XPO1/CRM1), the major nuclear export protein, causing nuclear accumulation of tumor suppressor proteins and pro-apoptotic factors. It is approved for relapsed/refractory multiple myeloma and diffuse large B-cell lymphoma, and is under investigation for multiple other malignancies. By trapping p53, p21, and other tumor suppressors in the nucleus, selinexor restores their antiproliferative and pro-apoptotic functions.

Berat Molekul

443,3000 g/mol

LogP

3,00

TPSA

97,60 Ų

Lipinski RO5

Lulus

Area Terapeutik

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Struktur 2D

SVG PNG

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SMILES

O=C(/C=C\n1cnc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)n1)NNc1cnccn1

InChI

InChI=1S/C17H11F6N7O/c18-16(19,20)11-5-10(6-12(7-11)17(21,22)23)15-26-9-30(29-15)4-1-14(31)28-27-13-8-24-2-3-25-13/h1-9H,(H,25,27)(H,28,31)/b4-1-

Molecular Formula

C17H11F6N7O

HBD / HBA

2 / 12

Ikatan yang Dapat Dirotasi

5

Atom Berat

31

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.

Pertanyaan yang Sering Diajukan

Selinexor is a first-in-class selective inhibitor of nuclear export (SINE) compound that blocks exportin 1 (XPO1/CRM1), the major nuclear export protein, causing nuclear accumulation of tumor suppressor proteins and pro-apoptotic factors. It is approved for relapsed/refractory multiple myeloma and diffuse large B-cell lymphoma, and is under investigation for multiple other malignancies. By trapping p53, p21, and other tumor suppressors in the nucleus, selinexor restores their antiproliferative and pro-apoptotic functions.

Yes, Selinexor 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). CHEMBL3545185. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 71481097. Chemical information database.

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

Penyangkalan Medis

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.