Velpatasvir

CHEMBL3545062 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
883.0 g/mol
LogP
6.2
Phase
4

Velpatasvir is a pan-genotypic NS5A inhibitor that blocks the nonstructural protein 5A of hepatitis C virus (HCV), which is essential for viral RNA replication and virion assembly. It is used in combination with sofosbuvir (Epclusa) or sofosbuvir and voxilaprevir (Vosevi) for the treatment of chronic HCV infection across all six major genotypes. Its pan-genotypic activity simplifies treatment by eliminating the need for genotype testing before initiating therapy.

Khối lượng phân tử

883,0000 g/mol

LogP

6,20

TPSA

193,00 Ų

Lipinski RO5

Không đạt

Lĩnh vực điều trị

Cơ chế tác dụng

Inhibits the NS5A protein of hepatitis C virus, disrupting viral RNA replication and virion assembly.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Inhibits the NS5A protein of hepatitis C virus, disrupting viral RNA replication and virion assembly.

Cấu trúc 2D

SVG PNG

Cite this structure


                        

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SMILES

COC[C@H]1C[C@@H](c2nc(-c3ccc4c(c3)COc3cc5c(ccc6nc([C@@H]7CC[C@H](C)N7C(=O)[C@@H](NC(=O)OC)C(C)C)[nH]c65)cc3-4)c[nH]2)N(C(=O)[C@H](NC(=O)OC)c2ccccc2)C1

InChI

InChI=1S/C49H54N8O8/c1-26(2)41(54-48(60)63-5)47(59)57-27(3)12-17-38(57)45-51-36-16-14-30-20-35-33-15-13-31(19-32(33)25-65-40(35)21-34(30)43(36)53-45)37-22-50-44(52-37)39-18-28(24-62-4)23-56(39)46(58)42(55-49(61)64-6)29-10-8-7-9-11-29/h7-11,13-16,19-22,26-28,38-39,41-42H,12,17-18,23-25H2,1-6H3,(H,50,52)(H,51,53)(H,54,60)(H,55,61)/t27-,28-,38-,39-,41-,42+/m0/s1

Molecular Formula

C49H54N8O8

HBD / HBA

4 / 10

Liên kết có thể quay

13

Nguyên tử nặng

65

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.

Câu hỏi thường gặp

Velpatasvir is a pan-genotypic NS5A inhibitor that blocks the nonstructural protein 5A of hepatitis C virus (HCV), which is essential for viral RNA replication and virion assembly. It is used in combination with sofosbuvir (Epclusa) or sofosbuvir and voxilaprevir (Vosevi) for the treatment of chronic HCV infection across all six major genotypes. Its pan-genotypic activity simplifies treatment by eliminating the need for genotype testing before initiating therapy.

Inhibits the NS5A protein of hepatitis C virus, disrupting viral RNA replication and virion assembly.

Yes, Velpatasvir 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). CHEMBL3545062. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 67683363. Chemical information database.

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

Tuyên bố miễn trách y tế

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.