Daclatasvir Dihydrochloride

CHEMBL2303621 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
811.8 g/mol
LogP
Phase
4

The dihydrochloride salt form of daclatasvir, a hepatitis C NS5A inhibitor used in combination antiviral regimens. The salt formulation provides improved stability and bioavailability.

Khối lượng phân tử

811,8000 g/mol

TPSA

175,00 Ų

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

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SMILES

COC(=O)N[C@H](C(=O)N1CCC[C@H]1c1ncc(-c2ccc(-c3ccc(-c4cnc([C@@H]5CCCN5C(=O)[C@@H](NC(=O)OC)C(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C.Cl.Cl

InChI

InChI=1S/C40H50N8O6.2ClH/c1-23(2)33(45-39(51)53-5)37(49)47-19-7-9-31(47)35-41-21-29(43-35)27-15-11-25(12-16-27)26-13-17-28(18-14-26)30-22-42-36(44-30)32-10-8-20-48(32)38(50)34(24(3)4)46-40(52)54-6;;/h11-18,21-24,31-34H,7-10,19-20H2,1-6H3,(H,41,43)(H,42,44)(H,45,51)(H,46,52);2*1H/t31-,32-,33-,34-;;/m0../s1

Molecular Formula

C40H52Cl2N8O6

HBD / HBA

6 / 8

Liên kết có thể quay

13

Nguyên tử nặng

56

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

The dihydrochloride salt form of daclatasvir, a hepatitis C NS5A inhibitor used in combination antiviral regimens. The salt formulation provides improved stability and bioavailability.

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

Yes, Daclatasvir Dihydrochloride 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). CHEMBL2303621. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 25154713. Chemical information database.

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

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.