Viomycin Sulfate

CHEMBL3989823 Phase 4 Onaylandı Protein
Half-Life
Bioavailability
Protein Binding
Molecular Weight
783.8 g/mol
LogP
Phase
4

Viomycin sulfate is the sulfate salt of viomycin, a cyclic peptide antibiotic with antimycobacterial activity used as a second-line agent for drug-resistant tuberculosis. The sulfate salt form was used in parenteral formulations for intramuscular administration. Like the free base, it inhibits bacterial protein synthesis by targeting ribosomal translocation but causes significant nephrotoxicity and ototoxicity.

Moleküler Ağırlık

783,8000 g/mol

TPSA

476,00 Ų

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Yapı

SVG PNG

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SMILES

NCCC[C@H](N)CC(=O)N[C@H]1CNC(=O)[C@H]([C@H]2C[C@H](O)NC(N)=N2)NC(=O)/C(=C/NC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC1=O.O=S(=O)(O)O

InChI

InChI=1S/C25H43N13O10.H2O4S/c26-3-1-2-10(27)4-16(41)32-12-6-30-23(47)18(11-5-17(42)37-24(28)36-11)38-20(44)13(7-31-25(29)48)33-21(45)14(8-39)35-22(46)15(9-40)34-19(12)43;1-5(2,3)4/h7,10-12,14-15,17-18,39-40,42H,1-6,8-9,26-27H2,(H,30,47)(H,32,41)(H,33,45)(H,34,43)(H,35,46)(H,38,44)(H3,28,36,37)(H3,29,31,48);(H2,1,2,3,4)/b13-7-;/t10-,11+,12-,14-,15-,17-,18-;/m0./s1

Molecular Formula

C25H45N13O14S

HBD / HBA

17 / 17

Döndürülebilir Bağlar

10

Ağır Atomlar

53

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.

Sıkça Sorulan Sorular

Viomycin sulfate is the sulfate salt of viomycin, a cyclic peptide antibiotic with antimycobacterial activity used as a second-line agent for drug-resistant tuberculosis. The sulfate salt form was used in parenteral formulations for intramuscular administration. Like the free base, it inhibits bacterial protein synthesis by targeting ribosomal translocation but causes significant nephrotoxicity and ototoxicity.

Yes, Viomycin Sulfate is an approved drug. It has reached clinical phase 4. It is classified as a Protein.

{# 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). CHEMBL3989823. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 135524783. Chemical information database.

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

Tıbbi Sorumluluk Reddi

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.