Capreomycin
A cyclic peptide antibiotic used to treat multidrug-resistant tuberculosis, particularly when first-line drugs have failed or cannot be used. It works by inhibiting bacterial protein synthesis at the ribosomal level. It must be given by injection and requires monitoring for kidney toxicity and hearing loss.
Molecular Weight
1321.4000 g/mol
TPSA
737.00 Ų
Therapeutic Areas
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D Structure
Cite this structure
Embed this structure
SMILES
C[C@@H]1NC(=O)[C@@H](N)CNC(=O)[C@H](C2CCNC(=N)N2)NC(=O)/C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)CC(N)CCCN)NC1=O.N=C1NCCC([C@@H]2NC(=O)/C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)CC(N)CCCN)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CNC2=O)N1
InChI
InChI=1S/C25H44N14O8.C25H44N14O7/c26-4-1-2-11(27)6-17(41)32-8-14-20(43)35-15(9-34-25(30)47)21(44)39-18(13-3-5-31-24(29)38-13)23(46)33-7-12(28)19(42)37-16(10-40)22(45)36-14;1-11-19(41)36-15(9-32-17(40)7-12(27)3-2-5-26)21(43)37-16(10-34-25(30)46)22(44)39-18(14-4-6-31-24(29)38-14)23(45)33-8-13(28)20(42)35-11/h9,11-14,16,18,40H,1-8,10,26-28H2,(H,32,41)(H,33,46)(H,35,43)(H,36,45)(H,37,42)(H,39,44)(H3,29,31,38)(H3,30,34,47);10-15,18H,2-9,26-28H2,1H3,(H,32,40)(H,33,45)(H,35,42)(H,36,41)(H,37,43)(H,39,44)(H3,29,31,38)(H3,30,34,46)/b15-9-;16-10-/t11?,12-,13?,14-,16-,18-;11-,12?,13-,14?,15-,18-/m00/s1
Molecular Formula
C50H88N28O15
HBD / HBA
27 / 23
Rotatable Bonds
19
Heavy Atoms
93
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.
Frequently Asked Questions
A cyclic peptide antibiotic used to treat multidrug-resistant tuberculosis, particularly when first-line drugs have failed or cannot be used. It works by inhibiting bacterial protein synthesis at the ribosomal level. It must be given by injection and requires monitoring for kidney toxicity and hearing loss.
Yes, Capreomycin is an approved drug. It has reached clinical phase 4. It is classified as a Protein.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2221250. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3000502. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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