Capreomycin sulfate

For research use only. Not for therapeutic Use.

  • CAT Number: I001559
  • CAS Number: 1405-37-4
  • PubChem Substance ID: 22836615
  • Molecular Formula: C24H42N14O8 • H2SO4
  • Molecular Weight: 752.80
  • Purity: 99%
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Capreomycin sulfate(Cat No.:I001559)is an injectable antibiotic used primarily to treat multidrug-resistant tuberculosis (MDR-TB). It belongs to the class of polypeptide antibiotics and is derived from the bacterium Streptomyces capreolus. Capreomycin works by inhibiting protein synthesis in mycobacteria, effectively stopping bacterial growth. It’s often used in combination with other anti-TB drugs to enhance treatment efficacy and prevent resistance. Due to potential side effects, including nephrotoxicity and ototoxicity, its use is generally reserved for cases where other treatments have failed. Capreomycin sulfate remains an important option in TB management worldwide.


Catalog Number I001559
CAS Number 1405-37-4
Synonyms

(2S)-2,5-diamino-N-(((2S,5R,11S,15R,Z)-15-amino-11-(2-amino-3,4,5,6-tetrahydropyrimidin-4-yl)-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-8-(ureidomethylene)-1,4,7,10,13-pentaazacyclohexadecan-5-yl)methyl)pentanamide, monosulfate

Molecular Formula C24H42N14O8 • H2SO4
Purity 99%
Solubility H2O: ≥ 37 mg/mL
Appearance White solid
Storage -20°C
Analysis method HPLC
IUPAC Name (2S)-2,5-diamino-N-[[(5S,8Z,15S)-15-amino-11-(2-amino-1,4,5,6-tetrahydropyrimidin-6-yl)-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentazacyclohexadec-5-yl]methyl]pentanamide;sulfuric acid
InChI InChI=1S/C24H42N14O8.H2O4S/c25-4-1-2-10(26)17(40)32-7-13-19(42)34-14(8-33-24(29)46)20(43)38-16(12-3-5-30-23(28)37-12)22(45)31-6-11(27)18(41)36-15(9-39)21(44)35-13;1-5(2,3)4/h8,10-13,15-16,39H,1-7,9,25-27H2,(H,31,45)(H,32,40)(H,34,42)(H,35,44)(H,36,41)(H,38,43)(H3,28,30,37)(H3,29,33,46);(H2,1,2,3,4)/b14-8-;/t10-,11-,12?,13-,15?,16?;/m0./s1
InChIKey LFFNIXQXRKNZCE-BSPPLRILSA-N
SMILES C1CN=C(NC1C2C(=O)NC[C@@H](C(=O)NC(C(=O)N[C@H](C(=O)N/C(=C\NC(=O)N)/C(=O)N2)CNC(=O)[C@H](CCCN)N)CO)N)N.OS(=O)(=O)O
Reference

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[1]. Johansen SK, et al. Capreomycin binds across the ribosomal subunit interface using tlyA-encoded 2/&#39;-O-methylations in 16S and 23S rRNAs. Mol Cell. 2006 Jul 21;23(2):173-82.</p>

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