Antibiotic; inhibits bacterial DNA synthesis
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Key Product Details
Description: | Antibiotic; inhibits bacterial DNA synthesis |
Chemical Name: | (S)-3,6-Diamino-N-((3S,9S,12S,15S,Z)3((2R,4S)-6-amino-4-hydroxy-1,2,3,4-tetrahydropyridin-2-yl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-6-(ureidomethylene)-1,4,7,10,13-pentaazacyclohexadecan-15-yl)hexanamide disulfate |
Molecular Weight: | 881.85 |
Citations for Viomycin (5)
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Citations are publications that use Bio-Techne products. Selected citations for Viomycin include:
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Matilde E et al.
(2019)
Common Metabolic Pathways Implicated in Resistance to Chemotherapy Point to a Key Mitochondrial Role in Breast Cancer.
Mol Cell Proteomics.
18:231-244
PMID: 33451433 -
Abad et al.
(2018)
Common metabolic pathways implicated in resistance to chemotherapy point to a key mitochondrial role in breast cancer.
Mol Cell Proteomics.
2018;
PMID: 30373788 -
Freihofer et al.
(2016)
Nonmutational compensation of the fitness cost of antibiotic resistance in mycobacteria by overexpression of tlyA rRNA methylase.
RNA.
22:1836
PMID: 27698071 -
Samokhvalov et al.
(2015)
PPARδ signaling mediates the cytotoxicity of DHA in H9c2 cells.
PLoS One.
232:44105
PMID: 25300478 -
Akbergenov et al.
(2011)
Molecular basis for the selectivity of antituberculosis compounds capreo. and vio.
Antimicrob Agents Chemother.
55:4712
PMID: 21768509
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Species: HumanViomycin and streptomycin were compared in inhibition of bacterial protein production.Cross-resistance between streptomycin and other aminoglycosides and polypeptides observed.
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