Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C22H34FN7O4.CH4O3S |
Molecular Weight | 575.654 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(O)(=O)=O.[H][C@]12COCCN1CCN(C2)C3=C(F)C(NNC(=O)[C@H](CC4CCCC4)CN(O)C=O)=NC(C)=N3
InChI
InChIKey=UNGNACZMQRGYNV-URBRKQAFSA-N
InChI=1S/C22H34FN7O4.CH4O3S/c1-15-24-20(19(23)21(25-15)29-7-6-28-8-9-34-13-18(28)12-29)26-27-22(32)17(11-30(33)14-31)10-16-4-2-3-5-16;1-5(2,3)4/h14,16-18,33H,2-13H2,1H3,(H,27,32)(H,24,25,26);1H3,(H,2,3,4)/t17-,18+;/m1./s1
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Antibiotics in development targeting protein synthesis. | 2011 Dec |
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Determination of disk diffusion and MIC quality control ranges for GSK1322322, a novel peptide deformylase inhibitor. | 2011 Nov |
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Single-dose safety, tolerability, and pharmacokinetics of the antibiotic GSK1322322, a novel peptide deformylase inhibitor. | 2013 May |
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Comparative analysis of the antibacterial activity of a novel peptide deformylase inhibitor, GSK1322322. | 2013 May |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23478958
Lanopepden (GSK1322322) had an MIC90 of 1 μg/ml against M. catarrhalis and 4 μg/ml against H. influenzae, with 88.8% of beta-lactamase-positive strains showing growth inhibition at that concentration. All S. pneumoniae strains were inhibited by ≤ 4 μg/ml of GSK1322322, with an MIC90 of 2 μg/ml. GSK1322322 was very potent against S. pyogenes strains, with an MIC90 of 0.5 μg/ml, irrespective of their macrolide resistance phenotype. It was also active against S. aureus strains regardless of their susceptibility to methicillin, macrolides, or levofloxacin, with an MIC90 of 4 μg/ml in all cases.
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CHEMBL3301608
Created by
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300000044500
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DBSALT002104
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1441390-17-5
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71571564
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C170093
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YW25HPP501
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BC-71
Created by
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ACTIVE MOIETY
SUBSTANCE RECORD