Nemonoxacin
CAS No. 378746-64-6
Nemonoxacin( —— )
Catalog No. M36615 CAS No. 378746-64-6
Nemonoxacin (TG-873870) is an orally available non-fluorinated quinolone antibiotic with broad-spectrum antimicrobial activity against staphylococci, streptococci, and enterococci, as well as against Neisseria gonorrhoeae and Haemophilus influenzae.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameNemonoxacin
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NoteResearch use only, not for human use.
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Brief DescriptionNemonoxacin (TG-873870) is an orally available non-fluorinated quinolone antibiotic with broad-spectrum antimicrobial activity against staphylococci, streptococci, and enterococci, as well as against Neisseria gonorrhoeae and Haemophilus influenzae.
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DescriptionNemonoxacin (TG-873870) is an orally active and potent broad-spectrum antibiotic. Nemonoxacin shows good inhibitory activity against different species of staphylococci, streptococci, and enterococci, Neisseria gonorrhoeae, and Haemophilus influenza. Nemonoxacin can be used in the study of bacterial infections and community-acquired pneumonia.
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In VitroNemonoxacin (0-5.51 μM; 24 h) shows good antibacterial activity in vitro.Cell Viability Assay Cell Line:MSSA, MRSA Concentration:0-5.51 μM (0-2048 μg/mL) Incubation Time:24 h Result:Inhibited MSSA and MRSA with MIC90 values of 0.12 and 4 μg/mL.
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In VivoNemonoxacin (p.o.; 15 min and 6 h after infection) shows potent and broad-spectrum in vivo activity against both Gram-positive (S. aureus, S. capitis, S. pneumonia and E. faecalis) and Gram-negative (E. coli) isolates.Nemonoxacin (p.o.; 6, 12 and 24 h after infection) shows potent activities towards (2.5, 5, 10, 20 mg/kg) S. pneumonia 0613 (PRSP) and (10, 20, 40, 80 mg/kg) K. pneumonia 0607 infections in mouse pulmonary infection model.Animal Model:CD-1 ICR mice (18-22 g; mouse systemic infection model).Dosage:1.6-4.0 mg/kg (S. aureus and S. capitis infections), 2.4-10.0 mg/kg (S. pneumonia infections), 5.0-22.6 mg/kg (E. faecalis infections), 1.6-10.0 mg/kg (E. coli infections)Administration:Oral administration; 15 min and 6 h after infection Result:Showed the ED50s of 2.08, 2.59 and 2.52 mg/kg to against S. aureus ATCC 29213 (MSSA), S. aureus 0705 (MRSA) and S. capitis 0687 (levofloxacin-resistant MRSC), respectively.Animal Model:CD-1 ICR mice (18-22 g; mouse pulmonary infection model).Dosage:2.5, 5, 10, 20 mg/kg (S. pneumonia 0613 (PRSP)); 10, 20, 40, 80 mg/kg (K. pneumonia 0607)Administration:Oral administration; 6, 12 and 24 h after infection Result:Significantly decreased colony counts in vivo.
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Synonyms——
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorAntibacterial
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Research Area——
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Indication——
Chemical Information
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CAS Number378746-64-6
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Formula Weight371.43
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Molecular FormulaC20H25N3O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 2 mg/mL (5.38 mM; Ultrasonic (<60°C)
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SMILESO(C)C1=C2N(C=C(C(O)=O)C(=O)C2=CC=C1N3C[C@@H](C)C[C@H](N)C3)C4CC4
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Temocillin disodium
Temocillin disodium (BRL 17421 disodium) is a carbapenem antibiotic with antimicrobial activity that can be used to study urinary tract infections, bloodstream infections, pneumonia, intra-abdominal infections, central nervous system infections, skin and soft tissue infections, surgical site infections and bone and joint infections.
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D-3-Phenyllactic aci...
D-3-Phenyllactic acid is an anti-bacterial agent excreted by Geotrichum candidum inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans.
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6-AZATHYMINE
6-azathymine is a potent inhibitors of D-3-aminoisobutyrate-pyruvate aminotransferase.?6-Azauracil acted as a competitive inhibitor with respect to beta-alanine, and was an uncompetitive inhibitor with respect to pyruvic acid with a Ki of approximately 8.9 mM.
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