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Nilofabicin
CAS No. 934628-27-0
Nilofabicin( CG-400549 | CG 400549 | CG400549 | CG-0549 | CG 0549 | CG0549 | )
Catalog No. M27115 CAS No. 934628-27-0
Nilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 50 | Get Quote |
|
| 10MG | 72 | Get Quote |
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| 25MG | 120 | Get Quote |
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| 50MG | 177 | Get Quote |
|
| 100MG | 295 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameNilofabicin
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NoteResearch use only, not for human use.
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Brief DescriptionNilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute.
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DescriptionNilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute. (In Vitro):Nilofabicin had an MIC90 of 0.5 μg/ml for Staphylococcus aureus strains and was more potent than either linezolid or vancomycin. Among 203 strains of Staphylococcus aureus, the MICs of Nilofabicin were 0.06 to 1.0 μg/ml, with MIC(50) and MIC(90) values of 0.25 μg/ml each. All strains were susceptible to linezolid and quinupristin-dalfopristin (MICs, 0.25 to 2.0 μg/ml).
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In Vitro——
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In Vivo——
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SynonymsCG-400549 | CG 400549 | CG400549 | CG-0549 | CG 0549 | CG0549 |
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorProstacyclin receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number934628-27-0
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Formula Weight340.44
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Molecular FormulaC19H20N2O2S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (293.74 mM)
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SMILESCc1c(N)cccc1Cn1ccc(OCCc2cccs2)cc1=O
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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
1.Bexis S, et, al. Vascular actions of the prostacyclin receptor antagonist BAY 73-1449 in the portal hypertensive rat. Eur J Pharmacol. 2008 Aug 20;590(1-3):322-6.
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