PK150
CAS No. 2165324-62-7
PK150( —— )
Catalog No. M21144 CAS No. 2165324-62-7
PK150 shows oral bioavailability and antibacterial activity against several pathogenic strains at submicromolar concentrations.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 67 | Get Quote |
|
| 5MG | 110 | Get Quote |
|
| 10MG | 178 | Get Quote |
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| 25MG | 340 | Get Quote |
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| 50MG | 512 | Get Quote |
|
| 100MG | 735 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NamePK150
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NoteResearch use only, not for human use.
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Brief DescriptionPK150 shows oral bioavailability and antibacterial activity against several pathogenic strains at submicromolar concentrations.
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DescriptionPK150 shows oral bioavailability and antibacterial activity against several pathogenic strains at submicromolar concentrations.
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In Vitro——
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In VivoThe in vivo efficacy of PK150 against methicillin-sensitive S. aureus (MSSA) (strain SH1000) is demonstrated in a murine bloodstream infection model. PK150 (20?mg/kg; p.o.) significantly reduces bacterial loads in the liver and heart.PK150 (10 and 20mg/kg orally; or 10mg/kg intravenously) shows no obvious signs of toxicity in mice. Higher i.v. dosing of 20mg/kg results in severe toxic effects and is thus avoided for subsequent therapeutic models. Animal Model:Pathogen-free 9-week old female C57BL/6J miceDosage:20?mg/kg Administration:Administered p.o.Result:Bacterial loads in the liver and heart were both significantly reduced by approximately 100-fold.Animal Model:Outbred male CD-1 mice, 4 weeks oldDosage:10 and 20 mg/kg (Pharmacokinetic Analysis) Administration:Administered by intragastric gavage at 10 and 20 mg/kg or intravenously at 10 mg/kg Result:Oral bioavailability was approximately 63% and the mean residence time was slightly enhanced via this administration route.T1/2=11.69±1.5, 9.67±0.2, and 9.37±0.5 hours for 10 mg/kg i.v., 10 mg/kg p.o., and 20 mg/kg p.o., respectively.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptorothers
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Research Area——
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Indication——
Chemical Information
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CAS Number2165324-62-7
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Formula Weight394.68
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Molecular FormulaC15H3ClF5N2O3
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Purity>98% (HPLC)
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SolubilityDMSO:250 mg/mL (633.42 mM; Need ultrasonic)
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SMILESO=C(Nc1ccc2c(c1)OC(F)(F)O2)Nc1ccc(Cl)c(C(F)(F)F)c1
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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.Le P et al. Repurposing human kinase inhibitors to create an antibiotic active against drug-resistant Staphylococcus aureus persisters and biofilms. Nat Chem. 2019 Dec 16.
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