Thiamphenicol
CAS No. 15318-45-3
Thiamphenicol( NSC 522822 | (+)-Thiamphenicol | Thiophenicol | WIN 5,603-2 )
Catalog No. M12153 CAS No. 15318-45-3
Thiamphenicol is an antimicrobial antibiotic and a methyl-sulfonyl analogue of chloramphenicol.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
50MG | 35 | In Stock |
|
100MG | 48 | In Stock |
|
200MG | 60 | In Stock |
|
500MG | 69 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
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Product NameThiamphenicol
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NoteResearch use only, not for human use.
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Brief DescriptionThiamphenicol is an antimicrobial antibiotic and a methyl-sulfonyl analogue of chloramphenicol.
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DescriptionThiamphenicol is an antimicrobial antibiotic and a methyl-sulfonyl analogue of chloramphenicol.(In Vitro):Thiamphenicol shows a significant post-antibiotic effect (PAE) (0.33 to 2.9h) on all pathogens studied (S. pneumoniae, S. aureus and Escherichia coli) and a powerful bactericidal effect against β-lactamase-positive and -negative H. influenzae. Thiamphenicol MICs for the microorganisms analyzed are: 32 mg/L (S. aureus and E. coli), 2 mg/L (S. pneumoniae) and 0.25 mg/L (H. influenzae). Thiamphenicol shows a good in vitro activity against difficult-to-treat multiply resistant pathogens.(In Vivo):The pharmacokinetics of Thiamphenicol (30 mg/kg) after single intravenous (IV) and oral (PO) administration is investigated in Mulard ducks. After IV administration, for Thiamphenicol, the mean residence time is 2.83 hours, the general half-life is 1.96 hours, the clearance is 0.04 L/hr/kg. Pharmacokinetics after PO administration is very similar for IV administration. Thiamphenicol shows rapid absorption and bioavailability of more than 70%.
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In VitroThiamphenicol shows a significant post-antibiotic effect (PAE) (0.33 to 2.9h) on all pathogens studied (S. pneumoniae, S. aureus and Escherichia coli) and a powerful bactericidal effect against β-lactamase-positive and -negative H. influenzae. Thiamphenicol MICs for the microorganisms analyzed are: 32 mg/L (S. aureus and E. coli), 2 mg/L (S. pneumoniae) and 0.25 mg/L (H. influenzae). Thiamphenicol shows a good in vitro activity against difficult-to-treat multiply resistant pathogens.
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In VivoThe pharmacokinetics of Thiamphenicol (30 mg/kg) after single intravenous (IV) and oral (PO) administration is investigated in Mulard ducks. After IV administration, for Thiamphenicol, the mean residence time is 2.83 hours, the general half-life is 1.96 hours, the clearance is 0.04 L/hr/kg. Pharmacokinetics after PO administration is very similar for IV administration. Thiamphenicol shows rapid absorption and bioavailability of more than 70%.
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SynonymsNSC 522822 | (+)-Thiamphenicol | Thiophenicol | WIN 5,603-2
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number15318-45-3
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Formula Weight356.22
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Molecular FormulaC12H15Cl2NO5S
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Purity>98% (HPLC)
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SolubilityDMSO: 71 mg/mL (199.31 mM)
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SMILESO=C(N[C@H](CO)[C@H](O)C1=CC=C(S(=O)(C)=O)C=C1)C(Cl)Cl
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Chemical Name2,2-dichloro-N-((1R,2R)-1,3-dihydroxy-1-(4-(methylsulfonyl)phenyl)propan-2-yl)acetamide
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.Berman HM, et al. Nucleic Acids Res. 2000 Jan 1; 28(1): 235-42.
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