An oxazolidinone antibiotic
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Labeled Version(s)
33290Tedizolid-13C-d3
Pro-drug Form(s)
23729Tedizolid Phosphate
Technical Support & Resources

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Tedizolid

Item No. 32952

Technical Information
Formal Name
(5R)-3-[3-fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-5-(hydroxymethyl)-2-oxazolidinone
CAS Number
856866-72-3
Synonyms
  • DA 7157
  • TR-700
Molecular Formula
C17H15FN6O3
Formula Weight
Purity
≥98%
A crystalline solid
DMF: Slightly solubleDMSO: Slightly solubleEthanol: Slightly soluble
λmax
234, 302 nm
SMILES
FC1=C(C2=CN=C(C3=NN(C)N=N3)C=C2)C=CC(N4C[C@H](CO)OC4=O)=C1
InChi Code
InChI=1S/C17H15FN6O3/c1-23-21-16(20-22-23)15-5-2-10(7-19-15)13-4-3-11(6-14(13)18)24-8-12(9-25)27-17(24)26/h2-7,12,25H,8-9H2,1H3/t12-/m1/s1
InChi Key
XFALPSLJIHVRKE-GFCCVEGCSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Tedizolid is an oxazolidinone antibiotic and active metabolite of the antibiotic tedizolid phosphate (Item No. 23729).1 Tedizolid phosphate is converted to tedizolid by phosphatases in vivo. It is active against a wide variety of clinical isolates, including isolates of methicillin-resistant S. aureus (MRSA), E. faecalis, and penicillin-susceptible S. pneumoniae (MICs = 0.5, 0.5, and 0.25 µg/ml, respectively), as well as isolates of anaerobic bacteria (MICs = 0.25-4 µg/ml). Tedizolid protects against mortality in a mouse model of systemic methicillin-susceptible S. aureus (MSSA) infection (ED50 = 8.8 mg/kg).2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Schaadt, R., Sweeney, D.A., Shinabarger, D., et alIn vitro activity of TR-700, the active ingredient of the antibacterial prodrug TR-701, a novel oxazolidinone antibacterial agent. Antimicrob. Agents Chemother. 53(8), 3236-3239 (2009).

    2. Im, W.B., Choi, S.H., Park, J.-Y., et alDiscovery of torezolid as a novel 5-hydroxymethyl-oxazolidinone antibacterial agent. Eur. J. Med. Chem. 46(4), 1027-1039 (2011).