Torezolid

CAS No. 856866-72-3

Torezolid( TR-701 | tedizolid )

Catalog No. M16213 CAS No. 856866-72-3

Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infections.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 51 In Stock
5MG 78 In Stock
10MG 136 In Stock
25MG 236 In Stock
50MG 362 In Stock
100MG 529 In Stock
200MG Get Quote In Stock
500MG 1107 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Torezolid
  • Note
    Research use only, not for human use.
  • Brief Description
    Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infections.
  • Description
    Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infections.(In Vitro):Tedizolid (0.25 μg/mL) inhibits all 28 clinical isolates of PRSP, and is 4-fold more potent than linezolid against PRSP.(In Vivo):For mice infected with PSSP type III, the 100% survival rate is achieved with tedizolid phosphate at a minimum total daily dose of 10 mg/kg. Lungs of infected mice treated with tedizolid phosphate show less severe inflammation and edema, as indicated by the mean scores for inflammation and edema.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    TR-701 | tedizolid
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    MAO
  • Recptor
    MAO-A| MAO-B
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    856866-72-3
  • Formula Weight
    370.34
  • Molecular Formula
    C17H15FN6O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 10 mM
  • SMILES
    O=C1O[C@@H](CO)CN1C2=CC=C(C3=CC=C(C4=NN(C)N=N4)N=C3)C(F)=C2
  • Chemical Name
    (5R)-3-(3-fluoro-4-(6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)phenyl)-5-(hydroxymethyl)oxazolidin-2-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Choi S, et al. Antimicrob Agents ChemOthers. 2012 Jun 19.
molnova catalog
related products
  • Ladostigil

    Ladostigil (Ladostigil free base) is an orally active dual inhibitor of cholinesterase and brain-selective monoamine oxidase (MAO) with inhibitory effects on MAO-B and AChE, with IC50 values of 37.1 and 31.8 μM, respectively.

  • Osthenol

    Osthenol is a natural product, and is selective, reversible, and competitive human monoamine oxidase-A (hMAO-A) inhibitor (Ki=0.26 μM).

  • AnnH31

    AnnH31 is a potent Dyrk1A inhibitor with an IC50 value of 81 nM.AnnH31 inhibits MAO-A with an IC50 of 3.2 μM.AnnH31 can be used as a probe to confirm the involvement of DYRK1A in cellular phosphorylation.