Decarboxy Moxifloxacin

CAS No. 1322062-57-6

Decarboxy Moxifloxacin( —— )

Catalog No. M26147 CAS No. 1322062-57-6

Decarboxylated moxifloxacin is a decarboxylated compound of moxifloxacin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 89 In Stock
5MG 82 In Stock
10MG 122 In Stock
25MG 204 In Stock
50MG 298 In Stock
100MG 423 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Decarboxy Moxifloxacin
  • Note
    Research use only, not for human use.
  • Brief Description
    Decarboxylated moxifloxacin is a decarboxylated compound of moxifloxacin.
  • Description
    Decarboxylated moxifloxacin is a decarboxylated compound of moxifloxacin. Moxifloxacin is an oral active 8-methoxy quinolone antibiotic used in acute bacterial sinusitis, chronic bronchitis, acute bacterial deterioration, and community-acquired pneumonia.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Trk
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1322062-57-6
  • Formula Weight
    357.429
  • Molecular Formula
    C20H24FN3O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    [H][C@]12CN(C[C@@]1([H])NCCC2)c1c(F)cc2c(c1OC)n(ccc2=O)C1CC1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Emiliano Cocco, et al. NTRK fusion-positive cancers and TRK inhibitor therapy. Nat Rev Clin Oncol. 2018 Dec;15(12):731-747.
molnova catalog
related products
  • 16alpha-Hydroxypredn...

    16alpha-Hydroxyprednisolone is a stereoselective metabolite of the 22(R) epimer of the glucocorticoid budesonide.

  • Raddeanoside R9

    The rhizomes of Anemone raddeana Regel.

  • V116517

    V116517 is a potent, orally active transient receptor potential vanilloid (TRPV1) antagonist. V116517 shows potent activity in inhibiting both capsaicin (CAP)- and acid (pH 5)-induced currents in rat DRG neurons expressing native TRPV (IC50=423.2 nM for CAP; IC50=180.3 nM for acid). V116517 can be used for the research of pain.