Moxalactam Disodium

CAS No. 64953-12-4

Moxalactam Disodium ( Moxalactam Disodium; Latamoxef, Sodium Salt )

Catalog No. M18954 CAS No. 64953-12-4

Moxalactam sodium salt is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
50MG 27 In Stock
100MG 41 In Stock
500MG 128 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Moxalactam Disodium
  • Note
    Research use only, not for human use.
  • Brief Description
    Moxalactam sodium salt is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
  • Description
    Moxalactam sodium salt is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
  • Synonyms
    Moxalactam Disodium; Latamoxef, Sodium Salt
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    Antibacterial
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    64953-12-4
  • Formula Weight
    564.44
  • Molecular Formula
    C20H18N6Na2O9S
  • Purity
    98%
  • Solubility
    DMSO : ≥ 38 mg/mL; 67.32 mM
  • SMILES
    [H][C@]12OCC(CSC3=NN=NN3C)=C(N1C(=O)[C@]2(NC(=O)[C@H](C(=O)O[Na])C1=CC=C(O)C=C1)OC)C(=O)O[Na]
  • Chemical Name
    sodium (6R,7R)-7-(2-carboxylato-2-(4-hydroxyphenyl)acetamido)-7-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

Shipping & Storage Information

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

Reference

1. Carmine AA, et al. Drugs. 1983 Oct;26(4):279-333.
molnova catalog
related products
  • (-)-(S)-B-973B

    (-)-(S)-B-973B is an effective allosteric agonist and a positive allosteric modulator of α7 nAChR.

  • Theobromine

    3,7-Dimethylxanthine. The principle alkaloid in Theobroma cacao (the cacao bean) and other plants.

  • TAE-1

    TAE-1 is an inhibitor of amyloid-β fibril formation and aggregation. It inhibits cholinesterases AChE and BuChE with IC50 of 0.3 μM and 3.9 μM, respectively.