Dicloxacillin Sodium

CAS No. 343-55-5

Dicloxacillin Sodium ( —— )

Catalog No. M18450 CAS No. 343-55-5

Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin and it has activity against gram-positive/negative aerobic and anaerobic bacteria.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 45 Get Quote
50MG 59 Get Quote
100MG 106 Get Quote
200MG 193 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Dicloxacillin Sodium
  • Note
    Research use only, not for human use.
  • Brief Description
    Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin and it has activity against gram-positive/negative aerobic and anaerobic bacteria.
  • Description
    Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin and it has activity against gram-positive/negative aerobic and anaerobic bacteria.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    343-55-5
  • Formula Weight
    510.32
  • Molecular Formula
    C19H17Cl2N3O5S·H2O·Na
  • Purity
    98%
  • Solubility
    ——
  • SMILES
    CC1=C(C(=NO1)C2=C(C=CC=C2Cl)Cl)C(=N[C@H]3[C@@H]4N(C3=O)[C@H](C(S4)(C)C)C(=O)O)[O-].[Na+]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Quijano R, et al. Proc Soc Exp Biol Med. 1979, 162(3), 442-444.
molnova catalog
related products
  • Isovanillic acid

    Isovanillic acidis is a natural product isolated from Senecio scandens and shows distinct anti -inflammatory activities.

  • Caesappanin C

    Caesappanin C, extracted from the heartwood of Indonesian Caesalpinia sappan L., shows strong proliferation stimulating activity against the primary osteoblastic cells in vitro.

  • [Pro3]-GIP (Mouse)

    GIP receptor antagonist (IC50 = 2.6μM). Inhibits GIP-stimulated insulin release from pancreatic β cells in vitro. In ob/ob mice, blocks the effects of GIP on insulin release and plasma glucose levels. Also improves intraperitoneal glucose tolerance, insulin sensitivity, and glucose response to feeding in ob/ob mice.