Cephradine

CAT:
804-HY-B1156-01
Size:
100 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Cephradine - image 1

Cephradine

  • Description :

    Cephradine (Cefradine) is a broad-spectrum and orally active cephalosporin. Cephradine is active against both gram-positive and gram-negative pathogens. Cephradine is effective in eradicating most penicillinase-producing organisms. Cephradine has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK[1][2][3].
  • CAS Number :

    [38821-53-3]
  • Product Name Alternative :

    Cefradine; SQ-11436
  • UNSPSC :

    12352005
  • Hazard Statement :

    H315, H317, H319, H334, H335
  • Target :

    Antibiotic; Bacterial; TOPK
  • Type :

    Reference compound
  • Related Pathways :

    Anti-infection; Cell Cycle/DNA Damage
  • Applications :

    COVID-19-anti-virus
  • Field of Research :

    Infection; Inflammation/Immunology
  • Assay Protocol :

    https://www.medchemexpress.com/Cefradine.html
  • Purity :

    95.11
  • Solubility :

    DMSO : ≥ 3.6 mg/mL|H2O : 8.33 mg/mL (ultrasonic)
  • Smiles :

    O=C(C(N12)=C(C)CS[C@]2([H])[C@H](NC([C@H](N)C3=CCC=CC3)=O)C1=O)O
  • Molecular Formula :

    C16H19N3O4S
  • Molecular Weight :

    349.40
  • Precautions :

    H315, H317, H319, H334, H335
  • References & Citations :

    [1]Schwinghammer TL, et al. Pharmacokinetics of cephradine administered intravenously and orally to young and elderly subjects. J Clin Pharmacol. 1990;30 (10) :893-899|[2]Caloza DL Jr, et al. Intravenous use of cephradine and cefazolin against serious infections. Antimicrob Agents Chemother. 1979;15 (1) :119-122.|[3]Fan X, et al. Cefradine blocks solar-ultraviolet induced skin inflammation through direct inhibition of T-LAK cell-originated protein kinase. Oncotarget. 2016;7 (17) :24633-24645|[4]Kang S, et al. In Vitro and In Vivo Antimicrobial Activity of Antibiotic-Conjugated Carriers with Rapid pH-Responsive Release Kinetics. Adv Healthc Mater. 2019;8 (14) :e1900247.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • Isoform :

    β-lactam

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