Leflunomide

CAT:
804-HY-B0083-01
Size:
100 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Leflunomide - image 1

Leflunomide

  • Description :

    Leflunomide is a pyrimidine synthesis inhibitor, inhibiting dihydroorotate dehydrogenase (DHODH), and acts as a disease-modifying antirheumatic agent.
  • CAS Number :

    [75706-12-6]
  • Product Name Alternative :

    HWA486; RS-34821; SU101
  • UNSPSC :

    12352005
  • Hazard Statement :

    H301, H315, H319, H335
  • Target :

    Bacterial; Dihydroorotate Dehydrogenase; Endogenous Metabolite
  • Type :

    Reference compound
  • Related Pathways :

    Anti-infection; Metabolic Enzyme/Protease
  • Applications :

    Cancer-Kinase/protease
  • Field of Research :

    Cancer
  • Assay Protocol :

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

    99.82
  • Solubility :

    DMSO : ≥ 50 mg/mL
  • Smiles :

    O=C(C1=C(C)ON=C1)NC2=CC=C(C(F)(F)F)C=C2
  • Molecular Formula :

    C12H9F3N2O2
  • Molecular Weight :

    270.21
  • Precautions :

    H301, H315, H319, H335
  • References & Citations :

    [1]Davis JP, et al. The immunosuppressive metabolite of leflunomide is a potent inhibitor of human dihydroorotate dehydrogenase. Biochemistry. 1996 Jan 30;35 (4) :1270-3.|[2]Xu X, et al. Inhibition of protein tyrosine phosphorylation in T cells by a novel immunosuppressive agent, leflunomide. J Biol Chem. 1995 May 26;270 (21) :12398-403.|[3]Fox RI, et al. Mechanism of action for leflunomide in rheumatoid arthritis. Clin Immunol. 1999 Dec;93 (3) :198-208.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    Launched

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