RWJ-67657

CAT:
804-HY-15505-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
RWJ-67657 - image 1

RWJ-67657

  • Description :

    RWJ-67657 (JNJ 3026582) is an orally active and selective p38α and p38β MAPK inhibitor with IC50s of 1 and 11 μM, respectively. RWJ-67657 displays no activity at p38γ and p38δ, and exhibits cardio protective effect. Anti-inflammatory and anti-tumor activity[1].
  • CAS Number :

    [215303-72-3]
  • Product Name Alternative :

    JNJ 3026582
  • UNSPSC :

    12352005
  • Target :

    P38 MAPK
  • Type :

    Reference compound
  • Related Pathways :

    MAPK/ERK Pathway
  • Applications :

    Cancer-Kinase/protease
  • Field of Research :

    Cancer; Inflammation/Immunology; Cardiovascular Disease
  • Assay Protocol :

    https://www.medchemexpress.com/rwj-67657.html
  • Purity :

    99.75
  • Solubility :

    DMSO : 125 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    OCCC#CC1=NC(C2=CC=C(F)C=C2)=C(C3=CC=NC=C3)N1CCCC4=CC=CC=C4
  • Molecular Formula :

    C27H24FN3O
  • Molecular Weight :

    425.50
  • References & Citations :

    [1]Shahin R, et al. Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment. Future Sci OA. 2017 Aug 8;3 (4) :FSO204.|[2]Wadsworth SA, et al. RWJ 67657, a potent, orally active inhibitor of p38 mitogen-activated protein kinase. J Pharmacol Exp Ther. 1999 Nov;291 (2) :680-7.|[3]Frigo DE, et al. p38 mitogen-activated protein kinase stimulates estrogen-mediated transcription and proliferation through the phosphorylation and potentiation of the p160 coactivator glucocorticoid receptor-interacting protein 1. Mol Endocrinol. 2006 May;20 (5) :971-83.|[4]Bai YY, et al. Synergistic Effects of Transplanted Endothelial Progenitor Cells and RWJ 67657 in Diabetic Ischemic Stroke Models. Stroke. 2015 Jul;46 (7) :1938-46.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    Phase 1
  • Isoform :

    P38α; p38β

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