Pirtobrutinib

CAS No. 2101700-15-4

Pirtobrutinib( LOXO-305 )

Catalog No. M28068 CAS No. 2101700-15-4

Pirtobrutinib (LOXO-305), a highly selective and non-covalent next generation BTK inhibitor, inhibits diverse BTK C481 substitution mutations.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 72 In Stock
5MG 68 In Stock
10MG 122 In Stock
25MG 282 In Stock
50MG 425 In Stock
100MG 625 In Stock
200MG Get Quote In Stock
500MG 1330 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Pirtobrutinib
  • Note
    Research use only, not for human use.
  • Brief Description
    Pirtobrutinib (LOXO-305), a highly selective and non-covalent next generation BTK inhibitor, inhibits diverse BTK C481 substitution mutations.
  • Description
    Pirtobrutinib (LOXO-305), a highly selective and non-covalent next generation BTK inhibitor, inhibits diverse BTK C481 substitution mutations. Pirtobrutinib causes regression of BTK-dependent lymphoma tumors in mouse xenograft models. Pirtobrutinib is also more than 300-fold selective for BTK versus 370 other kinases tested and shows no significant inhibition of non-kinase off-targets at 1 μM.(In Vitro):Pirtobrutinib potently inhibits both wild-type BTK and BTK C481S-mediated kinase activity with nanomolar potency. Pirtobrutinib inhibits WT BTK (Y223) autophosphorylation with an IC50 of 3.68 nM. Pirtobrutinib inhibits BTK C481S Y223, C481T Y223, and C481R Y223 autophosphorylation with IC50s of 8.45, 7.23, and 11.73 nM, respectively.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    LOXO-305
  • Pathway
    Tyrosine Kinase
  • Target
    BTK
  • Recptor
    8-oxoguanine DNA glycosylase 1 (OGG1)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2101700-15-4
  • Formula Weight
    479.43
  • Molecular Formula
    C22H21F4N5O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (104.29 mM)
  • SMILES
    N/A
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Baptiste BA, et al. Enhanced mitochondrial DNA repair of the common disease-associated variant, Ser326Cys, of hOGG1 through small molecule intervention. Free Radic Biol Med. 2018 Aug 20;124:149-162.
molnova catalog
related products
  • Tilfrinib

    Tilfrinib is an effective and selective inhibitor of breast tumor kinase (IC50: 3.15 nM), which displays anti-proliferative activity.

  • AVL-292

    AVL-292 (Spebrutinib, CC-292) is a highly selective, covalent Btk inhibitor with IC50 of <1 nM; also less potently inhibits Yes, c-Src, Brk, Lyn, and Fyn with IC50s of 723 nM, 1.729 uM, 2.43 uM, 4.4 uM, and 7.15 uM, rspectively.

  • ARQ-531

    ARQ-531 (ARQ531) is a potent, reversible, orally available inhibitor of both wild type and C481S-mutant BTK kinase with IC50 of 0.85 and 0.39 nM, respectively.