KX2-391

CAS No. 897016-82-9

KX2-391( KX 01 )

Catalog No. M16454 CAS No. 897016-82-9

KX2-391, the first clinical Src inhibitor (peptidomimetic class) that targets the peptide substrate site of Src, with GI50 of 9-60 nM in cancer cell lines.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 32 In Stock
5MG 51 In Stock
10MG 63 In Stock
25MG 129 In Stock
50MG 251 In Stock
100MG 435 In Stock
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Biological Information

  • Product Name
    KX2-391
  • Note
    Research use only, not for human use.
  • Brief Description
    KX2-391, the first clinical Src inhibitor (peptidomimetic class) that targets the peptide substrate site of Src, with GI50 of 9-60 nM in cancer cell lines.
  • Description
    KX2-391, the first clinical Src inhibitor (peptidomimetic class) that targets the peptide substrate site of Src, with GI50 of 9-60 nM in cancer cell lines. Phase 2.(In Vitro):Tirbanibulin (KX2-391) is a Src inhibitor that is directed to the Src substrate pocket. Tirbanibulin (KX2-391) shows steep dose-response curves against Huh7 (GI50=9 nM), PLC/PRF/5 (GI50=13 nM), Hep3B (GI50=26 nM), and HepG2 (GI50=60 nM), four hepatic cell cancer (HCC) cell lines. Tirbanibulin (KX2-391) is found to inhibit certain leukemia cells that are resistant to current commercially available drugs, such as those derived from chronic leukemia cells with the T3151 mutation. Tirbanibulin (KX2-391) is evaluated in engineered Src driven cell growth assays inNIH3T3/c-Src527F and SYF/c-Src527F cells and exhibits GI50 with 23 nM and 39 nM, respectively.(In Vivo):Orally administered Tirbanibulin (KX2-391) is shown to inhibit primary tumor growth and to suppress metastasis, in pre-clinical animal models of cancer.
  • In Vitro
    Tirbanibulin (KX2-391) is a Src inhibitor that is directed to the Src substrate pocket. Tirbanibulin (KX2-391) shows steep dose-response curves against Huh7 (GI50=9 nM), PLC/PRF/5 (GI50=13 nM), Hep3B (GI50=26 nM), and HepG2 (GI50=60 nM), four hepatic cell cancer (HCC) cell lines. Tirbanibulin (KX2-391) is found to inhibit certain leukemia cells that are resistant to current commercially available drugs, such as those derived from chronic leukemia cells with the T3151 mutation. Tirbanibulin (KX2-391) is evaluated in engineered Src driven cell growth assays inNIH3T3/c-Src527F and SYF/c-Src527F cells and exhibits GI50 with 23 nM and 39 nM, respectively.
  • In Vivo
    Orally administered Tirbanibulin (KX2-391) is shown to inhibit primary tumor growth and to suppress metastasis, in pre-clinical animal models of cancer.
  • Synonyms
    KX 01
  • Pathway
    Tyrosine Kinase
  • Target
    Src
  • Recptor
    Src (Hep 3B)| Src (Hep G2)| Src (HuH7)| Src (PLC/PRF/5)
  • Research Area
    Cancer
  • Indication
    Solid Tumors

Chemical Information

  • CAS Number
    897016-82-9
  • Formula Weight
    431.53
  • Molecular Formula
    C26H29N3O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:86 mg/mL (199.29 mM); Ethanol:<1 mg/mL (<1 mM); Water:<1 mg/mL (<1 mM)
  • SMILES
    O=C(NCC1=CC=CC=C1)C2=NC=C(C3=CC=C(OCCN4CCOCC4)C=C3)C=C2
  • Chemical Name
    N-benzyl-5-(4-(2-morpholinoethoxy)phenyl)picolinamide

Shipping & Storage Information

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

Reference

1.Lau GM, et al, Dig Dis Sci, 2009, 54(7), 1465-1474.
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