BMS-5

CAS No. 1338247-35-0

BMS-5( LIMKI-3 | LIMKI 3 | LIMKI3 | BMS-5 )

Catalog No. M17956 CAS No. 1338247-35-0

BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 45 In Stock
5MG 68 In Stock
10MG 113 In Stock
25MG 188 In Stock
50MG 282 In Stock
100MG 420 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
1 mL x 10 mM in DMSO 80 In Stock
2MG 48 In Stock
5MG 72 In Stock
10MG 119 In Stock
25MG 199 In Stock
50MG 291 In Stock
100MG 434 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    BMS-5
  • Note
    Research use only, not for human use.
  • Brief Description
    BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.
  • Description
    LIMKI-3, also known as BMS-3, is a Potent LIM kinase inhibitor (IC50 values are 7 and 8 nM for LIMK1 and LIMK2 respectively). Inhibits cofilin phosphorylation in MDA-MB-231 breast cancer cells. Reduces MDA-MB-231 tumor cell invasion in a 3D matrigel invasion assay.
  • In Vitro
    BMS-5 (LIMKi 3) inhibits cofilin-Ser3 phosphorylation in a dose-dependent manner in Nf2ΔEx2 mouse Schwann cells (MSCs) with an IC50 of ~2 μM. BMS-5 (LIMKi 3) reduces Nf2ΔEx2 MSC viability in a dose-dependent manner with an IC50 of 3.9 μM, but does not significantly reduce the viability of control Nf2flox2/flox2 MSCs at equivalent BMS-5 concentrations. At 10 μM BMS-5, Nf2ΔEx2 MSC viability is 40% compared to 83% for controls.
  • In Vivo
    BMS-5 (LIMKi 3) (20 or 200 μM/side) is bilaterally infused into the hippocampus of rats immediately after contextual fear conditioning training. Rats are tested for memory consolidation 48 h after fear conditioning. Post hoc analysis shows that the group treated with 200 μM BMS-5 express lower freezing levels compared to the 20 μM and vehicle groups (P<0.01).
  • Synonyms
    LIMKI-3 | LIMKI 3 | LIMKI3 | BMS-5
  • Pathway
    Angiogenesis
  • Target
    PDGFR
  • Recptor
    LIMK1|LIMK2
  • Research Area
    Inflammation/Immunology|Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    1338247-35-0
  • Formula Weight
    431.29
  • Molecular Formula
    C17H14Cl2F2N4OS
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 34 mg/mL; 78.83 mM
  • SMILES
    O=C(Nc1ncc(s1)c2cc(nn2c3c(Cl)cccc3Cl)C(F)F)C(C)C
  • Chemical Name
    N-[5-[1-(2,6-Dichlorophenyl)-3-(difluoromethyl)-1H-pyrazol-5-yl]-2-thiazolyl]-2-methylpropanamide

Shipping & Storage Information

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

Reference

1.Ross-Macdonald P, et al. Identification of a nonkinase target mediating cytotoxicity of novel kinase inhibitors. Mol Cancer Ther. 2008 Nov;7(11):3490-8.
molnova catalog
related products
  • SU16f

    SU16f is a potent and selective PDGFRβ inhibitor (IC50s: 10 nM, 140 nM, 2.29 μM for PDGFRβ, PDGFR1, PDGFR2, respectively).

  • PDGFRα kinase inhibi...

    PDGFRα kinase inhibitor 1 is a highly selective inhibitor of type II PDGFRα kinase (PDGFRα and PDGFRβ) with IC50 values of 132 nM and 6115 nM, respectively.

  • AG-1295

    A quinoxaline-type tyrphostin that acts as a potent and selective inhibitor of PDGFR kinase in vitro and in Swiss 3T3 cells with IC50 of 0.3-1 uM.