LB 42708 Chemical Properties

Boiling point:

769.6±60.0 °C(Predicted)

Density 

1.39±0.1 g/cm3(Predicted)

storage temp. 

Store at -20°C

solubility 

≥22.75 mg/mL in DMSO; insoluble in H2O; ≥47.5 mg/mL in EtOH

form 

solid

pka

5.67±0.13(Predicted)

LB 42708 Usage And Synthesis

Uses

LB 42708 is a selective nonpeptidic Farnesyltransferase (FTase) inhibitor.LB42708 suppresses tumor growth and tumor angiogenesis in both xenograft tumor models of Ras-mutated HCT116 cells and its wild-type Caco-2 cells, indicating its potential application in the treatment of both Ras-mutated and wild type tumors.

Biological Activity

lb42708 is a selective inhibitor of farnesyltransferase (ftase) with ic50 value of 0.8nm [1].lb42708 is a nonpeptide pyrrole-based ftase inhibitor with high potency and selectivity. it inhibits the farnesylation of h-ras, n-ras and k-ras4b in vitro with ic50 values of 0.8nm, 1.2nm and 2nm, respectively. to the related enzyme geranylgeranyltransferase i, lb42708 shows no significant inhibition with ic50 value of 100μm. in cultured raw264.7 cell line, lb42708 potently reduces the farnesylated p21ras stimulated by lps and ifn-γ with ic50 value of ~ 10nm. besides that, the huvec cells treated with lb42708 shows inhibition of cell proliferation and migration induced by vegf. lb42708 inhibits the vegf-induced dna synthesis with ic50 value of 75nm and also inhibits vegf-induced formation of the gtp-bound form of ras with ic50 values of 50nm. in addition, it affects the tube-like structure formation. furthermore, the administration of lb42708 can suppress tumor growth both in ras-mutated hct116 and wild-type caco-2 xenograft models [1, 2].

References

[1] na h j, lee s j, kang y c, et al. inhibition of farnesyltransferase prevents collagen-induced arthritis by down-regulation of inflammatory gene expression through suppression of p21ras-dependent nf-κb activation. the journal of immunology, 2004, 173(2): 1276-1283.
[2] kim c k, choi y k, lee h, et al. the farnesyltransferase inhibitor lb42708 suppresses vascular endothelial growth factor-induced angiogenesis by inhibiting ras-dependent mitogen-activated protein kinase and phosphatidylinositol 3-kinase/akt signal pathways. molecular pharmacology, 2010, 78(1): 142-150.

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