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LY2940680

LY2940680 (Taladegib) is potent Smoothened (SMO) receptor antagonist, potently inhibits Hedgehog (Hh) signaling with IC50 of 6.3 nM in Gli-luc reporter assyas; inhibits medulloblastoma cell proliferation isolated from Ptch+/–p53–/– mice with IC50 of 43.5 nM; demonstrates anti-tumor activity in vivo with advanced basal cell carcinoma (BCC) and other malignancies.Ovarian Cancer Phase 2 Clinical (In Vitro) :Taladegib, a small-molecule antagonist of the smoothened receptor, shows a slight inhibitory effect on cell proliferation without differences between mucin- (IC50: Taladegib=49.8±4.5 μM) and mixed- Cholangiocarcinoma (CCA) (IC50: Taladegib=61.2±21.1 μM) . The IC50 for Taladegib inhibition of [3H]MRT-92 binding is right shifted (3- to 100-fold) for the S387AECL2, L325F3.36f, and D473H6.54f mutants but did not differ from that of WT receptor for the other mutants. The ability of SANT-1 to inhibit [3H]MRT-92 binding to V329F3.40f and T466F6.47f mutants is abolished, and it is severely impaired for L325F3.40f, I408F5.51f, and M525G7.45f mutants (4- to 140-fold drop of the IC50), but is not modified for the S387AECL2 mutant. Taken together, these data confirm our docking hypothesis that MRT-92-binding mode differs from that of either Taladegib or SANT-1 by simultaneously occupying binding sites 1 and 2.

Product Specifications

CAS Number

1258861-20-9

Product Name Alternative

LY 2940680 | LY-2940680 | Taladegib

Purity

>98% (HPLC)

Solubility

DMSO: ≥ 5.2 mg/mL

Smiles

CN1C (=CC=N1) C2=NN=C (C3=CC=CC=C32) N4CCC (CC4) N (C) C (=O) C5=C (C=C (C=C5) F) C (F) (F) F

Molecular Formula

C26H24F4N6O

Molecular Weight

512.502

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

Benzamide, 4-fluoro-N-methyl-N-[1-[4- (1-methyl-1H-pyrazol-5-yl) -1-phthalazinyl]-4-piperidinyl]-2- (trifluoromethyl) -

Available Sizes

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