SGI-1776
SGI-1776 is a potent, selective, orally active Pim kinase inhibitor with IC50 of 7, 363 and 69 nM for Pim1, Pim2 and Pim3, respectively; exhibits promising selectivity against a panel of >300 kinases, shows inhibitory activity against two other kinases: Flt-3 (IC50=44 nM) and Haspin (IC50=34 nM) ; reduces cell viability of androgen-independent prostate cancer cell lines with IC50 of 2-4 uM, causes cell cycle arrest and caspase-dependent apoptosis in prostate cancer cells, marginally sensitizes prostate cancer cells to taxane-based therapeutics by inhibiting MDR1 activity and inducing apoptosis; shows efficacy in xenograft model bearing MV-4-11 tumors.Prostate Cancer Phase 1 Clinical.
Product Specifications
CAS Number
1025065-69-3
Product Name Alternative
SGI 1776 | SGI1776
Purity
>98% (HPLC)
Solubility
10 mM in DMSO
Smiles
FC (F) (F) OC1=CC=C (C2=CN=C3C=CC (NCC4CCN (C) CC4) =NN32) C=C1
Molecular Formula
C20H22F3N5O
Molecular Weight
405.42
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
Imidazo[1,2-b]pyridazin-6-amine, N-[ (1-methyl-4-piperidinyl) methyl]-3-[3- (trifluoromethoxy) phenyl]-
Available Sizes
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