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PD173074

SKU: orb1305225

Description

PD173074

Research Area

Cardiovascular Research, Cell Biology, Signal Transduction

Images & Validation

Key Properties

CAS Number219580-11-7
MW523.67
Purity98.21%
FormulaC28H41N7O3
SMILESCCN(CC)CCCCNc1ncc2cc(c(NC(=O)NC(C)(C)C)nc2n1)-c1cc(OC)cc(OC)c1
TargetVEGFR,Src,FGFR,Apoptosis,IGF-1R,EGFR
SolubilityEthanol:52.4 mg/mL (100.06 mM);DMSO:125 mg/mL (238.7 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (3.82 mM)

Bioactivity

Target IC50
VEGFR2:100 nM-200 nM|FGFR1:25 nM
In Vivo
PD173074 dose-dependently inhibite the autophosphorylation of VEGFR2 IC50 100-200 nM) and FGFR1 IC50 1-5 nM). PD173074 dose-dependently inhibited FGF-2-promoted granule neuron survival IC50 12 nM), which was more than 1,000-fold higher than SU 5402 activity. PD173074 specifically inhibited FGF-2-mediated cell proliferation, differentiation and MAPK activation in oligodendrocyte lineage cells.PD173074 was an ATP-competitive inhibitor of FGFR1 (Ki: 40 nM).PD173074 also dose-dependently and potently inhibite the autophosphorylation of FGFR3 IC50 5 nM). In multiple myeloma cell lines, PD173074 was active against wild-type and FGFR3 mutant types.PD173074 caused a significant decrease in the viability of FGFR3-expressing KMS11 and KMS18 cells IC50 20 nM).
In Vitro
PD173074 dose-dependently inhibite the autophosphorylation of VEGFR2 IC50 100-200 nM) and FGFR1 IC50 1-5 nM). PD173074 dose-dependently inhibited FGF-2-promoted granule neuron survival IC50 12 nM), which was more than 1,000-fold higher than SU 5402 activity. PD173074 specifically inhibited FGF-2-mediated cell proliferation, differentiation and MAPK activation in oligodendrocyte lineage cells.PD173074 was an ATP-competitive inhibitor of FGFR1 (Ki: 40 nM).PD173074 also dose-dependently and potently inhibite the autophosphorylation of FGFR3 IC50 5 nM). In multiple myeloma cell lines, PD173074 was active against wild-type and FGFR3 mutant types.PD173074 caused a significant decrease in the viability of FGFR3-expressing KMS11 and KMS18 cells IC50 20 nM).
Cell Research
Cells are incubated with increasing concentration of PD173074 in the presence of aFGF/heparin for 48 hours the percentage of viable cells is determined by MTT.(Only for Reference)

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
DisclaimerFor research use only

Alternative Names

c-Src, Apoptosis, PD173074, PD-173074, PD 173074, inhibit, Inhibitor, IGF1R, Insulin Receptor, EGFR, FGFR1, FGFR, Fibroblast growth factor receptor, VEGFR2, VEGFR, Vascular endothelial growth factor receptor

Similar Products

  • PD173074 [orb1225643]

    >98%(HPLC)

    219580-11-7

    523.7

    C28H41N7O3

    1 g, 10 mg, 50 mg, 100 mg, 200 mg, 5 mg, 25 mg, 500 mg
Quality Guarantee

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Key Properties

No computed properties available.

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Protocol Information

PD173074 (orb1305225)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

5 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 100.00
10 mg
$ 100.00
25 mg
$ 140.00
50 mg
$ 190.00
100 mg
$ 280.00
200 mg
$ 460.00
500 mg
$ 730.00
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