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GDC-0449 (Vismodegib)

Cat. No. M1713

All AbMole products are for research use only, cannot be used for human consumption.

GDC-0449 (Vismodegib) Structure
Synonym:

Vismodegib, HhAntag691

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
10mM*1mL in DMSO USD 40 In stock
5mg USD 35 In stock
10mg USD 46 In stock
50mg USD 65 In stock
100mg USD 84 In stock
200mg USD 120 In stock
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Quality Control & Documentation
Biological Activity

GDC-0449 (Vismodegib) is a potent and specific hedgehog (Hh) pathway, also inhibits ABCG2, Pgp and MRP1-important ABC transporters associated with MDR. The IC50 values of GDC-0449 for inhibition of ABCG2 and Pgp were 1.4 and 3.0μM, respectively. GDC-0449 (Vismodegib) has been used to treat medulloblastoma in animal models and has recently entered clinical trials for a variety of solid tumors.

Product Citations
Customer Product Validations & Biological Datas
Source Pharma Res (2017). Figure 7. GDC-0449
Method i.v.
Cell Lines mice
Concentrations 10 mg/kg
Incubation Time 15, 30, 60, 240, 720 and 1440 min
Results For the 20% M6P-conjugated micelles, GDC-0449 concentration increased by 30.60% compared to non targeted micelles in normal mice and by 50.36% in fibrotic mice liver
Source Pharma Res (2017). Figure 6. GDC-0449
Method i.v.
Cell Lines mice
Concentrations 10 mg/kg
Incubation Time 15, 30, 60, 240, 720 and 1440 min
Results Liver fibrosis results changes in the subendothelial space of Disse and sinusoid due to scar formation, which may affect the hepatic uptake of GDC-0449. The hepatic uptake of GDC-0449 after systemic administration of drug loaded micelles decreased from ~40% to ~30%
Protocol (for reference only)
Cell Experiment
Cell lines OM9;22 cell line
Preparation method Cell proliferation assay The cells were seeded in 24- or 96-well plates at a density of 2 *105 mL -1 in the presence or absence of S9 feeder cells. The cells were treated with the inhibitor drugs at the indicated concentrations: dasatinib, 1–100nM; and GDC-0449, 100nM to 10 mM. Viable cells were counted by trypan blue exclusion or fluorescence-activated cell sorting.
Concentrations 100nM to 10 µM
Incubation time 48h
Animal Experiment
Animal models Medulloblastoma allografts model in mice
Formulation 0.5% methyl-cellulose, 0.2% tween-80 (MCT)
Dosages 0.3 to 75 mg/kg daily
Administration oral gavage
Chemical Information
Molecular Weight 421.3
Formula C19H14Cl2N2O3S
CAS Number 879085-55-9
Solubility (25°C) DMSO 50 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Chang et al. Arch Dermatol. Initial Assessment of Tumor Regrowth After Vismodegib in Advanced Basal Cell Carcinoma.

[2] Dirix et al. Future Oncol. Vismodegib: a promising drug in the treatment of basal cell carcinomas.

[3] Keating GM. Drugs. Vismodegib: in locally advanced or metastatic Basal cell carcinoma.

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Keywords: GDC-0449 (Vismodegib), Vismodegib, HhAntag691 supplier, Smo, inhibitors, activators

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