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RO8994

Cat. No. M9184
RO8994 Structure
Synonym:

RO-8994

Size Price Availability Quantity
10mM*1mL USD 520  USD520 In stock
2mg USD 285  USD285 In stock
5mg USD 385  USD385 In stock
10mg USD 555  USD555 In stock
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Quality Control & Documentation
Biological Activity

RO8994 induces dose-dependent up-regulation of p53 target genes and apoptosis in wild-type p53 cancer cells, consistent with its non-genotoxic mechanism of p53 activation.

In vivo, RO8994 displays remarkable tumor growth inhibition in the wild-type p53, MDM2-amplified SJSA-1 osteosarcoma tumor xenograft model - exhibiting significant (>60%) tumor growth inhibition at the low dose of 1.56 mg/kg, tumor stasis at 3.125 mg/kg and regression at 6.25 mg/kg.

Chemical Information
Molecular Weight 613.51
Formula C31H31Cl2FN4O4
CAS Number 1309684-94-3
Solubility (25°C) DMSO: ≥ 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Zhang Z, et al. Bioorg Med Chem. Discovery of potent and selective spiroindolinone MDM2 inhibitor, RO8994, for cancer therapy.

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Keywords: RO8994, RO-8994 supplier, Mdm2, inhibitors, activators


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