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RG-7112 (RO-5045337)

This product is for research use only, not for human use. We do not sell to patients.

RG-7112 (RO-5045337)
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
250mg$1340Check With Us
500mg$1950Check With Us
1g$2925Check With Us

Cat #: V0045 CAS #: 939981-39-2 Purity ≥ 98%

Description: RG7112 (also known as RO5045337) is a novel, potent and highly selective antagonist/inhibitor of the p53-MDM2 protein-protein interaction with IC50 of 11 nM.

References: Vu B, et al. Discovery of RG7112: A Small-Molecule MDM2 Inhibitor in Clinical Development. ACS Med Chem Lett. 2013 Apr 2;4(5):466-9.

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Molecular Weight (MW)727.78
Molecular FormulaC38H48Cl2N4O4S
CAS No.939981-39-2
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 100 mg/mL (137.7 mM)r
Water:<1 mg/mL (slightly soluble or insoluble)r
Ethanol: N/A
Solubility In Vivo1% CMC Na:14 mg/mL
SMILES CodeO=C(N1[C@](C)(C2=CC=C(Cl)C=C2)[C@](C)(C3=CC=C(Cl)C=C3)N=C1C4=CC=C(C(C)(C)C)C=C4OCC)N5CCN(CCCS(=O)(C)=O)CC5
SynonymsRO5045337; RO 5045337; RO5045337; R7112 RG7112 RG 7112; RG7112;
ProtocolIn VitroRG7112 (0-5 μM) stabilizes wild-type p53 and induces p53 signaling in cancer cells. RG7112 effectively activates p53 functions in cancer cells.
In VivoRG7112 (25-200 mg/kg, single oral dose) activates p53 pathway and induces apoptosis in tumor cells in vivo.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM1.3740 mL6.8702 mL13.7404 mL27.4808 mL
5mM0.2748 mL1.3740 mL2.7481 mL5.4962 mL
10mM0.1374 mL0.6870 mL1.3740 mL2.7481 mL
20mM0.0687 mL0.3435 mL0.6870 mL1.3740 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.