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R547 (Ro 4584820)

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R547 (Ro 4584820)
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Size Price Stock
250mg$1950Check With Us
500mg$2925Check With Us
1g$4385Check With Us

Cat #: V1559 CAS #: 741713-40-6 Purity ≥ 98%

Description: R547 (R-547; Ro4584820; R 547; Ro-4584820) is a potent, selective and ATP-competitive inhibitor of CDK1/2/4 with potential antitumor activity.

References: DePinto, Wanda et al In vitro and in vivo activity of R547: a potent and selective cyclin-dependent kinase inhibitor currently in phase I clinical trials Molecular Cancer Therapeutics (2006), 5(11), 2644-2658

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Molecular Weight (MW)441.45
Molecular FormulaC18H21F2N5O4S
CAS No.741713-40-6
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 60 mg/mL (135.9 mM)r
Water: <1 mg/mLr
Ethanol: <1 mg/mL
Solubility In Vivo1% hydroxyethyl cellulose+0.2% Tween 80: 30 mg/mL
SynonymsR547; Ro4584820; R 547; Ro-4584820; R-547; Ro 4584820
ProtocolIn VitroR547 potently inhibits CDK1/cyclin B, CDK2/cyclin E, and CDK4/cyclin D1 (Ki=1-3 nM) and is inactive (Ki> 120,5 nM) of > unrelated kinases in cells.
In VivoR547 has significant in vivo efficacy and is administered orally daily and intravenously once weekly. R547 Inhibits phosphorylation of retinoblastoma proteins in tumors.
Animal model13-14 weeks old female immunodeficient nude mice (23-25 g), with HCT116/H460a/MDA-MB-435/DU145/LOX/A549 cells xenograft.
Dosages 40 mg/kg
AdministrationOral administration; daily; for 3-weeks
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
1mM2.2653 mL11.3263 mL22.6526 mL45.3052 mL
5mM0.4531 mL2.2653 mL4.5305 mL9.0610 mL
10mM0.2265 mL1.1326 mL2.2653 mL4.5305 mL
20mM0.1133 mL0.5663 mL1.1326 mL2.2653 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.