VU6015929

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

VU6015929
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Size Price Stock
250mg$1650Check With Us
500mg$2450Check With Us
1g$3675Check With Us

Cat #: V34659 CAS #: N/A Purity ≥ 99%

Description: VU6015929 is a selective and orally bioavailable dual inhibitor of discoidin domain receptor 1/2 (DDR1/2) with IC50s of 4.67 nM and 7.39 nM, respectively.

References: Daniel E. Jeffries, et al. Discovery of VU6015929: A Selective Discoidin Domain Receptor 1/2 (DDR1/2) Inhibitor to Explore the Role of DDR1 in Antifibrotic Therapy. ACS Med. Chem. Lett. 2019.

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Molecular Weight (MW)485.43
Molecular FormulaC24H19F4N5O2
CAS No.N/A
SMILES Code FC1=CC=C(C(NC2=CC=CC(OC(F)(F)F)=C2)=O)C=C1NCC3=CC(C4=NN(C)C=C4)=CN=C3
SynonymsVU6015929; VU 6015929; VU-6015929
ProtocolIn VitroVU6015929 (Compound 7e; 4-100 nM; 24 hours; HEK293-DDR1b cells) treatment inhibits collagen I-induced DDR1 phosphorylation in a dose dependent manner. Analysis of the phosphorylated DDR1/total DDR1 ratio reveals an IC50 for VU6015929 of 0.7078 nM.
In VivoVU6015929 (Compound 7e) is further evaluated in a rat IV (0.5 mg/kg)/PO (3 mg/kg) PK study in a 10% EtOH/40% PEG400/50% saline vehicle. VU6015929 displays a good in vitro:in vivo correlation (IVIC), with moderate in vivo clearance (CLp = 34.2 mL/min/kg), an ~3 hour half-life, moderate volume of distribution at steady state (Vss = 4.3 L/kg) and 12.5% oral bioavailability with a rapid Tmax (0.75 hr).
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
1mM2.0600 mL10.3001 mL20.6003 mL41.2006 mL
5mM0.4120 mL2.0600 mL4.1201 mL8.2401 mL
10mM0.2060 mL1.0300 mL2.0600 mL4.1201 mL
20mM0.1030 mL0.5150 mL1.0300 mL2.0600 mL
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
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Concentration
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Volume
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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.