KY19382

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

KY19382
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Cat #: V2448 CAS #: 2226664-93-1 Purity ≥ 99%

Description: KY-19382 is a novel, potent and orally active dual inhibitor of CXXC5-DVL( IC50s =19) and GSK3β( IC50s = 10 nM). It can be used for the research of high fat diet (HFD) induced metabolic diseases.

References: Choi S, et, al. CXXC5 mediates growth plate senescence and is a target for enhancement of longitudinal bone growth. Life Sci Alliance. 2019 Apr 10; 2(2): e201800254.

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Molecular Weight (MW)360.19
Molecular FormulaC17H11Cl2N3O2
CAS No.2226664-93-1
SMILES CodeO=C1NC2=C(C=C(Cl)C(Cl)=C2)/C1=C3NC4=C(C=CC=C4)C/3=N/OC
SynonymsKY19382; KY 19382; KY-1938
ProtocolIn VitroKY19382 (0.1 μM; 48 h) elevates nuclear translocation of β-catenin in ATDC5 cells. KY19382 (0.001-10 μM; 18 h) enhances the TOPFlash activity in HEK293 reporter cells. KY19382 (0.1 μM; 4 h) interrupts the CXXC5-DVL interaction in ATDC5 cells. KY19382 (0.01 and 0.1 μM; 24 h) inactivates GSK3α/β in ATDC5 cells. KY19382 (0.1 μM; 3 d) up-regulates the mRNA levels of chondrogenic differentiation markers in ATDC5 and C28/I2 cells. KY19382 (0.01 and 0.1 μM; 48 h) promotes ATDC5 cells proliferation.
In VivoKY19382 (5 mg/kg; i.p.) displays a relatively favorable bioavailability (F=16.74%), showing half-life of 16.20 h and an exposure level of 6,555.79 ng•h/ml. KY19382 (0.1 mg/kg; i.p. once daily for 10 weeks) significantly increases the length of tibiae in mice. KY19382 (0.1 mg/kg; i.p. once daily for 2 weeks) delays growth plate senescence in older mice and promotes growth plate maturation in rapidly growing young mice.
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
1mM2.7763 mL13.8816 mL27.7631 mL55.5263 mL
5mM0.5553 mL2.7763 mL5.5526 mL11.1053 mL
10mM0.2776 mL1.3882 mL2.7763 mL5.5526 mL
20mM0.1388 mL0.6941 mL1.3882 mL2.7763 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.