MLN0905

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

MLN0905
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
250mg$1550Check With Us
500mg$2550Check With Us
1g$3825Check With Us

Cat #: V1578 CAS #: 1228960-69-7 Purity ≥ 98%

Description: MLN0905 (MLN-0905; MLN 0905) is a novel, potent and selective small-molecule inhibitor of polo-like kinase-1 (PLK1) with potential antineoplastic activity.

References: Duffey MO, et al. Discovery of a potent and orally bioavailable benzolactam-derived inhibitor of Polo-like kinase 1 (MLN0905). J Med Chem. 2012 Jan 12; 55(1):197-208.

Top Publications Citing Invivochem Products
Publications Citing InvivoChem Products

Product Promise

Promise
Molecular Weight (MW)486.56
Molecular FormulaC24H25F3N6S
CAS No.1228960-69-7
Storage-20℃ for 3 years in powder formrr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 97 mg/mL (199.4 mM)rr
Water:<1 mg/mLrr
Ethanol: <1 mg/mL
SynonymsPLK1 inhibitor; MLN0905; MLN 0905; MLN-0905
ProtocolIn VitroMLN0905 (compound 12c) has inhibitory effect on PLK1, IC50 The value is 2 nM. MLN0905 has potent activity against Cdc25C, EC50 The value is 33 nM。 MLN0905 has inhibitory effects on HT29, HCT116, H460, and A375 cell lines, LD50 The values are 22 nM, 56 nM, 89 nM, and 34 nM, respectively. MLN0905 (125 nM) exhibits intense mitotic arrest and unipolar spindle formation in HT-29 cells.
In VivoMLN0905 (p.o.; 50 mg/kg) demonstrated a highly sustained PD response in nude mouse HT29 xenograft tumors
Animal modelTumor (HT29) xenograft model
Dosages0-50 mg/kg
AdministrationP.O; daily, QD×3/week
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
1mM2.0552 mL10.2762 mL20.5524 mL41.1049 mL
5mM0.4110 mL2.0552 mL4.1105 mL8.2210 mL
10mM0.2055 mL1.0276 mL2.0552 mL4.1105 mL
20mM0.1028 mL0.5138 mL1.0276 mL2.0552 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.