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881970-80-5

881970-80-5 Structure

881970-80-5 Structure
IdentificationBack Directory
[Name]

iMDK
[CAS]

881970-80-5
[Synonyms]

iMDK
3-[2-(4-Fluoro-benzyl)-imidazo[2,1-b]thiazol-6-yl]-chromen-2-one
2H-1-Benzopyran-2-one, 3-[2-[(4-fluorophenyl)methyl]imidazo[2,1-b]thiazol-6-yl]-
inhibit,iMDK,midkine,factor,PI3K,NSCLC,growth,Inhibitor,Phosphoinositide 3-kinase,MDK
[Molecular Formula]

C21H13FN2O2S
[MDL Number]

MFCD07528492
[MOL File]

881970-80-5.mol
[Molecular Weight]

376.4
Chemical PropertiesBack Directory
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C, protect from light
[solubility ]

Limited solubility
[form ]

Solid
[pka]

5.71±0.40(Predicted)
[color ]

Off-white to yellow
[InChI]

InChI=1S/C21H13FN2O2S/c22-15-7-5-13(6-8-15)9-16-11-24-12-18(23-21(24)27-16)17-10-14-3-1-2-4-19(14)26-20(17)25/h1-8,10-12H,9H2
[InChIKey]

IWFKQTWYILKFGE-UHFFFAOYSA-N
[SMILES]

C1(=O)OC2=CC=CC=C2C=C1C1=CN2C=C(CC3=CC=C(F)C=C3)SC2=N1
Hazard InformationBack Directory
[Uses]

iMDK is a small molecule inhibitor used to bind to midkine (MDK), a heparin binding growth factor that is expressed in malignant tumors.
[Biological Activity]

Cell permeable: yes''Primary Target
Midkine''Reversible: yes
[in vivo]

The combination treatment of iMDK ( (9 mg/kg/day; intraperitoneally injected with 100 μl) and PD0325901 (5 mg/kg; orally administered) effectively reduced lung tumor growth in a xenograft mouse model[1].

Animal Model:female BALB/c nude mice (6 week old) bearing H441 human lung cancer xenografts[1]
Dosage:iMDK (9 mg/kg) and PD0325901 (5 mg/kg)
Administration:Intraperitoneally injected with 100 μL iMDK everyday and/or orally administered PD0325901 five times per week (on days 1, 2, 3, 4, 5, 7, 8, 9, 10, 11)
Result:Reduced significantly volume of the tumors derived from H441 lung adenocarcinoma cells after the combination treatment with iMDK and PD0325901 compared to that of single compound in a xenograft mouse model.
[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

iMDK(881970-80-5)1HNMR
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