iMDK

iMDK Suppliers list
Company Name: Angel Pharmatech, Ltd.  Gold
Tel: 17317130613
Email: 3358272972@qq.com
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Beijing Solarbio Science & Tecnology Co., Ltd.  
Tel: 17801761073 18101056239
Email: 3193328036@qq.com
Company Name: BOC Sciences  
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com

iMDK manufacturers

  • iMDK
  • iMDK pictures
  • $54.00
  • 2026-07-27
  • CAS:881970-80-5
  • Purity: 99.99%
  • Supply Ability: 10g
iMDK Basic information
Product Name:iMDK
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;3-[2-[(4-Fluorophenyl)methyl]imidazo[2,1-b]thiazol-6-yl]-2H-1-benzopyran-2-one;3-(2-(4-Fluorobenzyl)imidazo[2,1-b]thiazol-6-yl)-2H-chromen-2-one;iMDK, 10 mM in DMSO
CAS:881970-80-5
MF:C21H13FN2O2S
MW:376.4
EINECS:
Product Categories:
Mol File:881970-80-5.mol
iMDK Structure
iMDK Chemical Properties
density 1.42±0.1 g/cm3(Predicted)
storage temp. Store at -20°C, protect from light
solubility Limited solubility
pka5.71±0.40(Predicted)
form Solid
color Off-white to yellow
InChIInChI=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
InChIKeyIWFKQTWYILKFGE-UHFFFAOYSA-N
SMILESC1(=O)OC2=CC=CC=C2C=C1C1=CN2C=C(CC3=CC=C(F)C=C3)SC2=N1
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
iMDK Usage And Synthesis
UsesiMDK is a small molecule inhibitor used to bind to midkine (MDK), a heparin binding growth factor that is expressed in malignant tumors.
Biological ActivityCell 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.
storageStore at +4°C
iMDK Preparation Products And Raw materials
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