iMDK
CAS No. 881970-80-5
iMDK ( —— )
Catalog No. M28701 CAS No. 881970-80-5
iMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 115 | Get Quote |
|
10MG | 177 | Get Quote |
|
25MG | 410 | Get Quote |
|
50MG | 605 | Get Quote |
|
100MG | 860 | Get Quote |
|
500MG | 1728 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
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Product NameiMDK
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NoteResearch use only, not for human use.
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Brief DescriptioniMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice.
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DescriptioniMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice.(In Vitro):Administration of iMDK (50-500 nM) for 72 h quarterhydrate suppressed AKT phosphorylation in H441 lung adenocarcinoma cells after treatment dose-dependently. In contrast, iMDK quarterhydrate robustly increases p-ERK.(In Vivo):Intraperitoneally injection with 100 μl of iMDK ( (9 mg/kg/day) and ; oral administion of PD0325901 (5 mg/kg) effectively reduced lung tumor growth in a xenograft mouse model.
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Synonyms——
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PathwayPI3K/Akt/mTOR signaling
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TargetPI3K
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RecptorTRPV1
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Research Area——
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Indication——
Chemical Information
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CAS Number881970-80-5
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Formula Weight376.4
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Molecular FormulaC21H13FN2O2S
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Purity>98% (HPLC)
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Solubility——
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SMILESFc1ccc(Cc2cn3cc(nc3s2)-c2cc3ccccc3oc2=O)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Gomtsyan A, et al. Identification of (R)-1-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-3-(1H-indazol-4-yl)urea (ABT-102) as a potent TRPV1 antagonist for pain management. J Med Chem. 2008 Feb 14;51(3):392-5.
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