ATM Inhibitor-1
ATM Inhibitor-1 is a highly potent, selective and orally active ATM inhibitor, with an IC50 of 0.7 nM, shows weak activity against mTOR (IC50, 21 μM), DNAPK (IC50, 2.8 μM), PI3Kα (IC50, 3.8 μM), PI3Kβ (IC50, 10.3 μM), PI3Kγ (IC50, 3 μM) and PI3Kδ (IC50, 0.73 μM). ATM Inhibitor-1 exhibits anti-tumor activity.
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- CAS No.: 2135639-94-8
- Formule: C27H36N6O3
- Masse moléculaire:492.61
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
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ATM 0.7 nM (IC50) |
ATM 2.8 nM (IC50, Cellular assay) |
PI3Kδ 0.73 μM (IC50) |
PI3Kγ 3 μM (IC50) |
PI3Kα 3.8 μM (IC50) |
PI3Kβ 10.3 μM (IC50) |
DNAPK 2.8 μM (IC50) |
mTOR 21 μM (IC50) |
ATM Inhibitor-1 (Compound 21) is a highly potent, selective and orally active ATM Inhibitor, with an IC50 of 0.7 nM, shows weak activity against mTOR (IC50, 21 μM), DNAPK (IC50, 2.8 μM), PI3Kα (IC50, 3.8 μM), PI3Kβ (IC50, 10.3 μM), PI3Kγ (IC50, 3 μM) and PI3Kδ (IC50, 0.73 μM)[1].
In cellular assays, ATM Inhibitor-1 exhibits IC50s of 2.8 nM, >30 μM and >19 μM for ATM, ATR/PI3Kα and PI3Kβ/mTOR, respectively[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:SW620 mice model[1]
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Dosage:50 mg/kg
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Administration:P.O., once daily for 3 days every week starting 24 h post-irinotecan dosing, 21 days
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Result:Inhibited the growth of tumor combined with 50 mg/kg irinotecan in SW620 mice model.
Chemical Information
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CAS No. 2135639-94-8
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Masse moléculaire 492.61
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Formule C27H36N6O3
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SMILES
C[C@@H](C1CCOCC1)NC2=C(C(NC)=O)N=NC3=CC=C(C4=CC=C(OCCCN(C)C)N=C4)C=C32
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)