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EPZ011989

Catalog No.GC19141

EPZ011989 est un inhibiteur Zeste Homolog 2 (EZH2) puissant et actif par voie orale avec une stabilité métabolique. EPZ011989 a une inhibition inhibitrice pour EZH2 avec une valeur Ki <3 nM. EPZ011989 montre une inhibition robuste de la marque méthyle et une activité anti-tumorale. EPZ011989 peut être utilisé pour la recherche de divers cancers.

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EPZ011989 Chemical Structure

Cas No.: 1598383-40-4

Taille Prix Stock Qté
5mg
75,00 $US
En stock
10mg
131,00 $US
En stock
50mg
459,00 $US
En stock
100mg
637,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description of EPZ011989

EPZ011989 is a potent, selective orally bioavailable EZH2 inhibitor with Ki 3000-fold selectivity over other HMTase.IC50 value: 15-fold selectivity over EZH1 and >3000-fold selectivity relative to the Ki of 20 other histone methyltransferases (HMTs) tested. EPZ011989 also exhibits metabolic stability. Furthermore, EPZ011989 reduces cellular H3K27 methylation in the Y641F, mutant-bearing human lymphoma cell line, WSU-DLCL2, with an IC50 below 100 nM. This functional response translates to activity in a long-term proliferation assay where EPZ011989 demonstrates an average lowest cytotoxic concentration (LCC) in WSU-DLCL2 cells of 208 nM. In vivo: The LCC parameter, when corrected for plasma protein-binding, predicts an efficacious plasma level in mouse for EPZ011989 of 158 ng/mL. The pharmacokinetics in SCID mice following oral administration of 125, 250, 500, and 1000 mg/kg indicated that the 1000 mg/kg dose provided coverage over the LCC for 24 h, while the 250 and 500 mg/kg doses provided coverage over this value for approximately 8 h. EPZ011989 demonstrates significant tumor growth inhibition in a mouse xenograft model of human B cell lymphoma.

References:
[1]. Campbell JE, et al. EPZ011989, A Potent, Orally-Available EZH2 Inhibitor with Robust in Vivo Activity. ACS Med Chem Lett. 2015 Mar 4;6(5):491-495.

Chemical Properties of EPZ011989

Cas No. 1598383-40-4 SDF
Canonical SMILES O=C(NCC1=C(C)C=C(C)NC1=O)C2=CC(C#CCN3CCOCC3)=CC(N(CC)[C@H]4CC[C@H](N(CCOC)C)CC4)=C2C
Formula C35H51N5O4 M.Wt 605.81
Solubility DMSO : ≥ 33 mg/mL (54.47 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of EPZ011989

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1 mg 5 mg 10 mg
1 mM 1.6507 mL 8.2534 mL 16.5068 mL
5 mM 0.3301 mL 1.6507 mL 3.3014 mL
10 mM 0.1651 mL 0.8253 mL 1.6507 mL
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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 addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Average Rating: 5 ★★★★★ (Based on Reviews and 12 reference(s) in Google Scholar.)

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