Tazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >4,500-fold selectivity relative to 14 other HMTs.TargetsEZH2 (Cell-free assay) 2.5 nM(Ki)In vitroEPZ-6438 concentration-dependently reduces global H3K27Me3 levels in wild-type or SMARCB1 mutant cells, and induces strong antiproliferative effects with IC50 ranging from 32 nM to 1000 nM in SMARCB1-deleted MRT cell lines. EPZ-6438 induces gene expression of neuronal differentiation and cell cycle inhibition, while inhibtis expression of Hedgehog pathway genes, MYC and EZH2. The antiproliferative effect of EPZ-6438 is enhanced by either prednisolone or dexamethasone in several EZH2 mutant lymphoma cell lines.In vivoIn SCID mice bearing s.c. G401 xenografts, EPZ-6438 induces tumor stasis during the administration period and produces a significant tumor growth delay with minimal effect on body weight.Cell Research(from reference)Cell lines:Mutant cell lines (G401, A204, G402, KYM-1), Wild type cell line (RD, 293, SJCRH30) Concentrations:~10 μM Incubation Time:7 days
EZH1/2 Inhibitors
Specifications & Purity: Tazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >4,500-fold selectivity relative to 14 other HMTs.TargetsEZH2 (Cell-free assay) 2.5 nM(Ki)In vitroEPZ-6438 concentration-dependently reduces global H3K27Me3 levels in wild-type or SMARCB1 mutant cells, and induces strong antiproliferative effects with IC50 ranging from 32 nM to 1000 nM in SMARCB1-deleted MRT cell lines. EPZ-6438 induces gene expression of neuronal differentiation and cell cycle inhibition, while inhibtis expression of Hedgehog pathway genes, MYC and EZH2. The antiproliferative effect of EPZ-6438 is enhanced by either prednisolone or dexamethasone in several EZH2 mutant lymphoma cell lines.In vivoIn SCID mice bearing s.c. G401 xenografts, EPZ-6438 induces tumor stasis during the administration period and produces a significant tumor growth delay with minimal effect on body weight.Cell Research(from reference)Cell lines:Mutant cell lines (G401, A204, G402, KYM-1), Wild type cell line (RD, 293, SJCRH30) Concentrations:~10 μM Incubation Time:7 days
Grade: Moligand™
Molecular Formula: C34H44N4O4
Molecular Weight: 572.74
PubChem CID: 66558664
Isomeric SMILES: CCN(C1CCOCC1)C2=CC(=CC(=C2C)C(=O)NCC3=C(C=C(NC3=O)C)C)C4=CC=C(C=C4)CN5CCOCC5
Storage Temperature: Store at -20°C
Shipped in: Ice chest + Ice pads
More Information: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/T413712-SCI_ed1f43195b987ef3226a2e1dee0c4ca1.pdf
- UPC:
- 41112802
- HazmatClass:
- Yes
- WeightUOM:
- LB
- MPN:
- T413712-50mg
- Country of Origin:
- China
- CAS:
- 1403254-99-8
- Product Size:
- 50mg
- Harmonized Tariff Code:
- 2931.90.90
- Hazard Statement Codes:
- H302;H315;H319;H335
- Precautionary Statement Codes:
- P261;P305+P351+P338
akash.verma@cenmed.com
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