DCH36_06
Modify Date: 2024-01-08 12:56:38
DCH36_06 structure
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Common Name | DCH36_06 | ||
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| CAS Number | 593273-05-3 | Molecular Weight | 372.83 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C18H13ClN2O3S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of DCH36_06DCH36_06 is a potent and selective p300/CBP inhibitor with IC50s of 0.6 μM and 3.2 μM for p300 and CBP, respectively. DCH36_06 mediated p300/CBP inhibition leading to hypoacetylation on H3K18 in leukemic cells. Anti-tumor activity[1]. |
| Name | DCH36_06 |
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| Description | DCH36_06 is a potent and selective p300/CBP inhibitor with IC50s of 0.6 μM and 3.2 μM for p300 and CBP, respectively. DCH36_06 mediated p300/CBP inhibition leading to hypoacetylation on H3K18 in leukemic cells. Anti-tumor activity[1]. |
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| Related Catalog | |
| In Vitro | DCH36_06 (6.7-20 μM; 24-48 hours) treatment arrests cell cycle at G1 phase and induces apotosis in a dose-dependent manner in leukemic cells[1]. DCH36_06 (5-10 μM; 24 hours) treatment significantly activates the cleavage of pro-caspase 3, pro-caspase 9 and PARP1 at dose-dependent manner[1]. DCH36_06 shows potent antiproliferative activity against tested leukemia cell lines (CEM, MOLT3, MOLT4, Jurkat, MV4-11, THP-1, RS4; 11, KOPN8, Kasumi-1 and K562 cells) in a dose-dependent manner with IC50 values at single-digit micromolar range[1]. Cell Cycle Analysis[1] Cell Line: MV4-11 cells Concentration: 6.7 μM, 20 μM Incubation Time: 24 hours, 48 hours Result: Dose-dependently arrested cell cycle at G1 phase. Apoptosis Analysis[1] Cell Line: MV4-11 cells Concentration: 6.7 μM, 20 μM Incubation Time: 24 hours, 48 hours Result: Significantly induced apoptosis. Western Blot Analysis[1] Cell Line: MV4-11 cells Concentration: 5 μM, 10 μM Incubation Time: 24 hours Result: Significantly activated the cleavage of pro-caspase 3, pro-caspase 9 and PARP1 at dose-dependent manner. |
| In Vivo | DCH36_06 (25-50 mg/kg; intraperitoneal injection; every two days; for 20 days) blocks the leukemic xenograft growth in mice[1]. Animal Model: MV4-11 xenograft nude mice[1] Dosage: 25 mg/kg, 50 mg/kg Administration: Intraperitoneal injection; every two days; for 20 days Result: The tumor growth rate showed significant reduction in dose-dependent manner. |
| References |
| Molecular Formula | C18H13ClN2O3S |
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| Molecular Weight | 372.83 |