CDK4/6-IN-10
Modify Date: 2024-01-24 10:42:38
CDK4/6-IN-10 structure
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Common Name | CDK4/6-IN-10 | ||
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| CAS Number | 2688098-11-3 | Molecular Weight | 418.47 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C22H23FN8 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of CDK4/6-IN-10CDK4/6-IN-10 is a potent, selective and orally active CDK4 and CDK6 inhibitor with IC50s of 22 nM and 10 nM, respectively. CDK4/6-IN-10 shows antitumor activity. CDK4/6-IN-10 has the potential for the research of Multiple myeloma (MM)[1]. |
| Name | CDK4/6-IN-10 |
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| Description | CDK4/6-IN-10 is a potent, selective and orally active CDK4 and CDK6 inhibitor with IC50s of 22 nM and 10 nM, respectively. CDK4/6-IN-10 shows antitumor activity. CDK4/6-IN-10 has the potential for the research of Multiple myeloma (MM)[1]. |
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| Related Catalog | |
| Target |
CDK4:22 nM (IC50) CDK6/cyclinD1:10 nM (IC50) |
| In Vitro | CDK4/6-IN-10 (compouns 32) (1 µM) shows kinase selectivity with IC50s of 22 nM and 10 nM for CDK4 and CDK6, respectively[1]. CDK4/6-IN-10 (72 h) shows antiproliferative activity (GI50s of 2.028, 5.802, 2.286, 2.238, 1.526, 11.381 µM for RPMI-8226, U266, K562, HL-60, 22RV1, HEK-293 cells, respectively)[1]. CDK4/6-IN-10 (0, 1.5, 3, 6 µM, 24 h) induces cell cycle arrest at the G1 phase in a concentration-dependent manner[1]. CDK4/6-IN-10 ( 0, 1, 2, 3 µM, 24 h) induces apoptosis of RPMI-8226 cells in a concentration-dependent manner[1]. CDK4/6-IN-10 (0, 1.5, 3, 6 µM, 24 h) reduces the CDK4/6 activity by decreases the expression level of p-RB, c-MYC and BCL-2[1]. Cell Proliferation Assay[1] Cell Line: RPMI-8226, U266, K562, HL-60, 22RV1, HEK-293 cells Concentration: Incubation Time: 72 h Result: Shows antiproliferative activity (GI50s of 2.028, 5.802, 2.286, 2.238, 1.526, 11.381 µM for RPMI-8226, U266, K562, HL-60, 22RV1, HEK-293 cells, respectively). Cell Cycle Analysis[1] Cell Line: RPMI-8226 cells Concentration: 0, 1.5, 3, 6 µM Incubation Time: 24 h Result: Cells were arrested at the G1 phase in a concentration-dependent manner. Apoptosis Analysis[1] Cell Line: RPMI-8226 cells Concentration: 0, 1.5, 3, 6 µM Incubation Time: 24 h Result: Reduced the CD4/K activity by decreased the expression level of p-RB, c-MYC and BCL-2. |
| In Vivo | CDK4/6-IN-10 (1000, 5000, 10000 mg/kg; p.o.) shows safety profile with LD50 much higher than 10,000 mg/kg[1]. CDK4/6-IN-10 (10 mg/kg; p.o.) shows oral bioavailability (F=51%) in SD rats[1]. CDK4/6-IN-10 (100, 200 mg/kg; p.o., once a day for 19 days) shows antitumor potency and favorable safety profile[1]. Pharmacokinetic Parameters of CDK4/6-IN-10 in SpragueeDawley rats[1]. Compd Admin. Cmax (ng/mL) AUC0-t (h·ng/mL) MRT0-t (h) Tmax (h) t1/2 (h) CL (mL/h/kg) F (%) 32 i.v. 355 960 5.9 0.033 8.9 641 - p.o. 257 4,878 12.8 10.7 >24 524 51SpragueeDawley rats, 10 mg/kg, p.o. Animal Model: ICR mice[1] Dosage: 1000, 5000, 10000 mg/kg Administration: p.o. Result: Showed safety profile with LD50 much higher than 10,000 mg/kg. Animal Model: SpragueeDawley rats[1] Dosage: 10 mg/kg Administration: p.o. Result: Showed oral bioavailability (F=51%). Animal Model: BALB/c nude mice (6-8 weeks) (MM xenograft model)[1] Dosage: 100, 200 mg/kg Administration: p.o., once a day, 19 days Result: Showed antitumor potency and favorable safety profile. |
| References |
| Molecular Formula | C22H23FN8 |
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| Molecular Weight | 418.47 |