| 包装 | 价格(元) |
| 5mg | 电议 |
| 25mg | 电议 |
Preparation Method | Purified CHK1 was incubated with LY2606368 and substrate was added to detect whether LY2606368 was inhibited. |
Reaction Conditions | 10-6-10nM LY2606368 |
Applications | LY2606368 is an ATP-competitive protein kinase inhibitor with a Ki of 0.9 nmol/L against purified CHK1. |
Cell lines | HeLa cells |
Preparation Method | Cells were treated with LY2606368 for 7 hours and stained for evidence of DNA DSB using both TUNEL and an antibody for H2AX phosphorylated on serine 139. |
Reaction Conditions | 33 nmol/L LY2606368 for 7 hours |
Applications | LY2606368 triggered S-phase DNA damage, such as pH2AX (S139) and TUNEL positive staining cells significantly increased in S-phase cells. LY2606368 also requires CDC25A and CDK2 to trigger DNA damage. In addition, LY2606368 causes replication catastrophe. |
Animal models | Female CD-1nu-/nu mice carrying CALU-6 tumors (26-28 g) |
Preparation Method | Vehicle consisting of 20% Captisol (CyDex Inc) pH4 or LY2606368 was administered by subcutaneous injection in a volume of 200 ml(10 mmol/L). 4,8, 12, 24, and 48 hours after drug administration, blood for plasma drug exposure was extracted |
Dosage form | 1, 3.3, or 10 mg/kg LY2606368 twice daily for 2 days |
Applications | Up to 72.3% inhibition of tumor growth was observed in the three doses of LY2606368 tested, and mice lost no more than 3% of their body weight, indicating that LY2606368 was well tolerated in any treatment group. In addition, tumor regrowth was slow in the highest dose group during the 28-day recovery period, indicating a durable tumor response to LY2606368. |
| 产品描述 | LY2606368, an ATP-competitive CHK1 inhibitor, is currently in the clinical stage with a Ki of 0.9 nM and an IC50 of<1 nm. ly2606368 inhibits chk2 (ic50=8 nm) and rsk1 nm)[2]. Treatment of cells with LY2606368 results in the rapid appearance of TUNEL and pH2AX-positive double-stranded DNA breaks in the S-phase cell population. Inhibition of apoptosis by the caspase inhibitor Z-VAD-FMK had no effect on chromosome fragmentation, indicating that LY2606368 causes replication catastrophe[1].LY2606368 triggered S-phase DNA damage, such as pH2AX (S139) and TUNEL positive staining cells significantly increased in S-phase cells. LY2606368 also requires CDC25A and CDK2 to trigger DNA damage. In addition, LY2606368 causes replication catastrophe[1]. In primary patient-derived osteosarcoma cells, LY2606368 alone results in strongly reduced clonogenic survival at low nanomolar concentrations and acts by affecting cell cycle progression, induction of apoptosis and induction of double-stranded DNA breakage at concentrations that are well below clinically tolerable and safe plasma concentrations[3]. To investigate the combined effect of the Chk1 inhibitor LY2606368and antitumor drugs (GEM and S 1) on pancreatic cancer cell line SUIT 2. Acombination of LY2606368 and GS showed effective induction of apoptosis[4]. HGSOC cell lines were also sensitive to LY2606368, associated with induction of DNA damage and replication stress. LY2606368 also sensitized these cell lines to PARP inhibition and compromised both HR repair and replication fork stability[5]. BRCAwt HGSOC develops resistance to LY2606368 monotherapy via a prolonged G2 delay induced by lower CDK1/CyclinB1 activity, thus preventing cells from mitotic catastrophe and cell death[6]. PLK1 or CHEK1 inhibitors (BI-2536 or LY2606368) were found to exert a superior anticancer effect against cell lines at low nanomolar concentrations and induce cell-cycle arrest[7]. Up to 72.3% inhibition of tumor growth was observed in the three doses of LY2606368 tested, and mice lost no more than 3% of their body weight, indicating that LY2606368 was well tolerated in any treatment group. In addition, tumor regrowth was slow in the highest dose group during the 28-day recovery period, indicating a durable tumor response to LY2606368[1]. References: |
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