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A-674563
Catalog Number: E1KS2670
Amount: 2mg1​ PHYSICAL AND CHEMICAL PROPERTIES
Applications: Reactivity:
产品类型: Unconjugated
发货周期: 现货
说明书:     PDF
总价格:    513.6元
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概述
  • Catalog Number:

    E1KS2670
  • Amount:

    2mg1​ PHYSICAL AND CHEMICAL PROPERTIES

2​ Biological Activity
A-674563 is a potent selective protein kinase B/Akt inhibitor with an IC50 of 14 nM. A-674563 also shows inhibitory activity against PKA and CDK2 with IC50 of 16 and 46 nM, respectively. While promising efficacy was observed in vivo, A-674563 indicated significantly effects on depolarization of purkinje fiber in an in vitro assay and severe CV toxicity (e.g. hypotension) in vivo. An X-ray structure of A-674563 bound to protein kinase A, which has 80% homology with Akt in the kinase domain, suggested the phenyl group is not tightly bound in the ligand-protein complex. The Akt inhibitor A-674563 displayed proliferation of tumor cells with an EC50 of 0.4 μM. When given in combination, A-674563 enhanced the efficacy of paclitaxel in a PC-3 xenograft model.[1][2]
3​ References:
Potent and selective inhibitors of Akt kinases slow the progress of tumors in vivo. Luo Y et al. Mol Cancer Ther. 2005 Jun;4(6):977-86
MEDI 144 Jianchun Gong1 et al. March 2005;
The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

2​ Biological Activity A-674563 is a potent selective protein kinase B/Akt inhibitor with an IC50 of 14 nM. A-674563 also shows inhibitory activity against PKA and CDK2 with IC50 of 16 and 46 nM, respectively. While promising efficacy was observed in vivo, A-674563 indicated significantly effects on depolarization of purkinje fiber in an in vitro assay and severe CV toxicity (e.g. hypotension) in vivo. An X-ray structure of A-674563 bound to protein kinase A, which has 80% homology with Akt in the kinase domain, suggested the phenyl group is not tightly bound in the ligand-protein complex. The Akt inhibitor A-674563 displayed proliferation of tumor cells with an EC50 of 0.4 μM. When given in combination, A-674563 enhanced the efficacy of paclitaxel in a PC-3 xenograft model.[1][2] 3​ References: Potent and selective inhibitors of Akt kinases slow the progress of tumors in vivo. Luo Y et al. Mol Cancer Ther. 2005 Jun;4(6):977-86 MEDI 144 Jianchun Gong1 et al. March 2005; The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

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