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PF-06873600

SKU: orb1298913

描述

PF-06873600 is an orally bioavailable, selective CDK2/4/6 inhibitor with low nanomolar Ki values. It exhibits antineoplastic activity and has been investigated in preclinical studies for cancer research, demonstrating effects in both cellular and animal models of various malignancies.

研究领域

Cell Biology

图片与验证

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关键属性

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CAS 号2185857-97-8
MW471.52
纯度99.58% (May vary between batches)
分子式C20H27F2N5O4S
SMILESC[C@@]1(O)CCC[C@H]1n1c2nc(NC3CCN(CC3)S(C)(=O)=O)ncc2cc(C(F)F)c1=O
靶点CDK
溶解性DMSO:150 mg/mL (318.12 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:3.3 mg/mL (7 mM)

生物活性

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靶点 IC50
CDK6:0.16 nM (Ki)|CDK4:0.13 nM (Ki)|CDK2:0.09 nM (Ki)
体外
PF-06873600 selectively targets, binds to and inhibits the activity of CDKs. Inhibition of these kinases leads to cell cycle arrest, induction of apoptosis and inhibition of tumor cell proliferation. CDKs, ATP-dependent serine/threonine kinases that are important regulators of cell cycle progression and cellular proliferation, are frequently overexpressed in tumor cells.

储存与操作

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储存-20°C
有效期12 months from date of receipt.
免责声明For research use only

别名

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CDK2, PF 06873600, PF06873600, PF-06873600, PF3600

相似产品

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  • (S)-PF-06873600 [orb1708609]

    99.12% (May vary between batches)

    2185859-59-8

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  • (S)-PF-06873600 [orb2901716]

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    C20H27F2N5O4S

    10 mg, 25 mg, 50 mg, 100 mg, 2 mg, 5 mg, 500 mg, 1 g
质量保证

质量保证

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our 条款与条件和选购指南.

关键属性

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暂无计算属性。

实验方案信息

可选规格

请在下方选择规格

1 mg
¥ 1,300.00
5 mg
¥ 2,210.00
1 ml x 10 mM (in DMSO)
¥ 2,210.00
10 mg
¥ 3,120.00
25 mg
¥ 5,460.00
50 mg
¥ 8,580.00
100 mg
¥ 13,390.00
200 mg
¥ 17,810.00
发货Usually dispatched within 5-10 working days
批量询价