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PD 0332991-d8 Sale

(Synonyms: 帕博西尼-D8,PD 0332991-d8) 目录号 : GC40092

An internal standard for the quantification of PD 0332991

PD 0332991-d8 Chemical Structure

Cas No.:1628752-83-9

规格 价格 库存 购买数量
500μg
¥4,046.00
现货
1mg
¥7,658.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

PD 0332991-d8 is intended for use as an internal standard for the quantification of PD 0332991 by GC- or LC-MS. PD 0332991 is an orally active, selective inhibitor of the cyclin D kinases Cdk4 (IC50 = 11 nM) and Cdk6 (IC50= 16 nM) with no activity against a panel of 36 additional protein kinases. It has been reported to have antiproliferative activity against retinoblastoma-positive tumor cells, blocking retinoblastoma phosphorylation and inducing G1 arrest at nanomolar concentrations. PD 0332991 can inhibit the growth of certain ER-positive or HER2-amplified breast cancer cells (IC50s as low as 4 nM) and demonstrates synergy with tamoxifen and trastuzumab, respectively. PD 0332991 inhibition of Cdk4 activity has been used to demonstrate a role for insulin-activated cyclin D1-Cdk4 signaling in the control of glucose metabolism that is independent of cell cycle progression.

化学性质

Cas No. 1628752-83-9 SDF
别名 帕博西尼-D8,PD 0332991-d8
Canonical SMILES O=C1N(C2CCCC2)C3=NC(NC4=NC=C(N5C([2H])([2H])C([2H])([2H])NC([2H])([2H])C5([2H])[2H])C=C4)=NC=C3C(C)=C1C(C)=O
分子式 C24H21D8N7O2 分子量 455.6
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

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1 mg 5 mg 10 mg
1 mM 2.1949 mL 10.9745 mL 21.9491 mL
5 mM 0.439 mL 2.1949 mL 4.3898 mL
10 mM 0.2195 mL 1.0975 mL 2.1949 mL
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