BX-795

目录号: A11148

PDK-1 抑制剂

BX-795

BX-795 Chemical Structure

CAS NO. 702675-74-9

BX-795是有效的PDK1抑制剂,可阻断肿瘤细胞中的PDK1/Akt信号传导并抑制培养物中多种肿瘤细胞系的锚定依赖性生长或诱导凋亡。

库存: 现货

规格 价格 数量
10 mg
¥ 840.00
25 mg
¥ 1,750.00
50 mg
¥ 2,940.00
100 mg
¥ 5,600.00
10mM * 1mL in DMSO
¥ 910.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

BX-795是有效的PDK1抑制剂,可阻断肿瘤细胞中的PDK1/Akt信号传导并抑制培养物中多种肿瘤细胞系的锚定依赖性生长或诱导凋亡。
Targets
Target Value
TBK1/IKK?
PDK-1IC50: 6nM
c-KitIC50: 320nM
CDK2/CyclinEIC50: 430nM
Chk1IC50: 510nM
GSK-3βIC50: 620nM
PKAIC50: 840nM
KDRIC50: 1.1μM
T-FynIC50: 6.4μM
PKCIC50: 9.3μM
EGFRIC50: >10μM
Insulin ReceptorIC50: >10μM
In vitro (25°C) DMSO 88 mg/mL (148.78 mM)
Water Insoluble
Ethanol Insoluble
In vivo 2% DMSO+30% PEG +2% Tween 80+ddH2O 3 mg/mL
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 16.91 mL 84.53 mL 169.06 mL
0.5 mM 3.38 mL 16.91 mL 33.81 mL
1 mM 1.69 mL 8.45 mL 16.91 mL
5 mM 0.34 mL 1.69 mL 3.38 mL

*The above data is based on the productmolecular weight 591.5 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A11148
作用机制 Inhibitor (抑制剂)
M. Wt 591.5
Formula C23H26IN7O2S
Purity >99%
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

CAS No. 702675-74-9
Synonyms BX795
SMILES C1CCN(C1)C(=O)NC2=CC=CC(=C2)NC3=NC=C(C(=N3)NCCCNC(=O)C4=CC=CS4)I

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