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CID 2011756 Sale

目录号 : GC15718

An inhibitor of protein kinase D

CID 2011756 Chemical Structure

Cas No.:638156-11-3

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥405.00
现货
5mg
¥360.00
现货
10mg
¥639.00
现货
50mg
¥2,700.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

CID-2011756 is a novel and potent inhibitor of protein kinase D1 (PKD1), one of three PKD isoforms of a novel family of serine/threonine kinases involved in cell proliferation, survival, invasion and protein transport, with a value of 50% inhibition concentration IC50 of 3.2 μM in vitro. CID-2011756 also exhibits pan-PKD inhibitory effects that ATP-competitively inhibits PKD2 and PDK3 with values of IC50 of 0.6 μM and 0.7 μM respectively. Study results have shown that CID-2011756 is a cell active PKD1 inhibitor that concentration-dependently inhibits phorbolester-induced endogenous PKD1 activation in LNCap prostate cancer cells with a value of half maximal effective concentration EC50 of 10 μM.

Reference

[1].Sharlow ER, Mustata Wilson G, Close D, Leimgruber S, Tandon M, Reed RB, Shun TY, Wang QJ, Wipf P, Lazo JS. Discovery of diverse small molecule chemotypes with cell-based PKD1 inhibitory activity. PLoS One. 2011;6(10):e25134.

化学性质

Cas No. 638156-11-3 SDF
化学名 5-(3-chlorophenyl)-N-[4-(morpholin-4-ylmethyl)phenyl]furan-2-carboxamide
Canonical SMILES C1COCCN1CC2=CC=C(C=C2)NC(=O)C3=CC=C(O3)C4=CC(=CC=C4)Cl
分子式 C22H21ClN2O3 分子量 396.87
溶解度 ≥ 39.7mg/mL in DMSO with gentle warming, ≥ 2.34 mg/mL in EtOH with ultrasonic and warming 储存条件 Store at RT
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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。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.5197 mL 12.5986 mL 25.1972 mL
5 mM 0.5039 mL 2.5197 mL 5.0394 mL
10 mM 0.252 mL 1.2599 mL 2.5197 mL
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