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PRL-3 Inhibitor I

更新时间:2025-08-22 21:41:47

PRL-3 Inhibitor I结构式
PRL-3 Inhibitor I结构式
品牌特惠专场
常用名 PRL-3 Inhibitor I 英文名 BR1
CAS号 893449-38-2 分子量 485.21300
密度 N/A 沸点 N/A
分子式 C17H11Br2NO2S2 熔点 N/A
MSDS 中文版 美版 闪点 N/A
符号 GHS07 GHS09
GHS07, GHS09
信号词 Warning

 PRL-3 Inhibitor I用途


PRL-3抑制剂I是一种有效的PRL-3抑制剂,IC50为0.9μM。在基于细胞的分析中,PRL-3抑制剂I显示侵袭性降低[1]。

 PRL-3 Inhibitor I名称

英文名 4-Thiazolidinone, 5-[[5-bromo-2-[(2-bromophenyl)methoxy]phenyl]methylene]-2-thioxo
英文别名 更多

 PRL-3 Inhibitor I生物活性

描述 PRL-3抑制剂I是一种有效的PRL-3抑制剂,IC50为0.9μM。在基于细胞的分析中,PRL-3抑制剂I显示侵袭性降低[1]。
相关类别
靶点实验

IC50: 0.9 μM (PRL-3)[1]

体外研究 在基于细胞的试验中,PRL-3抑制剂I可减少小鼠黑色素瘤B16F10细胞的侵袭[1]。
参考文献

[1]. Ahn JH, et al. Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors. Bioorg Med Chem Lett. 2006;16(11):2996-2999.

 PRL-3 Inhibitor I物理化学性质

分子式 C17H11Br2NO2S2
分子量 485.21300
精确质量 482.86000
PSA 95.72000
LogP 5.60820
InChIKey HXNBAOLVPAWYLT-NVNXTCNLSA-N
SMILES O=C1NC(=S)SC1=Cc1cc(Br)ccc1OCc1ccccc1Br
储存条件 -20°C,密闭,干燥

 PRL-3 Inhibitor I安全信息

符号 GHS07 GHS09
GHS07, GHS09
信号词 Warning
危害声明 H315-H319-H335-H410
警示性声明 P261-P273-P305 + P351 + P338-P501
个人防护装备 dust mask type N95 (US);Eyeshields;Gloves
危险品运输编码 UN 3077 9 / PGIII

 PRL-3 Inhibitor I文献1

更多文献
Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors.

Bioorg. Med. Chem. Lett. 16 , 2996-2999, (2006)

A series of rhodanine derivatives was synthesized and evaluated for their ability to inhibit PRL-3. Benzylidene rhodanine derivative showed good biological activity, while compound 5e was the most act...

 PRL-3 Inhibitor I靶点实验

查看更多实验

实验名称:Ability to reduce the invasiveness of tumor in B16F10 cells
来源:ChEMBL
靶标:B16-F10
External Id:CHEMBL866952
实验名称:Antimigratory activity against human DLD1 cells overexpressing PRL3 at 20 uM after 20...
来源:ChEMBL
靶标:DLD-1
External Id:CHEMBL2400557
实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
实验名称:Antimigratory activity against human DLD1 cells overexpressing PRL3 by crystal violet...
来源:ChEMBL
靶标:DLD-1
External Id:CHEMBL2400556
实验名称:Antiinvasive activity against human DLD1 cells overexpressing PRL3 at 20 uM after 20 ...
来源:ChEMBL
靶标:DLD-1
External Id:CHEMBL2400555
实验名称:Cytotoxicity against human DLD1 cells overexpressing PRL3 assessed as cell viability ...
来源:ChEMBL
靶标:DLD-1
External Id:CHEMBL2400554
实验名称:Inhibition of human His6-tagged full length PRL3 assessed as inhibition of DiFMUP dep...
来源:ChEMBL
靶标:Protein tyrosine phosphatase type IVA 3
External Id:CHEMBL2400560
实验名称:Antimigratory activity against human DLD1 cells overexpressing PRL3 at 10 ug/ml after...
来源:ChEMBL
靶标:DLD-1
External Id:CHEMBL2400559
实验名称:Inhibition of human His6-tagged full length PRL3 assessed as inhibition of DiFMUP dep...
来源:ChEMBL
靶标:Protein tyrosine phosphatase type IVA 3
External Id:CHEMBL2400558
实验名称:Inhibition of SHP2 (unknown origin) using DiFMUP as substrate at 5 uM relative to con...
来源:ChEMBL
靶标:Tyrosine-protein phosphatase non-receptor type 11
External Id:CHEMBL2399953
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 PRL-3 Inhibitor I英文别名

prl-3 inhibitor i
prl-3 inhibitor
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