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4,6-二(苯甲酰氨基)-1,3-苯二羧酸

更新时间:2025-08-27 10:26:22

4,6-二(苯甲酰氨基)-1,3-苯二羧酸结构式
4,6-二(苯甲酰氨基)-1,3-苯二羧酸结构式
品牌特惠专场
常用名 4,6-二(苯甲酰氨基)-1,3-苯二羧酸 英文名 NS 3763
CAS号 70553-45-6 分子量 404.37200
密度 1.485g/cm3 沸点 490.7ºC at 760 mmHg
分子式 C22H16N2O6 熔点 N/A
MSDS 中文版 美版 闪点 250.6ºC
符号 GHS07 GHS09
GHS07, GHS09
信号词 Warning

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸用途


NS3763是一种选择性、非竞争性的GLUK5受体拮抗剂,IC50为1.6µM。NS3763对GLUK6、AMPA或NMDA受体没有明显的拮抗作用[1]。

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸名称

中文名 4,6-二(苯甲酰氨基)-1,3-苯二羧酸
英文名 4,6-dibenzamidobenzene-1,3-dicarboxylic acid
中文别名 4,6-双(苯甲酰氨基)-1,3-苯二羧酸
英文别名 更多

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸生物活性

描述 NS3763是一种选择性、非竞争性的GLUK5受体拮抗剂,IC50为1.6µM。NS3763对GLUK6、AMPA或NMDA受体没有明显的拮抗作用[1]。
相关类别
靶点实验

IC50: 1.6 µM (GLUK5 receptor)[1]

体外研究 在表达同源GLUK5或GLUK6受体的人类胚胎肾HEK293细胞中,与GLUK6亚型(IC50>30µM)相比,NS3763显示出选择性,可抑制通过GLUK5亚型(IC50=1.6µM)红藻氨酸受体介导的多莫酸诱导的细胞内钙增加[1]。NS3763通过HEK293细胞中的GLUK5受体选择性抑制l-谷氨酸和多莫酸诱发电流[1]。
参考文献

[1]. Jeppe K Christensen, et al. In vitro characterization of 5-carboxyl-2,4-di-benzamidobenzoic acid (NS3763), a noncompetitive antagonist of GLUK5 receptors. J Pharmacol Exp Ther. 2004 Jun;309(3):1003-10.

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸物理化学性质

密度 1.485g/cm3
沸点 490.7ºC at 760 mmHg
分子式 C22H16N2O6
分子量 404.37200
闪点 250.6ºC
精确质量 404.10100
PSA 132.80000
LogP 3.73360
InChIKey UUDYZUDTQPLDDP-UHFFFAOYSA-N
SMILES O=C(Nc1cc(NC(=O)c2ccccc2)c(C(=O)O)cc1C(=O)O)c1ccccc1
折射率 1.735

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸安全信息

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
危害码 (欧洲) Xi,N
风险声明 (欧洲) 36/37/38-50/53
安全声明 (欧洲) 26-36-60-61
危险品运输编码 UN 3077 9/PG 3

 4,6-二(苯甲酰氨基)-1,3-苯二羧酸文献7

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 4,6-二(苯甲酰氨基)-1,3-苯二羧酸靶点实验

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实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
实验名称:High Throughput Screening for Foot and Mouth Disease Virus Antivirals
来源:NCGC
靶标:N/A
External Id:StopGo1
实验名称:A screen for small molecules that modulate mitochondrial supercomplex formation
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1482
实验名称:qHTS for Inhibitors of Polymerase Kappa
来源:NCGC
靶标:DNA polymerase kappa [Homo sapiens]
External Id:PolK100
实验名称:Human GluK1 (Ionotropic glutamate receptors)
来源:IUPHAR-DB
靶标:GluK1 (Ionotropic glutamate receptors) [Homo sapiens]
External Id:450_Human
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
实验名称:Stabilization of p53 in human papillomavirus-positive cells
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Cellular tumor antigen p53
External Id:HMS1485
实验名称:qHTS for Inhibitors of binding or entry into cells for Marburg Virus
来源:NCGC
靶标:gene 4 small orf - Marburg virus
External Id:VSVM-OFFLINE
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 4,6-二(苯甲酰氨基)-1,3-苯二羧酸英文别名

NS3763
5-Carboxy-2,4-dibenzamidobenzoic acid
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