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NSC 15364

更新时间:2025-09-12 19:11:11

NSC 15364结构式
NSC 15364结构式
品牌特惠专场
常用名 NSC 15364 英文名 NSC 15364
CAS号 4550-72-5 分子量 242.277
密度 1.4±0.1 g/cm3 沸点 381.4±27.0 °C at 760 mmHg
分子式 C13H14N4O 熔点 N/A
MSDS N/A 闪点 184.5±23.7 °C

 NSC 15364用途


NSC 15364 是一种 VDAC1 寡聚化和细胞凋亡 (apoptosis) 抑制剂。

 NSC 15364名称

英文名 1,3-bis(4-aminophenyl)urea
英文别名 更多

 NSC 15364生物活性

描述 NSC 15364 是一种 VDAC1 寡聚化和细胞凋亡 (apoptosis) 抑制剂。
相关类别
体外研究 线粒体膜蛋白电压依赖性负离子通道1(VDAC1)齐聚是设计用于调节凋亡的药物的主要靶点[1]。
参考文献

[1]. Ben-Hail D, et al. Novel Compounds Targeting the Mitochondrial Protein VDAC1 Inhibit Apoptosis and Protect against Mitochondrial Dysfunction. J Biol Chem. 2016 Nov 25;291(48):24986-25003.

 NSC 15364物理化学性质

密度 1.4±0.1 g/cm3
沸点 381.4±27.0 °C at 760 mmHg
分子式 C13H14N4O
分子量 242.277
闪点 184.5±23.7 °C
精确质量 242.116760
PSA 93.17000
LogP -0.50
外观性状 白色固体
蒸汽压 0.0±0.9 mmHg at 25°C
折射率 1.785
储存条件 -20℃

 NSC 15364安全信息

海关编码 2924299090

 NSC 15364合成线路

~96%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Rodriguez, Fernando; Rozas, Isabel; Kaiser, Marcel; Brun, Reto; Nguyen, Binh; Wilson, W. David; Garcia, Rory Nelson; Dardonville, Christophe Journal of Medicinal Chemistry, 2008 , vol. 51, # 4 p. 909 - 923

~73%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Khan, S. Rehman; Gilani; Inayat, Asma; Waheed, Shaheena Pakistan Journal of Scientific and Industrial Research, 2006 , vol. 49, # 5 p. 319 - 323

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Turner, William R.; Werbel, Leslie M. Journal of Medicinal Chemistry, 1985 , vol. 28, # 11 p. 1728 - 1740

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Uno, Masaharu; Koma, Yosuke; Ban, Hyun Seung; Nakamura, Hiroyuki Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 16 p. 5169 - 5173

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Schiff,H.; Ostrogovich Justus Liebigs Annalen der Chemie, 1896 , vol. 293, p. 374 Chemische Berichte, 1894 , vol. 27, p. 398

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Soloduschenkow et al. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1957 , vol. 30, p. 1361,1365; engl.Ausg.S.1430,1432

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Schiff,H.; Ostrogovich Justus Liebigs Annalen der Chemie, 1896 , vol. 293, p. 374 Chemische Berichte, 1894 , vol. 27, p. 398

~%

NSC 15364结构式

NSC 15364

4550-72-5

文献:Schiff,H.; Ostrogovich Justus Liebigs Annalen der Chemie, 1896 , vol. 293, p. 374 Chemische Berichte, 1894 , vol. 27, p. 398

 NSC 15364海关

海关编码 2924299090
中文概述 2924299090. 其他环酰胺(包括环氨基甲酸酯)(包括其衍生物以及他们的盐). 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%
申报要素 品名, 成分含量, 用途, 包装
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 NSC 15364靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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 NSC 15364英文别名

1,3-Bis(p-aminophenyl)urea
N,N'-Bis(4-aminophenyl)urea
1,3-bis-(4-aminophenyl)urea
1,3-Bis(4-aminophenyl)urea
4,4'-diaminodiphenylurea
Carbanilide,4'-diamino
NSC 15364
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