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NSC-60339

更新时间:2025-08-27 14:10:51

NSC-60339结构式
NSC-60339结构式
品牌特惠专场
常用名 NSC-60339 英文名 NSC-60339
CAS号 70-09-7 分子量 486.95300
密度 N/A 沸点 N/A
分子式 C26H23ClN6O2 熔点 N/A
MSDS N/A 闪点 N/A

 NSC-60339用途


NSC-60339 是外排泵的抑制剂和 AcrAB-TolC 的底物,是聚对苯二甲酸衍生物,是一种潜在的癌症化疗化合物。

 NSC-60339名称

中文名 2-氯-N1,N4-双(4-(4,5-二氢-1H-咪唑-2-基)苯基)对苯二甲酰胺
英文名 2-chloro-1-N,4-N-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]benzene-1,4-dicarboxamide
英文别名 更多

 NSC-60339生物活性

描述 NSC-60339 是外排泵的抑制剂和 AcrAB-TolC 的底物,是聚对苯二甲酸衍生物,是一种潜在的癌症化疗化合物。
相关类别
体外研究 NSC 60339与7个肿瘤细胞系对邻苯二甲酰胺的敏感性、耐药性或交叉耐药性相关。敏感肿瘤(L1210、L1210/MTX、L1210/ara-C和P815)迅速吸收药物,并在24小时实验期间主要作为脂质结合药物保留。耐药肿瘤L1210/NSC 60339和2个交叉耐药肿瘤P388/VCR和P815/VLB在0.5小时内所需药物与敏感肿瘤相同,但在24小时内有脂质结合药物从这些耐药肿瘤中流出[3]。
参考文献

[1]. D. W. Yesair, et al. Relationship of Phthalanilide-Lipid Complexes to Uptake and Retention of 2-Chloro-4′,4″-di(2-imidazolin-2-yl)terephthalanilide (NSC 60339) by Sensitive and Resistant P388 Leukemia Cells. CANCER RESEARCH 26 Part 1: 202-207, February 1966.

[2]. Yesair DW, et al. The retention or efflux of phthalanilide (NSC 60339)-lipid complexes by sensitive or resistant murine tumor cells and Escherichia coli B. Cancer Res. 1968 Feb;28(2):314-9.

[3]. Haynes KM, et al. Identification and Structure-Activity Relationships of Novel Compounds that Potentiate the Activities of Antibiotics in Escherichia coli. J Med Chem. 2017 Jul 27;60(14):6205-6219.

[4]. Abdali N, et al. Reviving Antibiotics: Efflux Pump Inhibitors That Interact with AcrA, a Membrane Fusion Protein of the AcrAB-TolC Multidrug Efflux Pump. ACS Infect Dis. 2017 Jan 13;3(1):89-98.

 NSC-60339物理化学性质

分子式 C26H23ClN6O2
分子量 486.95300
精确质量 486.15700
PSA 106.98000
LogP 3.21900
InChIKey UJQGBYRKCZQJJS-UHFFFAOYSA-N
SMILES O=C(Nc1ccc(C2=NCCN2)cc1)c1ccc(C(=O)Nc2ccc(C3=NCCN3)cc2)c(Cl)c1
储存条件 -20°C

 NSC-60339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:Single Concentration Validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase U...
来源:Burnham Center for Chemical Genomics
靶标:COP9 signalosome complex subunit 5 [Homo sapiens]
External Id:SBCCG-A995-CSN5-CP-Assay
实验名称:Single concentration validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase H...
来源:Burnham Center for Chemical Genomics
靶标:72 kDa type IV collagenase isoform a preproprotein [Homo sapiens]
External Id:SBCCG-A996-CSN5-MMP2-CP-Assay
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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4296184
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:Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4296185
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 NSC-60339英文别名

Glycopeptide,3b
Wander
HR 2198
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