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整合素拮抗剂27

更新时间:2026-07-05 10:38:11

整合素拮抗剂27结构式
整合素拮抗剂27结构式
品牌特惠专场
常用名 整合素拮抗剂27 英文名 Integrin Antagonists 27
CAS号 593274-97-6 分子量 444.44
密度 N/A 沸点 N/A
分子式 C24H20N4O5 熔点 N/A
MSDS N/A 闪点 N/A

 整合素拮抗剂27用途


Integrin Antagonists 27是一种小分子整合蛋白αvβ3拮抗剂, 亲和力为18 nM, 用作抗癌剂。

 整合素拮抗剂27名称

中文名 整合素拮抗剂27
英文名 Integrin Antagonists 27

 整合素拮抗剂27生物活性

描述 Integrin Antagonists 27是一种小分子整合蛋白αvβ3拮抗剂, 亲和力为18 nM, 用作抗癌剂。
相关类别
参考文献

[1]. Dayam R, et al. Discovery of small molecule integrin alphavbeta3 antagonists as novel anticancer agents. J Med Chem. 2006 Jul 27;49(15):4526-4534.

 整合素拮抗剂27物理化学性质

分子式 C24H20N4O5
分子量 444.44
InChIKey BJCKKLXERBMNHP-MOSHPQCFSA-N
SMILES Cc1ccc(NC(=O)CN2C(=O)NC(=Cc3cccn3-c3cccc(C(=O)O)c3)C2=O)cc1
储存条件 2-8℃

 整合素拮抗剂27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: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: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: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
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
实验名称:MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint...
来源:Broad Institute
靶标:N/A
External Id:2084-01_Activator_SinglePoint_HTS_Activity
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