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SLEC-11

更新时间:2026-03-13 16:05:22

SLEC-11结构式
SLEC-11结构式
品牌特惠专场
常用名 SLEC-11 英文名 SLEC-11
CAS号 863761-17-5 分子量 296.34
密度 N/A 沸点 N/A
分子式 C18H17FN2O 熔点 N/A
MSDS N/A 闪点 N/A

 SLEC-11用途


SLEC-11作为一种潜在的合成致命铅用于胃癌的治疗。AL-GDa62显示等基因乳腺上皮细胞MCF10A-WT(野生型)和MCF10A-CDH1-/-[1]的EC50分别为12.2μM和8.2μM。

 SLEC-11名称

英文名 SLEC-11

 SLEC-11生物活性

描述 SLEC-11作为一种潜在的合成致命铅用于胃癌的治疗。AL-GDa62显示等基因乳腺上皮细胞MCF10A-WT(野生型)和MCF10A-CDH1-/-[1]的EC50分别为12.2μM和8.2μM。
相关类别
参考文献

[1]. Andreas Luxenburger, et al. Discovery of AL-GDa62 as a Potential Synthetic Lethal Lead for the Treatment of Gastric Cancer. J Med Chem. 2021 Dec 23;64(24):18114-18142.

 SLEC-11物理化学性质

分子式 C18H17FN2O
分子量 296.34

 SLEC-11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:Specificity screen against TRPC6 for compounds that activate transient receptor poten...
来源:Johns Hopkins Ion Channel Center
靶标:short transient receptor potential channel 6 [Mus musculus]
External Id:TRPC4_AG_Counter_C6
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:Specificity screen against TRPC6 for compounds that inhibit transient receptor potent...
来源:Johns Hopkins Ion Channel Center
靶标:short transient receptor potential channel 6 [Mus musculus]
External Id:TRPC4_Inh_Counter_C6
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: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:Specificity screen against TRPC6 for compounds that allosterically potentiate transie...
来源:Johns Hopkins Ion Channel Center
靶标:short transient receptor potential channel 6 [Mus musculus]
External Id:TRPC4_Alo_Counter_C6
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