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BC-1382

更新时间:2026-08-06 06:30:03

BC-1382结构式
BC-1382结构式
品牌特惠专场
常用名 BC-1382 英文名 BC-1382
CAS号 1013753-99-5 分子量 459.559
密度 1.3±0.1 g/cm3 沸点 N/A
分子式 C23H29N3O5S 熔点 N/A
MSDS N/A 闪点 N/A

 BC-1382用途


一种有效的泛素E3连接酶HECTD2抑制剂,特异性破坏HECTD2/PIAS1与IC50的相互作用5 nM;显着增加PIAS1蛋白水平,IC50为100 nM,改善PIAS1蛋白稳定性,对PIAS3,PIAS4和HECTD2蛋白没有影响水平;抑制LPS诱导的PIAS1降解并恢复800nM的PIAS1蛋白水平,以及PBMC释放的促炎细胞因子;减弱LPS-和铜绿假单胞菌诱导的肺部炎症

 BC-1382名称

中文名 N-{(2S)-1-[(2-methoxybenzyl)amino]-1-oxopropan-2-yl}-1-(phenylsulfonyl)piperidine-4-carboxamide
英文名 N-{(2S)-1-[(2-Methoxybenzyl)amino]-1-oxo-2-propanyl}-1-(phenylsulfonyl)-4-piperidinecarboxamide
英文别名 更多

 BC-1382生物活性

描述 一种有效的泛素E3连接酶HECTD2抑制剂,特异性破坏HECTD2/PIAS1与IC50的相互作用5 nM;显着增加PIAS1蛋白水平,IC50为100 nM,改善PIAS1蛋白稳定性,对PIAS3,PIAS4和HECTD2蛋白没有影响水平;抑制LPS诱导的PIAS1降解并恢复800nM的PIAS1蛋白水平,以及PBMC释放的促炎细胞因子;减弱LPS-和铜绿假单胞菌诱导的肺部炎症
参考文献 References 1. Coon TA, et al. Sci Transl Med. 2015 Jul 8;7(295):295ra109. View Related Products by Target E3 Ubiquitin Ligase

 BC-1382物理化学性质

密度 1.3±0.1 g/cm3
分子式 C23H29N3O5S
分子量 459.559
精确质量 459.182800
LogP 2.13
InChIKey RCWXKFCEGKXUIN-KRWDZBQOSA-N
SMILES COc1ccccc1CNC(=O)C(C)NC(=O)C1CCN(S(=O)(=O)c2ccccc2)CC1
折射率 1.584
储存条件 2-8°C,密封,干燥

 BC-1382安全信息

危害码 (欧洲) Xi

 BC-1382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: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: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:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
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 BC-1382英文别名

N-{(2S)-1-[(2-Methoxybenzyl)amino]-1-oxo-2-propanyl}-1-(phenylsulfonyl)-4-piperidinecarboxamide
MFCD08290616
MFCD30470656
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