5J-4

• 常用名: 5J-4
• 英文名: 5J-4
• CAS号: 827001-82-1
• 分子量: 312.34
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₆H₁₂N₂O₃S
• 熔点: N/A
• 闪点: N/A

5J-4用途

5J-4是一种有效的CRAC抑制剂。5J-4可减少浸润到中枢神经系统的单个核细胞数量,并显著减少浸润的CD4+细胞数量。5J-4在小鼠炎症模型中减轻症状并延缓EAE(实验性自身免疫性脑脊髓炎)的发病【1】。

5J-4名称

• 英文名: 5J-4

5J-4生物活性

• 描述: 5J-4是一种有效的CRAC抑制剂。5J-4可减少浸润到中枢神经系统的单个核细胞数量,并显著减少浸润的CD4+细胞数量。5J-4在小鼠炎症模型中减轻症状并延缓EAE(实验性自身免疫性脑脊髓炎)的发病【1】。
• 相关类别:
  信号通路 >> 跨膜转运 >> CRAC频道
  研究领域 >> 炎症/免疫
• 体内研究: 5J-4可减少IL-17的产生,并降低RORα和RORγt的表达【1】。5J-4(2毫克/千克；腹腔注射；连续30天每隔一天)可减轻症状并延缓EAE的发作[1]。动物模型：C57BL/6小鼠(MOG35-55肽免疫小鼠)[1]剂量：2 m/kg给药：腹腔注射,每隔一天,连续30天结果：显著减轻症状,延缓EAE的发作,减少浸润到中枢神经系统的单个核细胞数量,显著减少浸润的CD4+细胞数量。
• 参考文献:

  [1]. Kim KD, et al. Calcium signaling via Orai1 is essential for induction of the nuclear orphan receptor pathway to drive Th17 differentiation. J Immunol. 2014 Jan 1;192(1):110-22.

5J-4物理化学性质

• 分子式: C₁₆H₁₂N₂O₃S
• 分子量: 312.34
• InChIKey: WMUSJLJASFXGHN-UHFFFAOYSA-N
• SMILES: O=C(NC(=S)Nc1cccc2cc(O)ccc12)c1ccco1

5J-4靶点实验

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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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