Neuropeptide Y5 receptor ligand-1

• 常用名: Neuropeptide Y5 receptor ligand-1
• 英文名: Neuropeptide Y5 receptor ligand-1
• CAS号: 322723-35-3
• 分子量: 319.36
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₉H₁₇N₃O₂
• 熔点: N/A
• 闪点: N/A

Neuropeptide Y5 receptor ligand-1用途

神经肽Y5受体配体-1(化合物54)是一种咔唑衍生物,是一种有效的神经肽Y2(NPY-5)受体拮抗剂[1]。

Neuropeptide Y5 receptor ligand-1名称

• 英文名: Neuropeptide Y5 receptor ligand-1

Neuropeptide Y5 receptor ligand-1生物活性

• 描述: 神经肽Y5受体配体-1(化合物54)是一种咔唑衍生物,是一种有效的神经肽Y2(NPY-5)受体拮抗剂[1]。
• 相关类别:
  研究领域 >> 神经疾病
  信号通路 >> G 蛋白偶联受体/G 蛋白 >> 神经肽Y受体
• 靶点实验:

  NPY Y5 receptor

• 参考文献:

  [1]. Howard BM, et, al. Carbazole derivatives and their use as neuropeptide Y5 receptor ligands. WO2001007409.

Neuropeptide Y5 receptor ligand-1物理化学性质

• 分子式: C₁₉H₁₇N₃O₂
• 分子量: 319.36
• InChIKey: IHLJGRKMODLXFG-UHFFFAOYSA-N
• SMILES: CCn1c2ccccc2c2cc(NC(=O)c3cc(C)on3)ccc21

Neuropeptide Y5 receptor ligand-1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：A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School External Id：HMS979

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：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：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

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