N,4-dicyclohexylpiperazine-1-carboxamide

• 常用名: N,4-dicyclohexylpiperazine-1-carboxamide
• 英文名: N,4-dicyclohexylpiperazine-1-carboxamide
• CAS号: 89011-68-7
• 分子量: 293.44800
• 密度: 1.08g/cm3
• 沸点: 477.7ºC at 760 mmHg
• 分子式: C₁₇H₃₁N₃O
• 熔点: N/A
• 闪点: 242.7ºC

N,4-dicyclohexylpiperazine-1-carboxamide名称

• 英文名: N,4-dicyclohexylpiperazine-1-carboxamide

N,4-dicyclohexylpiperazine-1-carboxamide物理化学性质

• 密度: 1.08g/cm3
• 沸点: 477.7ºC at 760 mmHg
• 分子式: C₁₇H₃₁N₃O
• 分子量: 293.44800
• 闪点: 242.7ºC
• 精确质量: 293.24700
• PSA: 39.07000
• LogP: 3.05920
• InChIKey: LRAUBOSEUOPEDA-UHFFFAOYSA-N
• SMILES: O=C(NC1CCCCC1)N1CCN(C2CCCCC2)CC1
• 折射率: 1.548

N,4-dicyclohexylpiperazine-1-carboxamide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：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

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

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N,4-dicyclohexylpiperazine-1-carboxamide英文别名

• N,4-Dicyclohexyl-1-piperazinecarboxamide
• 1-Piperazinecarboxamide,N,4-dicyclohexyl
• 1-Cyclohexyl-4-(cyclohexylaminocarbonyl)piperazine