9H-吡啶并[3,4-b]吲哚-3-羧酸

• 常用名: 9H-吡啶并[3,4-b]吲哚-3-羧酸
• 英文名: 9H-pyrido[3,4-b]indole-3-carboxylic acid
• CAS号: 74214-63-4
• 分子量: 212.20400
• 密度: 1.497g/cm3
• 沸点: 538.7ºC at 760 mmHg
• 分子式: C₁₂H₈N₂O₂
• 熔点: N/A
• 闪点: 279.6ºC

9H-吡啶并[3,4-b]吲哚-3-羧酸名称

• 中文名: 9H-吡啶并[3,4-b]吲哚-3-羧酸
• 英文名: 9H-pyrido[3,4-b]indole-3-carboxylic acid

9H-吡啶并[3,4-b]吲哚-3-羧酸物理化学性质

• 密度: 1.497g/cm3
• 沸点: 538.7ºC at 760 mmHg
• 分子式: C₁₂H₈N₂O₂
• 分子量: 212.20400
• 闪点: 279.6ºC
• 精确质量: 212.05900
• PSA: 65.98000
• LogP: 2.41430
• InChIKey: ARLVFKCLBYUINL-UHFFFAOYSA-N
• SMILES: O=C(O)c1cc2c(cn1)[nH]c1ccccc12
• 折射率: 1.814
• 储存条件: 室温

9H-吡啶并[3,4-b]吲哚-3-羧酸靶点实验

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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：Concentration that inhibits specific [3H]flunitrazepam binding to benzodiazepine rece... 来源：ChEMBL 靶标：Gamma-aminobutyric acid receptor subunit alpha-4 External Id：CHEMBL651487

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：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：qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen 来源：NCGC External Id：tdp43-p2-repeat

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9H-吡啶并[3,4-b]吲哚-3-羧酸英文别名

• 9H-pyrido<3,4-b>indole-3-carboxylic acid
• Carboline-3-carboxylic acid