3-(2-羧基乙基)-1H-吲哚-2-羧酸结构式
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常用名 | 3-(2-羧基乙基)-1H-吲哚-2-羧酸 | 英文名 | 4,6,6-TRIMETHYL-6H-[1,3]THIAZIN-2-YLAMINE |
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| CAS号 | 31529-28-9 | 分子量 | 233.22000 | |
| 密度 | 1.472g/cm3 | 沸点 | 533.1ºC at 760mmHg | |
| 分子式 | C12H11NO4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 276.2ºC |
| 中文名 | 3-(2-羧基乙基)-1H-吲哚-2-羧酸 |
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| 英文名 | 3-(2-Carboxyethyl)-1H-indole-2-carboxylic acid |
| 英文别名 | 更多 |
| 密度 | 1.472g/cm3 |
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| 沸点 | 533.1ºC at 760mmHg |
| 分子式 | C12H11NO4 |
| 分子量 | 233.22000 |
| 闪点 | 276.2ºC |
| 精确质量 | 233.06900 |
| PSA | 90.39000 |
| LogP | 1.88330 |
| InChIKey | BYJQAPYDPPKJGH-UHFFFAOYSA-N |
| SMILES | O=C(O)CCc1c(C(=O)O)[nH]c2ccccc12 |
| 折射率 | 1.7 |
| 海关编码 | 2933990090 |
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3-(2-羧基乙基)-1H-吲... 31529-28-9 |
| 文献:Salituro, Francesco G.; Harrison, Boyd L.; Baron, Bruce M.; Nyce, Philip L.; Stewart, Kenneth T.; et al. Journal of Medicinal Chemistry, 1992 , vol. 35, # 10 p. 1791 - 1799 |
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3-(2-羧基乙基)-1H-吲... 31529-28-9 |
| 文献:Salituro, Francesco G.; Harrison, Boyd L.; Baron, Bruce M.; Nyce, Philip L.; Stewart, Kenneth T.; McDonald, Ian A. Journal of Medicinal Chemistry, 1990 , vol. 33, # 11 p. 2944 - 2946 |
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3-(2-羧基乙基)-1H-吲... 31529-28-9 |
| 文献:Gray, Nancy M.; Dappen, Michael S.; Cheng, Brian K.; Cordi, Alexis A.; Biesterfeldt, John P.; et al. Journal of Medicinal Chemistry, 1991 , vol. 34, # 4 p. 1283 - 1292 |
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3-(2-羧基乙基)-1H-吲... 31529-28-9 |
| 文献:Tokmakov, G. P.; Zemlyanova, T. G.; Grandberg, I. I. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1986 , vol. 22, # 12 p. 1345 - 1349 Khimiya Geterotsiklicheskikh Soedinenii, 1986 , vol. 22, # 12 p. 1662 - 1667 |
| 3-(2-羧基乙基)-1H-吲哚-2-羧酸上游产品 4 | |
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| 3-(2-羧基乙基)-1H-吲哚-2-羧酸下游产品 1 | |
| 海关编码 | 2933990090 |
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| 中文概述 | 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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实验名称:Ability to compete with [3H]glycine for strychnine-insensitive binding sites on rat c...
来源:ChEMBL
靶标:Glutamate receptor ionotropic, NMDA 3A
External Id:CHEMBL752489
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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
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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
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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
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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
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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
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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
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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.
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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
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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
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| 1H-Indole-3-propanoic acid,2-carboxy |
| 2-carboxy-3-indolepropanoic acid |
| CIPA |