2-(5-苄氧基-1H-吲哚-3-基)-乙醇结构式
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常用名 | 2-(5-苄氧基-1H-吲哚-3-基)-乙醇 | 英文名 | 2-(5-phenylmethoxy-1H-indol-3-yl)ethanol |
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| CAS号 | 41339-61-1 | 分子量 | 267.32200 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C17H17NO2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 2-(5-苄氧基-1H-吲哚-3-基)-乙醇 |
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| 英文名 | 2-(5-phenylmethoxy-1H-indol-3-yl)ethanol |
| 英文别名 | 更多 |
| 分子式 | C17H17NO2 |
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| 分子量 | 267.32200 |
| 精确质量 | 267.12600 |
| PSA | 45.25000 |
| LogP | 3.28170 |
| InChIKey | SQAUQUOZCKVQND-UHFFFAOYSA-N |
| SMILES | OCCc1c[nH]c2ccc(OCc3ccccc3)cc12 |
| 海关编码 | 2933990090 |
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~%
2-(5-苄氧基-1H-吲哚-... 41339-61-1 |
| 文献:John Wyeth and Brother Limited Patent: US4062869 A1, 1977 ; |
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~94%
2-(5-苄氧基-1H-吲哚-... 41339-61-1 |
| 文献:Lounasmaa, Mauri; Jokela, Reija; Tiainen, Lasse-Pekka Tetrahedron, 1990 , vol. 46, # 23 p. 7873 - 7884 |
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~46%
2-(5-苄氧基-1H-吲哚-... 41339-61-1 |
| 文献:Kamiya; Shirahase; Nakamura; Kanda; Matsui; Yoshimi; Kasai; Takahashi; Kurahashi Chemical and Pharmaceutical Bulletin, 2001 , vol. 49, # 5 p. 563 - 571 |
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~68%
2-(5-苄氧基-1H-吲哚-... 41339-61-1 |
| 文献:Wood, Paul M.; Woo, L. W. Lawrence; Labrosse, Jean-Robert; Thomas, Mark P.; Mahon, Mary F.; Chander, Surinder K.; Purohit, Atul; Reed, Michael J.; Potter, Barry V. L. ChemMedChem, 2010 , vol. 5, # 9 p. 1577 - 1593 |
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~%
2-(5-苄氧基-1H-吲哚-... 41339-61-1 |
| 文献:Koo et al. Journal of Organic Chemistry, 1959 , vol. 24, p. 179,183 |
| 2-(5-苄氧基-1H-吲哚-3-基)-乙醇上游产品 5 | |
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| 2-(5-苄氧基-1H-吲哚-3-基)-乙醇下游产品 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: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: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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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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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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