3-(4-苯基-1-哌嗪)-1-丙胺结构式
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常用名 | 3-(4-苯基-1-哌嗪)-1-丙胺 | 英文名 | 3-(4-Phenylpiperazin-1-yl)propan-1-amine |
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| CAS号 | 20529-19-5 | 分子量 | 219.32600 | |
| 密度 | 1.041g/cm3 | 沸点 | 355.3ºC at 760 mmHg | |
| 分子式 | C13H21N3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 166.2ºC |
| 中文名 | 3-(4-苯基-1-哌嗪)-1-丙胺 |
|---|---|
| 英文名 | 3-(4-Phenylpiperazin-1-yl)propan-1-amine |
| 英文别名 | 更多 |
| 密度 | 1.041g/cm3 |
|---|---|
| 沸点 | 355.3ºC at 760 mmHg |
| 分子式 | C13H21N3 |
| 分子量 | 219.32600 |
| 闪点 | 166.2ºC |
| 精确质量 | 219.17400 |
| PSA | 32.50000 |
| LogP | 1.86060 |
| InChIKey | KNLCRNWJXCLJHQ-UHFFFAOYSA-N |
| SMILES | NCCCN1CCN(c2ccccc2)CC1 |
| 蒸汽压 | 3.15E-05mmHg at 25°C |
| 折射率 | 1.554 |
| 海关编码 | 2933599090 |
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~72%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Biswas, Swati; Zhang, Suhong; Fernandez, Fernando; Ghosh, Balaram; Zhen, Juan; Kuzhikandathil, Eldo; Reith, Maarten E. A.; Dutta, Aloke K. Journal of Medicinal Chemistry, 2008 , vol. 51, # 1 p. 101 - 117 |
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~72%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Nagarapu, Lingaiah; Mateti, Jhansi; Gaikwad, Hanmant K.; Bantu, Rajashaker; Sheeba Rani; Prameela Subhashini Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 14 p. 4138 - 4140 |
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~%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Bioorganic and Medicinal Chemistry, , vol. 14, # 22 p. 7539 - 7550 |
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~54%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Synaptic Pharmaceutical Corporation Patent: US5767131 A1, 1998 ; |
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~%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Bioorganic and Medicinal Chemistry, , vol. 6, # 6 p. 849 - 868 |
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~%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Bioorganic and Medicinal Chemistry Letters, , vol. 7, # 18 p. 2399 - 2402 |
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~%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Yakugaku Zasshi, , vol. 76, p. 644,647, 648 Chem.Abstr., , p. 425 |
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~%
3-(4-苯基-1-哌嗪)-1-丙胺 20529-19-5 |
| 文献:Yakugaku Zasshi, , vol. 76, p. 644,647, 648 Chem.Abstr., , p. 425 |
| 3-(4-苯基-1-哌嗪)-1-丙胺上游产品 7 | |
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| 3-(4-苯基-1-哌嗪)-1-丙胺下游产品 2 | |
| 海关编码 | 2933599090 |
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| 中文概述 | 2933599090. 其他结构上有嘧啶环的化合物(包括其他结构上有哌嗪环的化合物. 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 | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. 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: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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