4-(吡咯烷-1-基)吡啶-2-甲酸结构式
|
常用名 | 4-(吡咯烷-1-基)吡啶-2-甲酸 | 英文名 | 2-Pyridinecarboxylicacid, 4-(1-pyrrolidinyl) |
|---|---|---|---|---|
| CAS号 | 66933-69-5 | 分子量 | 192.21400 | |
| 密度 | 1.283g/cm3 | 沸点 | 416.1ºC at 760mmHg | |
| 分子式 | C10H12N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 205.5ºC |
| 中文名 | 4-吡咯烷基-1-吡啶-2-羧酸盐酸盐 |
|---|---|
| 英文名 | 4-pyrrolidin-1-ylpyridine-2-carboxylic acid |
| 英文别名 | 更多 |
| 密度 | 1.283g/cm3 |
|---|---|
| 沸点 | 416.1ºC at 760mmHg |
| 分子式 | C10H12N2O2 |
| 分子量 | 192.21400 |
| 闪点 | 205.5ºC |
| 精确质量 | 192.09000 |
| PSA | 53.43000 |
| LogP | 1.44500 |
| InChIKey | BFBSDJMGXPOZJS-UHFFFAOYSA-N |
| SMILES | O=C(O)c1cc(N2CCCC2)ccn1 |
| 折射率 | 1.603 |
| 储存条件 | 室温, 密封, 干燥 |
| 海关编码 | 2933990090 |
|---|
|
~%
4-(吡咯烷-1-基)吡啶-2-甲酸 66933-69-5 |
| 文献:Wieprecht, Torsten; Schlingloff, Gunther; Xia, Juntao; Heinz, Uwe; Schneider, Abert; Dubs, Marie-Josee; Bachmann, Frank; Hazekamp, Menno; Dannacher, Josef Patent: US2006/19853 A1, 2006 ; Location in patent: Page/Page column 20 ; |
|
~67%
4-(吡咯烷-1-基)吡啶-2-甲酸 66933-69-5 |
| 文献:Bogdanowicz, Agnieszka; Foks, Henryk; Gobis, Katarzyna; Augustynowicz-Kopec, Ewa Heteroatom Chemistry, 2012 , vol. 23, # 2 p. 223 - 230 |
|
~%
4-(吡咯烷-1-基)吡啶-2-甲酸 66933-69-5 |
| 文献:Bogdanowicz, Agnieszka; Foks, Henryk; Gobis, Katarzyna; Augustynowicz-Kopec, Ewa Heteroatom Chemistry, 2012 , vol. 23, # 2 p. 223 - 230 |
| 4-(吡咯烷-1-基)吡啶-2-甲酸上游产品 4 | |
|---|---|
| 4-(吡咯烷-1-基)吡啶-2-甲酸下游产品 0 | |
| 海关编码 | 2933990090 |
|---|---|
| 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% |
|
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:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
|
|
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
|
|
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
|
|
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:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
|
| 4-(pyrrolidin-1-yl)picolinic acid |
| 4-(1-Pyrrolidinyl)picolinsaeure |
| 4-pyrrolidin-1-yl-pyridine-2-carboxylic acid |