2-氨基-4-苯基嘧啶-5-羧酸结构式
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常用名 | 2-氨基-4-苯基嘧啶-5-羧酸 | 英文名 | 5-Pyrimidinecarboxylicacid, 2-amino-4-phenyl |
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| CAS号 | 91093-42-4 | 分子量 | 215.20800 | |
| 密度 | 1.379g/cm3 | 沸点 | 488.1ºC at 760mmHg | |
| 分子式 | C11H9N3O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 249ºC |
| 中文名 | 2-氨基-4-苯基嘧啶-5-羧酸 |
|---|---|
| 英文名 | 2-amino-4-phenylpyrimidine-5-carboxylic acid |
| 英文别名 | 更多 |
| 密度 | 1.379g/cm3 |
|---|---|
| 沸点 | 488.1ºC at 760mmHg |
| 分子式 | C11H9N3O2 |
| 分子量 | 215.20800 |
| 闪点 | 249ºC |
| 精确质量 | 215.06900 |
| PSA | 89.10000 |
| LogP | 2.00520 |
| InChIKey | QYMSHUCTVIQCSI-UHFFFAOYSA-N |
| SMILES | Nc1ncc(C(=O)O)c(-c2ccccc2)n1 |
| 折射率 | 1.668 |
| 海关编码 | 2933599090 |
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~93%
2-氨基-4-苯基嘧啶-5-羧酸 91093-42-4 |
| 文献:Schenone, Pietro; Sansebastiano, Laura; Mosti, Luisa Journal of Heterocyclic Chemistry, 1990 , vol. 27, # 2 p. 295 - 305 |
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~%
2-氨基-4-苯基嘧啶-5-羧酸 91093-42-4 |
| 文献:Schenone, Pietro; Sansebastiano, Laura; Mosti, Luisa Journal of Heterocyclic Chemistry, 1990 , vol. 27, # 2 p. 295 - 305 |
| 2-氨基-4-苯基嘧啶-5-羧酸上游产品 2 | |
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| 2-氨基-4-苯基嘧啶-5-羧酸下游产品 1 | |
| 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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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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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: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
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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
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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
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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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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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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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
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| 2-amino-4-phenyl-pyrimidine-5-carboxylic acid |
| 2-Amino-4-phenyl-pyrimidin-carbonsaeure-(5) |