ASINEX-REAG BAS 03375399结构式
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常用名 | ASINEX-REAG BAS 03375399 | 英文名 | ASINEX-REAG BAS 03375399 |
|---|---|---|---|---|
| CAS号 | 38580-22-2 | 分子量 | 184.14900 | |
| 密度 | 1.384g/cm3 | 沸点 | N/A | |
| 分子式 | C7H8N2O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 2-(6-methyl-2,4-dioxo-1H-pyrimidin-5-yl)acetic acid |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.384g/cm3 |
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| 分子式 | C7H8N2O4 |
| 分子量 | 184.14900 |
| 精确质量 | 184.04800 |
| PSA | 103.02000 |
| InChIKey | GFWWREGOTNQVGC-UHFFFAOYSA-N |
| SMILES | Cc1[nH]c(=O)[nH]c(=O)c1CC(=O)O |
| 折射率 | 1.522 |
| 危险品运输编码 | NONH for all modes of transport |
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| 海关编码 | 2933599090 |
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~79%
ASINEX-REAG BAS... 38580-22-2 |
| 文献:KATHOLIEKE UNIVERSITEIT LEUVEN; CHALTIN, Patrick; DEBYSER, Zeger; DE MAEYER, Marc; MARCHAND, Arnaud; MARCHAND, Damien; SMETS, Wim; VOET, Arnout; CHRIST, Frauke Patent: WO2011/15641 A1, 2011 ; Location in patent: Page/Page column 91; 92 ; |
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~31%
ASINEX-REAG BAS... 38580-22-2 |
| 文献:Itahara, Toshio; Ide, Naoko Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1990 , # 4 p. 1225 - 1226 |
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~%
ASINEX-REAG BAS... 38580-22-2 |
| 文献:KATHOLIEKE UNIVERSITEIT LEUVEN; CHALTIN, Patrick; DEBYSER, Zeger; DE MAEYER, Marc; MARCHAND, Arnaud; MARCHAND, Damien; SMETS, Wim; VOET, Arnout; CHRIST, Frauke Patent: WO2011/15641 A1, 2011 ; |
| ASINEX-REAG BAS 03375399上游产品 4 | |
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| ASINEX-REAG BAS 03375399下游产品 0 | |
| 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:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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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:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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| 6-Methyl-uracil-5-essigsaeure |
| (6-Methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-essigsaeure |
| 2-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acetic acid |
| 5-pyrimidineacetic acid,1,2,3,4-tetrahydro-6-methyl-2,4-dioxo |
| 5-Carboxymethyl-6-methyluracil |
| (6-Methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-acetic acid |