4-甲基烟酰胺结构式
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常用名 | 4-甲基烟酰胺 | 英文名 | 4-Methylnicotinamide |
|---|---|---|---|---|
| CAS号 | 7250-52-4 | 分子量 | 136.15100 | |
| 密度 | 1.157 g/cm3 | 沸点 | 294.1ºC at 760 mmHg | |
| 分子式 | C7H8N2O | 熔点 | 102-105ºC | |
| MSDS | N/A | 闪点 | 131.6ºC |
| 中文名 | 4-甲基烟酰胺 |
|---|---|
| 英文名 | 4-methylpyridine-3-carboxamide |
| 英文别名 | 更多 |
| 密度 | 1.157 g/cm3 |
|---|---|
| 沸点 | 294.1ºC at 760 mmHg |
| 熔点 | 102-105ºC |
| 分子式 | C7H8N2O |
| 分子量 | 136.15100 |
| 闪点 | 131.6ºC |
| 精确质量 | 136.06400 |
| PSA | 56.97000 |
| LogP | 1.37310 |
| InChIKey | SXKLOQCGXUTBNP-UHFFFAOYSA-N |
| SMILES | Cc1ccncc1C(N)=O |
| 外观性状 | 白色到类白色固体 |
| 折射率 | 1.561 |
| 储存条件 | 室温,惰性气氛 |
| 海关编码 | 2933399090 |
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~76%
4-甲基烟酰胺 7250-52-4 |
| 文献:Galli, Ubaldina; Mesenzani, Ornella; Coppo, Camilla; Sorba, Giovanni; Canonico, Pier Luigi; Tron, Gian Cesare; Genazzani, Armando A. European Journal of Medicinal Chemistry, 2012 , vol. 55, p. 58 - 66,9 |
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~49%
4-甲基烟酰胺 7250-52-4 |
| 文献:ANORMED INC. Patent: WO2006/138350 A2, 2006 ; Location in patent: Page/Page column 114 ; WO 2006/138350 A2 |
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~86%
4-甲基烟酰胺 7250-52-4 |
| 文献:Di Rienzo, Barbara; Mellini, Paolo; Tortorella, Silvano; De Vita, Daniela; Scipione, Luigi Synthesis, 2010 , # 22 art. no. P11510SS, p. 3835 - 3838 |
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~%
4-甲基烟酰胺 7250-52-4 |
| 文献:Journal of the American Chemical Society, , vol. 66, p. 1456,1458 |
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~%
4-甲基烟酰胺 7250-52-4 |
| 文献:Canadian Journal of Chemistry, , vol. 73, # 4 p. 531 - 538 |
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~16%
4-甲基烟酰胺 7250-52-4
详细
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| 文献:Bulletin of the Chemical Society of Japan, , vol. 61, # 8 p. 2837 - 2846 |
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~%
4-甲基烟酰胺 7250-52-4 |
| 文献:Bulletin of the Chemical Society of Japan, , vol. 55, # 9 p. 3055 - 3056 |
| 海关编码 | 2933399090 |
|---|---|
| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 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 | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) 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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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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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实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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| 4-Methyl-pyridin-carbonsaeure-(3)-amid |
| 4-Methyl-nicotinsaeure-amid |
| 4-methyl-nicotinamide |
| 4-methyl-nicotinic acid amide |
| 4-Methyl-3-pyridinecarboxamide |