L-Histidine β-naphthylamide结构式
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常用名 | L-Histidine β-naphthylamide | 英文名 | L-Histidine β-naphthylamide |
|---|---|---|---|---|
| CAS号 | 7424-15-9 | 分子量 | 280.32400 | |
| 密度 | 1.338g/cm3 | 沸点 | 661.6ºC at 760mmHg | |
| 分子式 | C16H16N4O | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | 353.9ºC |
L-Histidine β-naphthylamide用途L-组氨酸β-萘胺是组氨酸衍生物[1]。 |
| 英文名 | h-his-betana |
|---|---|
| 英文别名 | 更多 |
| 描述 | L-组氨酸β-萘胺是组氨酸衍生物[1]。 |
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| 相关类别 | |
| 体外研究 | 氨基酸和氨基酸衍生物已被商业化用作能量补充剂。它们影响合成代谢激素的分泌、运动期间的燃料供应、压力相关任务期间的精神表现,并防止运动引起的肌肉损伤。它们被认为是有益的能生膳食物质[1]。 |
| 参考文献 |
| 密度 | 1.338g/cm3 |
|---|---|
| 沸点 | 661.6ºC at 760mmHg |
| 分子式 | C16H16N4O |
| 分子量 | 280.32400 |
| 闪点 | 353.9ºC |
| 精确质量 | 280.13200 |
| PSA | 83.80000 |
| LogP | 2.84470 |
| InChIKey | DKDILZBBFKZMRO-HNNXBMFYSA-N |
| SMILES | NC(Cc1cnc[nH]1)C(=O)Nc1ccc2ccccc2c1 |
| 折射率 | 1.728 |
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Purification and characterization of a halotolerant intracellular protease from Bacillus subtilis strain FP-133.
J. Basic Microbiol. 46 , 294-304, (2006) A halotolerant strain FP-133, able to grow at concentrations of 0-12.5% (w/v) NaCl, was isolated from a fish paste and identified as Bacillus subtilis . B. subtilis strain FP-133 produced an intracell... |
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Histidines, histamines and imidazoles as glycosidase inhibitors.
Biochem. J. 274 , 885-889, (1991) This present study reports the ability of a range of derivatives of L-histidine, histamine and imidazole to act as inhibitors of sweet-almond beta-glucosidase, yeast alpha-glucosidase and Escherichia ... |
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Histidine 450 plays a critical role in catalysis and, with Ca2+, contributes to the substrate specificity of aminopeptidase A.
Biochemistry 39 , 3061-3068, (2000) Aminopeptidase A (EC 3.4.11.7, APA) is a 130 kDa membrane-bound protease that contains the HEXXH consensus sequence found in the zinc metalloprotease family, the zincins. In addition to the catalytic ... |
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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: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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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
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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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实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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| HISTIDINE-BETANA |
| H-His-bNA |
| L-histidine B-naphthylamide |