N-(二苯甲基)甲胺
N-(二苯甲基)甲胺结构式
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常用名 | N-(二苯甲基)甲胺 | 英文名 | N-(Diphenylmethyl) methylamine |
|---|---|---|---|---|
| CAS号 | 14683-47-7 | 分子量 | 197.27600 | |
| 密度 | 1.04 g/cm3 | 沸点 | 310.4ºC at 760 mmHg | |
| 分子式 | C14H15N | 熔点 | 38-42ºC | |
| MSDS | 美版 | 闪点 | N/A | |
| 符号 |
GHS05 |
信号词 | Danger |
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Quantification of plasma HIV RNA using chemically engineered peptide nucleic acids.
Nat. Commun. 5 , 5079, (2014) The remarkable stability of peptide nucleic acids (PNAs) towards enzymatic degradation makes this class of molecules ideal to develop as part of a diagnostic device. Here we report the development of chemically engineered PNAs for the quantitative detection o... |
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Design, synthesis and characterisation of mannosylated ovalbumin lipid core peptide self-adjuvanting vaccine delivery system.
Drug Deliv Transl Res 4(3) , 246-55, (2014) Peptide-based vaccine delivery can be hampered by rapid peptidase activity and poor inherent immunogenicity. The self-adjuvanting lipid core peptide system (LCP) has been shown to confer improved stability and immunogenicity on peptide epitopes of group A Str... |
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Label-free measurement of histone lysine methyltransferases activity by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
Anal. Biochem. 456 , 25-31, (2014) Histone lysine methyltransferases (HKMTs) are enzymes that play an essential role in epigenetic regulation. Thus, identification of inhibitors specifically targeting these enzymes represents a challenge for the development of new antitumor therapeutics. Sever... |
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N-Diphenylmethyl-2-propenamide: theoretical study of the structure and interaction with a DNA model system. Barone G, et al.
J. Mol. Struct. 572(1) , 113-19, (2001)
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An Improved Iron-Catalyzed Epoxidation of Aromatic and Aliphatic Olefins with Hydrogen Peroxide as Oxidant. Bitterlich B, et al.
European J. Org. Chem. 29 , 4867-70, (2008)
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Discovery, biological evaluation, and structure-activity and -selectivity relationships of 6'-substituted (E)-2-(benzofuran-3(2H)-ylidene)-N-methylacetamides, a novel class of potent and selective monoamine oxidase inhibitors.
J. Med. Chem. 56(6) , 2651-64, (2013) The use of selective inhibitors of monoamine oxidase A (MAO-A) and B (MAO-B) holds a therapeutic relevance in the treatment of depressive disorders and Parkinson's disease (PD), respectively. Here, the discovery of a new class of compounds acting as monoamine... |