O-三苯甲基羟胺
O-三苯甲基羟胺结构式
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常用名 | O-三苯甲基羟胺 | 英文名 | O-Tritylhydroxylamine |
|---|---|---|---|---|
| CAS号 | 31938-11-1 | 分子量 | 275.344 | |
| 密度 | 1.1±0.1 g/cm3 | 沸点 | 443.2±44.0 °C at 760 mmHg | |
| 分子式 | C19H17NO | 熔点 | 79-81ºC(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 235.1±22.1 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
Bioorg. Med. Chem. 18 , 2225-31, (2010) There are many of pathogen parasite species with different susceptibility profile to antiparasitic drugs. Unfortunately, almost QSAR models predict the biological activity of drugs against only one parasite species. Consequently, predicting the probability wi... |
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Antimalarial and antileishmanial activities of histone deacetylase inhibitors with triazole-linked cap group.
Bioorg. Med. Chem. 18(1) , 415-25, (2010) Histone deacetylase inhibitors (HDACi) are endowed with plethora of biological functions including anti-proliferative, anti-inflammatory, anti-parasitic, and cognition-enhancing activities. Parsing the structure-activity relationship (SAR) for each disease co... |
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Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide
Bioorg. Med. Chem. Lett. 19(23) , 6588-90, (2009) We describe herein the synthesis and characterization of a new class of histone deacetylase (HDAC) inhibitors derived from conjugation of a suberoylanilide hydroxamic acid-like aliphatic-hydroxamate pharmacophore to a nuclear localization signal peptide. We f... |