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1.
Comput Intell Neurosci ; 2022: 1415713, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35586098

RESUMEN

Numerous internal and external intrusion attacks have appeared one after another, which has become a major problem affecting the normal operation of the power system. The power system is the infrastructure of the national economy, ensuring that the information security of its network not only is an aspect of computer information security but also must consider high-standard security requirements. This paper analyzes the intrusion threat brought by the power information network and conducts in-depth research and investigation combined with the intrusion detection technology of the power information network. It analyzes the structure of the power knowledge network and cloud computing through deep learning-based methods and provides a network interference detection model. The model combines the methods of abuse detection and anomaly detection, which solves the problem that the abuse analysis model does not detect new attack variants. At the same time, for big data network data retrieval, it retrieves and analyzes data flow quickly and accurately with the help of deep learning of data components. It uses a fuzzy integral method to optimize the accuracy of power information network intrusion prediction, and the accuracy reaches 98.11%, with an increase of 0.6%.


Asunto(s)
Nube Computacional , Aprendizaje Profundo , Seguridad Computacional , Recolección de Datos , Almacenamiento y Recuperación de la Información
2.
Org Lett ; 24(14): 2689-2693, 2022 04 15.
Artículo en Inglés | MEDLINE | ID: mdl-35362316

RESUMEN

The Diels-Alder (DA) reaction and hetero-Diels-Alder (HDA) reaction are among the most powerful methods for the construction of carbocycles and heterocycles. Herein, an integrated building block of DA and HDA reactions is described. The triazenyl dienes could undergo a DA reaction, while the newly released alkene moiety and the triazene were able to engage in a HDA reaction. In these processes, the triazene group could facilitate the electron-demand DA reaction and also act as a fragment of diazadiene.


Asunto(s)
Alquenos , Electrones , Reacción de Cicloadición
3.
Ann Neurol ; 90(3): 377-390, 2021 09.
Artículo en Inglés | MEDLINE | ID: mdl-34288031

RESUMEN

OBJECTIVE: Unidentified mechanisms largely restrict the viability of effective therapies in pharmacoresistant epilepsy. Our previous study revealed that hyperactivity of the subiculum is crucial for the genesis of pharmacoresistance in temporal lobe epilepsy (TLE), but the underlying molecular mechanism is not clear. METHODS: Here, we examined the role of subicular caspase-1, a key neural pro-inflammatory enzyme, in pharmacoresistant TLE. RESULTS: We found that the expression of activated caspase-1 in the subiculum, but not the CA1, was upregulated in pharmacoresistant amygdaloid-kindled rats. Early overexpression of caspase-1 in the subiculum was sufficient to induce pharmacoresistant TLE in rats, whereas genetic ablation of caspase-1 interfered with the genesis of pharmacoresistant TLE in both kindled rats and kainic acid-treated mice. The pro-pharmacoresistance effect of subicular caspase-1 was mediated by its downstream inflammasome-dependent interleukin-1ß. Further electrophysiological results showed that inhibiting caspase-1 decreased the excitability of subicular pyramidal neurons through influencing the excitation/inhibition balance of presynaptic input. Importantly, a small molecular caspase-1 inhibitor CZL80 attenuated seizures in pharmacoresistant TLE models, and decreased the neuronal excitability in the brain slices obtained from patients with pharmacoresistant TLE. INTERPRETATION: These results support the subicular caspase-1-interleukin-1ß inflammatory pathway as a novel alternative mechanism hypothesis for pharmacoresistant TLE, and present caspase-1 as a potential target. ANN NEUROL 2021;90:377-390.


Asunto(s)
Caspasa 1/biosíntesis , Inhibidores de Caspasas/uso terapéutico , Epilepsia Refractaria/enzimología , Epilepsia del Lóbulo Temporal/enzimología , Hipocampo/enzimología , Adulto , Animales , Caspasa 1/genética , Inhibidores de Caspasas/farmacología , Niño , Epilepsia Refractaria/tratamiento farmacológico , Epilepsia del Lóbulo Temporal/tratamiento farmacológico , Femenino , Hipocampo/efectos de los fármacos , Humanos , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Persona de Mediana Edad , Técnicas de Cultivo de Órganos , Ratas , Ratas Wistar
4.
Org Lett ; 23(13): 5197-5202, 2021 07 02.
Artículo en Inglés | MEDLINE | ID: mdl-34157840

RESUMEN

Herein, the sulfonyl fluoro isocyanides were first developed as a new type of SuFExable synthon, and they are used as building blocks in the Ugi reaction (U-4CR). The Ugi reaction was established and the substrate scope was investigated, and various sulfonyl fluoro α-amino amides and peptides could be reached in a one-step synthesis. Therefore, this protocol opens a new vision for SuFExable building blocks and click chemistry, and it also provides a distinct approach to sulfonyl fluoro peptides.


Asunto(s)
Cianuros/química , Péptidos/síntesis química , Amidas/química , Química Clic , Estructura Molecular , Péptidos/química
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