Rudrawar相关文献与解析，生知库 | 链接生命科学的每一步

Mishra, Biswa P; Loyo, Christian L; Cai, Yanyao; Litfin, Thomas; Miraj, Gause; Brillault, Lou; Masic, Veronika; Mosaiab, Tamim; Rajaratnam, Premraj; Rudrawar, Santosh; Gu, Weixi; Kobe, Bostjan; Gerdt, Joseph P; Grossman, Alan D; Shi, Yun; Ve, Thomas

发表日期：2025

文献求助收藏

Design, synthesis, in silico, and in vitro evaluation of pyrrol-2-yl-phenyl allylidene hydrazine carboximidamide derivatives as AChE/BACE 1 dual inhibitors

设计、合成、计算机模拟和体外评估吡咯-2-基苯基烯丙基肼甲酰亚胺衍生物作为 AChE/BACE 1 双重抑制剂的效果

期刊:RSC Advances

影响因子:3.9

doi:10.1039/d4ra03589e

Amit Sharma, Santosh Rudrawar, Ankita Sharma, Sandip B Bharate, Hemant R Jadhav

信号转导

发表日期：2024

文献求助收藏

Unveiling the potential of novel indol-3-yl-phenyl allylidene hydrazine carboximidamide derivatives as AChE/BACE 1 dual inhibitors: a combined in silico, synthesis and in vitro study

揭示新型吲哚-3-基苯基烯丙基肼甲酰亚胺衍生物作为 AChE/BACE 1 双重抑制剂的潜力：计算机模拟、合成和体外研究

期刊:RSC Advances

影响因子:3.9

doi:10.1039/d4ra04315d

Amit Sharma, Santosh Rudrawar, Ankita Sharma, Sandip B Bharate, Hemant R Jadhav

信号转导

发表日期：2024

文献求助收藏

Advances in the development of imaging probes and aggregation inhibitors for alpha-synuclein

α-突触核蛋白成像探针和聚集抑制剂的研发进展

期刊:Acta Pharmacologica Sinica

影响因子:8.4

doi:10.1038/s41401-019-0304-y

Xu, Ming-Ming; Ryan, Philip; Rudrawar, Santosh; Quinn, Ronald J; Zhang, Hai-Yan; Mellick, George D

神经科学

发表日期：2020

文献求助收藏

Atypical group 1 neuraminidase pH1N1-N1 bound to a group 1 inhibitor

非典型1型神经氨酸酶pH1N1-N1与1型抑制剂结合

期刊:Protein & Cell

影响因子:12.8

doi:10.1007/s13238-015-0197-6

Wu, Ying; Vavricka, Christopher J; Wu, Yan; Li, Qing; Rudrawar, Santosh; Thomson, Robin J; von Itzstein, Mark; Gao, George F; Qi, Jianxun

发表日期：2015

文献求助收藏

In silico and in vitro investigations of novel Siglec-1 inhibitors in a microglial cell model

在小胶质细胞模型中对新型Siglec-1抑制剂进行计算机模拟和体外研究

Molecular characterisation of the Bacillus subtilis SpbK antiphage defence system

枯草芽孢杆菌SpbK抗噬菌体防御系统的分子特征

Design, synthesis, in silico, and in vitro evaluation of pyrrol-2-yl-phenyl allylidene hydrazine carboximidamide derivatives as AChE/BACE 1 dual inhibitors

设计、合成、计算机模拟和体外评估吡咯-2-基苯基烯丙基肼甲酰亚胺衍生物作为 AChE/BACE 1 双重抑制剂的效果

Unveiling the potential of novel indol-3-yl-phenyl allylidene hydrazine carboximidamide derivatives as AChE/BACE 1 dual inhibitors: a combined in silico, synthesis and in vitro study

揭示新型吲哚-3-基苯基烯丙基肼甲酰亚胺衍生物作为 AChE/BACE 1 双重抑制剂的潜力：计算机模拟、合成和体外研究

Advances in the development of imaging probes and aggregation inhibitors for alpha-synuclein

α-突触核蛋白成像探针和聚集抑制剂的研发进展

Atypical group 1 neuraminidase pH1N1-N1 bound to a group 1 inhibitor

非典型1型神经氨酸酶pH1N1-N1与1型抑制剂结合