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- Halogen bonding in halocarbon–protein complexes: a structural survey. Emilio Parisini, Pierangelo Metrangolo, Tullio Pilati, Giuseppe Resnati, Giancarlo Terraneo
, Chem. Soc. Rev.
, 2011
, 40
, 2267
- Design, synthesis and molecular modelling of novel methyl[4-oxo-2-(aroylimino)-3-(substituted phenyl)thiazolidin-5-ylidene]acetates as potent and selective aldose reductase inhibitors. Sher Ali, Aamer Saeed, Naeem Abbas, Mohammad Shahid, Michael Bolte, Jamshed Iqbal
, Med. Chem. Commun.
, 2012
, 3
, 1428
- Selective synthesis and comparative activity of olefinic isomers of 1,2-benzothiazine-1,1-dioxide carboxylates as aldose reductase inhibitors. Shagufta Parveen, Saghir Hussain, Shaojuan Zhu, Xiangyu Qin, Xin Hao, Shuzhen Zhang, Jianglu Lu, Changjin Zhu
, RSC Adv.
, 2014
, 4
, 21134
- Multifunctional aldose reductase inhibitors based on 2H-benzothiazine 1,1-dioxide. Zhongfei Han, Xin Hao, Zehong Gao, Bing Ma, Changjin Zhu
, RSC Adv.
, 2016
, 6
, 12761
- Identification of novel pyrazole–rhodanine hybrid scaffolds as potent inhibitors of aldose reductase: design, synthesis, biological evaluation and molecular docking analysis. Hina Andleeb, Yildiz Tehseen, Syed Jawad Ali Shah, Imtiaz Khan, Jamshed Iqbal, Shahid Hameed
, RSC Adv.
, 2016
, 6
, 77688
- Heterocyclic compounds as a magic bullet for diabetes mellitus: a review. Umme Farwa, Muhammad Asam Raza
, RSC Adv.
, 2022
, 12
, 22951
- Synthesis of optically pure (S)-2-amino-5-arylpent-4-ynoic acids by Sonogashira reactions and their potential use as highly selective potent inhibitors of aldose reductase. Silvio Parpart, Andranik Petrosyan, Syed Jawad Ali Shah, Raji Akeem Adewale, Peter Ehlers, Tatevik Grigoryan, Anna F. Mkrtchyan, Zorayr Z. Mardiyan, Ani J. Karapetyan, Avetis H. Tsaturyan, Ashot S. Saghyan, Jamshed Iqbal, Peter Langer
, RSC Adv.
, 2015
, 5
, 107400