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首页> Chemical biology & drug design> Design, synthesis, and molecular docking studies of benzimidazole-1,3,4-triazole hybrids as carbonic anhydrase I and II inhibitors.

Design, synthesis, and molecular docking studies of benzimidazole-1,3,4-triazole hybrids as carbonic anhydrase I and II inhibitors.

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第一作者： İsmail,Çelik

第一单位： Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Erciyes University, Kayseri, Turkey.

作者： İsmail,Çelik ^[1] ; Ulviye,Acar Çevik ^[2] ; Kaan,Küçükoğlu ^[3] ; Hayrunnisa,Nadaroglu ^[4] ; Hayrani Eren,Bostancı ^[5] ; Ayşen,Işık ^[6] ; Yusuf,Özkay ^[2] ; Zafer Asım,Kaplancıklı ^[2]

作者单位： Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Erciyes University, Kayseri, Turkey. ^[1] Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey. ^[2] Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Selçuk University, Konya, Turkey. ^[3] Department of Food Technology, ErzurumVocational Training School, Ataturk University, Erzurum, Turkey. ^[4] Department of Biochemistry, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Turkey. ^[5] Department of Biochemistry, Faculty of Science, Selçuk University, Konya, Turkey. ^[6]

关键词 1,3,4-triazole antioxidant benzimidazole carbonic anhydrase molecular docking

主题词小鼠(Mice);动物(Animals);碳酸酐酶Ⅰ(Carbonic Anhydrase I);碳酸酐酶抑制剂(Carbonic Anhydrase Inhibitors);碳酸酐酶Ⅱ(Carbonic Anhydrase II);苯咪唑类(Benzimidazoles);构效关系(Structure-Activity Relationship);分子结构(Molecular Structure)

DOI 10.1111/cbdd.14351

PMID 37697918

发布时间 2024-03-25

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Chemical biology & drug design

Chemical biology & drug design

2024年103卷1期

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