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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors
Sercan Askin, Hakan Tahtacı, Cüneyt Türkeş, et al.
Bioorganic Chemistry (2021) Vol. 113, pp. 105009-105009
Closed Access | Times Cited: 92

Showing 51-75 of 92 citing articles:

Synthesis, Biological Evaluation, Molecular Docking, and Acid Dissociation Constant of New Bis‐1,2,3‐triazole Compounds
Yahya Nural, Sadin Özdemir, M. Serkan Yalçın, et al.
ChemistrySelect (2021) Vol. 6, Iss. 28, pp. 6994-7001
Closed Access | Times Cited: 16
Recent updates in the development of small molecules as potential clinical candidates for Alzheimer's disease: A review
Tarana Umar, Rampratap Meena, Mustehasan, et al.
Chemical Biology & Drug Design (2022) Vol. 100, Iss. 5, pp. 674-681
Closed Access | Times Cited: 11
Screening of in vitro and in silico effect of Fluorophenylthiourea compounds on glucose 6‐phosphate dehydrogenase and 6‐phosphogluconate dehydrogenase enzymes
Muhammed Lütfü Yıldız, Yeliz Demir, Ömer İrfan Küfrevioğlu
Journal of Molecular Recognition (2022) Vol. 35, Iss. 12
Closed Access | Times Cited: 10
Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review
Anjaneyulu Bendi, Taruna, Rajni Rajni, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 1
Exploring etofenamate hydrazide-hydrazone/copper(II) complexes: Synthesis, anticancer activity, carbonic anhydrase IX inhibition and docking studies
S. Cakmak, Ömer Erdoğan, Faika Başoğlu, et al.
Journal of Molecular Structure (2024) Vol. 1312, pp. 138555-138555
Closed Access | Times Cited: 1
Bisbenzimidazole salts and their in silico–in vitro inhibitory abilities on hCA I, hCA II, and AChE enzymes
Ülkü Yılmaz, Yeliz Demir, Tuğba Taşkın‐Tok, et al.
Monatshefte für Chemie - Chemical Monthly (2024) Vol. 155, Iss. 6, pp. 653-662
Open Access | Times Cited: 1
Synthesis, Properties, and Biological Applications of 1,3,4-Thiadiazoles
Kalyani Sonawane, Rushikesh Said, Navnath T. Hatvate
Royal Society of Chemistry eBooks (2024), pp. 163-223
Closed Access | Times Cited: 1
The biguanide–sulfonamide derivatives: synthesis, characterization and investigation of anticholinesterase inhibitory, antioxidant and DNA/BSA binding properties
Özge Güngör, Muhammet Köse
Journal of Biomolecular Structure and Dynamics (2023) Vol. 41, Iss. 24, pp. 14952-14967
Closed Access | Times Cited: 4
Discovery of N-(1,3,4-thiadiazol-2-yl)benzamide derivatives containing a 6,7-methoxyquinoline structure as novel EGFR/HER-2 dual-target inhibitors against cancer growth and angiogenesis
Xinyang Li, De-pu Wang, Shuai Li, et al.
Bioorganic Chemistry (2021) Vol. 119, pp. 105469-105469
Closed Access | Times Cited: 12
2‐Amino thiazole derivatives as inhibitors of some metabolic enzymes: An in vitro and in silico study
Işıl Nihan Korkmaz
Biotechnology and Applied Biochemistry (2022) Vol. 70, Iss. 2, pp. 659-669
Closed Access | Times Cited: 7
Synthesis, anticholinesterase activity, molecular docking, and molecular dynamic simulation studies of 1,3,4‐oxadiazole derivatives
Şeyma Durmaz, Asaf Evrim Evren, Begüm Nurpelin Sağlık, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 11
Closed Access | Times Cited: 7
Recombinant human carbonic anhydrase VII: Purification, characterization, inhibition, and molecular docking studies
Hatice Esra Duran, Şükrü Beydemir
Biotechnology and Applied Biochemistry (2022) Vol. 70, Iss. 1, pp. 415-428
Closed Access | Times Cited: 6
Benzimidazolium Salts Containing Trifluoromethoxybenzyl: Synthesis, Characterization, Crystal Structure, Molecular Docking Studies and Enzymes Inhibitory Properties
Mahmut Hamide, Yetkın Gök, Yeliz Demir, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 12
Closed Access | Times Cited: 6
Novel Thioether‐Bridged 2,6‐Disubstituted and 2,5,6‐Trisubstituted Imidazothiadiazole Analogues: Synthesis, Antiproliferative Activity, ADME, and Molecular Docking Studies
Ibrahim Ozcan, Senem Akkoç, Hakan Alıcı, et al.
Chemistry & Biodiversity (2022) Vol. 20, Iss. 1
Closed Access | Times Cited: 6
Pyrimidines: Molecular docking and inhibition studies on carbonic anhydrase and cholinesterases
Hatice Esra Duran
Biotechnology and Applied Biochemistry (2022) Vol. 70, Iss. 1, pp. 68-82
Closed Access | Times Cited: 5
Access to new phosphonate- and imidazolidine-benzopyrimidinone derivatives as antityrosinase and anti-acetylcholinesterase agents: Design, synthesis and molecular docking
Sarra Chortani, Amel Hajlaoui, Salma Jlizi, et al.
Journal of Molecular Structure (2022) Vol. 1268, pp. 133693-133693
Closed Access | Times Cited: 5
Recent synthetic strategies of medicinally important imidazothiadiazoles
Tooba Jabeen, Sana Aslam, Muhammad Yaseen, et al.
Journal of Saudi Chemical Society (2023) Vol. 27, Iss. 4, pp. 101679-101679
Open Access | Times Cited: 2
Sappanin-type homoisoflavonoids from Scilla nervosa inhibits acetylcholinesterase enzyme: a combined in silico and in vitro approach
Samson O. Famuyiwa, Rajesh B. Patil, Kolade O. Faloye, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 41, Iss. 20, pp. 10957-10968
Closed Access | Times Cited: 2
Antipsychotics Induced Reproductive Toxicity by Stimulating Oxidative Stress: A Comparative in Vivo and in Silico Study
Büşra Dinçer, Ahmet Bülent Yazıcı, İrfan Çınar, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 5
Closed Access | Times Cited: 2
Metal-free synthesis of imidazoles and 2-aminoimidazoles
Nirjhar Saha, Pravin J. Wanjari, Gurudutt Dubey, et al.
Journal of Molecular Structure (2022) Vol. 1272, pp. 134092-134092
Closed Access | Times Cited: 4
1,3,4‐Thiadiazole and 1,2,4‐triazole‐5‐thione derivatives bearing 2‐pentyl‐5‐phenyl‐2,4‐dihydro‐3H‐1,2,4‐triazole‐3‐one ring: Synthesis, molecular docking, urease inhibition, and crystal structure
Ergün Gültekin, Olcay Bekircan, Yakup Kara, et al.
Archiv der Pharmazie (2022) Vol. 356, Iss. 1
Closed Access | Times Cited: 4
Acetylphenyl-substituted imidazolium salts: synthesis, characterization, in silico studies and inhibitory properties against some metabolic enzymes
Özlem Demirci, Burcu Tezcan, Yeliz Demir, et al.
Molecular Diversity (2022) Vol. 27, Iss. 6, pp. 2767-2787
Closed Access | Times Cited: 4
Synthesis, in vitro acetylcholinesterase inhibitory activity and molecular modeling studies of imidazo[2,1-b]thiazole derivatives bearing thiosemicarbazide moiety
Efe Doğukan DİNCEL, Gözde Hasbal Çelikok, Tugba YILMAZ OZDEN Nuray ULUSOY GÜZELDEMİRCİ
Journal of Research in Pharmacy (2024) Vol. 28(1), Iss. 28(1), pp. 155-163
Open Access
Thiadiazoles

Royal Society of Chemistry eBooks (2024)
Closed Access
Synthesis and evaluation of isoxazole derivatives of lapachol as inhibitors of pyruvate kinase M2
Deepak Mali, Barkha Darra Wadhwani, Vandana Nunia, et al.
Synthetic Communications (2024) Vol. 54, Iss. 16, pp. 1311-1320
Closed Access

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