OpenAlex Citation Counts

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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:

A new exploration towards aminothiazolquinolone oximes as potentially multi-targeting antibacterial agents: Design, synthesis and evaluation acting on microbes, DNA, HSA and topoisomerase IV
Liangliang Wang, Narsaiah Battini, Rammohan R. Yadav Bheemanaboina, et al.
European Journal of Medicinal Chemistry (2019) Vol. 179, pp. 166-181
Closed Access | Times Cited: 85

Showing 26-50 of 85 citing articles:

Design and biological evaluation of a novel type of potential multi-targeting antimicrobial sulfanilamide hybrids in combination of pyrimidine and azoles
Yan‐Fei Sui, Di Li, Juan Wang, et al.
Bioorganic & Medicinal Chemistry Letters (2020) Vol. 30, Iss. 6, pp. 126982-126982
Closed Access | Times Cited: 53

Design and Synthesis of Sulfanilamide Aminophosphonates as Novel Antibacterial Agents towards Escherichia coli
Juan Wang, Mohammad Fawad Ansari, Jian‐Mei Lin, et al.
Chinese Journal of Chemistry (2021) Vol. 39, Iss. 8, pp. 2251-2263
Closed Access | Times Cited: 52

Novel carbazole-oxadiazoles as potential Staphylococcus aureus germicides
Yun‐Peng Xie, Mohammad Fawad Ansari, Shaolin Zhang, et al.
Pesticide Biochemistry and Physiology (2021) Vol. 175, pp. 104849-104849
Closed Access | Times Cited: 48

Molecular design and preparation of 2-aminothiazole sulfanilamide oximes as membrane active antibacterial agents for drug resistant Acinetobacter baumannii
Juan Wang, Pengli Zhang, Mohammad Fawad Ansari, et al.
Bioorganic Chemistry (2021) Vol. 113, pp. 105039-105039
Closed Access | Times Cited: 48

An unanticipated discovery towards novel naphthalimide corbelled aminothiazoximes as potential anti-MRSA agents and allosteric modulators for PBP2a
Pengli Zhang, Lavanya Gopala, Shaolin Zhang, et al.
European Journal of Medicinal Chemistry (2021) Vol. 229, pp. 114050-114050
Closed Access | Times Cited: 46

Discovery of novel purinylthiazolylethanone derivatives as anti-Candida albicans agents through possible multifaceted mechanisms
Yan‐Fei Sui, Mohammad Fawad Ansari, Bo Fang, et al.
European Journal of Medicinal Chemistry (2021) Vol. 221, pp. 113557-113557
Closed Access | Times Cited: 45

One-pot strategy for thiazole tethered 7-ethoxy quinoline hybrids: Synthesis and potential antimicrobial agents as dihydrofolate reductase (DHFR) inhibitors with molecular docking study
Yousry A. Ammar, Sondos M. A. Abd El‐Hafez, Sadia A. Hessein, et al.
Journal of Molecular Structure (2021) Vol. 1242, pp. 130748-130748
Closed Access | Times Cited: 42

Design, synthesis, molecular modeling, and antimicrobial potential of novel 3‐[(1H‐pyrazol‐3‐yl)imino]indolin‐2‐one derivatives as DNA gyrase inhibitors
Abdullah Yahya Abdullah Alzahrani, Yousry A. Ammar, Mohamed A. Salem, et al.
Archiv der Pharmazie (2021) Vol. 355, Iss. 1
Closed Access | Times Cited: 39

Recent insight into the biological activities and SAR of quinolone derivatives as multifunctional scaffold
Vishal Sharma, Rina Das, Dinesh Kumar Mehta, et al.
Bioorganic & Medicinal Chemistry (2022) Vol. 59, pp. 116674-116674
Closed Access | Times Cited: 33

An unanticipated discovery of novel naphthalimidopropanediols as potential broad-spectrum antibacterial members
Pengli Zhang, Mouna Hind Laiche, Yanliang Li, et al.
European Journal of Medicinal Chemistry (2022) Vol. 241, pp. 114657-114657
Closed Access | Times Cited: 31

Novel metronidazole-derived three-component hybrids as promising broad-spectrum agents to combat oppressive bacterial resistance
Fenfen Li, Pengli Zhang, Vijai Kumar Reddy Tangadanchu, et al.
Bioorganic Chemistry (2022) Vol. 122, pp. 105718-105718
Closed Access | Times Cited: 30

Structure-activity relationship studies of thiazole agents with potential anti methicillin-resistance Staphylococcus aureus (MRSA) activity
Xinyi Wang, Sihui Long, Ziwei Liu, et al.
Process Biochemistry (2023) Vol. 132, pp. 13-29
Closed Access | Times Cited: 19

Thiazolyl hydrazineylidenyl indolones as unique potential multitargeting broad-spectrum antimicrobial agents
Wenhao Zhao, Jiahe Xu, Vijai Kumar Reddy Tangadanchu, et al.
European Journal of Medicinal Chemistry (2023) Vol. 256, pp. 115452-115452
Closed Access | Times Cited: 18

Thiazole-based analogues as potential antibacterial agents against methicillin-resistant Staphylococcus aureus (MRSA) and their SAR elucidation
Jiaojiao Guo, Zhouling Xie, Wei Ruan, et al.
European Journal of Medicinal Chemistry (2023) Vol. 259, pp. 115689-115689
Closed Access | Times Cited: 18

Sulfur (SⅥ)-containing heterocyclic hybrids as antibacterial agents against methicillin-resistant Staphylococcus aureus (MRSA) and its SAR
Santosh Kumar Verma, Shobith Rangappa, Rameshwari Verma, et al.
Bioorganic Chemistry (2024) Vol. 145, pp. 107241-107241
Closed Access | Times Cited: 5

Discovery of indolylacryloyl-derived oxacins as novel potential broad-spectrum antibacterial candidates
Yue-Gao Hu, Narsaiah Battini, Bo Fang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 270, pp. 116392-116392
Closed Access | Times Cited: 4

Synthesis and Biological Evaluation of Quinazolonethiazoles as New Potential Conquerors towards Pseudomonas Aeruginosa
Jie Wang, Narsaiah Battini, Mohammad Fawad Ansari, et al.
Chinese Journal of Chemistry (2020) Vol. 39, Iss. 5, pp. 1093-1103
Closed Access | Times Cited: 46

Unique para-aminobenzenesulfonyl oxadiazoles as novel structural potential membrane active antibacterial agents towards drug-resistant methicillin resistant Staphylococcus aureus
Juan Wang, Mohammad Fawad Ansari, Cheng‐He Zhou
Bioorganic & Medicinal Chemistry Letters (2021) Vol. 41, pp. 127995-127995
Closed Access | Times Cited: 37

Aloe-emodin derived azoles as a new structural type of potential antibacterial agents: design, synthesis, and evaluation of the action on membrane, DNA, and MRSA DNA isomerase
Xinyuan Liang, Narsaiah Battini, Yan‐Fei Sui, et al.
RSC Medicinal Chemistry (2021) Vol. 12, Iss. 4, pp. 602-608
Open Access | Times Cited: 36

Pyrimidinetrione‐imidazoles as a Unique Structural Type of Potential Agents towards Candida Albicans: Design, Synthesis and Biological Evaluation
Yan‐Fei Sui, Mohammad Fawad Ansari, Cheng‐He Zhou
Chemistry - An Asian Journal (2021) Vol. 16, Iss. 11, pp. 1417-1429
Closed Access | Times Cited: 36

Novel chalcone-conjugated, multi-flexible end-group coumarin thiazole hybrids as potential antibacterial repressors against methicillin-resistant Staphylococcus aureus
Yuanyuan Hu, Chunfang Hu, Guangxing Pan, et al.
European Journal of Medicinal Chemistry (2021) Vol. 222, pp. 113628-113628
Closed Access | Times Cited: 36

Natural aloe emodin-hybridized sulfonamide aminophosphates as novel potential membrane-perturbing and DNA-intercalating agents against Enterococcus faecalis
Zhao Deng, Hang Sun, Rammohan R. Yadav Bheemanaboina, et al.
Bioorganic & Medicinal Chemistry Letters (2022) Vol. 64, pp. 128695-128695
Closed Access | Times Cited: 24

Current scenario of quinolone hybrids with potential antibacterial activity against ESKAPE pathogens
Jingyue Gao, Haodong Hou, Feng Gao
European Journal of Medicinal Chemistry (2022) Vol. 247, pp. 115026-115026
Closed Access | Times Cited: 24

Benzopyrone-mediated quinolones as potential multitargeting antibacterial agents
Shu-Rui Li, Chun-Mei Zeng, Xin-Mei Peng, et al.
European Journal of Medicinal Chemistry (2023) Vol. 262, pp. 115878-115878
Closed Access | Times Cited: 13

Discovery of benzopyridone cyanoacetates as new type of potential broad-spectrum antibacterial candidates
Jing Zhang, Yi-Min Tan, Shu-Rui Li, et al.
European Journal of Medicinal Chemistry (2023) Vol. 265, pp. 116107-116107
Closed Access | Times Cited: 12

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