Minhang Xin

2.1k total citations · 1 hit paper
71 papers, 1.8k citations indexed

About

Minhang Xin is a scholar working on Molecular Biology, Organic Chemistry and Genetics. According to data from OpenAlex, Minhang Xin has authored 71 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 23 papers in Organic Chemistry and 21 papers in Genetics. Recurrent topics in Minhang Xin's work include PI3K/AKT/mTOR signaling in cancer (22 papers), Chronic Lymphocytic Leukemia Research (20 papers) and Quinazolinone synthesis and applications (14 papers). Minhang Xin is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (22 papers), Chronic Lymphocytic Leukemia Research (20 papers) and Quinazolinone synthesis and applications (14 papers). Minhang Xin collaborates with scholars based in China, United States and India. Minhang Xin's co-authors include San‐Qi Zhang, Hongyi Zhao, Shuai Mao, Chengyuan Liang, Hao Zhang, Suresh Thareja, Junjie Zhang, Feng Tang, Weiming Duan and Jiajia Sun and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Organic Letters.

In The Last Decade

Minhang Xin

70 papers receiving 1.7k citations

Hit Papers

Small molecule selenium-containing compounds: Recent deve... 2021 2026 2022 2024 2021 50 100 150

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Minhang Xin China 22 1.0k 582 427 291 183 71 1.8k
Jinyun Dong China 24 1.1k 1.0× 479 0.8× 733 1.7× 182 0.6× 136 0.7× 65 2.1k
Linjiang Tong China 30 1.5k 1.4× 689 1.2× 604 1.4× 100 0.3× 113 0.6× 99 2.3k
San‐Qi Zhang China 25 1000 1.0× 776 1.3× 356 0.8× 92 0.3× 118 0.6× 100 1.8k
Anna Kruczynski France 26 1.3k 1.3× 313 0.5× 779 1.8× 96 0.3× 110 0.6× 71 2.1k
Jinlei Bian China 26 1.1k 1.0× 441 0.8× 392 0.9× 57 0.2× 85 0.5× 98 1.9k
Kevin Kish United States 20 930 0.9× 381 0.7× 265 0.6× 295 1.0× 433 2.4× 38 2.0k
Elaine Willmore United Kingdom 23 1.4k 1.3× 208 0.4× 778 1.8× 129 0.4× 84 0.5× 54 1.7k
Hong Ding China 26 1.7k 1.7× 311 0.5× 349 0.8× 52 0.2× 98 0.5× 80 2.3k
Ramesh Ummanni India 25 756 0.7× 494 0.8× 167 0.4× 92 0.3× 68 0.4× 64 1.6k
Donghwa Kim South Korea 19 764 0.7× 140 0.2× 313 0.7× 80 0.3× 119 0.7× 42 1.3k

Countries citing papers authored by Minhang Xin

Since Specialization
Citations

This map shows the geographic impact of Minhang Xin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Minhang Xin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Minhang Xin more than expected).

Fields of papers citing papers by Minhang Xin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Minhang Xin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Minhang Xin. The network helps show where Minhang Xin may publish in the future.

Co-authorship network of co-authors of Minhang Xin

This figure shows the co-authorship network connecting the top 25 collaborators of Minhang Xin. A scholar is included among the top collaborators of Minhang Xin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Minhang Xin. Minhang Xin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Yuan, Bo, Mengyan Ma, Yujie Wu, et al.. (2025). Discovery of novel covalent PI3Kδ inhibitors bearing alaninamide moiety by lysine-targeted covalent strategy. European Journal of Medicinal Chemistry. 297. 117948–117948. 1 indexed citations
2.
Wang, Fang, et al.. (2024). Menin-MLL protein–protein interaction inhibitors: a patent review (2021-present). Expert Opinion on Therapeutic Patents. 35(1). 65–78. 1 indexed citations
3.
Gao, Li, Mengyan Ma, San‐Qi Zhang, et al.. (2023). Design, synthesis and bioactivity evaluation of selenium-containing PI3Kδ inhibitors. Bioorganic Chemistry. 140. 106815–106815. 3 indexed citations
4.
Zhao, Hongyi, Minhang Xin, & San‐Qi Zhang. (2023). Progress of small molecules for targeted protein degradation: PROTACs and other technologies. Drug Development Research. 84(2). 337–394. 19 indexed citations
5.
Zhang, San‐Qi, et al.. (2021). Recent Progress of Small Molecule Menin–MLL Interaction Inhibitors as Therapeutic Agents for Acute Leukemia. Journal of Medicinal Chemistry. 64(21). 15519–15533. 14 indexed citations
6.
Zhao, Hongyi, Xueyan Yang, Shemin Lu, et al.. (2020). Discovery of potent small molecule PROTACs targeting mutant EGFR. European Journal of Medicinal Chemistry. 208. 112781–112781. 75 indexed citations
7.
Wang, Yazhou, Wei Huang, Minhang Xin, et al.. (2019). Discovery of potent anti-inflammatory 4-(4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-yl) pyrimidin-2-amines for use as Janus kinase inhibitors. Bioorganic & Medicinal Chemistry. 27(12). 2592–2597. 8 indexed citations
8.
Zhang, San‐Qi, Yifan Feng, Jin Wang, et al.. (2019). Alkylsulfonamide-containing quinazoline derivatives as potent and orally bioavailable PI3Ks inhibitors. Bioorganic & Medicinal Chemistry. 27(20). 114930–114930. 15 indexed citations
9.
Lei, Hao, Hao Zhang, Yanjie Liu, et al.. (2019). Discovery of novel 9-heterocyclyl substituted 9H-purines as L858R/T790M/C797S mutant EGFR tyrosine kinase inhibitors. European Journal of Medicinal Chemistry. 186. 111888–111888. 54 indexed citations
10.
Liang, Chengyuan, et al.. (2018). The development of Bruton's tyrosine kinase (BTK) inhibitors from 2012 to 2017: A mini-review. European Journal of Medicinal Chemistry. 151. 315–326. 137 indexed citations
11.
Zhang, Hao, Hongyi Zhao, Xueyan Yang, et al.. (2018). Synthesis and biological evaluation of irreversible EGFR tyrosine kinase inhibitors containing pyrido[3,4-d]pyrimidine scaffold. Bioorganic & Medicinal Chemistry. 26(12). 3619–3633. 18 indexed citations
12.
Wang, Huiyan, et al.. (2017). Discovery of 2-(pyridin-2-yl)aniline as a directing group for the sp2 C–H bond amination mediated by cupric acetate. Organic & Biomolecular Chemistry. 15(31). 6622–6631. 12 indexed citations
13.
Xin, Minhang, Jun Wen, Han Shen, et al.. (2016). Synthesis and pharmacological evaluation of trifluoromethyl containing 4-(2-pyrimidinylamino)benzamides as Hedgehog signaling pathway inhibitors. Bioorganic & Medicinal Chemistry. 24(5). 1079–1088. 9 indexed citations
14.
Xin, Minhang, et al.. (2016). Discovery of novel 4-(2-pyrimidinylamino)benzamide derivatives as highly potent and orally available hedgehog signaling pathway inhibitors. European Journal of Medicinal Chemistry. 110. 115–125. 10 indexed citations
15.
Zhang, Hao, et al.. (2015). Synthesis and antitumor activity evaluation of PI3K inhibitors containing 3-substituted quinazolin-4(3H)-one moiety. Bioorganic & Medicinal Chemistry. 23(24). 7765–7776. 22 indexed citations
16.
Xin, Minhang, et al.. (2015). Synthesis and antitumor activities evaluation of m-(4-morpholinoquinazolin-2-yl)benzamides in vitro and in vivo. European Journal of Medicinal Chemistry. 96. 382–395. 32 indexed citations
17.
Xin, Minhang, Wei Huang, Jin Qiu, et al.. (2015). Synthesis and biological evaluation of novel 7-substituted 3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amines as potent Bruton’s tyrosine kinase (BTK) inhibitors. Bioorganic & Medicinal Chemistry. 23(19). 6250–6257. 10 indexed citations
18.
Xin, Minhang. (2015). Hedgehog inhibitors: a patent review (2013 – present). Expert Opinion on Therapeutic Patents. 25(5). 549–565. 26 indexed citations
19.
Wang, Xiaomeng, Shuai Mao, Lei Cao, et al.. (2015). Modification of N-(6-(2-methoxy-3-(4-fluorophenylsulfonamido)pyridin-5-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)acetamide as PI3Ks inhibitor by replacement of the acetamide group with alkylurea. Bioorganic & Medicinal Chemistry. 23(17). 5662–5671. 14 indexed citations
20.
Xin, Minhang, Jun Wen, Feng Tang, et al.. (2013). Synthesis and evaluation of 4-(2-pyrimidinylamino) benzamides inhibitors of hedgehog signaling pathway. Bioorganic & Medicinal Chemistry Letters. 24(3). 983–988. 15 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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