Evidence map›Paper›PMID 41099752›Full record

ReviewMolecular diversity2026

Recent advances in Pyrazolo[3,4-d]pyrimidine-based dual inhibitors in the treatment of cancers.

Hanrui Jiang, Nan Li, Ruosong Qin, Siyu Lin, Xuelian Wang, Chunyan Li, Jiwei Shen, Ye Chen, Ju Liu, Shi Ding

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hanrui JiangCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Nan LiCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Ruosong QinCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Siyu LinCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Xuelian WangCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Chunyan LiShenyang Xingqi Pharmaceutical Co., Ltd., 68 Sishui Street, Hunnan District, Shenyang, 110163, China.
Jiwei ShenCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Ye ChenCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China.
Ju LiuCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China. liuju1216@126.com.
Shi DingCollege of Pharmacy of Liaoning University, Shenyang, 110036, Liaoning, People's Republic of China. dingshi_destiny@163.com.

Funding

General Projects of Education Department of Liaoning Province LJ212410140038Shenyang Natural Science Foundation of Key Laboratory 23-503-6-12
6 · The paper itself

Abstract

Cancer remains a paramount threat to global health and constitutes a critical frontier in contemporary drug discovery. The pyrazolo[3,4-d]pyrimidine scaffold represents a unique chemical architecture that merges purine and pyrimidine pharmacophores, enabling profound exploration and clinical translation across anti-cancer therapeutic domains. The development of dual-target inhibitors represented a compelling strategy. This combinatorial approach not only amplified pharmacological efficacy through synergistic pathway suppression but also reduced the likelihood of resistance development by disrupting redundant survival networks. This review focused on the emerging paradigm of pyrazolo[3,4-d]pyrimidine-based dual-target inhibitors in oncology. Specifically, we systematically analyzed seven distinct dual-inhibition paradigms: AK/CDK1, HDAC/Topo II, CDK2/GSK-3β, Src/Bcr-Abl, BRAF V600E/VEGFR2, EGFR/PDE5, and EGFR T790M/HER2. Comprehensive insights were provided into the rational design principles, the structure-activity relationships (SARs), and molecular mechanisms underlying these innovative therapeutics. Furthermore, we proposed forward-looking strategies for design, ADME profiling, and toxicity mitigation to guide the translational development of pyrazolo[3,4-d]pyrimidine derivatives in cancer therapy.

Indexed as

Antineoplastic AgentsNeoplasmsProtein Kinase InhibitorsPyrazolesPyrimidinesAnimalsHumansStructure-Activity RelationshipAntineoplastic AgentsProtein Kinase InhibitorsPyrazolespyrazolo(3,4-d)pyrimidinePyrimidinesAnticancerDual target inhibitorsPyrazolo[3,4-d]pyrimidineSARs

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.