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Sankore

Named after the University of Sankore in Timbuktu — one of the world’s oldest centres of learning. Every figure here is computed from work-level records in our own graph, never copied from a source’s summary count.

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Discovery of new 2,4-diaminopyrimidines derivatives as EGFRT790M kinase inhibitors: a structure-based approach with DFT calculation, drug-likeness, ADME-toxicity properties evaluation and MD simulation

2024Journal of Umm Al-Qura University for Applied SciencesJournalOpen access

10.1007/s43994-023-00099-6 Full text16 citations

Authors

6 authors across 5 institutions in 2 countries.

Muhammad Tukur IbrahimFirst authorCorresponding
- Ahmadu Bello University (NG)
Kamal Tabti
- Université Moulay Ismail de Meknes (MA)
Safiya Abdulsalam
- Ahmadu Bello University (NG)
Abdulsalam Salisu Tahir
- Kaduna State University (NG)
Abdulhamid Mahmoud
- Sa'adu Zungur University (NG)
Aisha Muhammad DanmallamSenior author
- Federal University Birnin Kebbi (NG)

Fields

Assignment is probabilistic — a work belongs to several fields in proportions.

Computational Drug Discovery Methodslevel 3 · 1.00
Cancer therapeutics and mechanismslevel 3 · 1.00
Quinazolinone synthesis and applicationslevel 3 · 1.00

Sources

Several sources describing one work is the point — it means the record rests on more than one authority.

openalexseen September 9, 2026
2024 · Journal of Umm Al-Qura University for Applied Sciences · 16 citations
https://openalex.org/W4390903962

Discovery of new 2,4-diaminopyrimidines derivatives as EGFRT790M kinase inhibitors: a structure-based approach with DFT calculation, drug-likeness, ADME-toxicity properties evaluation and MD simulation · Sankore