Bahaa G. M. Youssif - Concepedia

Author

Bahaa G. M. Youssif

Also Known As

B. G. M. Youssif, Baha G.M. Youssif, Bahaa G.M. Youssif, Bahaa G. M. Youssif, Bahaa G. M. Youssif, Bahaa G.M. Youssif, Bahaa GM Youssif, Bahaa Gamal Mohamed Youssif, Bahaa Youssif, Bahaa  G.  M. Youssif

152

Publications

Citations

H-Index

Concepts

All Affiliations

Assiut University Jouf University Minia University Al-Azhar University Deraya University

About

Bahaa G. M. Youssif is an author at Assiut University specializing in pharmacology, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	40	2.2K
2	Natural Sciences	15	18	891
3	Biochemistry	13	14	554
4	Engineering	3	3	239
5	Health Sciences	3	3	255

Bahaa G. M. Youssif

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
Synthesis, anticancer activity and molecular modeling studies of 1,2,4-triazole derivatives as EGFR inhibitors Hany A.M. El-Sherief, Bahaa G. M. Youssif, Syed Nasir Abbas Bukhari, European Journal of Medicinal Chemistry Medicinal ChemistryMedicineRational Drug Design1,2,4-Triazole DerivativesEgfr Inhibitors	2018	176
Novel 1,2,4-triazole derivatives as potential anticancer agents: Design, synthesis, molecular docking and mechanistic studies Hany A.M. El-Sherief, Bahaa G. M. Youssif, Syed Nasir Abbas Bukhari, Bioorganic Chemistry Combinatorial ChemistryMedicinal ChemistryMedicineNatural SciencesPharmacology	2017	171
2-Nitroimidazole-Tricarbocyanine Conjugate as a Near-Infrared Fluorescent Probe for <i>in Vivo</i> Imaging of Tumor Hypoxia K Okuda, Yasuyuki Okabe, Tetsuya Kadonosono, Bioconjugate Chemistry Near-infrared Fluorescent ProbeTumor HypoxiaEngineeringOncologic ImagingImaging Agent	2012	166
EGFR inhibitors and apoptotic inducers: Design, synthesis, anticancer activity and docking studies of novel xanthine derivatives carrying chalcone moiety as hybrid molecules Hesham A. Abou‐Zied, Bahaa G. M. Youssif, Mamdouh F. A. Mohamed, Bioorganic Chemistry Medicinal ChemistryMedicineNovel Xanthine DerivativesEgfr InhibitorsChalcone Moiety	2019	137
Design and synthesis of novel quinoline/chalcone/1,2,4-triazole hybrids as potent antiproliferative agent targeting EGFR and BRAFV600E kinases Aliaa M. Mohassab, Heba A. Hassan, Dalia Abdelhamid, Bioorganic Chemistry Combinatorial ChemistryMedicinal ChemistryPotent Antiproliferative AgentMedicineBrafv600e Kinases	2020	111
Design, synthesis, mechanistic and histopathological studies of small-molecules of novel indole-2-carboxamides and pyrazino[1,2-a]indol-1(2H)-ones as potential anticancer agents effecting the reactive oxygen species production Bahaa G. M. Youssif, Mostafa Abdelrahman, Ahmed H. Abdelazeem, European Journal of Medicinal Chemistry Medicinal ChemistryBiochemistryNatural SciencesHistopathological StudiesOrganic Chemistry	2018	88
Synthesis and biological evaluation of novel xanthine derivatives as potential apoptotic antitumor agents Mohamed Hisham, Bahaa G. M. Youssif, Essam Eldin A. Osman, European Journal of Medicinal Chemistry Medicinal ChemistryPharmaceutical ScienceMedicineNovel Xanthine DerivativesPharmacological Agent	2019	88
Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors Lamya H. Al-Wahaibi, Ahmed M. Gouda, Ola F. Abou‐Ghadir, Bioorganic Chemistry Medicinal ChemistryNatural SciencesAntiproliferative EgfrDiversity-oriented SynthesisMedicine	2020	75
Design, synthesis, and antibacterial evaluation of new quinoline-1,3,4-oxadiazole and quinoline-1,2,4-triazole hybrids as potential inhibitors of DNA gyrase and topoisomerase IV Heba A. Hofny, Mamdouh F. A. Mohamed, Hesham A. M. Gomaa, Bioorganic Chemistry Medicinal ChemistryAntibacterial EvaluationMedicineDrug DiscoveryTopoisomerase Iv	2021	73
Synthesis, biological evaluation, docking study and ulcerogenicity profiling of some novel quinoline-2-carboxamides as dual COXs/LOX inhibitors endowed with anti-inflammatory activity Mostafa Abdelrahman, Bahaa G. M. Youssif, Mohamed A. Abdelgawad, European Journal of Medicinal Chemistry Medicinal ChemistryAnti-inflammatoryBiochemistryDual Coxs/lox InhibitorsMedicine	2016	69

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