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901

Biologically Potent Benzimidazole-Based-Substituted Benzaldehyde Derivatives as Potent Inhibitors for Alzheimer’s Disease along with Molecular Docking Study

by Adalat B.; Rahim F.; Rehman W.; Ali Z.; Rasheed L.; Khan Y.; Farghaly T.A.; Shams S.; Taha M.; Wadood A.; Shah S.A.A.; Abdellatif M.H.
Published in Pharmaceuticals (2023)

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902

Quality of life among caregivers of children with special needs in kelantan, malaysia: The importance of psychosocial mediators

by Isa S.N.I.; Ishak I.; Rahman A.A.; Saat N.Z.M.; Din N.C.; Lubis S.H.; Ismail M.F.M.; Suradi N.R.M.
Published in Malaysian Journal of Medical Sciences (2021)

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903

Simulation and experimental study on distortion of butt and T-joints using WELD PLANNER

by Sulaiman M.S.; Manurung Y.H.P.; Haruman E.; Rahim M.R.A.; Redza M.R.; Lidam R.N.A.; Abas S.K.; Tham G.; Chau C.Y.
Published in Journal of Mechanical Science and Technology (2011)

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904

Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases

by Rahim F.; Ullah H.; Taha M.; Wadood A.; Javed M.T.; Rehman W.; Nawaz M.; Ashraf M.; Ali M.; Sajid M.; Ali F.; Khan M.N.; Khan K.M.
Published in Bioorganic Chemistry (2016)

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905

Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents

by Rahim F.; Zaman K.; Ullah H.; Taha M.; Wadood A.; Javed M.T.; Rehman W.; Ashraf M.; Uddin R.; Uddin I.; Asghar H.; Khan A.A.; Khan K.M.
Published in Bioorganic Chemistry (2015)
“…, 5.75 ± 0.003, 8.81 ± 0.005, and 1.73 ± 0.001 μM, respectively, which is better than the standard…”

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906

Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities

by Taha M.; Ismail N.H.; Jamil W.; Rashwan H.; Kashif S.M.; Sain A.A.; Adenan M.I.; Anouar E.H.; Ali M.; Rahim F.; Khan K.M.
Published in European Journal of Medicinal Chemistry (2014)
“… and antioxidant activities. Compounds 1-7 and 11 showed excellent activities ranged 140-280 μM, better than…”

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907

Synthesis of benzimidazole derivatives and their antiglycation, antioxidant, antiurease and molecular docking study

by Taha, Muhammad; Rahim, Fazal; Adalath, Bushra; Imran, Syahrul; Khan, Khalid Mohammed; Shah, Syed Adnan Ali; Uddin, Nizam; Nawaz, Muhammad; Break, Mohammed Khaled Bin; Magam, Sami M.; Alqarni, Saad
Published in ARABIAN JOURNAL OF CHEMISTRY (2024)

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908

Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues

by Zaman K.; Rahim F.; Taha M.; Ullah H.; Wadood A.; Nawaz M.; Khan F.; Wahab Z.; Shah S.A.A.; Rehman A.U.; Kawde A.-N.; Gollapalli M.
Published in Bioorganic Chemistry (2019)

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909

Molecular modeling and synthesis of novel benzimidazole-derived thiazolidinone bearing chalcone derivatives: a promising approach to develop potential anti-diabetic agents

by Abbasi, Shahzad Ahmad; Rehman, Wajid; Rahim, Fazal; Hussain, Rafaqat; Hawsawi, Mohammed B.; Alluhaibi, Mustafa S.; Alharbi, Majed; Taha, Muhammad; Khan, Shoaib; Rasheed, Liaqat; Wadood, Abdul; Ali Shah, Syed Adnan
Published in ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES (2024)

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910

New biologically dynamic hybrid pharmacophore triazinoindole-based-thiadiazole as potent α-glucosidase inhibitors: In vitro and in silico study

by Khan A.A.; Rahim F.; Taha M.; Rehman W.; Iqbal N.; Wadood A.; Ahmad N.; Shah S.A.A.; Ghoneim M.M.; Alshehri S.; Salahuddin M.; Khan K.M.
Published in International Journal of Biological Macromolecules (2022)
“… in the series with fifteen folds more active than standard acarbose. Structure activity relationship (SAR…”

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911

Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase

by Rahim F.; Ullah H.; Javid M.T.; Wadood A.; Taha M.; Ashraf M.; Shaukat A.; Junaid M.; Hussain S.; Rehman W.; Mehmood R.; Sajid M.; Khan M.N.; Khan K.M.
Published in Bioorganic Chemistry (2015)
“… = 36.75 ± 0.05 μM) exhibited outstanding inhibitory potential much better than the standard acarbose (IC50…”

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912

Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton

by Khan K.M.; Rahim F.; Wadood A.; Kosar N.; Taha M.; Lalani S.; Khan A.; Fakhri M.I.; Junaid M.; Rehman W.; Khan M.; Perveen S.; Sajid M.; Choudhary M.I.
Published in European Journal of Medicinal Chemistry (2014)

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913

Investigation of novel benzimidazole-based indole/thiazole hybrids derivatives as effective anti-diabetics and anti-alzheimer's agents: Structure-activity relationship insight, in...

by Naz H.; Othman M.S.; Rahim F.; Hussain R.; Khan S.; Taha M.; Hafez M.M.; Abdel-Hafez L.J.; Ullah H.; Khan I.U.; Khan Y.; Shah S.A.A.
Published in Journal of Molecular Structure (2024)
“… and validates the possibility of these compounds as options for treating type-2 diabetes and Alzheimer's disease…”

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914

Synthesis, In Vitro Biological Evaluation and Molecular Modeling of Benzimidazole-Based Pyrrole/Piperidine Hybrids Derivatives as Potential Anti-Alzheimer Agents

by Tariq S.; Rahim F.; Ullah H.; Sarfraz M.; Hussain R.; Khan S.; Khan M.U.; Rehman W.; Hussain A.; Bhat M.A.; Farooqi M.K.; Shah S.A.A.; Iqbal N.
Published in Pharmaceuticals (2024)

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915

Synthesis, in vitro biological screening and docking study of benzo[d]oxazole bis Schiff base derivatives as a potent anti-Alzheimer agent

by Taha M.; Rahim F.; Zaman K.; Anouar E.H.; Uddin N.; Nawaz F.; Sajid M.; Khan K.M.; Shah A.A.; Wadood A.; Rehman A.U.; Alhibshi A.H.
Published in Journal of Biomolecular Structure and Dynamics (2023)
“… inhibitory potential than donepezil. Moreover, derivative 18 is the most potent one among the series in both…”

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916

Multipotent Cholinesterase Inhibitors for the Treatment of Alzheimer’s Disease: Synthesis, Biological Analysis and Molecular Docking Study of Benzimidazole-Based Thiazole Derivativ...

by Hussain R.; Ullah H.; Rahim F.; Sarfraz M.; Taha M.; Iqbal R.; Rehman W.; Khan S.; Shah S.A.A.; Hyder S.; Alhomrani M.; Alamri A.S.; Abdulaziz O.; Abdelaziz M.A.
Published in Molecules (2022)

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917

Synthesis of symmetrical bis-Schiff base-disulfide hybrids as highly effective anti-leishmanial agents

by Taha M.; Sain A.A.; Ali M.; Anouar E.H.; Rahim F.; Ismail N.H.; Adenan M.I.; Imran S.; Al-Harrasi A.; Nawaz F.; Iqbal N.; Khan K.M.
Published in Bioorganic Chemistry (2020)

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918

Synthesis, α-amylase inhibition and molecular docking study of bisindolylmethane sulfonamide derivatives

by Taha M.; Noreen T.; Imran S.; Nawaz F.; Chigurupati S.; Selvaraj M.; Rahim F.; Hadiani Ismail N.; Kumar A.; Mosaddik A.; Alghamdi A.M.; Abdulrahman nasser alqahtani Y.; Abdulrahman nasser alqahtani A.
Published in Medicinal Chemistry Research (2019)

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919

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions

by Taha M.; Ismail N.H.; Javaid K.; Imran S.; Anouar E.H.; Wadood A.; Atia-Tul-Wahab; Ali M.; Khan K.M.; Saad S.M.; Rahim F.; Choudhary M.I.
Published in Bioorganic Chemistry (2015)

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920

Synthesis, In Vitro Enzymatic Inhibition, and Molecular Modeling of Novel Piperazine-Based Bis-Schiff Base Derivatives as Promising Anti-urease Agents

by Masood, Najat; Hussain, Rafaqat; Khan, Shoaib; Rahim, Fazal; Mumtaz, Sundas; Taha, Muhammad; Abid, Obaid Ur Rahman; Iqbal, Tayyiaba; Shah, Syed Adnan Ali; Al Wesabi, Esam Omar; Magam, Seami M.
Published in CHEMISTRYSELECT (2024)

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