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801

Synthesis and in vitro study of benzofuran hydrazone derivatives as novel alpha-amylase inhibitor

by Taha M.; Shah S.A.A.; Imran S.; Afifi M.; Chigurupati S.; Selvaraj M.; Rahim F.; Ullah H.; Zaman K.; Vijayabalan S.
Published in Bioorganic Chemistry (2017)
“…The α-amylase acts as attractive target to treat type-2 diabetes mellitus. Therefore in discovering…”

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802

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors

by Taha M.; Ismail N.H.; Imran S.; Selvaraj M.; Rashwan H.; Farhanah F.U.; Rahim F.; Kesavanarayanan K.S.; Ali M.
Published in Bioorganic Chemistry (2015)
“… have IC50 values ranging between 4.48 and 46.12 μM and showing better than standard d-saccharic acid…”

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803

Combined PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis

by Philip N.; Affendy N.B.; Masri S.N.; Muhamad Y.Y.; Than L.T.L.; Sekawi Z.; Neela V.K.
Published in PLoS ONE (2020)
“… gene in 63 (38%) patients. The use of more than one target gene for PCR increased the detection rates…”

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804

Syuf'ah in Islamic laws and its significance under the land law of Malaysia

by Taha M.M.; Awang M.B.; Sulong J.; Ruzulan Z.; Mohamed A.; Jusoh M.K.A.; Ayub M.N.
Published in Journal of Social Sciences Research (2019)

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805

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

by Khan K.M.; Qurban S.; Salar U.; Taha M.; Hussain S.; Perveen S.; Hameed A.; Ismail N.H.; Riaz M.; Wadood A.
Published in Bioorganic Chemistry (2016)

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806

2-(2′-Pyridyl) benzimidazole derivatives and their urease inhibitory activity

by Saify Z.S.; Kamil A.; Akhtar S.; Taha M.; Khan A.; Khan K.M.; Jahan S.; Rahim F.; Perveen S.; Choudhary M.I.
Published in Medicinal Chemistry Research (2014)
“… inhibition comparable to thiourea (IC50 = 21.00 ± 0.01 μM) and twofold more active than acetohydroxamic acid…”

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807

Synthesis, evaluation of antioxidant activity and crystal structure of 2,4-dimethylbenzoylhydrazones

by Taha M.; Ismail N.H.; Jamil W.; Yousuf S.; Jaafar F.M.; Ali M.I.; Kashif S.M.; Hussain E.
Published in Molecules (2013)
“… values of 25.6, 28.1, 29.3, 29.8, 30.0 and 30.1 μM respectively, showing better activity than an n-propyl…”

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808

Chemical and pharmacognostical characterization of two Malaysian plants both known as Ajisamat

by Mohamad T.A.S.T.; Naz H.; Jalal R.S.; Hussin K.; Rahman M.R.A.; Adam A.; Weber J.-F.F.
Published in Revista Brasileira de Farmacognosia (2013)

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809

Addressing preliminary challenges in upscaling the recovery of lithium from spent lithium ion batteries by the electrochemical method: a review

by Kasri, Mohamad Arif; Mohd Halizan, Muhammad Zharfan; Harun, Irina; Bahrudin, Fadzli Irwan; Daud, Nuraini; Aizamddin, Muhammad Faiz; Amira Shaffee, Siti Nur; Rahman, Norazah Abd; Shafiee, Saiful Arifin; Mahat, Mohd Muzamir
Published in RSC ADVANCES (2024)

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810

Cooking oil waste from AYAMAS as a carbon source in forming multilayer graphene films

by Nurfazianawatie M.Z.; Omar H.; Rosman N.F.; Malek N.S.A.; Afaah A.N.; Buniyamin I.; Salifairus M.J.; Malek M.F.; Mahat M.M.; Rusop M.; Asli N.A.
Published in Energy Sources, Part A: Recovery, Utilization and Environmental Effects (2023)
“… spectroscopy analysis of the graphene obtained revealed an I2D/IG ratio of less than 0.5, indicating its…”

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811

Forming multilayer graphene at different precursor temperature using cooking oil waste from AYAMAS via chemical vapour deposition

by Nurfazianawatie M.Z.; Omar H.; Rosman N.F.; S. A. Malek N.; Afaah A.N.; Buniyamin I.; Salifairus M.J.; Malek M.F.; Mahat M.M.; Rusop M.; Asli N.A.
Published in Materials Today: Proceedings (2023)

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812

Addressing preliminary challenges in upscaling the recovery of lithium from spent lithium ion batteries by the electrochemical method: a review

by Kasri M.A.; Mohd Halizan M.Z.; Harun I.; Bahrudin F.I.; Daud N.; Aizamddin M.F.; Amira Shaffee S.N.; Rahman N.A.; Shafiee S.A.; Mahat M.M.
Published in RSC Advances (2024)

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813

Synthesis, β-Glucuronidase Inhibition, and Molecular Docking Studies of 1,2,4-Triazole Hydrazones

by Jamil W.; Kumari D.; Taha M.; Khan M.N.; Baharudin M.S.; Ali M.; Kanwal M.; Lashari M.S.; Khan K.M.
Published in Journal of the Iranian Chemical Society (2018)
“… remarkable activity and found to be far more potent than the standard d-saccharic acid 1,4-lactone (IC50…”

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814

Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies

by Taha M.; Ismail N.H.; Lalani S.; Fatmi M.Q.; Atia-Tul-Wahab; Siddiqui S.; Khan K.M.; Imran S.; Choudhary M.I.
Published in European Journal of Medicinal Chemistry (2015)

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815

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors

by Ali F.; Khan K.M.; Salar U.; Iqbal S.; Taha M.; Ismail N.H.; Perveen S.; Wadood A.; Ghufran M.; Ali B.
Published in Bioorganic and Medicinal Chemistry (2016)
“…) found to be more potent than the standard D-saccharic acid 1,4-lactone (IC50 = 48.4 ± 1.25 μM…”

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816

Bis(indolyl)methanes synthesis through sodium iodate and sodium hydrogen sulfite in water

by Khan K.M.; Rahim F.; Shah S.A.A.; Taha M.; Ismail N.H.; Manzoor M.; Miana G.A.; Perveen S.
Published in Journal of the Chemical Society of Pakistan (2015)

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817

Synthesis and structure-activity relationship of thiobarbituric acid derivatives as potent inhibitors of urease

by Khan K.M.; Rahim F.; Khan A.; Shabeer M.; Hussain S.; Rehman W.; Taha M.; Khan M.; Perveen S.; Choudhary M.I.
Published in Bioorganic and Medicinal Chemistry (2014)
“… ± 0.18 μM, respectively, much better than the standard urease inhibitor thiourea (IC50 = 21 ± 0.11 μM…”

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818

Relationship of screen time with anxiety, depression, and sleep quality among adolescents: a cross-sectional study

by Mohd Saat N.Z.; Hanawi S.A.; Hanafiah H.; Ahmad M.; Farah N.M.F.; Abdul Rahman N.A.A.
Published in Frontiers in Public Health (2024)
“… of these relationships and investigate potential intervention strategies. Copyright © 2024 Mohd Saat, Hanawi, Hanafiah…”

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819

Discovering biological efficacy of new thiadiazole as effective inhibitors of urease, glycation, and (DPPH) scavengers: Biochemical and in silico study

by Taha M.; Imran S.; Rahim F.; Uddin N.; Iqbal N.; Khan K.M.; Farooq R.K.; Alomari M.; Islam I.; Algheribe S.
Published in Journal of Molecular Structure (2023)

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820

Synthesis and Molecular Docking of New Bis-Thiazolidinone-Based Chalcone Analogs as Effective Inhibitors of Acetylcholinesterase and Butyrylcholinesterase

by Hussain R.; Rahim F.; Rehman W.; Taha M.; Khan S.; Zaman K.; Adnan Ali Shah S.; Wadood A.; Imran S.; Abdellatif M.H.
Published in Chemistry and Biodiversity (2022)
“… a better selectivity index (2.60) than standard Donepezil drug (2.083) for AChE over BuChE…”

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