Nor Hadiani Ismail
Nor Hadiani Ismail
Professor of Chemistry, Universiti Teknologi Mara, Malaysia
Verified email at
TitleCited byYear
Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of Morinda elliptica
AM Ali, NH Ismail, MM Mackeen, LS Yazan, SM Mohamed, ASH Ho, ...
Pharmaceutical Biology 38 (4), 298-301, 2000
Antioxidant, radical-scavenging, anti-inflammatory, cytotoxic and antibacterial activities of methanolic extracts of some Hedyotis species
R Ahmad, AM Ali, DA Israf, NH Ismail, K Shaari, NH Lajis
Life Sciences 76 (17), 1953-1964, 2005
Antiviral and Cytotoxic Activities of Som. e Plants Used in Malaysian Indigenous Medicine
Pertanika J. Trop. Agric. Sci 19 (2/3), 129-136, 1996
Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies
M Taha, NH Ismail, S Lalani, MQ Fatmi, S Siddiqui, KM Khan, S Imran, ...
European journal of medicinal chemistry 92, 387-400, 2015
Analysis of essential oils of leaves, stems, flowers and rhizomes of Etlingera elatior (Jack) RM Smith
FM Jaafar, CP Osman, NH Ismail, K Awang
The Malaysian Journal of Analytical Sciences 11 (1), 269-273, 2007
Xanthones from Garcinia mangostana (Guttiferae)
GCL Ee, S Daud, YH Taufiq-Yap, NH Ismail, M Rahmani
Natural Product Research 20 (12), 1067-1073, 2006
Anthraquinones from Morinda elliptica
NH Ismail, AM Ali, N Aimi, M Kitajima, H Takayama, NH Lajis
Phytochemistry 45 (8), 1723-1725, 1997
The prediction of students’ academic performance using classification data mining techniques
F Ahmad, NH Ismail, AA Aziz
Applied Mathematical Sciences 9 (129), 6415-6426, 2015
Orang Asli in Peninsular Malaysia: population, spatial distribution and socio-economic condition
T Masron, F Masami, N Ismail
J Ritsumeikan Soc Sci Humanit 6, 75-115, 2013
Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors
M Taha, NH Ismail, S Imran, MQB Rokei, SM Saad, KM Khan
Bioorganic & medicinal chemistry 23 (15), 4155-4162, 2015
Comparison of reduced-intensity and myeloablative conditioning regimens for allogeneic hematopoietic stem cell transplantation in patients with acute myeloid leukemia and acute …
SF Abdul Wahid, NA Ismail, MR Mohd-Idris, FW Jamaluddin, NR Tumian, ...
Stem cells and development 23 (21), 2535-2552, 2014
Antioxidant properties of phenolic Schiff bases: structure–activity relationship and mechanism of action
S Raweh, I Bayach, M Taha, MS Baharudin, F Di Meo, MH Hasan, ...
Journal of computer-aided molecular design 27 (11), 951-964, 2013
Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities
M Taha, NH Ismail, W Jamil, H Rashwan, SM Kashif, AA Sain, MI Adenan, ...
European journal of medicinal chemistry 84, 731-738, 2014
Synthesis of novel bisindolylmethane Schiff bases and their antibacterial activity
S Imran, M Taha, N Ismail, K Khan, F Naz, M Hussain, S Tauseef
Molecules 19 (8), 11722-11740, 2014
Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica
A Wibowo, N Ahmat, AS Hamzah, AS Sufian, NH Ismail, R Ahmad, ...
Fitoterapia 82 (4), 676-681, 2011
Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth.(Rubiaceae)
CP Osman, NH Ismail, R Ahmad, N Ahmat, K Awang, FM Jaafar
Molecules 15 (10), 7218-7226, 2010
A modified toxicity testing method using tropical marine microalgae
M Ismail, SM Phang, SL Tong, MT Brown
Environmental monitoring and assessment 75 (2), 145-154, 2002
Synthesis crystal structure of 2-methoxybenzoylhydrazones and evaluation of their α-glucosidase and urease inhibition potential
M Taha, NH Ismail, MS Baharudin, S Lalani, S Mehboob, KM Khan, ...
Medicinal Chemistry Research 24 (3), 1310-1324, 2015
Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies
S Imran, M Taha, NH Ismail, SM Kashif, F Rahim, W Jamil, M Hariono, ...
European journal of medicinal chemistry 105, 156-170, 2015
4-Phenylcoumarins from Mesua elegans with acetylcholinesterase inhibitory activity
K Awang, G Chan, M Litaudon, NH Ismail, MT Martin, F Gueritte
Bioorganic & medicinal chemistry 18 (22), 7873-7877, 2010
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