Tiyyaba Furqan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Tiyyaba Furqan has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
Abid Ali Khan
Department of Biosciences, Comsats University, Islamabad campus, Pakistan
1 shared publication- Ahmed Hassan Al-Marzouqi
Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain 15551, United Arab Emirates
1 shared publication - Alya A. Arabi
Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box: 15551, Al Ain, United Arab Emirates
1 shared publication Amira Bekdash
Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box: 15551, Al Ain, United Arab Emirates
1 shared publication- Eugenie Nepovimova
Department of Chemistry, Faculty of Science, University of Hradec Kralove
1 shared publication - Ferenc Darvas
ComInnex Inc., 1031 Budapest, Hungary
1 shared publication
Latest Publications
- Open Access
- 10 October 2025
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 301, 118074
BRITE-338733: From RecA inhibition to cancer treatment
- 10 October 2025
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 301, 118074
Open AccessBRITE-338733: From RecA inhibition to cancer treatment
- Open Access
- 28 May 2021
- Published by Science Repository OU in Neurology and Neurobiology
- Vol. 2021 (2) , 1-6
In silico Analysis of Alkaloids for Therapeutic Use in Treatment of Alzheimer's Disease by Targeting Acetylcholinesterase Enzyme
Alzheimer’s is a progressive mental deterioration associated with the degeneration of the cognition activities and memory loss. It is considered to be a multifactorial disease. One of the causes of the Alzheimer’s disease is the low concentration of the neurotransmitter named acetylcholine (ACh) at the synaptic cleft. Thus, inhibitor of Acetylcholinesterase (AChE), an enzyme whose function is to degrade the acetylcholine, is proved to be a promising candidate to treat this disease. Among the inhibitors are the natural alkaloids that also have an inhibitory effect on the AChE. In this study we have focused on the simple derivates of beta carbolime (a group of alkaloids) and studied their interaction with AChE via rigid protein-ligand docking approach.
- 28 May 2021
- Published by Science Repository OU in Neurology and Neurobiology
- Vol. 2021 (2) , 1-6
Open AccessIn silico Analysis of Alkaloids for Therapeutic Use in Treatment of Alzheimer's Disease by Targeting Acetylcholinesterase Enzyme
Alzheimer’s is a progressive mental deterioration associated with the degeneration of the cognition activities and memory loss. It is considered to be a multifactorial disease. One of the causes of the Alzheimer’s disease is the low concentration of the neurotransmitter named acetylcholine (ACh) at the synaptic cleft. Thus, inhibitor of Acetylcholinesterase (AChE), an enzyme whose function is to degrade the acetylcholine, is proved to be a promising candidate to treat this disease. Among the inhibitors are the natural alkaloids that also have an inhibitory effect on the AChE. In this study we have focused on the simple derivates of beta carbolime (a group of alkaloids) and studied their interaction with AChE via rigid protein-ligand docking approach.
- Open Access
- 13 May 2020
- Published by MDPI AG in Biomolecules
- Vol. 10 (5) , 758
Cannabis Constituents and Acetylcholinesterase Interaction: Molecular Docking, In Vitro Studies and Association with CNR1 rs806368 and ACHE rs17228602
The study documented here was aimed to find the molecular interactions of some of the cannabinoid constituents of cannabis with acetylcholinesterase (AChE). Molecular docking and LogP determination were performed to predict the AChE inhibitory effect and lipophilicity. AChE enzyme activity was measured in the blood of cannabis addicted human subjects. Further, genetic predisposition to cannabis addiction was investigated by association analysis of cannabinoid receptor 1 (CNR1) single nucleotide polymorphism (SNP) rs806368 and ACHE rs17228602 using restriction fragment length polymorphism (RFLP) method. All the understudied cannabis constituents showed promising binding affinities with AChE and are lipophilic in nature. The AChE activity was observed to be indifferent in cannabis addicted and non-addicted healthy controls. There was no significant association with CNR1 SNP rs806368 and ACHE rs17228602. The study concludes that in silico prediction for individual biomolecules of cannabis is different from in vivo physiological action in human subjects when all are present together. However, for a deeper mechanistic insight into these interactions and association, multi-population studies are suggested. Further studies to explore the inhibitory potential of different cannabis constituents for intended AChE inhibitor-based drug are warranted.
- 13 May 2020
- Published by MDPI AG in Biomolecules
- Vol. 10 (5) , 758
Open AccessCannabis Constituents and Acetylcholinesterase Interaction: Molecular Docking, In Vitro Studies and Association with CNR1 rs806368 and ACHE rs17228602
The study documented here was aimed to find the molecular interactions of some of the cannabinoid constituents of cannabis with acetylcholinesterase (AChE). Molecular docking and LogP determination were performed to predict the AChE inhibitory effect and lipophilicity. AChE enzyme activity was measured in the blood of cannabis addicted human subjects. Further, genetic predisposition to cannabis addiction was investigated by association analysis of cannabinoid receptor 1 (CNR1) single nucleotide polymorphism (SNP) rs806368 and ACHE rs17228602 using restriction fragment length polymorphism (RFLP) method. All the understudied cannabis constituents showed promising binding affinities with AChE and are lipophilic in nature. The AChE activity was observed to be indifferent in cannabis addicted and non-addicted healthy controls. There was no significant association with CNR1 SNP rs806368 and ACHE rs17228602. The study concludes that in silico prediction for individual biomolecules of cannabis is different from in vivo physiological action in human subjects when all are present together. However, for a deeper mechanistic insight into these interactions and association, multi-population studies are suggested. Further studies to explore the inhibitory potential of different cannabis constituents for intended AChE inhibitor-based drug are warranted.
- Open Access
- 1 October 2019
- Published by ResearchersLinks Ltd in Novel Research in Microbiology Journal
- Vol. 3 (5) , 464-470
Microalgae as sources of biofuel production through waste water treatment
The shortage of fuel in the near future and the change in climate due to greenhouse gases are serious challenges of a global concern, thus it is imperious to explore new sustainable ways to overwhelm these challenges. The need of a new sustainable energy sources has increased the importance of the third generation biofuel produced from non-food stocks such as algae, which possibly represent a great opportunity in the long term. The major challenge of the algae based bio-fuel production is their extraordinary cultivation costs, which make their commercialization economically infeasible. Algal spp. especially Chlorella spp. are capable of thriving in waste water and can accumulate high lipid contents. The aim of the current review was to highlight the possible integration of waste water treatment and algae based bio-fuel production, as a sustainable option for cost effective bio-fuel production along with lower environmental impact.
- 1 October 2019
- Published by ResearchersLinks Ltd in Novel Research in Microbiology Journal
- Vol. 3 (5) , 464-470
Open AccessMicroalgae as sources of biofuel production through waste water treatment
The shortage of fuel in the near future and the change in climate due to greenhouse gases are serious challenges of a global concern, thus it is imperious to explore new sustainable ways to overwhelm these challenges. The need of a new sustainable energy sources has increased the importance of the third generation biofuel produced from non-food stocks such as algae, which possibly represent a great opportunity in the long term. The major challenge of the algae based bio-fuel production is their extraordinary cultivation costs, which make their commercialization economically infeasible. Algal spp. especially Chlorella spp. are capable of thriving in waste water and can accumulate high lipid contents. The aim of the current review was to highlight the possible integration of waste water treatment and algae based bio-fuel production, as a sustainable option for cost effective bio-fuel production along with lower environmental impact.