Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Dhrubo Jyoti Sen"'
Publikováno v:
Food Hydrocolloids for Health, Vol 4, Iss , Pp 100163- (2023)
Oxidative stress is widely acknowledged as a key contributor to a wide range of human illness. Although certain aspects of signaling pathways are being studied, comprehensive metabolic pathways for illness have been identified. Antioxidant treatment
Externí odkaz:
https://doaj.org/article/6039894f7f564a34bf35c559110d2476
Publikováno v:
Carbohydrate Polymer Technologies and Applications, Vol 5, Iss , Pp 100321- (2023)
The present research intends at investigating the extraction and characterization of linseed polysaccharide to explore its haematocompatibility and antioxidant properties. In this research, a light brown colored, odorless, tasteless, and aqueous-solu
Externí odkaz:
https://doaj.org/article/a08352c0cac94fa28b22feb9d5248aee
Publikováno v:
Sensors International, Vol 3, Iss , Pp 100158- (2022)
Since past few years, a number of polysaccharides are being extracted from different herbal sources, which have already been investigated for biomedical activities. Nowadays, antioxidant activities of numerous herbal polysaccharides are being extensi
Externí odkaz:
https://doaj.org/article/4d3ed4ef7d054a66893c20b938823106
Publikováno v:
Journal of Biochemicals and Phytomedicine. 1:8-12
Introduction: A growing tendency to the administration of medicinal plants is observed because of their amazing influence on human health. Pharmaceutical and food industries recommend the use of medicinal plants due to their antioxidant properties. H
Autor:
null Sipra Banerjee, null Kushal Nandi, null R. Badmanaban, null Sudip Kumar Mandal, null Dhrubo Jyoti Sen, null Kishor Kumar Dholwani, null Dhananjoy Saha
Publikováno v:
International Journal of Science and Research Archive. 7:013-035
In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered by identifying the active ingredient from traditional remedies or by seren
Autor:
Anand Nayyar, Hanan Ahabrach, Nisrin El Mlili, Mohammed Errami, Mohamed Eddouks, Arash Khojasteh, Meng Liu, Lichao Ma, Rajesh Kumar Singh, Fei Sun , Guohe Li, Qi Zhang, Neda Izadi Mahboubeh Bouhlouli, Saurabh S Pandya, Mohammad Gholami, Shikha Sharma, Shweta Sharma, Vaishali Pathak, Parwinder Kaur, Rachna Jain Rajalakshmi Krishnamurthi, Surabhi Jain , Smriti Sharma, Dhrubo Jyoti Sen, Omar Cauli
Publikováno v:
Current Analytical Chemistry. 18:518-528
Background: Speciation analysis is defined as the analytical activities of identifying and/or measuring the quantities of one or more individual chemical species in a sample. The knowledge of elemental species provides more complete information about
Publikováno v:
INTERNATIONAL RESEARCH JOURNAL OF PHARMACY. 12:1-7
Activation of the oncogenes and inhibition of the apoptotic function of the p53 protein is a gateway for the cancer genesis. Interaction of the MDM2 protein with p53 protein is responsible for the inhibition of the p53 function. Inhibiting the p53-MD
Autor:
Dhananjoy Saha, Supradip Mandal, R Badmanaban, Susmita Basak, Arpita Biswas, Dhrubo Jyoti Sen
Publikováno v:
Research Journal of Pharmacy and Technology. :5540-5550
Most of us know turmeric (Curcuma longa) as the vibrant orange powder located in the spice section between thyme and vanilla beans. And many of us use turmeric root powder in our cooking, particularly if we have an affinity for preparing Indian–ins
Publikováno v:
Anti-Infective Agents. 20
Aim: To ascertain the binding manner and drug-likeliness profile of imidazo[1,2-a]pyridine derivatives as antitubercular agents on ATP synthase protein. Background: : Field-based 3D-QSAR, Homology modelling, Molecular Docking and ADME-T studies have
Publikováno v:
International Journal of Pharmaceutical Chemistry and Analysis. 8:41-44
MDM2 inhibitors class of anti-neoplastic drugs has been evolve after the successful discovery of the nutlins and other potent inhibitors. MDM2 inhibitors can specifically target the tumour cells in the body, by selectively reactivating the inhibited