Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Mohd, Shahbaaz"'
Autor:
Mohd Yousuf, Parvez Khan, Anas Shamsi, Mohd Shahbaaz, Gulam Mustafa Hasan, Qazi Mohd Rizwanul Haque, Alan Christoffels, Asimul Islam, Md. Imtaiyaz Hassan
Publikováno v:
ACS Omega, Vol 5, Iss 42, Pp 27480-27491 (2020)
Externí odkaz:
https://doaj.org/article/029763e1410f4eac90b0b290955b7f4a
Autor:
Aleksey A. Vatlin, Egor A. Shitikov, Mohd Shahbaaz, Dmitry A. Bespiatykh, Ksenia M. Klimina, Alan Christoffels, Valery N. Danilenko, Dmitry A. Maslov
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
Tuberculosis (TB), caused by the Mycobacterium tuberculosis complex bacteria, is one of the most pressing health problems. The development of new drugs and new therapeutic regimens effective against the pathogen is one of the greatest challenges in t
Externí odkaz:
https://doaj.org/article/56fe4d7741e348d6b8b3a7799460730b
Autor:
Perumal Gobinath, Ponnusamy Packialakshmi, Kaliappillai Vijayakumar, Magda H. Abdellattif, Mohd Shahbaaz, Akbar Idhayadhulla, Radhakrishnan Surendrakumar
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Externí odkaz:
https://doaj.org/article/47cfab422a6e4c9f9f47772672f1b6c5
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
A rapid and increasing spread of COVID-19 pandemic disease has been perceived worldwide in 2020. The current COVID-19 disease outbreak is due to the spread of SARS-CoV-2. SARS-CoV-2 is a new strain of coronavirus that has spike protein on the envelop
Externí odkaz:
https://doaj.org/article/a437b8d2829e453082edc403213eff7c
Autor:
Perumal Gobinath, Ponnusamy Packialakshmi, Kaliappillai Vijayakumar, Magda H. Abdellattif, Mohd Shahbaaz, Akbar Idhayadhulla, Radhakrishnan Surendrakumar
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
This work investigated the interaction of indole with SARS-CoV-2. Indole is widely used as a medical material owing to its astounding biological activities. Indole and its derivatives belong to a significant category of heterocyclic compounds that ha
Externí odkaz:
https://doaj.org/article/3dd106f6f74f49c8ac5c163e3ac8e2cb
Publikováno v:
PLoS ONE, Vol 16, Iss 11 (2021)
Nicotinamide-nucleotide adenylyl transferase (Rv2421c) was selected as a potential drug target, because it has been shown, in vitro, to be essential for Mycobacterium tuberculosis growth. It is conserved between mycobacterium species, is up-regulated
Externí odkaz:
https://doaj.org/article/393aefbf68c04d198c9f8b1248274d9d
Autor:
Souleymane Diallo, Mohd Shahbaaz, Baldwyn Torto, Alan Christoffels, Daniel Masiga, Merid N. Getahun
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Insects that transmit many of the world’s deadliest animal diseases, for instance trypanosomosis, find their suitable hosts and avoid non-preferred hosts mostly through olfactory cues. The waterbuck repellent blend (WRB) comprising geranylacetone,
Externí odkaz:
https://doaj.org/article/29552c93cf394899abf8b42d4cbea670
Autor:
Mohd Shahbaaz, Dmitry A. Maslov, Aleksey A. Vatlin, Valery N. Danilenko, Maria Grishina, Alan Christoffels
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 333 (2022)
In the current era of a pandemic, infections of COVID-19 and Tuberculosis (TB) enhance the detrimental effects of both diseases in suffering individuals. The resistance mechanisms evolving in Mycobacterium tuberculosis are limiting the efficiency of
Externí odkaz:
https://doaj.org/article/8967a1cb602247fa8ab52d79eb7f859a
Publikováno v:
Molecules, Vol 26, Iss 18, p 5482 (2021)
In this study, we used oxazinethione as a perfect precursor to synthesize new pyrimidine and pyrazole derivatives with potent biological activities. Biological activities were determined for all compounds against A. flavus, E. coli, S. aureus, and F.
Externí odkaz:
https://doaj.org/article/04fcd14ad2614ee5a00c433e1d668f38
Autor:
Amena Ali, Magda H. Abdellattif, Abuzer Ali, Ola AbuAli, Mohd Shahbaaz, Mohamed Jawed Ahsan, Mostafa A. Hussien
Publikováno v:
Molecules, Vol 26, Iss 19, p 5932 (2021)
In the present in-silico study, various computational techniques were applied to determine potent compounds against TRAP1 kinase. The pharmacophore hypothesis DHHRR_1 consists of important features required for activity. The 3D QSAR study showed a st
Externí odkaz:
https://doaj.org/article/8db0e20b629f4f9686dea020b384b7e0