Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Emmanuel A. Iwuchukwu"'
Autor:
Uchechukwu C. Ogbodo, Ojochenemi A. Enejoh, Chinelo H. Okonkwo, Pranavathiyani Gnanasekar, Pauline W. Gachanja, Shamim Osata, Halimat C. Atanda, Emmanuel A. Iwuchukwu, Ikechukwu Achilonu, Olaitan I. Awe
Publikováno v:
Frontiers in Chemistry, Vol 11 (2023)
Introduction: Despite improved treatment options, colorectal cancer (CRC) remains a huge public health concern with a significant impact on affected individuals. Cell cycle dysregulation and overexpression of certain regulators and checkpoint activat
Externí odkaz:
https://doaj.org/article/cbb31e45095f490c8bd27b27a8c27c35
Publikováno v:
African Journal of Hospitality, Tourism and Leisure, Vol 8, Iss special edition (2019)
Given the fact that South Africa is one of the global emerging markets, many of the emerging small businesses are transiting from informal to formal businesses. The importance and contribution of these ventures in economic growth and job creation can
Externí odkaz:
https://doaj.org/article/4fff3938324c47c5aea94f868cd97d17
Publikováno v:
Computational Biology and Chemistry. 104:107851
Autor:
Olamide Jeje, Reabetswe Maake, Ruan van Deventer, Veruschka Esau, Emmanuel Amarachi Iwuchukwu, Vanessa Meyer, Thandeka Khoza, Ikechukwu Achilonu
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 116
International Journal of Molecular Sciences, Vol 23, Iss 116, p 116 (2022)
International Journal of Molecular Sciences, Vol 23, Iss 116, p 116 (2022)
The continuous threat of drug-resistant Klebsiella pneumoniae justifies identifying novel targets and developing effective antibacterial agents. A potential target is nicotinate nucleotide adenylyltransferase (NNAT), an indispensable enzyme in the bi
Autor:
Clement Agoni, Fisayo A. Olotu, Emmanuel A. Iwuchukwu, Kehinde F. Omolabi, Mahmoud E. S. Soliman
Publikováno v:
Journal of Molecular Modeling. 27
Compound P131 has been established to inhibit Cryptosporidium parvum's inosine monophosphate dehydrogenase (CpIMPDH). Its inhibitory activity supersedes that of paromomycin, which is extensively used in treating cryptosporidiosis. Through the per-res
Autor:
Kehinde F, Omolabi, Emmanuel A, Iwuchukwu, Clement, Agoni, Fisayo A, Olotu, Mahmoud E S, Soliman
Publikováno v:
Journal of molecular modeling. 27(2)
Compound P131 has been established to inhibit Cryptosporidium parvum's inosine monophosphate dehydrogenase (CpIMPDH). Its inhibitory activity supersedes that of paromomycin, which is extensively used in treating cryptosporidiosis. Through the per-res
Publikováno v:
Computational biology and chemistry. 90
Most notable Kinetoplastids are of the genus Trypanosoma and Leishmania, affecting several millions of humans in Africa and Latin America. Current therapeutic options are limited by several drawbacks, hence the need to develop more efficacious inhibi
Autor:
Ikechukwu Achilonu, Emmanuel Amarachi Iwuchukwu, Okechinyere Juliet Achilonu, Manuel Antonio Fernandes
The SARS-CoV-2 main protease (Mpro) is an attractive target towards discovery of drugs to treat COVID-19 because of its key role in virus replication. The atomic structure of Mpro in complex with an α-ketoamide inhibitor (Lig13b) is available (PDB I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30b5d1f2e2de9f334090681c42ef72c9
https://doi.org/10.21203/rs.3.rs-30382/v1
https://doi.org/10.21203/rs.3.rs-30382/v1
Autor:
Collins U. Ibeji, Joyce Oloaigbe Ogidigo, Emmanuel A. Iwuchukwu, Mahmoud E. S. Soliman, Okiemute Ajiroghene Okpalefe
Publikováno v:
Journal of Biomolecular Structure and Dynamics
Journal of Biomolecular Structure & Dynamics
article-version (VoR) Version of Record
Journal of Biomolecular Structure & Dynamics
article-version (VoR) Version of Record
At present, there is no cure or vaccine for the devastating new highly infectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that has affected people globally. Herein, we identified potent phytocompounds from two antiviral plants Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862af6a5c022fac38ccda60ae1eaed63
Publikováno v:
Journal of Molecular Structure. 1223:128892
The inhibition of the 26-kDa glutathione transferase from Schistosoma japonicum (Sj26GST) by bromosulfophthalein (BSP) and indanaloxyacetic acid-94 (IAA-94) was investigated using a systematic combination of empirical and theoretical approaches. Acti