Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Nishal Parbhoo"'
Autor:
Thandeka Moyo-Gwete, Frances Ayres, Nonkululeko B. Mzindle, Zanele Makhado, Nelia P. Manamela, Simone I. Richardson, Dale Kitchin, Strauss van Graan, Joritha van Heerden, Nishal Parbhoo, Gerald K. Chege, Penny L. Moore
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract African Green (Vervet) monkeys have been extensively studied to understand the pathogenesis of infectious diseases. Using vervet monkeys as pre-clinical models may be an attractive option for low-resourced areas as they are found abundantly
Externí odkaz:
https://doaj.org/article/30ec06a32f9b4efdab78102e98d23a75
Publikováno v:
Bioinformatics and Biology Insights, Vol 12 (2018)
Orbiviruses are double-stranded RNA viruses that have profound economic and veterinary significance, 3 of the most important being African horse sickness virus (AHSV), bluetongue virus (BTV), and epizootic hemorrhagic disease virus (EHDV). Currently,
Externí odkaz:
https://doaj.org/article/7437179d06dd48718ff3caa5efcf515c
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 9, p 2552 (2018)
A series of 2-arylbenzo[c]furan-chalcone hybrids 3a–y have been synthesized and evaluated for antiproliferative effects against the human breast cancer (MCF-7) cell line and for its potential to induce apoptosis and also to inhibit tubulin polymeri
Externí odkaz:
https://doaj.org/article/1963383a75c948d8aaec4f0586ae5e0a
Autor:
Malose J. Mphahlele, Nishal Parbhoo
Publikováno v:
Pharmaceuticals, Vol 11, Iss 2, p 59 (2018)
The 3-trifluoroacetyl–substituted 7-acetamido-2-aryl-5-bromoindoles 5a–h were prepared and evaluated for potential antigrowth effect in vitro against human lung cancer (A549) and cervical cancer (HeLa) cells and for the potential to inhibit tubul
Externí odkaz:
https://doaj.org/article/1dd76f389fd24a2db81a048f824dc2fc
Publikováno v:
Molecules, Vol 22, Iss 11, p 1719 (2017)
In this paper, we describe the synthesis of the 5-styryltetrazolo[1,5-c]quinazolines substituted at the 9-position with a 4-fluorophenyl ring directly or via a conjugated π-spacer (C=C or C≡C bond) based on the 6-bromo-4-chloro-2-styrylquinazoline
Externí odkaz:
https://doaj.org/article/da0bc1575ecd4c87a13d1aaa57408164
Publikováno v:
Europe PubMed Central
Rotavirus is the major cause of severe virus-associated gastroenteritis worldwide in children aged 5 and younger. Many children lose their lives annually due to this infection and the impact is particularly pronounced in developing countries. The mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55a4f634ae3ea450c8db04c7c4553d64
https://doi.org/10.4149/av_2016_03_260
https://doi.org/10.4149/av_2016_03_260
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 9, p 2552 (2018)
International Journal of Molecular Sciences
Volume 19
Issue 9
International Journal of Molecular Sciences
Volume 19
Issue 9
A series of 2-arylbenzo[c]furan-chalcone hybrids 3a&ndash
y have been synthesized and evaluated for antiproliferative effects against the human breast cancer (MCF-7) cell line and for its potential to induce apoptosis and also to inhibit tubulin
y have been synthesized and evaluated for antiproliferative effects against the human breast cancer (MCF-7) cell line and for its potential to induce apoptosis and also to inhibit tubulin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88d5c45d512e887b31cf07a39014071e
http://www.mdpi.com/1422-0067/19/9/2552
http://www.mdpi.com/1422-0067/19/9/2552
Autor:
Malose J. Mphahlele, Nishal Parbhoo
Structurally related 7-acetyl-2-aryl-5-bromoindoles 2a–d and the 7-acetamido-2-aryl-5-bromoindoles 4a–d as well as their corresponding 3-trifluoroacetyl–substituted derivatives 5a–d and 5e–h were evaluated for potential antigrowth effect in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9933a02682758382c1b83e35bdcdcde
https://doi.org/10.20944/preprints201805.0085.v1
https://doi.org/10.20944/preprints201805.0085.v1
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 22; Issue 11; Pages: 1719
Molecules, Vol 22, Iss 11, p 1719 (2017)
Molecules; Volume 22; Issue 11; Pages: 1719
Molecules, Vol 22, Iss 11, p 1719 (2017)
In this paper, we describe the synthesis of the 5-styryltetrazolo[1,5-c]quinazolines substituted at the 9-position with a 4-fluorophenyl ring directly or via a conjugated π-spacer (C=C or C≡C bond) based on the 6-bromo-4-chloro-2-styrylquinazoline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e235f93e5ff331bd5a907a9ab81d5fb9
http://europepmc.org/articles/PMC6150304
http://europepmc.org/articles/PMC6150304
Autor:
Nishal Parbhoo, Malose J. Mphahlele
Publikováno v:
Pharmaceuticals
Volume 11
Issue 2
Pharmaceuticals, Vol 11, Iss 2, p 59 (2018)
Volume 11
Issue 2
Pharmaceuticals, Vol 11, Iss 2, p 59 (2018)
The 3-trifluoroacetyl&ndash
substituted 7-acetamido-2-aryl-5-bromoindoles 5a&ndash
h were prepared and evaluated for potential antigrowth effect in vitro against human lung cancer (A549) and cervical cancer (HeLa) cells and for the potentia
substituted 7-acetamido-2-aryl-5-bromoindoles 5a&ndash
h were prepared and evaluated for potential antigrowth effect in vitro against human lung cancer (A549) and cervical cancer (HeLa) cells and for the potentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dc196103c286fede52ede47bb5b05f4
https://doi.org/10.3390/ph11020059
https://doi.org/10.3390/ph11020059