Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lois Muiva-Mutisya"'
Autor:
Yoseph Atilaw, Lois Muiva-Mutisya, Albert Ndakala, Hoseah M. Akala, Redemptah Yeda, Yu J. Wu, Paolo Coghi, Vincent K. W. Wong, Máté Erdélyi, Abiy Yenesew
Publikováno v:
Molecules, Vol 22, Iss 9, p 1514 (2017)
Four new flavones with modified prenyl groups, namely (E)-5-hydroxytephrostachin (1), purleptone (2), (E)-5-hydroxyanhydrotephrostachin (3), and terpurlepflavone (4), along with seven known compounds (5–11), were isolated from the CH2Cl2/MeOH (1:1)
Externí odkaz:
https://doaj.org/article/2b70d6a40e61495a9188a90f65a0f522
Autor:
Yoseph Atilaw, Sandra Duffy, Matthias Heydenreich, Lois Muiva-Mutisya, Vicky M. Avery, Máté Erdélyi, Abiy Yenesew
Publikováno v:
Molecules, Vol 22, Iss 2, p 318 (2017)
In our search for new antiplasmodial agents, the CH2Cl2/CH3OH (1:1) extract of the roots of Tephrosia aequilata was investigated, and observed to cause 100% mortality of the chloroquine-sensitive (3D7) strain of Plasmodium falciparum at a 10 mg/mL co
Externí odkaz:
https://doaj.org/article/5da01b3e7f1f478489d2a77151c0ec36
Autor:
Atilaw, Yoseph, Lois, Muiva-Mutisya, Bogaerts, Jonathan, Duffy, Sandra, Arto Valkonen, Heydenreich, Matthias, Avery, Vicky M., Rissanen, Kari, Erdelyi, Mate, Yenesew, Abiy
NMReDATA for compound 1-5, and FIDs for all compounds in the publication "Prenylated Flavonoids from the roots of Tephroisa rhodesica". MS and X-ray data.
NMReDATA files for compounds 1-5
NMReDATA files for compounds 1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50ff0a9b1f566de8aeeba8d85c6fc154
Autor:
Jonathan Bogaerts, Yoseph Atilaw, Lois Muiva-Mutisya, Máté Erdélyi, Kari Rissanen, Matthias Heydenreich, Arto Valkonen, Abiy Yenesew, Sandra Duffy, Vicky M. Avery
Publikováno v:
Journal of natural products
Journal of Natural Products
Journal of Natural Products
Five new compounds—rhodimer (1), rhodiflavan A (2), rhodiflavan B (3), rhodiflavan C (4), and rhodacarpin (5)—along with 16 known secondary metabolites, were isolated from the CH2Cl2–CH3OH (1:1) extract of the roots of Tephrosia rhodesica. They
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34273d50e7db1be1fbe9ac42237584e7
http://urn.fi/URN:NBN:fi:jyu-202008175553
http://urn.fi/URN:NBN:fi:jyu-202008175553
Autor:
Yenesew, Yoseph Atilaw, Lois Muiva-Mutisya, Albert Ndakala, Hoseah Akala, Redemptah Yeda, Yu Wu, Paolo Coghi, Vincent Wong, Máté Erdélyi, Abiy
Publikováno v:
Molecules; Volume 22; Issue 9; Pages: 1514
Four new flavones with modified prenyl groups, namely (E)-5-hydroxytephrostachin (1), purleptone (2), (E)-5-hydroxyanhydrotephrostachin (3), and terpurlepflavone (4), along with seven known compounds (5–11), were isolated from the CH2Cl2/MeOH (1:1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::a066d11fdef75677ba011995a744d150
Autor:
Lois Muiva-Mutisya, Matthias Heydenreich, Máté Erdélyi, Abiy Yenesew, Sandra Duffy, Yoseph Atilaw, Vicky M. Avery
Publikováno v:
Molecules; Volume 22; Issue 2; Pages: 318
Molecules, Vol 22, Iss 2, p 318 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 2, p 318 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
In our search for new antiplasmodial agents, the CH2Cl2/CH3OH (1:1) extract of the roots of Tephrosia aequilata was investigated, and observed to cause 100% mortality of the chloroquine-sensitive (3D7) strain of Plasmodium falciparum at a 10 mg/mL co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ba6b50dc156f9b376425c3aa68be3c
Autor:
Solomon Derese, Agnes C. Cheruiyot, Matthew L. Brown, Beatrice Irungu, Matthias Heydenreich, Lois Muiva-Mutisya, Charles Mutai, Abiy Yenesew, Andreas Koch, Yoseph Atilaw, Faith A. Okalebo, Hoseah M. Akala
The CH2Cl2/MeOH (1:1) extract of the aerial parts of Tephrosia subtriflora afforded a new flavanonol, named subtriflavanonol (1), along with the known flavanone spinoflavanone B, and the known flavanonols MS-II (2) and mundulinol. The structures were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cd9e1564d7aea9dc682068dbb3c7b05
Autor:
Matthias Heydenreich, Andreas Koch, Bernard Macharia, Lois Muiva-Mutisya, Amir O. Yusuf, Leonidah Kerubo Omosa, Solomon Derese, Abiy Yenesew, Hoseah M. Akala, Edwin Kamau
The CH2Cl2/MeOH (1: 1) extract of the roots of Tephrosia villosa showed good antiplasmodial activity against the chloroquine-sensitive (D6) and chloroquine-resistant (W2) strains of Plasmodium falciparum with IC50 values of 3.1 +/- 0.4 and 1.3 +/- 0.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb22618bb0462ea24cb4fff3c27c15fd
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/37317
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/37317