Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Jean, Fotie"'
Publikováno v:
Tetrahedron Green Chem, Vol 2, Iss , Pp 100027- (2023)
The cooperative activity of two proximal metal ions is well-known to exhibit highly efficient and synergistic catalytic activities in living organisms. Owing to this knowledge, tandem Cu–Zn systems have been widely used to catalyze a diversity of c
Externí odkaz:
https://doaj.org/article/53c0766727a64a9e846675484079f1f6
Autor:
Jean Fotie
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 1, p 641 (2024)
As mortality rates for other leading causes of death, such as stroke and coronary heart disease, decline in many parts of the world, cancer is becoming the leading cause of death worldwide, with the number of yearly new cases expected to rise to abou
Externí odkaz:
https://doaj.org/article/70497a9c818147958b2441031537c96a
Autor:
Jean Fotie, Caitlyn M. Matherne, Jasmine B. Mather, Jordan E. Wroblewski, Khaitlynn Johnson, Lara G. Boudreaux, Alba A. Perez
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 23, p 16854 (2023)
The present review explores the critical role of oxime and oxime ether moieties in enhancing the physicochemical and anticancer properties of structurally diverse molecular frameworks. Specific examples are carefully selected to illustrate the distin
Externí odkaz:
https://doaj.org/article/7ac837801f5f4d6888a227fbc1b4cf41
Autor:
Tithi Roy, Samuel T. Boateng, Sergette Banang-Mbeumi, Pankaj K. Singh, Pratik Basnet, Roxane-Cherille N. Chamcheu, Federico Ladu, Isabel Chauvin, Vladimir S. Spiegelman, Ronald A. Hill, Konstantin G. Kousoulas, Bolni Marius Nagalo, Anthony L. Walker, Jean Fotie, Siva Murru, Mario Sechi, Jean Christopher Chamcheu
Publikováno v:
Data in Brief, Vol 35, Iss , Pp 106858- (2021)
This article contains supplemental datasets of the recently published related research article “Synthesis, Inverse Docking-Assisted Identification and in vitro Biological Characterization of Flavonol-based Analogs of Fisetin as c-Kit, CDK2 and mTOR
Externí odkaz:
https://doaj.org/article/8f9eb6ff82c7476a93275e6a6773652e
Autor:
Julio Issah Mawouma, Pagna, Tengu, Awazi, Paul Etoga, Mbarga, Ines Michèle Kanko, Mbekou, Pierre, Mkounga, Jean, Fotie, Marcel, Frese, Fekam Boyom, Fabrice, Bruno Ndjakou, Lenta, Norbert, Sewald, Ephrem Augustin, Nkengfack
Publikováno v:
Journal of Asian natural products research. 24(11)
As part of our search for new secondary metabolites from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09dcb595cd24e960218dde4cc0948f91
https://pubmed.ncbi.nlm.nih.gov/34984935
https://pubmed.ncbi.nlm.nih.gov/34984935
Autor:
Samuel T. Boateng, Tithi Roy, Mercy E. Agbo, Sergette Banang-Mbeumi, Roxane-Cherille N. Chamcheu, Marion Bramwell, Long K. Pham, Keith E. Jackson, Ronald A. Hill, Bolni Marius Nagalo, Tatiana Efimova, Jean Fotie, Jean Christopher Chamcheu
Publikováno v:
SSRN Electronic Journal.
Melanoma and non-melanoma skin cancers are the most-lethal and commonest forms of skin cancers, that affecting one-fifth of the US population. With the aim of identifying new lead compounds as starting point for attaining cost-effective therapies, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d84360d32b18e7137c113c778231643
https://doi.org/10.2139/ssrn.4102562
https://doi.org/10.2139/ssrn.4102562
Autor:
Julio Issah Mawouma Pagna, Tengu Awazi, Paul Etoga Mbarga, Ines Michèle Kanko Mbekou, Pierre Mkounga, Jean Fotie, Marcel Frese, Fekam Boyom Fabrice, Bruno Ndjakou Lenta, Norbert Sewald, Ephrem Augustin Nkengfack
As part of our search for new secondary metabolites from Macaranga hurifolia Beille, a phytochemical investigation was carried out on the fruits that led to the isolation and characterization of two new prenylated flavonol derivatives named macafolia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed09dc9d195cc8f9365a6d9a8366b4fc
https://doi.org/10.1080/10286020.2021.2019223
https://doi.org/10.1080/10286020.2021.2019223
Publikováno v:
Tetrahedron Letters. 60:1636-1639
Silylated derivatives of oximes are important intermediates in organic synthesis, and have found application in the preparation of various nitrogen containing compounds including nitriles, amines, nitrones, and hydroxylamines. An efficient method for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97a8e70486817ca779a7c34bb1827168
https://doi.org/10.1016/j.tetlet.2019.05.033
https://doi.org/10.1016/j.tetlet.2019.05.033
Autor:
Pankaj Singh, Ronald A. Hill, Isabel Chauvin, Roxane Cherille N. Chamcheu, Mario Sechi, Konstantin G. Kousoulas, Jean Christopher Chamcheu, Pratik Basnet, Vladimir S. Spiegelman, Tithi Roy, Anthony L. Walker, Siva Murru, Samuel T. Boateng, Federico Ladu, Sergette Banang-Mbeumi, Jean Fotie, Bolni Marius Nagalo
Publikováno v:
Data in Brief, Vol 35, Iss, Pp 106858-(2021)
Data in Brief
Data in Brief
This article contains supplemental datasets of the recently published related research article “Synthesis, Inverse Docking-Assisted Identification and in vitro Biological Characterization of Flavonol-based Analogs of Fisetin as c-Kit, CDK2 and mTOR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8579f4ae24b51384835d183ae76a372d
http://www.sciencedirect.com/science/article/pii/S2352340921001426
http://www.sciencedirect.com/science/article/pii/S2352340921001426
Autor:
Pierre Mkounga, Maurice Tsaffack, Augustin Ephrem Nkengfack, Valerie Tedjon Sielinou, Hayato Ishikawa, Jules Clement Nguedia Assob, Blandine Marlyse Wache Ouahouo, Eric Gustave Bobda Gompe, Jean Fotie
Publikováno v:
Phytochemistry Letters. 26:154-158
Phytochemical investigation of the roots, stems and leaves of Mostuea thomsonii (Loganiaceae) resulted in the isolation of two new alkaloids of indolic and quinolinic types, named Thomsonines A (1) and B (2) respectively. Eleven additional known comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5baea4ea761d91a28ce7a957e10b3588
https://doi.org/10.1016/j.phytol.2018.05.024
https://doi.org/10.1016/j.phytol.2018.05.024