Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fante, Bamba"'
Autor:
COULIBALY, Bamoro, DIOMANDE, Se kou, SANGARE, Kassoum, ABLE, Anoh Valentin, Aurélie, Vallin, FANTE, Bamba
Publikováno v:
Journal of Drug Delivery & Therapeutics; Oct2024, Vol. 14 Issue 10, p24-30, 7p
Autor:
Robby Vroemans, Fante Bamba, Jonas Winters, Joice Thomas, Jeroen Jacobs, Luc Van Meervelt, Jubi John, Wim Dehaen
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 626-633 (2018)
A practical three-step protocol for the assembly of triazolobenzodiazepine-fused diketopiperazines and hydantoins has been developed. The synthesis of these tetracyclic ring systems was initiated by an Ugi reaction, which brought together all necessa
Externí odkaz:
https://doaj.org/article/16305acdaf874f1ea8689baf7767eba4
Autor:
Fante, Bamba, Ambeu-Loko, N'ta Christelle Mélissa, Coulibaly, Souleymane, Soro, Yaya, Coustard, Jean-Marie
Publikováno v:
Organic Preparations & Procedures International; 2023, Vol. 55 Issue 5, p411-420, 10p
Autor:
Fante, Bamba1 (AUTHOR), Ambeu-Loko, N'ta Christelle Mélissa1 (AUTHOR), Coulibaly, Souleymane1 (AUTHOR), Soro, Yaya2 (AUTHOR), Coustard, Jean-Marie3 (AUTHOR)
Publikováno v:
Organic Preparations & Procedures International. 2023, Vol. 55 Issue 5, p411-420. 10p.
Akademický článek
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Publikováno v:
Medicinal Chemistry Research. 30:1334-1340
SecA, a key component of the bacterial Sec-dependent secretion pathway, is an attractive target for the development of new antimicrobial agents. We have previously reported pyrimidine analogs as SecA inhibitors. Herein, we report an extension of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93c157eb64363a7deb04760885c48234
https://doi.org/10.1007/s00044-021-02717-6
https://doi.org/10.1007/s00044-021-02717-6
Autor:
Koffi Téki Dindet Steve-Evanes, Vincent Chagnault, Coulibaly Bamoro, Fante Bamba, Aurélie Vallin
Publikováno v:
Open Journal of Medicinal Chemistry. 11:17-26
Due to the continuous emergence and rapid spread of drug-resistant strains of bacteria, there is an urgent need for the development of novel antimicrobials. Along this line, the synthesis and antibacterial activity of 4,5-diphenylimidazol-2-thiol der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d003d69fccd8c72edf7947b910c0f471
https://doi.org/10.4236/ojmc.2021.112002
https://doi.org/10.4236/ojmc.2021.112002
Synthesis and biological evaluation of novel 4-oxo-5-cyano thiouracil derivatives as SecA inhibitors
Publikováno v:
Heterocyclic Communications, Vol 26, Iss 1, Pp 76-83 (2020)
The continuous emergence of drug-resistant strains of bacteria poses an urgent risk to human health and dictates the need for new antimicrobials. Along this line, we have been working on developing inhibitors of SecA, a key component of the bacterial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e726748422ae540ac33aadccb18137cb
https://doi.org/10.1515/hc-2020-0100
https://doi.org/10.1515/hc-2020-0100
Design, Synthesis and Antibacterial Activities of Triazole-pyrimidine Derivatives as SecA Inhibitors
Background: To highlight the magnitude of the important challenge now facing scientists, drug resistance needs exploration of novel antimicrobial agents. The identification of new and vital target in bacteria and then designing their inhibitors can b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1da73f4fe13157ce9d5c03cddf94161f
https://doi.org/10.21203/rs.3.rs-476874/v1
https://doi.org/10.21203/rs.3.rs-476874/v1
SecA, a key component of the bacterial Sec-dependent secretion pathway, is an attractive target for the development of new antimicrobial agents. We have previously reported pyrimidine analogs as SecA inhibitors. Herein, we report an extension of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e53787e6f20aad2c99cdb0f6c7a39eaf
https://doi.org/10.21203/rs.3.rs-188471/v1
https://doi.org/10.21203/rs.3.rs-188471/v1