Zobrazeno 1 - 10
of 1 306
pro vyhledávání: '"acylhydrazone"'
Autor:
Victoria V. Lipson, Fedyr G. Yaremenko, Volodymyr M. Vakula, Svitlana V. Kovalenko, Alexander V. Kyrychenko, Sergiy M. Desenko, Petro О. Borysko, Sergiy O. Zozulya
Publikováno v:
SynOpen, Vol 08, Iss 02, Pp 100-108 (2024)
Externí odkaz:
https://doaj.org/article/12eb0a35b15e4b65a764fa5b44b7b381
Publikováno v:
Arabian Journal of Chemistry, Vol 17, Iss 9, Pp 105913- (2024)
A series of N-acylhydrazone 4(a-f) were prepared by condensation of 2-hydroxybenzohydrazide with substituted benzaldehyde derivatives and catalytic amount of acetic acid via a simple method using microwave-assisted synthesis. Reaction conditions such
Externí odkaz:
https://doaj.org/article/bb96c72e6beb498c8ee970bdd6782a35
Autor:
Isabella Dib Ferreira Gremião, Gabriela Reis Pereira-Oliveira, Sandro Antonio Pereira, Maria Lopes Corrêa, Luana Pereira Borba-Santos, Alessandra Lifsitch Viçosa, Ashna Garg, Krupanandan Haranahalli, Deveney Dasilva, Nivea Pereira de Sa, Gabriel S. Matos, Vanessa Silva, Cristina Lazzarini, Caroline Mota Fernandes, Kildare Miranda, Jhon Jhamilton Artunduaga Bonilla, Anna Letícia Nunes, Leonardo Nimrichter, Iwao Ojima, John Mallamo, John B. McCarthy, Maurizio Del Poeta
Publikováno v:
Microbiology Spectrum, Vol 12, Iss 6 (2024)
ABSTRACT Acylhydrazone (AH) derivatives represent a novel category of anti-fungal medications that exhibit potent activity against Sporothrix sp., both in vitro and in a murine model of sporotrichosis. In this study, we demonstrated the anti-fungal e
Externí odkaz:
https://doaj.org/article/9a2aba0c9d7847cbb62ff4a8532b18f8
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1923-1932 (2023)
A straightforward synthetic protocol for the efficient construction of diazepine-containing spiroindolines has been developed and proceeds through a by base-promoted annulation reaction of α-halogenated N-acylhydrazones and isatin-derived MBH carbon
Externí odkaz:
https://doaj.org/article/3a3601cc6f4f4304b4f956fffd4ed997
Publikováno v:
Molecules, Vol 29, Iss 15, p 3569 (2024)
In our ongoing work to create potential antifungal agents, we synthesized and tested a group of C1-substituted acylhydrazone β-carboline analogues 9a–o and 10a–o for their effectiveness against Valsa mali, Fusarium solani, Fusarium oxysporum, an
Externí odkaz:
https://doaj.org/article/feaa8fccd4b14f4482ce8893c8347a65
Publikováno v:
Molecules, Vol 29, Iss 14, p 3330 (2024)
Adult neurogenesis involves the generation of functional neurons from neural progenitor cells, which have the potential to complement and restore damaged neurons and neural circuits. Therefore, the development of drugs that stimulate neurogenesis rep
Externí odkaz:
https://doaj.org/article/12e6d00845574635b31fc60f7df422db
Autor:
Juncheng Liang, Xin Fu, Jing Zhang, Haixin Ding, Zhiyuan Xu, Huochun Ye, Fadi Zhu, Chao Yan, Xiuhai Gan, Gang Feng
Publikováno v:
Arabian Journal of Chemistry, Vol 17, Iss 1, Pp 105389- (2024)
Plant diseases caused by bacteria lead to enormous yield and economic losses in agricultural production. To develop innovative bactericides for controlling plant disease, a series of coumarin-3-carboxylic acid derivatives containing acylhydrazone thi
Externí odkaz:
https://doaj.org/article/164983bdb1934eeba53c0f32dcc1aeac
Autor:
Tianzhu Shi, Zhengfeng Xie, Xinliang Mo, Yulong Feng, Tao Peng, Fuyong Wu, Mei Yu, Jingjing Zhao, Li Zhang, Ju Guo
Publikováno v:
Molecules, Vol 29, Iss 9, p 2032 (2024)
Using the aldehyde amine condensation procedure and the triphenylamine group as the skeleton structure, the new triphenylamine-aromatic aldehyde-succinylhydrazone probe molecule DHBYMH was created. A newly created acylhydrazone probe was structurally
Externí odkaz:
https://doaj.org/article/7b53b151797e4134b935e3a360c9e604
Autor:
Abdelfattah Hassan, Fawzy A. F. Mubarak, Ihsan A. Shehadi, Ahmed M. Mosallam, Hussain Temairk, Mohamed Badr, Aboubakr H. Abdelmonsef
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 38, Iss 1 (2023)
The dual c-Met/vascular endothelial growth factor receptor 2 (VEGFR-2) TK inhibition is a good strategy to overcome therapeutic resistance to small molecules VEGFR-2 inhibitors. In this study, we designed 3-substituted quinazoline-2,4(1H,3H)-dione de
Externí odkaz:
https://doaj.org/article/3768d35228f6460582feda1e7e03f2fd
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 59 (2023)
Abstract Someoxoquinoline-acylhydrazonederivativesshowedactivityagainst HumanImmunodeficiency Virus type 1 (HIV-1). These compounds must also be active against Herpes Simplex Virus type 1 (HSV-1) by an inhibition mechanism where they interact with th
Externí odkaz:
https://doaj.org/article/ce5c6c4238b248c3974794312c74b87f