Divergent strategy for the synthesis of α-aryl-substituted fosmidomycin analogues [PDF]
Fosmidomycin is the first representative of a new class of antimalarial drugs acting through inhibition of 1-deoxy-D-xylulose 5-phosphate ( DOXP) reductoisomerase (DXR), an essential enzyme in the non-mevalonate pathway for the synthesis of isoprenoids ...
Devreux, Vincent +5 more
core +2 more sources
The bromotyrosine derivative Ianthelline isolated from the Arctic marine sponge Stryphnus fortis inhibits marine micro- and macrobiofouling [PDF]
International audienceThe inhibition of marine biofouling by the bromotyrosine derivative ianthelline, isolated from the Arctic marine sponge Stryphnus fortis, is described. All major stages of the fouling process are investigated.
Andersen, Jeanette H. +9 more
core +3 more sources
Dynamic modelling of a fractionation process for a liquid mixture using supercritical carbon dioxide [PDF]
This work presents a simple dynamic modelling of a process of separation of a quaternary mixture using supercritical CO2. Thermodynamic description is accomplished using efficient available models (SRK equation of state with MHV2 mixing rules).
Abrams +18 more
core +3 more sources
Pollution of the marine environment with organotin compounds is a serious environmental problem due to their extreme toxicity to a wide range of organisms.
Kuzikova I.L. +2 more
doaj +1 more source
Imposex in Plicopurpura pansa (Neogastropoda: Thaididae) in Nayarit and Sinaloa, Mexico
Imposex is the development of male features in female prosobranch gastropods, caused by organotin compounds. In the Mexican Pacific coast, imposex was observed in Plicopurpura pansa.
Delia Domínguez-Ojeda +4 more
doaj +1 more source
ABSTRACT The N‐acylhydrazone scaffold is recognized as a privileged structure for the design of bioactive substances with increasing applications in medicinal chemistry research. Ensuring the safety of newly developed molecules is a critical step for both human health and environmental protection. Accordingly, this study aimed to evaluate the cytotoxic
Larissa Ribeiro Canuto Santos +4 more
wiley +1 more source
Organotin(IV) derivatives with 5,7-disubstituted-1,2,4-triazolo[1,5-a]pyrimidine and their cytotoxic activities: the importance of being conformers. [PDF]
The organotin(IV) compounds Me2SnCl2(dbtp)(1), Me2SnCl2(dbtp)2 (2), Et2SnCl2(dbtp) (3), Et2SnCl2(dbtp)2 (4), Et2SnCl2(dptp) (5), nBu2SnCl2(dbtp)2 (6), nBu2SnCl2(dptp) (7), Ph2SnCl2(dbtp) (8), Ph2SnCl2(dptp)2 (9), where dbtp = 5,7-di-tert-butyl-1,2,4 ...
Alessandro Attanzio +36 more
core +1 more source
Biological Evaluation of Triorganotin Derivatives as Potential Anticancer Agents
Metal-derived platinum complexes are widely used to treat solid tumors. However, systemic toxicity and tumor resistance to these drugs encourage further research into similarly effective compounds.
Valeria Stefanizzi +13 more
doaj +1 more source
ABSTRACT Prostate cancer (PCa) is an endocrine‐related cancer highly dependent on androgenic signaling. Beyond hormone dependence, extrinsic factors play a significant role in the risk of developing PCa, which raises concern about the influence of environmental compounds such as endocrine‐disrupting chemicals (EDCs). Tributyltin (TBT) is an EDC used in
Mariana Feijó +9 more
wiley +1 more source
Ionic Liquid Supported Organotin Reagents: Green Tools for Stille Cross-Coupling Reactions with Brominated Substrates [PDF]
Efficiency of ionic liquid supported organotin reagents in Stille cross-coupling reactions involving aryl bromides has been investigated. In a general manner, products were isolated with good yields by using a very simple catalytic system without the ...
A.S. Castanet +5 more
core +3 more sources

