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以硫代氨基脲为细胞毒剂的水溶性二茂钛基前药

Water-Soluble, Titanocene-Based Prodrugs with Thiosemicarbazones as Cytotoxic Agents.

作者信息

Schwitalla Kevin, Müller Marie-Carlotta, Fabra David, Schmidtmann Marc, Meyer Ulrike, Matesanz Ana I, Quiroga Adoracion G, Rauch Bernhard H, Beckhaus Rüdiger

机构信息

Institute of Chemistry, Carl von Ossietzky University, 26129 Oldenburg, Germany.

Pharmacology and Toxicology, University Medicine Oldenburg, Carl von Ossietzky University, 26129 Oldenburg, Germany.

出版信息

ACS Omega. 2025 Sep 3;10(36):41677-41687. doi: 10.1021/acsomega.5c05481. eCollection 2025 Sep 16.

Abstract

Prodrugs that improve drug delivery in the body are highly desirable because they increase drug solubility and activity, thereby reducing drug concentration and side effects compared to the actual active compound. In this work, we demonstrate the impact of titanocene scaffolds on active thiosemicarbazones (TSCN). Two routes toward cationic Ti-(IV) TSCN complexes were established either by the reaction of titanocene bis-(trimethylsilyl)-acetylene with TSCN and subsequent oxidation of the resulting Ti-(III) complex with ferrocenium triflate or by ligand exchange of the triflato ligands in titanocene-(IV) triflate with TSCN. The solubility and stability of the complexes in aqueous media were evaluated by NMR and ultraviolet/visible (UV/vis) spectroscopy. A selection of cationic Ti-(IV) TSCN complexes exhibit improved water solubility, stability and increased cytotoxicity at lower concentrations compared to pure TSCN, cisplatin and 5-FU in human colon cancer cells .

摘要

能够改善药物在体内递送的前药是非常理想的,因为它们能提高药物的溶解度和活性,从而与实际的活性化合物相比降低药物浓度和副作用。在这项工作中,我们展示了二茂钛支架对活性硫代半卡巴腙(TSCN)的影响。建立了两条通往阳离子Ti-(IV) TSCN配合物的路线,一条是通过二茂钛双(三甲基硅基)乙炔与TSCN反应,然后用三氟甲磺酸二茂铁氧化生成的Ti-(III)配合物;另一条是通过用TSCN进行二茂钛-(IV)三氟甲磺酸盐中三氟甲磺酸根配体的配体交换。通过核磁共振(NMR)和紫外/可见(UV/vis)光谱对配合物在水性介质中的溶解度和稳定性进行了评估。与纯TSCN、顺铂和5-氟尿嘧啶相比,一系列阳离子Ti-(IV) TSCN配合物在人结肠癌细胞中表现出改善的水溶性、稳定性,并在较低浓度下具有更高的细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4148/12444608/7b120cdbcc83/ao5c05481_0001.jpg

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