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用于生物研究的抗病毒磺酸盐碳硅烷树枝状大分子G2-S16及其荧光素标记衍生物的新合成方法。

New synthetic procedure for the antiviral sulfonate carbosilane dendrimer G2-S16 and its fluorescein-labelled derivative for biological studies.

作者信息

Gutiérrez-Ulloa Carlos, Peña-González Cornelia E, Barrios-Gumiel Andrea, Ceña-Díez Rafael, Serramía-Lobera M Jesús, Muñoz-Fernández M Ángeles, Javier de la Mata F, Sánchez-Nieves Javier, Gómez Rafael

机构信息

Dpto. de Química Orgánica y Química Inorgánica, Universidad de Alcalá (UAH), Campus Universitario E-28871 Alcalá de Henares Madrid Spain

Instituto de Investigación Química "Andrés M. del Río" (IQAR), Universidad de Alcalá (UAH) Spain.

出版信息

RSC Adv. 2020 May 27;10(34):20083-20088. doi: 10.1039/d0ra03448g. eCollection 2020 May 26.

Abstract

The anionic carbosilane (CBS) dendrimer with sulfonate groups G2-S16 is a promising compound for the preparation of a microbicide gel to prevent HIV infection. However, until now its synthesis required aggressive conditions. Hence, a reliable synthetic procedure is very important to face GMP conditions and clinical trials. In this study, G2-S16 has been prepared by a new approach that involves the addition of an amine-terminated dendrimer to ethenesulfonyl fluoride (CHSOF, ESF) and then transformation to the sulfonate dendrimer by treatment with a base. This strategy also makes feasible the synthesis of a labelled sulfonate dendrimer (G2-S16-FITC) to be used as a molecular probe for experiments. Interestingly, G2-S16-FITC enters into human peripheral blood mononuclear cells (PBMCs).

摘要

带有磺酸根基团的阴离子型碳硅烷(CBS)树枝状大分子G2-S16是一种很有前景的化合物,可用于制备预防HIV感染的杀微生物剂凝胶。然而,到目前为止,其合成需要苛刻的条件。因此,可靠的合成方法对于满足GMP条件和临床试验非常重要。在本研究中,G2-S16是通过一种新方法制备的,该方法包括将胺端基树枝状大分子添加到乙烯磺酰氟(CH₂SO₂F,ESF)中,然后用碱处理转化为磺酸根树枝状大分子。该策略还使合成标记的磺酸根树枝状大分子(G2-S16-FITC)成为可能,可将其用作实验的分子探针。有趣的是,G2-S16-FITC可进入人外周血单核细胞(PBMC)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5907/9054215/fbf727a79edc/d0ra03448g-s1.jpg

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