Literature DB >> 19128972

Synthesis and biological activities of high affinity taxane-based fluorescent probes.

Xuan Li1, Isabel Barasoain, Ruth Matesanz, J Fernando Díaz, Wei-Shuo Fang.   

Abstract

Three fluorescent probes 3a,3b, and 4 have been synthesized through conjugation of fluorescein and difluorescein groups to the 7-OH of C-2 modified paclitaxel and cephalomannine derivatives with very high affinity to microtubules. All these probes exhibited potent tubulin assembly promotion and tumor cell killing activities, thus may be useful as tools for the determination of thermodynamic parameters and exploration of ligand-microtubule interactions.

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Year:  2008        PMID: 19128972     DOI: 10.1016/j.bmcl.2008.12.018

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

Review 1.  Drug discovery targeting cell division proteins, microtubules and FtsZ.

Authors:  Iwao Ojima; Kunal Kumar; Divya Awasthi; Jacob G Vineberg
Journal:  Bioorg Med Chem       Date:  2014-03-05       Impact factor: 3.641

2.  Synthesis of a Fluorescent Analogue of Paclitaxel That Selectively Binds Microtubules and Sensitively Detects Efflux by P-Glycoprotein.

Authors:  Molly M Lee; Zhe Gao; Blake R Peterson
Journal:  Angew Chem Int Ed Engl       Date:  2017-05-09       Impact factor: 15.336

3.  Small-Scale Preparation of Fluorescently Labeled Chemical Probes from Marine Cyclic Peptides, Kapakahines A and F.

Authors:  Rie Kamihira; Yoichi Nakao
Journal:  Mar Drugs       Date:  2021-01-31       Impact factor: 5.118

  3 in total

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