نتایج جستجو برای: peptide analogue

تعداد نتایج: 199665  

1999
Srinivasa Rao Lifeng He Subrata Chakravarty Iwao Ojima George A. Orr

Photoaffinity labeling methods have allowed a definition of the sites of interaction between Taxol and its cellular target, the microtubule, specifically b-tubulin. Our previous studies have indicated that [H]3*-(pazidobenzamido)Taxol photolabels the N-terminal 31 amino acids of b-tubulin (Rao, S., Krauss, N. E., Heerding, J. M., Swindell, C. S., Ringel, I., Orr, G. A., and Horwitz, S. B. (1994...

Journal: :The Journal of biological chemistry 2008
Sébastien Dutertre Daniel Croker Norelle L Daly Asa Andersson Markus Muttenthaler Natalie G Lumsden David J Craik Paul F Alewood Gilles Guillon Richard J Lewis

We report the discovery of conopressin-T, a novel bioactive peptide isolated from Conus tulipa venom. Conopressin-T belongs to the vasopressin-like peptide family and displays high sequence homology to the mammalian hormone oxytocin (OT) and to vasotocin, the endogenous vasopressin analogue found in teleost fish, the cone snail's prey. Conopressin-T was found to act as a selective antagonist at...

Journal: :The Journal of biological chemistry 1999
S Rao L He S Chakravarty I Ojima G A Orr S B Horwitz

Photoaffinity labeling methods have allowed a definition of the sites of interaction between Taxol and its cellular target, the microtubule, specifically beta-tubulin. Our previous studies have indicated that [(3)H]3'-(p-azidobenzamido)Taxol photolabels the N-terminal 31 amino acids of beta-tubulin (Rao, S., Krauss, N. E., Heerding, J. M., Swindell, C. S., Ringel, I., Orr, G. A., and Horwitz, S...

2015
Keith A. Williams Peter T.M. Veenhuizen Beatriz G. de la Torre Ramon Eritja Cees Dekker

We have covalently coupled single-walled carbon nanotubes (SWNTs) to peptide nucleic acid (PNA, a synthetic DNA analogue [1]), and shown that the resulting macromolecular wires hybridize with complementary DNA. This provides a powerful tool to incorporate SWNTs into a recognition-based, massively parallel device assembly strategy, and permits sequence-specific attachment of SWNTs to biological ...

A new series of peptide-like derivatives containing different aromatic amino acids andpossessing pharmacophores of COX-2 inhibitors as SO2Me or N3 attached to the para positionof an end phenyl ring was synthesized for evaluation as selective cyclooxygenase-2 (COX-2)inhibitors. The synthetic reactions were based on the solid phase peptide synthesis methodusing Wang resin. One of the analogues, i...

2015
Zhongqiu Ni Lanxia Zhou Xu Li Jing Zhang Shouliang Dong Maxim Antopolsky

A novel amino acid derivative 3-(4-(1, 2, 4, 5-tetrazine-3-yl) phenyl)-2-aminopropanoic acid was synthesized in this study. The compound possessed better water-solubility and was synthesized more easily compared with the well-known and commercially available 3-(p-benzylamino)-1, 2, 4, 5-tetrazine. Tetrazine-containing amino acid showed excellent stability in biological media and might be used f...

Journal: :Molecular pharmaceutics 2006
Sharon Bloch Baogang Xu Yunpeng Ye Kexian Liang Gregory V Nikiforovich Samuel Achilefu

Biomolecules containing the RGD peptide sequence are known to bind integrins with high affinity. Studies of hexa-and hepta-peptides labeled with a near-infrared fluorescent probe (cypate) showed that rearranging the glycine in a linear RGD peptide sequence to form the GRD analogue favored the uptake of the GRD compound by alphavbeta3 integrin receptor (ABIR)-positive A549 tumor cells and tissue...

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