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Peptide 5Fam-RHKK-OH is a Research Peptide with significant interest within the field academic and medical research. Recent citations using 5Fam-RHKK-OH include the following: A fluorometric assay of SIRT1 deacetylation activity through quantification of nicotinamide adenine dinucleotide Y Feng , J Wu, L Chen, C Luo, X Shen, K Chen - Analytical , 2009 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0003269709005594 9-Fluorenylmethoxycarbonyl-labeled peptides as substrates in a capillary electrophoresis-based assay for sirtuin enzymes Y Fan, R Ludewig, GKE Scriba - Analytical biochemistry, 2009 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0003269709000682 5-((3-Amidobenzyl) oxy) nicotinamides as Sirtuin 2 Inhibitors T Ai, DJ Wilson, SS More , J Xie - Journal of medicinal , 2016 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.5b01376 Exemplification of the challenges associated with utilising fluorescence intensity based assays in discovery S Gul , P Gribbon - Expert Opinion on Drug Discovery, 2010 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.1517/17460441.2010.495748 Discovery of 1-hydroxypyridine-2-thiones as selective histone deacetylase inhibitors and their potential application for treating leukemia R Muthyala, WS Shin , J Xie, YY Sham - Bioorganic & medicinal chemistry , 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0960894X15007696 Anchor extension: a structure-guided approach to design cyclic peptides targeting enzyme active sites P Hosseinzadeh , PR Watson , TW Craven , X Li - Nature , 2021 - nature.comhttps://www.nature.com/articles/s41467-021-23609-8 A Novel Mechanism for SIRT1 Activators That Does Not Rely on the Chemical Moiety Immediately C-Terminal to the Acetyl-Lysine of the Substrate ND Yu, B Wang, XZ Li, HZ Han, D Liu - Molecules, 2022 - mdpi.comhttps://www.mdpi.com/1420-3049/27/9/2714 Guttiferone A aggregates modulate silent information regulator 1 (SIRT1) activity K Cottet, B Xu, P Coric, S Bouaziz - Journal of Medicinal , 2016 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.6b01182 Inhibition of histone deacetylase 6 suppresses inflammatory responses and invasiveness of fibroblast-like-synoviocytes in inflammatory arthritis JK Park , S Shon, HJ Yoo, DH Suh, D Bae - Arthritis Research & , 2021 - Springerhttps://link.springer.com/article/10.1186/s13075-021-02561-4 Discovery of macrocyclic peptides armed with a mechanism-based warhead: isoform-selective inhibition of human deacetylase SIRT2 J Morimoto , Y Hayashi , H Suga - Angewandte Chemie, 2012 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/ange.201108118 Kinetic Characterization of Human Histone Deacetylase 8 With Medium-Chain Fatty Acyl Lysine H Yoo, GA Polsinelli - Epigenetics Insights, 2021 - journals.sagepub.comhttps://journals.sagepub.com/doi/abs/10.1177/25168657211065685 Synthesis of indole inhibitors of silent information regulator 1 (SIRT1), and their evaluation as cytotoxic agents H Laaroussi, Y Ding, Y Teng, P Deschamps - European Journal of , 2020 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S022352342030533X Discovery of potent and selective sirtuin 2 (SIRT2) inhibitors using a fragment-based approach H Cui , Z Kamal, T Ai, Y Xu, SS More - Journal of medicinal , 2014 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm500777s Resveratrol is not a direct activator of SIRT1 enzyme activity D Beher, J Wu, S Cumine, KW Kim - Chemical biology & , 2009 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1747-0285.2009.00901.x

FAM标记说明:
Carboxyfluorescein (FAM) is fluorophor with an excitation at 492 nm ▉ and emission of 517 nm ▉. Donors like FAM and 5FAM are often paired together with acceptors (CPQ2) for FRET experiments.

FAM标记肽的相关文献:
Porous Silicon Nanoparticle Delivery of Tandem Peptide Anti-Infectives for the Treatment of Pseudomonas aeruginosa Lung Infections.
Kwon, Ester J., et al. Advanced Materials 29.35 (2017).

Ultrasensitive tumor-penetrating nanosensors of protease activity.
Kwon, Ester J., Jaideep S. Dudani, and Sangeeta N. Bhatia. Nature Biomedical Engineering 1 (2017): 0054.

Seneca Valley Virus 3C pro Substrate Optimization Yields Efficient Substrates for Use in Peptide-Prodrug Therapy.
Miles, Linde A., et al. PloS One 10.6 (2015): e0129103.

The function of the milk-clotting enzymes bovine and camel chymosin studied by a fluorescence resonance energy transfer assay.
Jensen, Jesper Langholm, et al. Journal of Dairy Science 98.5 (2015): 2853-2860.

A comparison of modular PEG incorporation strategies for stabilization of peptide-siRNA nanocomplexes.
Lo, Justin H., et al. Bioconjugate Chemistry (2016).