Literature DB >> 29039673

Rapid Access to a Broad Range of 6'-Substituted Firefly Luciferin Analogues Reveals Surprising Emitters and Inhibitors.

Deepak K Sharma1, Spencer T Adams1, Kate L Liebmann1, Stephen C Miller1.   

Abstract

Light-emitting firefly luciferin analogues contain electron-donating groups in the 6'-position, but the scope of known 6'-substitution remains narrow. A two-step route to a broad range of 6'-substituted luciferin analogues was developed to fill this void and enable more extensive study of the 6'-functionality. This chemistry allowed direct access to "caged" amide and bright azetidine analogues, but also revealed thioether inhibitors and unexpectedly luminogenic aryl amine derivatives.

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Year:  2017        PMID: 29039673      PMCID: PMC5836729          DOI: 10.1021/acs.orglett.7b02806

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  27 in total

1.  Ortho-substituent effect on fluorescence and electroluminescence of arylamino-substituted coumarin and stilbene.

Authors:  Chao-Tsen Chen; Chih-Long Chiang; Yu-Chung Lin; Li-Hsin Chan; Chien-Huang Huang; Zong-Wei Tsai; Chin-Ti Chen
Journal:  Org Lett       Date:  2003-04-17       Impact factor: 6.005

2.  4-Methyl-7-thioumbelliferyl-beta-D-cellobioside: a fluorescent, nonhydrolyzable substrate analogue for cellulases.

Authors:  Brian K Barr; Ronald J Holewinski
Journal:  Biochemistry       Date:  2002-04-02       Impact factor: 3.162

3.  Identification of mutant firefly luciferases that efficiently utilize aminoluciferins.

Authors:  Katryn R Harwood; David M Mofford; Gadarla R Reddy; Stephen C Miller
Journal:  Chem Biol       Date:  2011-12-23

4.  Robust light emission from cyclic alkylaminoluciferin substrates for firefly luciferase.

Authors:  Gadarla Randheer Reddy; Walter C Thompson; Stephen C Miller
Journal:  J Am Chem Soc       Date:  2010-10-06       Impact factor: 15.419

5.  New class of bioluminogenic probe based on bioluminescent enzyme-induced electron transfer: BioLeT.

Authors:  Hideo Takakura; Ryosuke Kojima; Mako Kamiya; Eiji Kobayashi; Toru Komatsu; Tasuku Ueno; Takuya Terai; Kenjiro Hanaoka; Tetsuo Nagano; Yasuteru Urano
Journal:  J Am Chem Soc       Date:  2015-03-19       Impact factor: 15.419

6.  A biocompatible condensation reaction for the labeling of terminal cysteine residues on proteins.

Authors:  Hongjun Ren; Fei Xiao; Ke Zhan; Young-Pil Kim; Hexin Xie; Zuyong Xia; Jianghong Rao
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

7.  Firefly Luciferase Mutants Allow Substrate-Selective Bioluminescence Imaging in the Mouse Brain.

Authors:  Spencer T Adams; David M Mofford; G S Kiran Kumar Reddy; Stephen C Miller
Journal:  Angew Chem Int Ed Engl       Date:  2016-03-17       Impact factor: 15.336

8.  Synthesis of rhodamines from fluoresceins using Pd-catalyzed C-N cross-coupling.

Authors:  Jonathan B Grimm; Luke D Lavis
Journal:  Org Lett       Date:  2011-11-17       Impact factor: 6.005

9.  A synthetic luciferin improves bioluminescence imaging in live mice.

Authors:  Melanie S Evans; Joanna P Chaurette; Spencer T Adams; Gadarla R Reddy; Miranda A Paley; Neil Aronin; Jennifer A Prescher; Stephen C Miller
Journal:  Nat Methods       Date:  2014-02-09       Impact factor: 28.547

10.  Aminoluciferins extend firefly luciferase bioluminescence into the near-infrared and can be preferred substrates over D-luciferin.

Authors:  David M Mofford; Gadarla Randheer Reddy; Stephen C Miller
Journal:  J Am Chem Soc       Date:  2014-09-11       Impact factor: 15.419

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  12 in total

1.  Sulfonamides Are an Overlooked Class of Electron Donors in Luminogenic Luciferins and Fluorescent Dyes.

Authors:  Deepak K Sharma; Spencer T Adams; Kate L Liebmann; Adam Choi; Stephen C Miller
Journal:  Org Lett       Date:  2019-03-05       Impact factor: 6.005

Review 2.  Lessons Learned from Luminous Luciferins and Latent Luciferases.

Authors:  Stephen C Miller; David M Mofford; Spencer T Adams
Journal:  ACS Chem Biol       Date:  2018-02-19       Impact factor: 5.100

3.  Bioluminescence imaging in mice with synthetic luciferin analogues.

Authors:  Xincai Ji; Spencer T Adams; Stephen C Miller
Journal:  Methods Enzymol       Date:  2020-05-31       Impact factor: 1.600

4.  Computational investigation into the fluorescence of luciferin analogues.

Authors:  Thom Vreven; Stephen C Miller
Journal:  J Comput Chem       Date:  2019-01-15       Impact factor: 3.376

5.  Building Biological Flashlights: Orthogonal Luciferases and Luciferins for in Vivo Imaging.

Authors:  Sierra J Williams; Jennifer A Prescher
Journal:  Acc Chem Res       Date:  2019-10-08       Impact factor: 22.384

6.  Luciferase Activity of Insect Fatty Acyl-CoA Synthetases with Synthetic Luciferins.

Authors:  David M Mofford; Kate L Liebmann; Ganapathy Subramanian Sankaran; G S Kiran Kumar Reddy; G Randheer Reddy; Stephen C Miller
Journal:  ACS Chem Biol       Date:  2017-11-07       Impact factor: 5.100

Review 7.  Seeing (and Using) the Light: Recent Developments in Bioluminescence Technology.

Authors:  Anna C Love; Jennifer A Prescher
Journal:  Cell Chem Biol       Date:  2020-08-13       Impact factor: 8.116

8.  Environment-Sensitive Fluorescent Labelling of Peptides by Luciferin Analogues.

Authors:  Marialuisa Siepi; Rosario Oliva; Antonio Masino; Rosa Gaglione; Angela Arciello; Rosita Russo; Antimo Di Maro; Anna Zanfardino; Mario Varcamonti; Luigi Petraccone; Pompea Del Vecchio; Marcello Merola; Elio Pizzo; Eugenio Notomista; Valeria Cafaro
Journal:  Int J Mol Sci       Date:  2021-12-10       Impact factor: 5.923

9.  Heterocyclic Cathinones as Inhibitors of Kynurenine Aminotransferase II-Design, Synthesis, and Evaluation.

Authors:  Michal Maryška; Lucie Svobodová; Wim Dehaen; Martina Hrabinová; Michaela Rumlová; Ondřej Soukup; Martin Kuchař
Journal:  Pharmaceuticals (Basel)       Date:  2021-12-10

10.  Computation-Guided Rational Design of a Peptide Motif That Reacts with Cyanobenzothiazoles via Internal Cysteine-Lysine Relay.

Authors:  Samantha G L Keyser; Ashley Utz; Carolyn R Bertozzi
Journal:  J Org Chem       Date:  2018-05-30       Impact factor: 4.354

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