These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
153 related articles for article (PubMed ID: 31808339)
1. Two-Photon Excitable Photoremovable Protecting Groups Based on the Quinoline Scaffold for Use in Biology. Hennig AK; Deodato D; Asad N; Herbivo C; Dore TM J Org Chem; 2020 Jan; 85(2):726-744. PubMed ID: 31808339 [TBL] [Abstract][Full Text] [Related]
2. Multi-Photon-Sensitive Chromophore for the Photorelease of Biologically Active Phenols. Asad N; Deodato D; Asad N; Gore S; Dore TM ACS Chem Neurosci; 2023 Dec; 14(23):4163-4175. PubMed ID: 37988406 [TBL] [Abstract][Full Text] [Related]
3. Substituent effects on the sensitivity of a quinoline photoremovable protecting group to one- and two-photon excitation. Davis MJ; Kragor CH; Reddie KG; Wilson HC; Zhu Y; Dore TM J Org Chem; 2009 Feb; 74(4):1721-9. PubMed ID: 19140722 [TBL] [Abstract][Full Text] [Related]
5. Sensitized 1-Acyl-7-nitroindolines with Enhanced Two-Photon Cross Sections for Release of Neurotransmitters. Puppala M; Carrothers JE; Asad N; Bernard MA; Kim DS; Widegren MB; Dore TM ACS Chem Neurosci; 2022 Dec; 13(24):3578-3596. PubMed ID: 36484374 [TBL] [Abstract][Full Text] [Related]
6. Development of a Two-Photon-Responsive Chromophore, 2-( Nguyen TP; Nguyen HD; Abe M J Org Chem; 2024 Apr; 89(7):4691-4701. PubMed ID: 38502935 [TBL] [Abstract][Full Text] [Related]
7. Photoactivatable AMPA for the study of glutamatergic neuronal transmission using two-photon excitation. Deodato D; Asad N; Dore TM Org Biomol Chem; 2021 Jun; 19(25):5589-5594. PubMed ID: 34086030 [TBL] [Abstract][Full Text] [Related]
8. Visible-light activatable coumarin-based phototriggers for fluorescence imaging with ultra-high photolysis efficiency. Zhou R; Yang L; Chen Z; Jiang L; Liu T; Wang Z; Huang X; Lin Q; Gong X; Yang Y; Zhu L Phys Chem Chem Phys; 2023 Apr; 25(16):11176-11184. PubMed ID: 37039244 [TBL] [Abstract][Full Text] [Related]
9. Photorearrangement of Quinoline-Protected Dialkylanilines and the Photorelease of Aniline-Containing Biological Effectors. Deodato D; Asad N; Dore TM J Org Chem; 2019 Jun; 84(11):7342-7353. PubMed ID: 31095378 [TBL] [Abstract][Full Text] [Related]
10. 8-Bromo-7-hydroxyquinoline as a photoremovable protecting group for physiological use: mechanism and scope. Zhu Y; Pavlos CM; Toscano JP; Dore TM J Am Chem Soc; 2006 Apr; 128(13):4267-76. PubMed ID: 16569001 [TBL] [Abstract][Full Text] [Related]
11. Unraveling the mechanism of the photodeprotection reaction of 8-bromo- and 8-chloro-7-hydroxyquinoline caged acetates. Ma J; Rea AC; An H; Ma C; Guan X; Li MD; Su T; Yeung CS; Harris KT; Zhu Y; Nganga JL; Fedoryak OD; Dore TM; Phillips DL Chemistry; 2012 May; 18(22):6854-65. PubMed ID: 22511356 [TBL] [Abstract][Full Text] [Related]
12. Synthesis and Characterization of Photoactivatable Doxycycline Analogues Bearing Two-Photon-Sensitive Photoremovable Groups Suitable for Light-Induced Gene Expression. Goegan B; Terzi F; Bolze F; Cambridge S; Specht A Chembiochem; 2018 Jun; 19(12):1341-1348. PubMed ID: 29341417 [TBL] [Abstract][Full Text] [Related]
13. The donor-acceptor biphenyl platform: a versatile chromophore for the engineering of highly efficient two-photon sensitive photoremovable protecting groups. Specht A; Bolze F; Donato L; Herbivo C; Charon S; Warther D; Gug S; Nicoud JF; Goeldner M Photochem Photobiol Sci; 2012 Mar; 11(3):578-86. PubMed ID: 22322902 [TBL] [Abstract][Full Text] [Related]
14. Photochemical Activation of Tertiary Amines for Applications in Studying Cell Physiology. Asad N; Deodato D; Lan X; Widegren MB; Phillips DL; Du L; Dore TM J Am Chem Soc; 2017 Sep; 139(36):12591-12600. PubMed ID: 28806084 [TBL] [Abstract][Full Text] [Related]
15. Efficient visible/NIR light-driven uncaging of hydroxylated thiazole orange-based caged compounds in aqueous media. Hashimoto R; Minoshima M; Sakata S; Ono F; Ishii H; Watakabe Y; Nemoto T; Yanaka S; Kato K; Kikuchi K Chem Sci; 2022 Jun; 13(25):7462-7467. PubMed ID: 35872806 [TBL] [Abstract][Full Text] [Related]