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.
156 related articles for article (PubMed ID: 26097262)
1. Computational studies of electronic circular dichroism spectra predict absolute configuration assignments for the guanine oxidation product 5-carboxamido-5-formamido-2-iminohydantoin. Fleming AM; Alshykhly O; Orendt AM; Burrows CJ Tetrahedron Lett; 2015 Jun; 56(23):3191-3196. PubMed ID: 26097262 [TBL] [Abstract][Full Text] [Related]
2. Guanine oxidation product 5-carboxamido-5-formamido-2-iminohydantoin induces mutations when bypassed by DNA polymerases and is a substrate for base excision repair. Alshykhly OR; Fleming AM; Burrows CJ Chem Res Toxicol; 2015 Sep; 28(9):1861-71. PubMed ID: 26313343 [TBL] [Abstract][Full Text] [Related]
3. Insights into the 5-Carboxamido-5-Formamido-2-Iminohydantoin Structural Isomerization Equilibria. Chabot MB; Fleming AM; Burrows CJ J Org Chem; 2022 Sep; 87(17):11865-11870. PubMed ID: 35960780 [TBL] [Abstract][Full Text] [Related]
4. Computational Study of the Oxidation of Guanine To Form 5-Carboxyamido-5-formamido-2-iminohydantoin (2Ih). Hebert SP; Schlegel HB Chem Res Toxicol; 2019 Nov; 32(11):2295-2304. PubMed ID: 31571479 [TBL] [Abstract][Full Text] [Related]
5. Reconciliation of chemical, enzymatic, spectroscopic and computational data to assign the absolute configuration of the DNA base lesion spiroiminodihydantoin. Fleming AM; Orendt AM; He Y; Zhu J; Dukor RK; Burrows CJ J Am Chem Soc; 2013 Dec; 135(48):18191-204. PubMed ID: 24215588 [TBL] [Abstract][Full Text] [Related]
6. Identification of the Major Product of Guanine Oxidation in DNA by Ozone. Chabot MB; Fleming AM; Burrows CJ Chem Res Toxicol; 2022 Oct; 35(10):1809-1813. PubMed ID: 35642826 [TBL] [Abstract][Full Text] [Related]
7. Determination of the absolute configurations of bicyclo[3.1.0]hexane derivatives via electronic circular dichroism, optical rotation dispersion and vibrational circular dichroism spectroscopy and density functional theory calculations. Yang G; Li J; Liu Y; Lowary TL; Xu Y Org Biomol Chem; 2010 Aug; 8(16):3777-83. PubMed ID: 20567790 [TBL] [Abstract][Full Text] [Related]
8. The 2Ih and Karwowski BT Molecules; 2023 Feb; 28(5):. PubMed ID: 36903425 [TBL] [Abstract][Full Text] [Related]
9. A 2-iminohydantoin from the oxidation of guanine. Ye W; Sangaiah R; Degen DE; Gold A; Jayaraj K; Koshlap KM; Boysen G; Williams J; Tomer KB; Ball LM Chem Res Toxicol; 2006 Apr; 19(4):506-10. PubMed ID: 16608161 [TBL] [Abstract][Full Text] [Related]
10. Absolute configurations of spiroiminodihydantoin and allantoin stereoisomers: comparison of computed and measured electronic circular dichroism spectra. Ding S; Jia L; Durandin A; Crean C; Kolbanovskiy A; Shafirovich V; Broyde S; Geacintov NE Chem Res Toxicol; 2009 Jun; 22(6):1189-93. PubMed ID: 19485408 [TBL] [Abstract][Full Text] [Related]
11. Determination of the absolute configuration of a chiral oxadiazol-3-one calcium channel blocker, resolved using chiral chromatography, via concerted density functional theory calculations of its vibrational circular dichroism, electronic circular dichroism, and optical rotation. Stephens PJ; Devlin FJ; Gasparrini F; Ciogli A; Spinelli D; Cosimelli B J Org Chem; 2007 Jun; 72(13):4707-15. PubMed ID: 17516678 [TBL] [Abstract][Full Text] [Related]
12. 5-Carboxamido-5-formamido-2-iminohydantoin, in Addition to 8-oxo-7,8-Dihydroguanine, Is the Major Product of the Iron-Fenton or X-ray Radiation-Induced Oxidation of Guanine under Aerobic Reducing Conditions in Nucleoside and DNA Contexts. Alshykhly OR; Fleming AM; Burrows CJ J Org Chem; 2015 Jul; 80(14):6996-7007. PubMed ID: 26092110 [TBL] [Abstract][Full Text] [Related]
13. Determination of absolute configuration using concerted ab Initio DFT calculations of electronic circular dichroism and optical rotation: bicyclo[3.3.1]nonane diones. Stephens PJ; McCann DM; Butkus E; Stoncius S; Cheeseman JR; Frisch MJ J Org Chem; 2004 Mar; 69(6):1948-58. PubMed ID: 15058939 [TBL] [Abstract][Full Text] [Related]
14. Characterization of 2'-deoxyguanosine oxidation products observed in the Fenton-like system Cu(II)/H2O2/reductant in nucleoside and oligodeoxynucleotide contexts. Fleming AM; Muller JG; Ji I; Burrows CJ Org Biomol Chem; 2011 May; 9(9):3338-48. PubMed ID: 21445431 [TBL] [Abstract][Full Text] [Related]
15. Computational prediction of one-electron reduction potentials and acid dissociation constants for guanine oxidation intermediates and products. Psciuk BT; Schlegel HB J Phys Chem B; 2013 Aug; 117(32):9518-31. PubMed ID: 23875631 [TBL] [Abstract][Full Text] [Related]
16. Electronic circular dichroism behavior of chiral Phthiobuzone. Li L; Wang L; Si Y Acta Pharm Sin B; 2014 Apr; 4(2):167-71. PubMed ID: 26579380 [TBL] [Abstract][Full Text] [Related]
17. Absolute configuration determination of donor-acceptor [2.2]paracyclophanes by comparison of theoretical and experimental vibrational circular dichroism spectra. Furo T; Mori T; Origane Y; Wada T; Izumi H; Inoue Y Chirality; 2006 Feb; 18(3):205-11. PubMed ID: 16432922 [TBL] [Abstract][Full Text] [Related]