Saha-Möller CR - Search Results

1

Formation of singlet oxygen in the thermal decomposition of 3-hydroxymethyl-3,4,4-trimethyl-1,2-dioxetane, a chemical source of triplet-excited ketones.

Briviba K, Saha-Möller CR, Adam W, Sies H. Briviba K, et al. Biochem Mol Biol Int. 1996 Apr;38(4):647-51. Biochem Mol Biol Int. 1996. PMID: 8728092

2

Formation of 7,8-dihydro-8-oxoguanine in the 1,2-dioxetane-induced oxidation of calf thymus DNA: evidence for photosensitized DNA damage by thermally generated triplet ketones in the dark.

Adam W, Saha-Möller CR, Schönberger A, Berger M, Cadet J. Adam W, et al. Photochem Photobiol. 1995 Aug;62(2):231-8. doi: 10.1111/j.1751-1097.1995.tb05263.x. Photochem Photobiol. 1995. PMID: 7480132

3

Photooxidative damage of guanine in DG and DNA by the radicals derived from the alpha cleavage of the electronically excited carbonyl products generated in the thermolysis of alkoxymethyl-substituted dioxetanes and the photolysis of alkoxyacetones.

Adam W, Arnold MA, Saha-Möller CR. Adam W, et al. J Org Chem. 2001 Jan 26;66(2):597-604. doi: 10.1021/jo0056491. J Org Chem. 2001. PMID: 11429836

4

Photochemical DNA modifications induced by 1,2-dioxetanes.

Epe B, Müller E, Adam W, Saha-Möller CR. Epe B, et al. Chem Biol Interact. 1992 Dec;85(2-3):265-81. doi: 10.1016/0009-2797(92)90067-u. Chem Biol Interact. 1992. PMID: 1337314

5

N-hydroxy-4-(4-chlorophenyl)thiazole-2(3H)-thione as a photochemical hydroxyl-radical source: photochemistry and oxidative damage of DNA (strand breaks) and 2'-deoxyguanosine (8-oxodG formation).

Adam W, Hartung J, Okamoto H, Saha-Möller CR, Spehar K. Adam W, et al. Photochem Photobiol. 2000 Nov;72(5):619-24. doi: 10.1562/0031-8655(2000)072<0619:nhctht>2.0.co;2. Photochem Photobiol. 2000. PMID: 11107846

6

A comparative photomechanistic study (spin trapping, EPR spectroscopy, transient kinetics, photoproducts) of nucleoside oxidation (dG and 8-oxodG) by triplet-excited acetophenones and by the radicals generated from alpha-oxy-substituted derivatives through Norrish-type I cleavage.

Adam W, Arnold MA, Nau WM, Pischel U, Saha-Möller CR. Adam W, et al. J Am Chem Soc. 2002 Apr 17;124(15):3893-904. doi: 10.1021/ja017600y. J Am Chem Soc. 2002. PMID: 11942826

7

Genotoxicity studies of benzofuran dioxetanes and epoxides with isolated DNA, bacteria and mammalian cells.

Adam W, Ahrweiler M, Saha-Möller CR, Sauter M, Schönberger A, Epe B, Müller E, Schiffmann D, Stopper H, Wild D. Adam W, et al. Toxicol Lett. 1993 Apr;67(1-3):41-55. doi: 10.1016/0378-4274(93)90045-y. Toxicol Lett. 1993. PMID: 8451770 Free article.

8

Spiroiminodihydantoin is a major product in the photooxidation of 2'-deoxyguanosine by the triplet states and oxyl radicals generated from hydroxyacetophenone photolysis and dioxetane thermolysis.

Adam W, Arnold MA, Grüne M, Nau WM, Pischel U, Saha-Möller CR. Adam W, et al. Org Lett. 2002 Feb 21;4(4):537-40. doi: 10.1021/ol017138m. Org Lett. 2002. PMID: 11843585

9

Peroxidase-catalyzed oxidative damage of DNA and 2'-deoxyguanosine by model compounds of lipid hydroperoxides: involvement of peroxyl radicals.

Adam W, Kurz A, Saha-Möller CR. Adam W, et al. Chem Res Toxicol. 2000 Dec;13(12):1199-207. doi: 10.1021/tx0001880. Chem Res Toxicol. 2000. PMID: 11123959

10

Synthesis of 4,6-dideoxyfuranoses through the regioselective and diastereoselective oxyfunctionalization of a dimethylphenylsilyl-substituted chiral homoallylic alcohol.

Adam W, Saha-Möller CR, Schmid KS. Adam W, et al. J Org Chem. 2001 Nov 2;66(22):7365-71. doi: 10.1021/jo010549w. J Org Chem. 2001. PMID: 11681949

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