141 related articles for article (PubMed ID: 35533186)
1. ThioCORMates: Tunable and Cost-Effective Carbon Monoxide-Releasing Molecules.
DeSimone CA; Naqvi SL; Tasker SZ
Chemistry; 2022 Jul; 28(41):e202201326. PubMed ID: 35533186
[TBL] [Abstract][Full Text] [Related]
2. Effects of frequently applied carbon monoxide releasing molecules (CORMs) in typical CO-sensitive model systems - A comparative in vitro study.
Stucki D; Krahl H; Walter M; Steinhausen J; Hommel K; Brenneisen P; Stahl W
Arch Biochem Biophys; 2020 Jul; 687():108383. PubMed ID: 32335048
[TBL] [Abstract][Full Text] [Related]
3. Development of Triggerable, Trackable, and Targetable Carbon Monoxide Releasing Molecules.
Lazarus LS; Benninghoff AD; Berreau LM
Acc Chem Res; 2020 Oct; 53(10):2273-2285. PubMed ID: 32929957
[TBL] [Abstract][Full Text] [Related]
4. Examining the antimicrobial activity and toxicity to animal cells of different types of CO-releasing molecules.
Nobre LS; Jeremias H; Romão CC; Saraiva LM
Dalton Trans; 2016 Jan; 45(4):1455-66. PubMed ID: 26673556
[TBL] [Abstract][Full Text] [Related]
5. Water-Soluble Carbon Monoxide-Releasing Molecules (CORMs).
Khan H; Faizan M; Niazi SUK; Madiha ; Muhammad N; Zhang W
Top Curr Chem (Cham); 2022 Dec; 381(1):3. PubMed ID: 36515756
[TBL] [Abstract][Full Text] [Related]
6. Carbon-monoxide-releasing molecules for the delivery of therapeutic CO in vivo.
García-Gallego S; Bernardes GJ
Angew Chem Int Ed Engl; 2014 Sep; 53(37):9712-21. PubMed ID: 25070185
[TBL] [Abstract][Full Text] [Related]
7. Carbon Monoxide and Its Controlled Release: Therapeutic Application, Detection, and Development of Carbon Monoxide Releasing Molecules (CORMs).
Ling K; Men F; Wang WC; Zhou YQ; Zhang HW; Ye DW
J Med Chem; 2018 Apr; 61(7):2611-2635. PubMed ID: 28876065
[TBL] [Abstract][Full Text] [Related]
8. Cytochrome bd-I in Escherichia coli is less sensitive than cytochromes bd-II or bo'' to inhibition by the carbon monoxide-releasing molecule, CORM-3: N-acetylcysteine reduces CO-RM uptake and inhibition of respiration.
Jesse HE; Nye TL; McLean S; Green J; Mann BE; Poole RK
Biochim Biophys Acta; 2013 Sep; 1834(9):1693-703. PubMed ID: 23624261
[TBL] [Abstract][Full Text] [Related]
9. Dicarbonyl-bis(cysteamine)iron(II): a light induced carbon monoxide releasing molecule based on iron (CORM-S1).
Kretschmer R; Gessner G; Görls H; Heinemann SH; Westerhausen M
J Inorg Biochem; 2011 Jan; 105(1):6-9. PubMed ID: 21134596
[TBL] [Abstract][Full Text] [Related]
10. Cell damage following carbon monoxide releasing molecule exposure: implications for therapeutic applications.
Winburn IC; Gunatunga K; McKernan RD; Walker RJ; Sammut IA; Harrison JC
Basic Clin Pharmacol Toxicol; 2012 Jul; 111(1):31-41. PubMed ID: 22269084
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and Biological Evaluation of Water-Soluble Esterase-Activated CO-Releasing Molecules Targeting Mitochondria.
Hemmersbach L; Schreiner Y; Zhang X; Dicke F; Hünemeyer L; Neudörfl JM; Fleming T; Yard B; Schmalz HG
Chemistry; 2022 Sep; 28(50):e202201670. PubMed ID: 35771078
[TBL] [Abstract][Full Text] [Related]
12. Intracellular CO release from composite of ferritin and ruthenium carbonyl complexes.
Fujita K; Tanaka Y; Sho T; Ozeki S; Abe S; Hikage T; Kuchimaru T; Kizaka-Kondoh S; Ueno T
J Am Chem Soc; 2014 Dec; 136(48):16902-8. PubMed ID: 25352251
[TBL] [Abstract][Full Text] [Related]
13. Interaction of carbon monoxide-releasing ruthenium carbonyl CORM-3 with plasma fibronectin.
Aki T; Unuma K; Noritake K; Kurahashi H; Funakoshi T; Uemura K
Toxicol In Vitro; 2018 Aug; 50():201-209. PubMed ID: 29580987
[TBL] [Abstract][Full Text] [Related]
14. A thiol-reactive Ru(II) ion, not CO release, underlies the potent antimicrobial and cytotoxic properties of CO-releasing molecule-3.
Southam HM; Smith TW; Lyon RL; Liao C; Trevitt CR; Middlemiss LA; Cox FL; Chapman JA; El-Khamisy SF; Hippler M; Williamson MP; Henderson PJF; Poole RK
Redox Biol; 2018 Sep; 18():114-123. PubMed ID: 30007887
[TBL] [Abstract][Full Text] [Related]
15. Ru(CO)3Cl(Glycinate) (CORM-3): a carbon monoxide-releasing molecule with broad-spectrum antimicrobial and photosensitive activities against respiration and cation transport in Escherichia coli.
Wilson JL; Jesse HE; Hughes B; Lund V; Naylor K; Davidge KS; Cook GM; Mann BE; Poole RK
Antioxid Redox Signal; 2013 Aug; 19(5):497-509. PubMed ID: 23186316
[TBL] [Abstract][Full Text] [Related]
16. Development of carbon monoxide-releasing molecules conjugated to polysaccharides (glyco-CORMs) for delivering CO during obesity.
Mohan S; Barel LA; Benrahla DE; Do B; Mao Q; Kitagishi H; Rivard M; Motterlini R; Foresti R
Pharmacol Res; 2023 May; 191():106770. PubMed ID: 37068532
[TBL] [Abstract][Full Text] [Related]
17. Interaction of the carbon monoxide-releasing molecule Ru(CO)3Cl(glycinate) (CORM-3) with Salmonella enterica serovar Typhimurium: in situ measurements of carbon monoxide binding by integrating cavity dual-beam spectrophotometry.
Rana N; McLean S; Mann BE; Poole RK
Microbiology (Reading); 2014 Dec; 160(Pt 12):2771-2779. PubMed ID: 25085864
[TBL] [Abstract][Full Text] [Related]
18. Carbon monoxide-releasing molecules (CO-RMs) attenuate the inflammatory response elicited by lipopolysaccharide in RAW264.7 murine macrophages.
Sawle P; Foresti R; Mann BE; Johnson TR; Green CJ; Motterlini R
Br J Pharmacol; 2005 Jul; 145(6):800-10. PubMed ID: 15880142
[TBL] [Abstract][Full Text] [Related]
19. Tetrachlorocarbonyliridates: water-soluble carbon monoxide releasing molecules rate-modulated by the sixth ligand.
Bikiel DE; González Solveyra E; Di Salvo F; Milagre HM; Eberlin MN; Corrêa RS; Ellena J; Estrin DA; Doctorovich F
Inorg Chem; 2011 Mar; 50(6):2334-45. PubMed ID: 21322575
[TBL] [Abstract][Full Text] [Related]
20. Silacarboxylic acids as efficient carbon monoxide releasing molecules: synthesis and application in palladium-catalyzed carbonylation reactions.
Friis SD; Taaning RH; Lindhardt AT; Skrydstrup T
J Am Chem Soc; 2011 Nov; 133(45):18114-7. PubMed ID: 22014278
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
