Results 101 to 110 of about 2,717 (170)

Regioselective and site-divergent synthesis of tetrahydropyridines by controlled reductive-oxidative dearomative hydroarylation of pyridinium salts. [PDF]

Nat Commun
Wei XF, Wang S, Li YL, Yu Q, Shu W.
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Functional and Morphological Changes in the Olfactory Epithelium of Mouse Models With Upper Respiratory Inflammation and Olfactory Dysfunction. [PDF]

Clin Exp Otorhinolaryngol
Yoo SH, Bae JS, Ventura R, Kim EH, Kim AY, Kim JH, Mo JH.   +6 more
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Brønstead Acid-Catalyzed Regiodivergent Hydroindolation of Indoles: Temperature-Controlled Markovnikov and Anti-Markovnikov Addition. [PDF]

Int J Mol Sci
Ganesan A, Kwon YU.
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Pd-Catalyzed Arylative Lossen Rearrangement: Synthesis of Secondary Amines from Aryl/Alkyl Carboxylic Acids and Aryl Halides. [PDF]

J Am Chem Soc
Luo Y, Zhou J, Mandler MD, Kwan EE, Liu RY.   +4 more
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Novel EP2 Antagonist Attenuates Microgliosis and Memory Deficits in Pilocarpine-Induced Status Epilepticus Mice. [PDF]

J Med Chem
Ganesh T, Pourkhodadad S, Heman-Bozadas P, Dingledine R, Wang W, Rawat V, Varvel NH, Herr RJ, Jiang Q, Johnson G.   +9 more
europepmc   +1 more source

Anomer-Selective Vorbrüggen Reaction for the Catalytic Synthesis of C₂-Deoxynucleoside Analogues. [PDF]

J Am Chem Soc
McMinn TL, Kozuszek CT, Owen BA, Legaux NM, Hearne WA, Leibfarth FA, Gagné MR.   +6 more
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Direct Fluoroformylation of the C3-Position of Indoles with 2,4-Dinitro(trifluoromethoxy)benzene as Fluorocarbonyl Source. [PDF]

ChemistryOpen
Wisson L, Hanquet G, Toulgoat F, Billard T, Leroux FR, Panossian A.   +5 more
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3-methylindole inhibits lipid peroxidation

Biochemical and Biophysical Research Communications, 1987
The mechanism of pneumotoxicity of 3-methylindole has been postulated to occur via protein alkylation or lipid peroxidation. This report describes the effects of the addition of 3-methylindole to goat lung microsomes to evaluate the possibility that this xenobiotic may increase NADPH-supported lipid peroxidation.
Garold S Yost, G S Yost
exaly   +3 more sources

Pharmacological modulation of the pneumotoxicity of 3-methylindole

Biochemical Pharmacology, 1982
The nature of the reactive metabolite of 3-methylindole is investigated using microsomal preparations prepared from the lungs of cattle. Nucleophilic thiol agents, glutathione, L-cysteine and N-acetyl-L-cysteine, protected microsomal proteins against alkylation by the reactive metabolite of 3-methylindole.
M S, Hanafy, J A, Bogan
openaire   +2 more sources