Results 241 to 250 of about 457,288 (287)

N-Acetyl-L-Cysteine (NAC) Blunts Axitinib-Related Adverse Effects in Preclinical Models of Glioblastoma. [PDF]

open access: yesCancer Med
Formato A   +14 more
europepmc   +1 more source

L-cysteine contributes to destructive activities of odontogenic cysts/tumor. [PDF]

open access: yesDiscov Oncol
Li J   +6 more
europepmc   +1 more source

Injectable hyaluronate-L- cysteine gel potentiates photothermal therapy in osteosarcoma via vorinostat-copper cell death. [PDF]

open access: yesMater Today Bio
Wang S   +10 more
europepmc   +1 more source
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L-Cysteine Nitrates

Journal of Structural Chemistry, 2023
The formation of salts in the l-cysteine–HNO3–H2O system was studied yielding three representatives as single crystals: anhydrous l-cysteinium nitrate (l-CysH)NO3 (I) and two new salts (l-CysH···l-Cys)NO3 (II) and (l-CysH···l-Cys)NO3∙0.5H2O (III) with the dimeric (l-CysH···l-Cys) cation.
Giester, G.   +4 more
openaire   +3 more sources

N-acetyl-l-cysteine

Journal of Cellular Biochemistry, 1993
The most commonly used chemopreventive agents in the prevention of oral leukoplakia, head and neck cancer, and lung cancer are beta-carotene, vitamin A, and other retinoids. One of the few chemopreventive agents not in this group and presently being used in a clinical trial is N-acetyl-l-cysteine (NAC).
N. D. Vries, DE FLORA, SILVIO
openaire   +3 more sources

S-Carboxymethyl-L-cysteine

Drug Metabolism Reviews, 2012
S-carboxymethyl-L-cysteine, the side-chain carboxymethyl derivative of the sulfur-containing amino acid, cysteine, has been known and available for almost 80 years. During this time, it has been put to a variety of uses, but it is within the field of respiratory medicine that, presently, it has found a clinical niche.
Mitchell, SC, Steventon, GB
openaire   +3 more sources

Mechanisms of L-Cysteine Neurotoxicity

Neurochemical Research, 2000
We review here the possible mechanisms of neuronal degeneration caused by L-cysteine, an odd excitotoxin. L-Cysteine lacks the omega carboxyl group required for excitotoxic actions via excitatory amino acid receptors, yet it evokes N-methyl-D-aspartate (NMDA) -like excitotoxic neuronal death and potentiates the Ca2+ influx evoked by NMDA.
R, Janáky   +4 more
openaire   +2 more sources

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