L-Valine (CAS 72-18-4)
L-Valine
CAS 72-18-4 · C5H11NO2 · MW 117.15 g/mol
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20 artykułów · 14 open access · Źródła: PubMed, OpenAlex, Semantic Scholar
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Fa Liu, Jung-Eun Park, Kyung S. Lee et al. (2009) · Tetrahedron
AI Summary
The application of 4 in the solid-phase synthesis of polo-like kinase 1 (Plk1) polo box domain (PBD)-binding peptides retain PBD binding efficacy similar to a parent pThr containing peptide should be a highly useful reagent for the preparation of signal transduction-directed peptides.
The application of 4 in the solid-phase synthesis of polo-like kinase 1 (Plk1) polo box domain (PBD)-binding peptides retain PBD binding efficacy similar to a parent pThr containing peptide should be a highly useful reagent for the preparation of signal transduction-directed peptides.
I. Cho, C. Kong (2024) · Animal bioscience
P. Strickland, Zheng Qian, M. Friesen et al. (2002) · Mutation research
AI Summary
It is indicated that significant amounts of PhIP are bioavailable from ingestion of fried or char-broiled meats, and that urinary PhIP metabolites reflect recent (12-24h) ingestion, and significant interindividual differences in the amounts of urine PhIP metabolite excreted are observed following ingestion of similar amounts ofPhIP.
It is indicated that significant amounts of PhIP are bioavailable from ingestion of fried or char-broiled meats, and that urinary PhIP metabolites reflect recent (12-24h) ingestion, and significant interindividual differences in the amounts of urine PhIP metabolite excreted are observed following ingestion of similar amounts ofPhIP.
L. Juknaitė, Yutaro Sugamata, K. Tokiwa et al. (2013) · Journal of Medicinal Chemistry
AI Summary
In vivo and in vitro neuronal activities of both enantiomers of IKM-159 prepared by enantioselective asymmetric synthesis are reported, consistent with a pharmacological action as competitive antagonist of AMPA receptors.
In vivo and in vitro neuronal activities of both enantiomers of IKM-159 prepared by enantioselective asymmetric synthesis are reported, consistent with a pharmacological action as competitive antagonist of AMPA receptors.
Amalendu Pal, Nalin Chauhan (2011) · Journal of Chemical & Engineering Data
Qu B, Zhao F, Song Y et al. (2024) · PloS one
Golsorkhi M, Koch J, Pedouim F et al. (2024) · Tremor and other hyperkinetic movements (New York, N.Y.)
Zhenning Yan, Yang Zhao, Ronghua Xing et al. (2010)
Zhenning Yan, Yang Zhao, Ronghua Xing et al. (2009) · Journal of Chemical & Engineering Data
U. Madsen, K. Frydenvang, B. Ebert et al. (1996) · Journal of Medicinal Chemistry
AI Summary
(R,S)-2-Amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid is a potent and selective agonist at the N- methyl-D-aspartic acid (NMDA) subtype of excitatory amino acid receptors.
(R,S)-2-Amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid is a potent and selective agonist at the N- methyl-D-aspartic acid (NMDA) subtype of excitatory amino acid receptors.
Keam SJ (2024) · Drugs
Xie M, Tang T, Liang H (2023) · Clinical cardiology
T. Kasim, Andrey G. Yavorsky, I. Mandel et al. (2026) · Journal of Clinical Practice
AI Summary
Perioperative intravenous infusion of a balanced amino acid solution safely reduces the incidence and severity of AKI and improves renal functional parameters after cardiac surgery with CPB, supporting its use as an early nephroprotective strategy.
Perioperative intravenous infusion of a balanced amino acid solution safely reduces the incidence and severity of AKI and improves renal functional parameters after cardiac surgery with CPB, supporting its use as an early nephroprotective strategy.
Maria Annunziata M. Capozzi, Cosimo Cardellicchio (2022) · Molbank
El-Hachem N, Leclercq M, Susaeta Ruiz M et al. (2024) · Nature cell biology
Wang ER, Cho K, Harrison GA et al. (2025) · Proceedings of the National Academy of Sciences of the United States of America
Kamali R, Rashki Ghaleno L, Izadi A et al. (2025) · Zygote (Cambridge, England)
Ianevski A, Frøysa IT, Lysvand H et al. (2024) · Antiviral research
Loggers ET, Chugh R, Federman N et al. (2024) · Cancer
Shu R, Tian S, Qu W et al. (2025) · Journal of lipid research
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