norvaline has been researched along with glycine in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (20.00) | 18.7374 |
1990's | 2 (20.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 5 (50.00) | 24.3611 |
2020's | 1 (10.00) | 2.80 |
Authors | Studies |
---|---|
Akamatsu, M; Asao, M; Fujita, T; Iwamura, H | 1 |
Brandsch, M; Gebauer, S; Laug, L; Schäfer, S; Thondorf, I; Voigt, V; Zebisch, K | 1 |
Friebele, E; Ponnamperuma, C; Shimoyama, A | 1 |
Goldsmith, JO; Kuo, LC | 1 |
Caprio, J; Valentincic, T | 1 |
Chao, P; Deshmukh, M; Gao, D; Kutscher, HL; Sinko, PJ | 1 |
Anufrieva, NV; Demidkina, TV; Faleev, NG; Fedorova, OS; Kuznetsov, NA; Kuznetsova, AA; Morozova, EA; Nikulin, AD; Revtovich, SV | 1 |
Barros, MC; Esteso, MA; Ribeiro, AC; Rodrigo, MM; Rodrigues, DF; Rodriguez, DM; Romero, CM; Verissimo, LM | 1 |
Bearne, SL; MacMillan, JWM; McCluskey, GD; Sorbara, NT | 1 |
Camacho-Davila, AA; Chavez-Flores, D; Espinoza-Hicks, JC; Zaragoza-Galan, G | 1 |
10 other study(ies) available for norvaline and glycine
Article | Year |
---|---|
Quantitative structure-activity relationships of the bitter thresholds of amino acids, peptides, and their derivatives.
Topics: Amino Acids; Humans; Mathematics; Peptides; Structure-Activity Relationship; Taste | 1987 |
Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1).
Topics: Amino Acid Transport Systems; Caco-2 Cells; Endocytosis; Humans; Kinetics; Models, Chemical; Models, Molecular; Molecular Conformation; Quantitative Structure-Activity Relationship; Substrate Specificity; Symporters | 2011 |
Adsorption of protein and non-protein amino acids on a clay mineral: a possible role of selection in chemical evolution.
Topics: Adsorption; Alanine; Amino Acids; Bentonite; Biological Evolution; Chemical Phenomena; Chemistry; gamma-Aminobutyric Acid; Glycine; Hydrogen-Ion Concentration; Isoleucine; Sarcosine; Valine | 1980 |
Protonation of arginine 57 of Escherichia coli ornithine transcarbamoylase regulates substrate binding and turnover.
Topics: Arginine; Carbamyl Phosphate; Catalysis; Electrochemistry; Escherichia coli; Glycine; Histidine; Hydrogen-Ion Concentration; Kinetics; Ornithine; Ornithine Carbamoyltransferase; Phosphates; Point Mutation; Protein Conformation; Protons; Structure-Activity Relationship; Substrate Specificity; Valine | 1993 |
Visual and chemical release of feeding behavior in adult rainbow trout.
Topics: Alanine; Amino Acids; Animals; Arginine; Betaine; Bites and Stings; Dose-Response Relationship, Drug; Feeding Behavior; Glycine; Leucine; Movement; Olfactory Pathways; Oncorhynchus mykiss; Photic Stimulation; Proline; Propionates; Reproducibility of Results; Stimulation, Chemical; Swimming; Taste; Valine | 1997 |
A series of alpha-amino acid ester prodrugs of camptothecin: in vitro hydrolysis and A549 human lung carcinoma cell cytotoxicity.
Topics: Alanine; Aminobutyrates; Antineoplastic Agents, Phytogenic; Camptothecin; Cell Proliferation; Cell Survival; Esters; Glycine; Humans; Hydrolysis; Lung Neoplasms; Prodrugs; Tumor Cells, Cultured; Valine | 2010 |
Pre-steady-state kinetic and structural analysis of interaction of methionine γ-lyase from Citrobacter freundii with inhibitors.
Topics: Alanine; Bacterial Proteins; Carbon-Sulfur Lyases; Catalytic Domain; Citrobacter freundii; Crystallography, X-Ray; Cycloserine; Cysteine; Enzyme Inhibitors; Escherichia coli; Gene Expression; Glycine; Imines; Kinetics; Models, Chemical; Pyridoxal Phosphate; Recombinant Proteins; Thermodynamics; Valine | 2015 |
Limiting values of diffusion coefficients of glycine, alanine, α-amino butyric acid, norvaline and norleucine in a relevant physiological aqueous medium.
Topics: Alanine; Butyric Acid; Diffusion; Glycine; Hydrophobic and Hydrophilic Interactions; Norleucine; Osmolar Concentration; Valine | 2017 |
Substrate-product analogue inhibitors of isoleucine 2-epimerase from Lactobacillus buchneri by rational design.
Topics: Binding Sites; Biocatalysis; Drug Design; Enzyme Inhibitors; Glycine; Isoleucine; Lactobacillus; Models, Molecular; Molecular Conformation; Racemases and Epimerases; Substrate Specificity; Valine | 2019 |
Stereoselective synthesis of S-norvaline and related amino acids through a common intermediate.
Topics: Allylglycine; Amino Acids; Catalysis; Glycine; Stereoisomerism; Valine | 2023 |