Results 101 to 110 of about 6,701 (204)

Effect of L-penicillamine Hydantoin, and Analog of Glutathione, On Rat-liver Glutathione-peroxidase, Reductase and Transferase Reactions

open access: yes, 1992
In soluble fractions prepared from rat liver homogenates, L-penicillamine hydantoin appeared to be, on the basis of SH consumption measurements, a substrate for glutathione peroxidase but not transferase reactions.
Hénichart, Jean-Pierre   +3 more
core   +1 more source

Diastereoselective synthesis of benzofuran-3(2H)-one-hydantoin dyads

open access: yes
a-convenient diastereoselective rearrangement of the racemic (R/S)-spirolchroman-2,4'-imidazolidine]-2',4,5'-triones 3a-c into (2'R,5S)- and (2'S,5R)-5-(3-oxo-2,3-dihydrobenzofuran-2-yl)imidazolidine-2,4-diones 4a-c under alkali conditions is described ...
Fernandes, Jose A.   +4 more
core   +1 more source

Polypeptide-Hydantoins [PDF]

open access: yesProceedings of the National Academy of Sciences, 1916
openaire   +2 more sources

Hydantoin and Its Derivatives Reduce the Viscosity of Concentrated Antibody Formulations by Inhibiting Associations via Hydrophobic Amino Acid Residues

open access: yes, 2019
Therapeutic antibodies for subcutaneous (SC) injection must be formulated at high concentrations because of the large therapeutic dose and volume restriction.
Tomoshi Kameda   +7 more
core   +1 more source

One-Pot Synthesis of Chiral, Spirocyclic 4‑Hydantoin-Proline Derivatives for Incorporation into Spiroligomer-Based Macromolecules

open access: yes, 2017
Derivatives of 4-hydantoin-proline have been synthesized via a direct two-step alkylation method. This method is valuable in the development of applications of N,N′-disubstituted hydantoin bearing α-amino acids by improving yields, reducing the time and ...
Christian E. Schafmeister (127045)   +2 more
core   +1 more source

Characterization of the hydantoin-hydrolysing system of Pseudomonas putida RU-KM3s [PDF]

open access: yes, 2005
The biocatalytic conversion of 5-monosubstituted hydantoin derivatives to optically pure amino acids involves two reaction steps: the hydrolysis of hydantoin to N-carbamylamino acid by an hydantoinase or dihydropyrimidinase enzyme, followed by conversion
Matcher, Gwynneth Felicity
core  

Chiral hydantoin resolution

open access: yes, 1990
A method for resolving chiral hydantoins having general formula (I), wherein R1 is a lower alkyl radical having 1-5 carbon atoms in a linear or branched chain; and R2 is a phenyl radical which is optionally mono-, di- or trisubstituted by lower alkoxy or
Coquerel, Gérard   +3 more
core  

Fetal Hydantoin Syndrome [PDF]

open access: yesThe Journal of Pediatrics, 2017
Avani Hegde   +7 more
openaire   +2 more sources

Total Synthesis and Biological Evaluation of Exiguamines. [PDF]

open access: yesJACS Au
Noh S   +6 more
europepmc   +1 more source

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