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  2. Peptide - Wikipedia

    en.wikipedia.org/wiki/Peptide

    A peptide hormone is a peptide that acts as a hormone. A proteose is a mixture of peptides produced by the hydrolysis of proteins. The term is somewhat archaic. A peptidergic agent (or drug) is a chemical which functions to directly modulate the peptide systems in the body or brain. An example is opioidergics, which are neuropeptidergics.

  3. Tripeptide - Wikipedia

    en.wikipedia.org/wiki/Tripeptide

    A tripeptide (example Val-Gly-Ala) with green marked amino end (L-Valine) and blue marked carboxyl end (L-Alanine) A tripeptide is a peptide derived from three amino acids joined by two or sometimes three peptide bonds. [1] As for proteins, the function of peptides is determined by the constituent amino acids and their sequence.

  4. Drug nomenclature - Wikipedia

    en.wikipedia.org/wiki/Drug_nomenclature

    Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs.In the majority of circumstances, drugs have 3 types of names: chemical names, the most important of which is the IUPAC name; generic or nonproprietary names, the most important of which are international nonproprietary names (INNs); and trade names, which are brand names. [1]

  5. Oligopeptide - Wikipedia

    en.wikipedia.org/wiki/Oligopeptide

    blue marked carboxyl end (L-Alanine) A tetrapeptide (example Val-Gly-Ser-Ala) with green marked amino end (L-valine) and blue marked carboxyl end (L-alanine) An oligopeptide (oligo-, "a few"), is a peptide consisting of two to twenty amino acids, including dipeptides, tripeptides, tetrapeptides, and other polypeptides.

  6. Tetrapeptide - Wikipedia

    en.wikipedia.org/wiki/Tetrapeptide

    [1] [2] Tetrapeptides may be cyclized by a fourth peptide bond or other covalent bonds. Examples of tetrapeptides are: Tuftsin (L-threonyl-L-lysyl-L-prolyl-L-arginine) is a peptide related primarily to the immune system function. Rigin (glycyl-L-glutaminyl-L-prolyl-L-arginine) is a tetrapeptide with functions similar to those of tuftsin.

  7. Peptide bond - Wikipedia

    en.wikipedia.org/wiki/Peptide_bond

    Peptide bond formation via dehydration reaction. When two amino acids form a dipeptide through a peptide bond, [1] it is a type of condensation reaction. [2] In this kind of condensation, two amino acids approach each other, with the non-side chain (C1) carboxylic acid moiety of one coming near the non-side chain (N2) amino moiety of the other.

  8. List of proteins - Wikipedia

    en.wikipedia.org/wiki/List_of_proteins

    The human genome, categorized by function of each gene product, given both as number of genes and as percentage of all genes. [7]Proteins may also be classified based on their cellular function.

  9. Dipeptide - Wikipedia

    en.wikipedia.org/wiki/Dipeptide

    Diphenylalanine is the most studied building block in peptide nanotechnology; Kyotorphin (L-tyrosyl-L-arginine) is a neuroactive dipeptide which plays a role in pain regulation in the brain. Balenine (or ophidine) (beta-alanyl-N tau-methyl histidine) has been identified in the muscles of several species of mammal (including man), and the chicken.