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Pharmacokinetics glucagon

The first and the second approaches have provided some positive results but, unfortunately, they depend upon the structure of the protein. Typical examples of sequence modifications to improve stability and pharmacokinetics are the preparation of humanized antibodies, where part of the mouse sequence is substituted by the human form, and the granulocyte colony-stimulating factor muteins, where up to seven amino acids are substituted. Examples of truncated sequence proteins with improved characteristic are the 7-36 analogues of glucagon-like peptides or the 1-29 sequence growth hormone-releasing factor [1, 2]. [Pg.271]

Pharmacokinetics, pharmacodynamics, safety, and tolerability of a single-dose of NN2211, a long-acting glucagon-like peptide 1 derivative, in healthy male subjects. Diabetes Care 2002 25(8) 1398 04. [Pg.1512]

Knudsen LB, Nielsen PF, Huusfeldt PO, Johansen NL, Madsen K, Pedersen FZ, et al. Potent derivatives of glucagon-hke peptide-1 with pharmacokinetic properties suitable for once daily administration. J Med Chem 2000 43 1664-1669. [Pg.136]


See other pages where Pharmacokinetics glucagon is mentioned: [Pg.179]    [Pg.356]    [Pg.224]    [Pg.387]    [Pg.17]    [Pg.634]    [Pg.10]    [Pg.2698]    [Pg.179]    [Pg.175]    [Pg.136]    [Pg.470]    [Pg.2166]    [Pg.18]    [Pg.40]    [Pg.179]    [Pg.268]    [Pg.398]    [Pg.87]   
See also in sourсe #XX -- [ Pg.387 ]




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Glucagon

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