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Semaglutide: difference between revisions

Diff·revision 16 → 17·22:02, 3 Jan 2025

Difference between revision 16 and revision 17 of Semaglutide. 2 lines changed; the page grew by 75 bytes.

Revision 16 — 04:56, 20 Dec 2024
ApoB_Aurelio (talk)
attribute the mechanism claim to the review rather than stating it flatly
6,658 bytes ±0
Revision 17 — 22:02, 3 Jan 2025
NewLabNell (talk)
expand §Pharmacokinetics
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20{{hatnote|For the oral formulation and its absorption enhancer, see [[Oral semaglutide]]. For the drug class, see [[GLP-1 receptor agonist]].}}20{{hatnote|For the oral formulation and its absorption enhancer, see [[Oral semaglutide]]. For the drug class, see [[GLP-1 receptor agonist]].}}
+21{{medical|talk=Scope of the research-material section}}
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22'''Semaglutide''' is an acylated analogue of [[Glucagon-like peptide-1]] and a [[GLP-1 receptor agonist]]. Three engineering changes to the native 31-residue sequence give it a circulating half-life of about seven days: α-aminoisobutyric acid at position 8 confers resistance to [[Dipeptidyl peptidase-4]], a C-18 fatty diacid attached at Lys26 confers [[Albumin binding half-life extension|albumin binding]], and an arginine substitution at position 34 leaves a single site available for acylation.{{r|lau2015}}23'''Semaglutide''' is an acylated analogue of [[Glucagon-like peptide-1]] and a [[GLP-1 receptor agonist]]. Three engineering changes to the native 31-residue sequence give it a circulating half-life of about seven days: α-aminoisobutyric acid at position 8 confers resistance to [[Dipeptidyl peptidase-4]], a C-18 fatty diacid attached at Lys26 confers [[Albumin binding half-life extension|albumin binding]], and an arginine substitution at position 34 leaves a single site available for acylation.{{r|lau2015}}
64* [[Oral semaglutide]]65* [[Oral semaglutide]]
65* [[STEP trial programme]]66* [[STEP trial programme]]
+67* [[SELECT trial]]
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67{{DEFAULTSORT:Semaglutide}}69{{DEFAULTSORT:Semaglutide}}