Teduglutide
Also called Gattex, Revestive
Part of the metabolic pathway of Teduglutide. See the timeline on the metabolic highway.
Overview
Teduglutide, sold under the brand names Revestive (EU) and Gattex (US), is a 33-membered polypeptide and glucagon-like peptide-2 (GLP-2) analog that is used for the treatment of short bowel syndrome. It works by promoting mucosal growth and possibly restoring gastric emptying and secretion. It was approved in both the European Union and the United States in 2012.[1]
Uses, dosage and effects
Medical uses
Up to a certain point, the gut can adapt to partial resections that result in short bowel syndrome. Still, parenteral substitution of water, minerals and vitamins (depending on which part of the gut has been removed) is often necessary. Teduglutide may reduce or shorten the necessity of such infusions by improving the intestinal mucosa and possibly by other mechanisms.[5] WP
Risks and side effects
Adverse effects
Common adverse effects in clinical studies included abdominal discomfort (49% of patients), respiratory infections (28%), nausea (27%) and vomiting (14%), local reactions at the injection site (21%), and headache (17%).[5] WP
Legal status
Legal status
It was approved in both the European Union (brand name Revestive) and the United States (brand name Gattex) in 2012. It was granted orphan drug designation by the European Medicines Agency (EMA).[2]
Chemistry
- Formula
- C164H252N44O55S PC
- CAS number
- 197922-42-2 PC
- Molar mass (g/mol)
- 3752.1 PC
- IUPAC name (computed by PubChem)
- (2S)
- PC2- [[(2S, 3R) - 2- [[(2S, 3S) - 2- [[(2S) - 6- amino- 2- [[(2S, 3R) - 2- [[(2S) - 5- amino- 2- [[(2S, 3S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 4- amino- 2- [[(2S, 3S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 4- amino- 2- [[(2S) - 2- [[(2S) - 2- [[(2S, 3S) - 2- [[(2S, 3R) - 2- [[(2S) - 4- amino- 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[(2S) - 2- [[2- [[(2S) - 2- [[2- [[(2S) - 2- amino- 3- (1H- imidazol- 5- yl) propanoyl] amino] acetyl] amino] - 3- carboxypropanoyl] amino] acetyl] amino] - 3- hydroxypropanoyl] amino] - 3- phenylpropanoyl] amino] - 3- hydroxypropanoyl] amino] - 3- carboxypropanoyl] amino] - 4- carboxybutanoyl] amino] - 4- methylsulfanylbutanoyl] amino] - 4- oxobutanoyl] amino] - 3- hydroxybutanoyl] amino] - 3- methylpentanoyl] amino] - 4- methylpentanoyl] amino] - 3- carboxypropanoyl] amino] - 4- oxobutanoyl] amino] - 4- methylpentanoyl] amino] propanoyl] amino] propanoyl] amino] - 5- carbamimidamidopentanoyl] amino] - 3- carboxypropanoyl] amino] - 3- phenylpropanoyl] amino] - 3- methylpentanoyl] amino] - 4- oxobutanoyl] amino] - 3- (1H- indol- 3- yl) propanoyl] amino] - 4- methylpentanoyl] amino] - 3- methylpentanoyl] amino] - 5- oxopentanoyl] amino] - 3- hydroxybutanoyl] amino] hexanoyl] amino] - 3- methylpentanoyl] amino] - 3- hydroxybutanoyl] amino] butanedioic acid - SMILES
- CC[C@H]
(C) PC[C@@H] (C(=O) N[C@@H] ([C@@H] (C) O) C(=O) N[C@@H] (CC(=O) O) C(=O) O) NC(=O) [C@H] (CCCCN) NC(=O) [C@H] ([C@@H] (C) O) NC(=O) [C@H] (CCC(=O) N) NC(=O) [C@H] ([C@@H] (C) CC) NC(=O) [C@H] (CC(C) C) NC(=O) [C@H] (CC1=CNC2=CC=CC=C21) NC(=O) [C@H] (CC(=O) N) NC(=O) [C@H] ([C@@H] (C) CC) NC(=O) [C@H] (CC3=CC=CC=C3) NC(=O) [C@H] (CC(=O) O) NC(=O) [C@H] (CCCNC(=N) N) NC(=O) [C@H] (C) NC(=O) [C@H] (C) NC(=O) [C@H] (CC(C) C) NC(=O) [C@H] (CC(=O) N) NC(=O) [C@H] (CC(=O) O) NC(=O) [C@H] (CC(C) C) NC(=O) [C@H] ([C@@H] (C) CC) NC(=O) [C@H] ([C@@H] (C) O) NC(=O) [C@H] (CC(=O) N) NC(=O) [C@H] (CCSC) NC(=O) [C@H] (CCC(=O) O) NC(=O) [C@H] (CC(=O) O) NC(=O) [C@H] (CO) NC(=O) [C@H] (CC4=CC=CC=C4) NC(=O) [C@H] (CO) NC(=O) CNC(=O) [C@H] (CC(=O) O) NC(=O) CNC(=O) [C@H] (CC5=CN=CN5) N - InChIKey
- CILIXQOJUNDIDU-
ASQIGDHWSA- PCN - PubChem CID
- 16139605
Harm reduction information
No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.
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Sources
- Journal / agency Jeppesen PB. Teduglutide, a novel glucagon-like peptide 2 analog, in the treatment of patients with short bowel syndrome. Therapeutic Advances in Gastroenterology. May 2012. doi:10.1177/1756283X11436318 · PMID 22570676 · PMC3342570
- Journal / agency Revestive EPAR. 11 December 2001
- Journal / agency Gattex- teduglutide injection, powder, lyophilized, for solution; Gattex- teduglutide kit. 28 February 2024
- Other Teduglutide Viatris Product information. 8 January 2026
- Journal / agency Klement A. Das Kurzdarmsyndrom ist erstmals behandelbar: Revestive. Österreichische Apothekerzeitung. 5 January 2015
- Other Revestive Product information. 4 September 2012
Text and values on this page are quoted from Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.