(D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt

Modify Date: 2024-01-17 17:58:22

(D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt Structure
(D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt structure
Common Name (D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt
CAS Number 444073-04-5 Molecular Weight N/A
Density N/A Boiling Point N/A
Molecular Formula C226H338N60O66S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of (D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt


[D-Ala2]-GIP (human) is a GIP receptor agonist. [D-Ala2]-GIP (human) improves glucose tolerance. [D-Ala2]-GIP (human) shows neuroprotective activity in MPTP-induced Parkinson's disease model. [D-Ala2]-GIP (human) also improves cognitive function and hippocampal synaptic plasticity in obese diabetic rats. [D-Ala2]-GIP (human) can be used for research of type 2 diabetes, Parkinson's disease, etc[1]

 Names

Name (D-Ala2)-Gastric Inhibitory Polypeptide (human) trifluoroacetate salt

  Biological Activity

Description [D-Ala2]-GIP (human) is a GIP receptor agonist. [D-Ala2]-GIP (human) improves glucose tolerance. [D-Ala2]-GIP (human) shows neuroprotective activity in MPTP-induced Parkinson's disease model. [D-Ala2]-GIP (human) also improves cognitive function and hippocampal synaptic plasticity in obese diabetic rats. [D-Ala2]-GIP (human) can be used for research of type 2 diabetes, Parkinson's disease, etc[1]
Related Catalog
References

[1]. Hinke SA, et al. Dipeptidyl peptidase IV-resistant [D-Ala(2)]glucose-dependent insulinotropic polypeptide (GIP) improves glucose tolerance in normal and obese diabetic rats. Diabetes. 2002 Mar;51(3):652-61.  

[2]. Porter DW,et al. Prolonged GIP receptor activation improves cognitive function, hippocampal synaptic plasticity and glucose homeostasis in high-fat fed mice. Eur J Pharmacol. 2011 Jan 15;650(2-3):688-93.  

[3]. Verma MK, et al. Effect of D-Ala2GIP, a stable GIP receptor agonist on MPTP-induced neuronal impairments in mice. Eur J Pharmacol. 2017 Jun 5;804:38-45.  

 Chemical & Physical Properties

Molecular Formula C226H338N60O66S