Diprotin A TFA (Ile-Pro-Pro (TFA))

Modify Date: 2024-01-21 13:00:39

Diprotin A TFA (Ile-Pro-Pro (TFA)) Structure
Diprotin A TFA (Ile-Pro-Pro (TFA)) structure
Common Name Diprotin A TFA (Ile-Pro-Pro (TFA))
CAS Number 209248-71-5 Molecular Weight 455.47
Density N/A Boiling Point N/A
Molecular Formula C19H32F3N3O6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Diprotin A TFA (Ile-Pro-Pro (TFA))


Diprotin A (TFA) is an inhibitor of dipeptidyl peptidase IV (DPP-IV).

 Names

Name Diprotin A TFA

 Diprotin A TFA (Ile-Pro-Pro (TFA)) Biological Activity

Description Diprotin A (TFA) is an inhibitor of dipeptidyl peptidase IV (DPP-IV).
Related Catalog
Target

DPP-IV[1].

In Vitro Diprotin A increases the phosphorylation of Src and vascular endothelial-cadherin (VE-cadherin) in human endothelial cells and disrupts endothelial cell-to-cell junctions, which are attenuated by CXCR4 (receptor of SDF-1α)-blocker or Src-inhibitor[1].
In Vivo In the model of retinopathy of prematurity, Diprotin A increases not only retinal vascularity but also leakage. Additionally, in the murine diabetic retinopathy model, Diprotin A increases the phosphorylation of Src and VE-cadherin and aggravates vascular leakage in the retinas. Collectively, Diprotin A induces vascular leakage by augmenting the SDF-1α/CXCR4/Src/VE-cadherin signaling pathway[1].
References

[1]. Lee CS, et al. Dipeptidyl Peptidase-4 Inhibitor Increases Vascular Leakage in Retina through VE-cadherin Phosphorylation. Sci Rep. 2016 Jul 6;6:29393.

 Chemical & Physical Properties

Molecular Formula C19H32F3N3O6
Molecular Weight 455.47
Storage condition 2-8℃
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