NVP DPP 728 dihydrochloride

Modify Date: 2024-01-28 11:16:26

NVP DPP 728 dihydrochloride Structure
NVP DPP 728 dihydrochloride structure
Common Name NVP DPP 728 dihydrochloride
CAS Number 207556-62-5 Molecular Weight 371.265
Density N/A Boiling Point N/A
Molecular Formula C15H20Cl2N6O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of NVP DPP 728 dihydrochloride


NVP-DPP728 dihydrochloride is a potent, selective and orally active dipeptidyl peptidase IV (DPP-IV) inhibitor with a Ki of 11 nM. NVP-DPP728 dihydrochloride can be used for the research of diabetes mellitus[1][2].

 Names

Name 6-{[2-({2-[(2S)-2-Cyano-1-pyrrolidinyl]-2-oxoethyl}amino)ethyl]am ino}nicotinonitrile dihydrochloride
Synonym More Synonyms

 NVP DPP 728 dihydrochloride Biological Activity

Description NVP-DPP728 dihydrochloride is a potent, selective and orally active dipeptidyl peptidase IV (DPP-IV) inhibitor with a Ki of 11 nM. NVP-DPP728 dihydrochloride can be used for the research of diabetes mellitus[1][2].
Related Catalog
Target

Ki: 11 nM (DPP-IV) [1]

In Vivo NVP-DPP728 inhibits DPP-IV and improves insulin secretion and glucose tolerance, probably through augmentation of the effects of endogenous GLP-1[2]. Animal Model: Obese (fa/fa) and lean (FA/?) Zucker rats[2] Dosage: 3.715 mg/kg Administration: Oral administration Result: Led to inhibition of plasma DPP-IV activity.
References

[1]. T E Hughes, et al. NVP-DPP728 (1-[[[2-[(5-cyanopyridin-2-yl)amino]ethyl]amino]acetyl]-2-cyano-(S)- pyrrolidine), a slow-binding inhibitor of dipeptidyl peptidase IV. Biochemistry. 1999 Sep 7;38(36):11597-603.

[2]. B Balkan, et al. Inhibition of dipeptidyl peptidase IV with NVP-DPP728 increases plasma GLP-1 (7-36 amide) concentrations and improves oral glucose tolerance in obese Zucker rats. Diabetologia. 1999 Nov;42(11):1324-31.

 Chemical & Physical Properties

Molecular Formula C15H20Cl2N6O
Molecular Weight 371.265
Exact Mass 370.107574
PSA 108.07000
LogP 1.82406

 Synonyms

3-Pyridinecarbonitrile, 6-[[2-[[2-[(2S)-2-cyano-1-pyrrolidinyl]-2-oxoethyl]amino]ethyl]amino]-, hydrochloride (1:2)
6-{[2-({2-[(2S)-2-Cyano-1-pyrrolidinyl]-2-oxoethyl}amino)ethyl]amino}nicotinonitrile dihydrochloride
6-{[2-({2-[(2S)-2-Cyanopyrrolidin-1-yl]-2-oxoethyl}amino)ethyl]amino}nicotinonitrile dihydrochloride
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