Chemistry:Tynorphin
From HandWiki
Short description: Synthetic opioid chemical compound
|  | |
| Clinical data | |
|---|---|
| ATC code | 
 | 
| Legal status | |
| Legal status | 
 | 
| Identifiers | |
| 
 | |
| PubChem CID | |
| ChemSpider | |
| Chemical and physical data | |
| Formula | C35H46N6O7 | 
| Molar mass | 662.788 g·mol−1 | 
| 3D model (JSmol) | |
| 
 | |
| 
 | |
Tynorphin is a synthetic opioid peptide which is a potent and competitive inhibitor of the enkephalinase class of enzymes which break down the endogenous enkephalin peptides.[1] It specifically inactivates dipeptidyl aminopeptidase III (DPP3) with very high efficacy, but also inhibits neutral endopeptidase (NEP), aminopeptidase N (APN), and angiotensin-converting enzyme (ACE) to a lesser extent.[1] It has a pentapeptide structure with the amino acid sequence Val-Val-Tyr-Pro-Trp (VVYPW).
Tynorphin was discovered in an attempt to develop an enkephalinase inhibitor of greater potency than spinorphin.[1]
See also
References
|  | 


