Substitution on the Phe3 aromatic ring in cyclic .delta. opioid receptor-selective dermorphin/deltorphin tetrapeptide analogs: electronic and lipophilic requirements for receptor affinity

1992 ◽  
Vol 35 (9) ◽  
pp. 1535-1541 ◽  
Author(s):  
Deborah L. Heyl ◽  
Henry I. Mosberg
1993 ◽  
Vol 115 (18) ◽  
pp. 8503-8504 ◽  
Author(s):  
Sharon D. Bryant ◽  
Severo Salvadori ◽  
Martti Attila ◽  
Lawrence H. Lazarus

2001 ◽  
Vol 48 (4) ◽  
pp. 1165-1168 ◽  
Author(s):  
A Olma ◽  
A Gniadzik ◽  
A W Lipkowski ◽  
M Lachwa

New analogues of deltorphin I (DT I), in which the phenylalanine residue in position 3 is substituted with amphiphilic alpha,alpha-disubstituted amino acid enantiomers, (R) and (S)-alpha-hydroxymethylnaphtylalanine, were synthesized and tested for mu and delta opioid receptor affinity and selectivity. Although both analogues have lower affinity to delta receptors than DT I, they both expressed specificity to delta receptors.


Analgesia ◽  
1995 ◽  
Vol 1 (3) ◽  
pp. 195-200 ◽  
Author(s):  
Benjamin Kest ◽  
Shirzad Jenab ◽  
Charles E. Inturrisi

1993 ◽  
Vol 268 (31) ◽  
pp. 23055-23058
Author(s):  
H Kong ◽  
K Raynor ◽  
K Yasuda ◽  
S.T. Moe ◽  
P.S. Portoghese ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document