The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27676089 |
35 |
A Cyclic Tetrapeptide ("Cyclodal") and Its Mirror-Image Isomer Are Both High-Affinityµ Opioid Receptor Antagonists. |
Clinical Research Institute of Montreal |
27301366 |
30 |
[Dmt(1)]DALDA analogues modified with tyrosine analogues at position 1. |
Nanjing Medical University |
27035422 |
46 |
Bifunctional Peptide-Based Opioid Agonist-Nociceptin Antagonist Ligands for Dual Treatment of Acute and Neuropathic Pain. |
Vrije Universiteit Brussel |
27234885 |
31 |
Evaluation of N-substituent structural variations in opioid receptor profile of LP1. |
University of Catania |
26713106 |
59 |
Dual Alleviation of Acute and Neuropathic Pain by Fused Opioid Agonist-Neurokinin 1 Antagonist Peptidomimetics. |
Vrije Universiteit Brussel |
26656913 |
85 |
Multitarget opioid ligands in pain relief: New players in an old game. |
University of Catania |
26712115 |
36 |
Design synthesis and structure-activity relationship of 5-substituted (tetrahydronaphthalen-2yl)methyl with N-phenyl-N-(piperidin-2-yl)propionamide derivatives as opioid ligands. |
University of Arizona |
26330078 |
51 |
Synthesis and biological evaluation of 2-alkyl-2-methoxymethyl-salvinorin ethers as selective¿-opioid receptor agonists. |
Harvard Medical School |
26323872 |
49 |
Design and synthesis of novel bivalent ligands (MOR and DOR) by conjugation of enkephalin analogues with 4-anilidopiperidine derivatives. |
University of Arizona |
26299827 |
43 |
Discovery of 5-substituted tetrahydronaphthalen-2yl-methyl with N-phenyl-N-(piperidin-4-yl)propionamide derivatives as potent opioid receptor ligands. |
University of Arizona |
26346669 |
53 |
Synthesis of new opioid derivatives with a propellane skeleton and their pharmacologies: Part 5, novel pentacyclic propellane derivatives with a 6-amide side chain. |
University of Tsukuba |
26252963 |
15 |
Novel diazabicycloalkane delta opioid agonists. |
Istituto Di Farmacologia Traslazionale |
25283554 |
43 |
Design, synthesis, and structure-activity relationship of novel opioid¿ receptor selective agonists:a-iminoamide derivatives with an azabicyclo[2.2.2]octene skeleton. |
Kitasato University |
25147605 |
52 |
Synthesis and Pharmacology of a Novel¿ Opioid Receptor (KOR) Agonist with a 1,3,5-Trioxazatriquinane Skeleton. |
Kitasato University |
25129170 |
20 |
'Carba'-carfentanil (trans isomer): aµ opioid receptor (MOR) partial agonist with a distinct binding mode. |
Clinical Research Institute of Montreal |
25544687 |
60 |
Synthesis and biological evaluation of compact, conformationally constrained bifunctional opioid agonist - neurokinin-1 antagonist peptidomimetics. |
Vrije Universiteit Brussel |
25783191 |
87 |
Design, syntheses, and pharmacological characterization of 17-cyclopropylmethyl-3,14ß-dihydroxy-4,5a-epoxy-6a-(isoquinoline-3'-carboxamido)morphinan analogues as opioid receptor ligands. |
Virginia Commonwealth University |
25562563 |
18 |
Methoxyflavones from Stachys glutinosa with binding affinity to opioid receptors: in silico, in vitro, and in vivo studies. |
National Research Council |
25248680 |
67 |
Synthesis of a novel universal opioid receptor agonist with the 1,3,5-trioxazatriquinane skeleton and its pharmacologies. |
Kitasato University |
25221662 |
24 |
Novel cyclic biphalin analogue with improved antinociceptive properties. |
Universit£ |
24900842 |
71 |
Novel delta opioid receptor agonists with oxazatricyclodecane structure. |
Kitasato University |
24839540 |
26 |
In Vitro Membrane Permeation Studies and in Vivo Antinociception of Glycosylated Dmt |
Vrije Universiteit Brussel |
24613457 |
64 |
Endomorphin analogues with mixedµ-opioid (MOP) receptor agonism/d-opioid (DOP) receptor antagonism and lackingß-arrestin2 recruitment activity. |
Nanjing Medical University |
24602401 |
40 |
[Dmt(1)]DALDA analogues with enhancedµ opioid agonist potency and with a mixedµ/¿ opioid activity profile. |
Nanjing Medical University |
23547584 |
19 |
Biological active analogues of the opioid peptide biphalin: mixeda/ß(3)-peptides. |
Universit£ |
23360448 |
18 |
Development of¿ opioid receptor antagonists. |
Research Triangle Institute |
23200250 |
36 |
The effect of 17-N substituents on the activity of the opioid¿ receptor in nalfurafine derivatives. |
Kitasato University |
16290934 |
51 |
Highly potent and selective zwitterionic agonists of the delta-opioid receptor. Part 1. |
Pfizer |
7154003 |
7 |
A quantitative structure-activity relationship study of the inhibitory action of a series of enkephalin-like peptides in the guinea pig ileum and mouse vas deferens bioassays. |
TBA |
11133082 |
32 |
Assessment of substitution in the second pharmacophore of Dmt-Tic analogues. |
University of Naples |
23131341 |
50 |
Synthesis of novel triplet drugs with 1,3,5-trioxazatriquinane skeletons and their pharmacologies. 3: synthesis of novel triplet drugs with the bis(epoxymethano) or bis(dimethylepoxymethano) structure (double-capped triplet). |
Kitasato University |
23116891 |
15 |
Synthesis of new opioid derivatives with a propellane skeleton and their pharmacologies: part 3, novel propellane derivatives with pentacyclic skeletons. |
Kitasato University |
23103094 |
39 |
Essential structure of opioid¿ receptor agonist nalfurafine for binding to the¿ receptor 3: synthesis of decahydro(iminoethano)phenanthrene derivatives with an oxygen functionality at the 3-position and their pharmacologies. |
Kitasato University |
22325949 |
28 |
Novel TIPP (H-Tyr-Tic-Phe-Phe-OH) analogues displaying a wide range of efficacies at thed opioid receptor. Discovery of two highly potent and selectived opioid agonists. |
Clinical Research Institute of Montreal |
23102273 |
60 |
Variation of the net charge, lipophilicity, and side chain flexibility in Dmt(1)-DALDA: Effect on Opioid Activity and Biodistribution. |
Vrije Universiteit Brussel |
22966938 |
20 |
cis-4-amino-L-proline residue as a scaffold for the synthesis of cyclic and linear endomorphin-2 analogues: part 2. |
Universit£ |
22734622 |
78 |
Synthesis and evaluation of aryl-naloxamide opiate analgesics targeting truncated exon 11-associatedµ opioid receptor (MOR-1) splice variants. |
Memorial Sloan-Kettering Cancer Center |
22724433 |
76 |
A new class of highly potent and selective endomorphin-1 analogues containinga-methylene-ß-aminopropanoic acids (map). |
Lanzhou University |
23585918 |
16 |
Tuned-Affinity Bivalent Ligands for the Characterization of Opioid Receptor Heteromers. |
TBA |
22967810 |
102 |
Synthesis of quinolinomorphinan derivatives as highly selectived opioid receptor ligands. |
Kitasato University |
22742909 |
24 |
Essential structure of opioid¿ receptor agonist nalfurafine for binding to the¿ receptor 2: synthesis of decahydro(iminoethano)phenanthrene derivatives and their pharmacologies. |
Kitasato University |
22445285 |
26 |
Design and synthesis of novel opioid ligands with an azabicyclo[2.2.2]octane skeleton and their pharmacologies. |
Kitasato University |
21128594 |
93 |
Development of potent µ and d opioid agonists with high lipophilicity. |
University of Arizona |
20547453 |
122 |
Design and synthesis of trivalent ligands targeting opioid, cholecystokinin, and melanocortin receptors for the treatment of pain. |
University of Arizona |
20218625 |
27 |
"Carba"-analogues of fentanyl are opioid receptor agonists. |
Clinical Research Institute of Montreal |
20560643 |
71 |
Improving metabolic stability by glycosylation: bifunctional peptide derivatives that are opioid receptor agonists and neurokinin 1 receptor antagonists. |
University of Arizona |
19211245 |
27 |
Synthesis and biological evaluation of C-12 triazole and oxadiazole analogs of salvinorin A. |
Harvard Medical School |
18990576 |
11 |
Synthesis of a novel 6,14-epoxymorphinan derivative and its pharmacology. |
Kitasato University |
18337104 |
7 |
Syntheses of 4,6'-epoxymorphinan derivatives and their pharmacologies. |
Kitasato University |
18370374 |
12 |
Blood-brain barrier penetration by two dermorphin tetrapeptide analogues: role of lipophilicity vs structural flexibility. |
Vrije Universiteit Brussel |
18311909 |
10 |
Synthesis of a potent and selective (18)F-labeled delta-opioid receptor antagonist derived from the Dmt-Tic pharmacophore for positron emission tomography imaging. |
Stanford University School of Medicine |
18178091 |
24 |
Role of benzimidazole (Bid) in the delta-opioid agonist pseudopeptide H-Dmt-Tic-NH-CH(2)-Bid (UFP-502). |
University of Ferrara |
18166466 |
12 |
Novel coumarin glycoside and phenethyl vanillate from Notopterygium forbesii and their binding affinities for opioid and dopamine receptors. |
Harvard Medical School |
17981041 |
79 |
Standard protecting groups create potent and selective kappa opioids: salvinorin B alkoxymethyl ethers. |
Mclean Hospital |
18293909 |
5 |
Toward a structure-based model of salvinorin A recognition of the kappa-opioid receptor. |
University of Minnesota |
17402725 |
9 |
Indium-labeled macrocyclic conjugates of naltrindole: high-affinity radioligands for in vivo studies of peripheral delta opioid receptors. |
University of Missouri-Columbia |
16942034 |
19 |
Effect of lysine at C-terminus of the Dmt-Tic opioid pharmacophore. |
University of Cagliari |
16789756 |
25 |
New 2',6'-dimethyl-L-tyrosine (Dmt) opioid peptidomimetics based on the Aba-Gly scaffold. Development of unique mu-opioid receptor ligands. |
Vrije Universiteit Brussels |
16509592 |
101 |
Design and synthesis of novel hydrazide-linked bifunctional peptides as delta/mu opioid receptor agonists and CCK-1/CCK-2 receptor antagonists. |
University of Arizona |
15857143 |
48 |
Synthesis and biological evaluation of 14-alkoxymorphinans. 22.(1) Influence of the 14-alkoxy group and the substitution in position 5 in 14-alkoxymorphinan-6-ones on in vitro and in vivo activities. |
Sapienza University of Rome |
15863299 |
8 |
Synthesis and biological evaluation of new biphalin analogues with non-hydrazine linkers. |
University of Arizona |
14998329 |
142 |
Identification of opioid ligands possessing mixed micro agonist/delta antagonist activity among pyridomorphinans derived from naloxone, oxymorphone, and hydromorphone [correction of hydropmorphone]. |
Southern Research Institute |
13678399 |
54 |
Peptide science: exploring the use of chemical principles and interdisciplinary collaboration for understanding life processes. |
University of Arizona |
12459023 |
46 |
Potent delta-opioid receptor agonists containing the Dmt-Tic pharmacophore. |
University of Cagliari |
11311071 |
53 |
Effect of N-alkyl and N-alkenyl substituents in noroxymorphindole, 17-substituted-6,7-dehydro-4,5alpha-epoxy-3,14-dihydroxy-6,7:2',3'-indolomorphinans, on opioid receptor affinity, selectivity, and efficacy. |
National Institute of Diabetes and Digestive and Kidney Diseases |
11300867 |
32 |
Investigation of the selectivity of oxymorphone- and naltrexone-derived ligands via site-directed mutagenesis of opioid receptors: exploring the"address" recognition locus. |
University of Minnesota |
11543672 |
24 |
[2',6'-Dimethyltyrosine]dynorphin A(1-11)-NH2 analogues lacking an N-terminal amino group: potent and selective kappa opioid antagonists. |
Clinical Research Institute of Montreal |
11405645 |
13 |
Transformation of a kappa-opioid receptor antagonist to a kappa-agonist by transfer of a guanidinium group from the 5'- to 6'-position of naltrindole. |
University of Minnesota |
11052799 |
10 |
Synthesis and evaluation of N,N-dialkyl enkephalin-based affinity labels for delta opioid receptors. |
University of Maryland |
10639287 |
62 |
Probes for narcotic receptor mediated phenomena. 26. Synthesis and biological evaluation of diarylmethylpiperazines and diarylmethylpiperidines as novel, nonpeptidic delta opioid receptor ligands. |
National Institute of Diabetes and Digestive and Kidney Diseases |
10479286 |
53 |
Synthesis, opioid receptor binding, and biological activities of naltrexone-derived pyrido- and pyrimidomorphinans. |
Southern Research Institute |
9667975 |
86 |
Synthesis, opioid receptor binding, and bioassay of naltrindole analogues substituted in the indolic benzene moiety. |
Southern Research Institute |
9057856 |
53 |
Probes for narcotic receptor mediated phenomena. 23. Synthesis, opioid receptor binding, and bioassay of the highly selective delta agonist (+)-4-[(alpha R)-alpha-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]- N,N-diethylbenzamide (SNC 80) and related novel nonpeptide delta opioid r |
National Institute of Diabetes and Digestive and Kidney Diseases |
9397176 |
28 |
Cyclic enkephalin analogues with exceptional potency and selectivity for delta-opioid receptors. |
University of Arizona |
9379438 |
31 |
Discovery of a novel class of substituted pyrrolooctahydroisoquinolines as potent and selective delta opioid agonists, based on an extension of the message-address concept. |
Smithkline Beecham |
9301674 |
60 |
Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary delta opioid antagonist activity. |
University of Ferrara |
9207938 |
15 |
Pyrrolomorphinans as delta opioid receptor antagonists. The role of steric hindrance in conferring selectivity. |
University of Minnesota |
9171881 |
17 |
7-Spiroindanyl derivatives of naltrexone and oxymorphone as selective ligands for delta opioid receptors. |
University of Minnesota |
8642567 |
64 |
Probes for narcotic receptor-mediated phenomena. 21. Novel derivatives of 3-(1,2,3,4,5,11-hexahydro-3-methyl-2,6-methano-6H-azocino[4,5-b]indol- 6-yl)-phenols with improved delta opioid receptor selectivity. |
National Institute of Diabetes and Digestive and Kidney Diseases |
7739011 |
90 |
Probes for narcotic receptor-mediated phenomena. 20. Alteration of opioid receptor subtype selectivity of the 5-(3-hydroxyphenyl)morphans by application of the message-address concept: preparation of delta-opioid receptor ligands. |
National Institute of Diabetes and Digestive and Kidney Diseases |
8035418 |
30 |
Probes for narcotic receptor mediated phenomena. 19. Synthesis of (+)-4-[(alpha R)-alpha-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3- methoxybenzyl]-N,N-diethylbenzamide (SNC 80): a highly selective, nonpeptide delta opioid receptor agonist. |
National Institute of Diabetes and Digestive and Kidney Diseases |
8021929 |
13 |
Synthesis and delta-opioid receptor antagonist activity of a naltrindole analogue with a regioisomeric indole moiety. |
University of Minnesota |
8021915 |
16 |
Newly discovered stereochemical requirements in the side-chain conformation of delta opioid agonists for recognizing opioid delta receptors. |
University of Arizona |
8201592 |
27 |
[L-Ala3]DPDPE: a new enkephalin analog with a unique opioid receptor activity profile. Further evidence of delta-opioid receptor multiplicity. |
University of Arizona |
8289188 |
30 |
Cyclic enkephalin analogs with exceptional potency at peripheral delta opioid receptors. |
University of Arizona |
8360887 |
9 |
Synthesis and kappa-opioid antagonist selectivity of a norbinaltorphimine congener. Identification of the address moiety required for kappa-antagonist activity. |
University of Minnesota |
1648137 |
30 |
Topographically designed analogues of [D-Pen,D-Pen5]enkephalin. |
University of Arizona |
1851843 |
96 |
Synthesis and structure-activity relationships of deltorphin analogues. |
University of Ferrara |
2832604 |
3 |
Binaltorphimine-related bivalent ligands and their kappa opioid receptor antagonist selectivity. |
University of Minnesota |
6296388 |
68 |
Synthesis and pharmacological characterization in vitro of cyclic enkephalin analogues: effect of conformational constraints on opiate receptor selectivity. |
TBA |
6276540 |
20 |
Evidence of the preferential involvement of mu receptors in analgesia using enkephalins highly selective for peripheral mu or delta receptors. |
TBA |
15115401 |
24 |
Oral bioavailability of a new class of micro-opioid receptor agonists containing 3,6-bis[Dmt-NH(CH(2))(n)]-2(1H)-pyrazinone with central-mediated analgesia. |
National Institutes of Environmental Health Sciences |
11755357 |
14 |
Synthesis and biological activities of YkFA analogues: effects of position 4 substitutions and altered ring size on in vitro opioid activity. |
University of Louisville |
10612597 |
31 |
Optically pure (-)-4-[(N-allyl-3-methyl-4-piperidinyl)phenyl-amino]-N,N-diethylbenzami de displays selective binding and full agonist activity for the delta opioid receptor. |
Research Triangle Institute |
10571174 |
25 |
(+/-)-4-[(N-allyl-cis-3-methyl-4-piperidinyl)phenylamino]-N,N-diethylbenzamide displays selective binding for the delta opioid receptor. |
Research Triangle Institute |
| 36 |
Pyrrolooctahydroisoquinolines as potent and selective opioid receptor ligands: SAR analysis and docking studies |
TBA |
22197670 |
51 |
Synthesis of quinolinomorphinan-4-ol derivatives asd opioid receptor agonists. |
Kitasato University |
21925887 |
10 |
Synthesis and biological evaluation of new opioid agonist and neurokinin-1 antagonist bivalent ligands. |
University of Arizona |
21889335 |
27 |
Synthesis of novel triplet drugs with 1,3,5-trioxazatriquinane skeletons and their pharmacologies. Part 2: Synthesis of novel triplet drugs with the epoxymethano structure (capped homotriplet). |
Kitasato University |
21413804 |
21 |
Design of novel neurokinin 1 receptor antagonists based on conformationally constrained aromatic amino acids and discovery of a potent chimeric opioid agonist-neurokinin 1 receptor antagonist. |
Vrije Universiteit Brussel |
21366266 |
66 |
Discovery of a potent and efficacious peptide derivative ford/µ opioid agonist/neurokinin 1 antagonist activity with a 2',6'-dimethyl-L-tyrosine: in vitro, in vivo, and NMR-based structural studies. |
University of Arizona |
20850307 |
27 |
Design and synthesis of KNT-127, ad-opioid receptor agonist effective by systemic administration. |
Kitasato University |
20692738 |
34 |
Synthesis and activity of endomorphin-2 and morphiceptin analogues with proline surrogates in position 2. |
Sapienza University of Rome |
20637637 |
46 |
Role of 2',6'-dimethyl-l-tyrosine (Dmt) in some opioid lead compounds. |
University of Cagliari |
20617791 |
70 |
Biological and conformational evaluation of bifunctional compounds for opioid receptor agonists and neurokinin 1 receptor antagonists possessing two penicillamines. |
University of Arizona |
20476738 |
14 |
Synthesis and evaluation of new endomorphin-2 analogues containing (Z)-alpha,beta-didehydrophenylalanine (Delta(Z)Phe) residues. |
Universit£ |
20137938 |
28 |
Novel multiple opioid ligands based on 4-aminobenzazepinone (Aba), azepinoindole (Aia) and tetrahydroisoquinoline (Tic) scaffolds. |
Vrije Universiteit Brussel |
19762245 |
69 |
The biological activity and metabolic stability of peptidic bifunctional compounds that are opioid receptor agonists and neurokinin-1 receptor antagonists with a cystine moiety. |
University of Arizona |
19646882 |
72 |
Novel delta opioid receptor agonists exhibit differential stimulation of signaling pathways. |
University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School and The Informatics Institute of Umdnj |
19540763 |
4 |
Synthesis and investigations of double-pharmacophore ligands for treatment of chronic and neuropathic pain. |
University of Arizona |
19827750 |
39 |
Agonist vs antagonist behavior of delta opioid peptides containing novel phenylalanine analogues in place of Tyr(1). |
Clinical Research Institute of Montreal |
19807094 |
45 |
The effects of C-terminal modifications on the opioid activity of [N-benzylTyr(1)]dynorphin A-(1-11) analogues. |
University of Kansas |
19715279 |
20 |
Design, synthesis, and pharmacological activities of dynorphin A analogues cyclized by ring-closing metathesis. |
The University of Kansas |
19642675 |
60 |
Influence of the side chain next to C-terminal benzimidazole in opioid pseudopeptides containing the Dmt-Tic pharmacophore. |
University of Cagliari |
19560919 |
28 |
Synthesis and evaluation of new endomorphin analogues modified at the Pro(2) residue. |
Universit£ |
| 12 |
The stereochemical requirements of the novel δ-opioid selective dipeptide antagonist TMT-Tic |
TBA |
| 8 |
Topographical requirements for delta opioid ligands: The synthesis and biological properties of a cyclic analogue of deltorphin I |
TBA |
19147366 |
60 |
Modification of the furan ring of salvinorin A: identification of a selective partial agonist at the kappa opioid receptor. |
Mclean Hospital |
19062273 |
41 |
Conformationally constrained opioid ligands: the Dmt-Aba and Dmt-Aia versus Dmt-Tic scaffold. |
Vrije Universiteit Brussel |
18821747 |
45 |
The importance of micelle-bound states for the bioactivities of bifunctional peptide derivatives for delta/mu opioid receptor agonists and neurokinin 1 receptor antagonists. |
University of Arizona |
18800771 |
26 |
Novel opioid peptide derived antagonists containing (2S)-2-methyl-3-(2,6-dimethyl-4-carbamoylphenyl)propanoic acid [(2S)-Mdcp]. |
National University of Singapore |
18701308 |
1 |
Design and synthesis of a metabolically stable and potent antitussive agent, a novel delta opioid receptor antagonist, TRK-851. |
Toray Industries |
18680274 |
44 |
Further studies on lead compounds containing the opioid pharmacophore Dmt-Tic. |
University of Cagliari |
18490168 |
32 |
Structure-activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy and molecular modeling. |
Lanzhou University |
17826995 |
48 |
Design and synthesis of opioidmimetics containing 2',6'-dimethyl-L-tyrosine and a pyrazinone-ring platform. |
Kobe Gakuin University |
17497839 |
72 |
Bifunctional [2',6'-dimethyl-L-tyrosine1]endomorphin-2 analogues substituted at position 3 with alkylated phenylalanine derivatives yield potent mixed mu-agonist/delta-antagonist and dual mu-agonist/delta-agonist opioid ligands. |
Kobe Gakuin University |
17350835 |
88 |
Further studies of tyrosine surrogates in opioid receptor peptide ligands. |
Adolor |
17315860 |
40 |
Dicarba analogues of the cyclic enkephalin peptides H-Tyr-c[D-Cys-Gly-Phe-D(or L)-Cys]NH(2) retain high opioid activity. |
Clinical Research Institute of Montreal |
17266203 |
29 |
Synthesis and characterization of potent and selective mu-opioid receptor antagonists, [Dmt(1), D-2-Nal(4)]endomorphin-1 (Antanal-1) and [Dmt(1), D-2-Nal(4)]endomorphin-2 (Antanal-2). |
Medical University |
17201419 |
93 |
Partial retro-inverso, retro, and inverso modifications of hydrazide linked bifunctional peptides for opioid and cholecystokinin (CCK) receptors. |
University of Arizona |
17188879 |
16 |
Endomorphin-1 analogs with enhanced metabolic stability and systemic analgesic activity: design, synthesis, and pharmacological characterization. |
Lanzhou University |
17142049 |
40 |
Transformation of mu-opioid receptor agonists into biologically potent mu-opioid receptor antagonists. |
Kobe Gakuin University |
16949282 |
12 |
Synthesis of 3,6-bis[H-Tyr/H-Dmt-NH(CH2)m,n]-2(1H)pyrazinone derivatives: function of alkyl chain length on opioid activity. |
Kobe Gakuin University |
16828552 |
20 |
Synthesis and evaluation of 3-aminopropionyl substituted fentanyl analogues for opioid activity. |
University of Arizona |
16759107 |
18 |
6-N,N-dimethylamino-2,3-naphthalimide: a new environment-sensitive fluorescent probe in delta- and mu-selective opioid peptides. |
Universidad De Santiago De Compostela |
16483774 |
66 |
Identification of potent phenyl imidazoles as opioid receptor agonists. |
Johnson & Johnson Pharmaceutical Research & Development |
16366592 |
33 |
Conversion of the potent delta-opioid agonist H-Dmt-Tic-NH-CH(2)-bid into delta-opioid antagonists by N(1)-benzimidazole alkylation(1). |
University of Cagliari |
16335927 |
48 |
Potent Dmt-Tic pharmacophoric delta- and mu-opioid receptor antagonists. |
Kobe Gakuin University |
16275086 |
18 |
Synthesis and biological activity of the first cyclic biphalin analogues. |
University of Arizona |
16183273 |
12 |
New series of potent delta-opioid antagonists containing the H-Dmt-Tic-NH-hexyl-NH-R motif. |
Kobe Gakuin University |
16107162 |
10 |
From the potent and selective mu opioid receptor agonist H-Dmt-d-Arg-Phe-Lys-NH(2) to the potent delta antagonist H-Dmt-Tic-Phe-Lys(Z)-OH. |
University of Cagliari |
15780619 |
15 |
Structure-activity relationship of the novel bivalent and C-terminal modified analogues of endomorphin-2. |
Lanzhou University |
15658871 |
28 |
Development of potent mu-opioid receptor ligands using unique tyrosine analogues of endomorphin-2. |
Kobe Gakuin University |
15324897 |
3 |
A novel cyclic enkephalin analogue with potent opioid antagonist activity. |
Clinical Research Institute of Montreal |
14711314 |
63 |
Synthesis and opioid activity of side-chain-to-side-chain cyclic dynorphin A-(1-11) amide analogues cyclized between positions 2 and 5. 1. Substitutions in position 3. |
University of Maryland |
12954053 |
39 |
Effects of the substitution of Phe4 in the opioid peptide [D-Ala8]dynorphin A-(1-11)NH2. |
University of Maryland |
12852751 |
34 |
Unique high-affinity synthetic mu-opioid receptor agonists with central- and systemic-mediated analgesia. |
Kobe Gakuin University |
12657261 |
32 |
Dermorphin tetrapeptide analogues with 2',6'-dimethylphenylalanine (Dmp) substituted for aromatic amino acids have high mu opioid receptor binding and biological activities. |
Tohoku Pharmaceutical University |
12408719 |
21 |
Synthesis and structure-activity relationships of an orally available and long-acting analgesic peptide, N(alpha)-amidino-Tyr-D-Arg-Phe-MebetaAla-OH (ADAMB). |
Daiichi Fine Chemical |
12190304 |
10 |
Solid phase synthesis and evaluation of Tyr-Tic-Phe-Phe(p-NHCOCH(2)Br) ([Phe(p-bromoacetamide)(4)]TIPP), a potent affinity label for delta opioid receptors. |
University of Maryland |
12166947 |
30 |
Synthesis and biological activities of cyclic lanthionine enkephalin analogues: delta-opioid receptor selective ligands. |
University of California |
11958984 |
24 |
Dermorphin and deltorphin heptapeptide analogues: replacement of Phe residue by Dmp greatly improves opioid receptor affinity and selectivity. |
Tohoku Pharmaceutical University |
11212102 |
24 |
Enkephalin analogues with 2',6'-dimethylphenylalanine replacing phenylalanine in position 4. |
Tohoku Pharmaceutical University |
11150176 |
9 |
Synthesis and evaluation of isothiocyanate-containing derivatives of the delta-opioid receptor antagonist Tyr-Tic-Phe-Phe (TIPP) as potential affinity labels for delta-opioid receptors. |
University of Maryland |
11150174 |
84 |
Synthesis and in vitro and in vivo activity of (-)-(1R,5R,9R)- and (+)-(1S,5S,9S)-N-alkenyl-, -N-alkynyl-, and -N-cyanoalkyl-5, 9-dimethyl-2'-hydroxy-6,7-benzomorphan homologues. |
Virginia Commonwealth University |
27556704 |
64 |
Mitragynine/Corynantheidine Pseudoindoxyls As Opioid Analgesics with Mu Agonism and Delta Antagonism, Which Do Not Recruit ?-Arrestin-2. |
Memorial Sloan Kettering Cancer Center |
10753473 |
14 |
Deltorphin II analogues with 6-hydroxy-2-aminotetralin-2-carboxylic acid in position 1. |
Hungarian Academy of Sciences |
10617088 |
15 |
Synthesis and biological activities of position one and three transposed analogs of the opioid peptide YKFA. |
University of Louisville |
9986710 |
28 |
Dermorphin and deltorphin glycosylated analogues: synthesis and antinociceptive activity after systemic administration. |
Sapienza University of Rome |
9871617 |
24 |
Modifications of the 4,4'-residues and SAR studies of Biphalin, a highly potent opioid receptor active peptide. |
University of Arizona |
9822547 |
41 |
De novo design, synthesis, and biological activities of high-affinity and selective non-peptide agonists of the delta-opioid receptor. |
The University of Arizona |
30608693 |
48 |
Design, Synthesis, and Biological Evaluation of the Third Generation 17-Cyclopropylmethyl-3,14?-dihydroxy-4,5?-epoxy-6?-[(4'-pyridyl)carboxamido]morphinan (NAP) Derivatives as ?/? Opioid Receptor Dual Selective Ligands. |
Virginia Commonwealth University |
9301669 |
24 |
7-spirobenzocyclohexyl derivatives of naltrexone, oxymorphone, and hydromorphone as selective opioid receptor ligands. |
University of Minnesota |
9258365 |
28 |
Helix-inducing alpha-aminoisobutyric acid in opioid mimetic deltorphin C analogues. |
National Institute of Environmental Health Sciences |
31782922 |
107 |
Application of Bivalent Bioisostere Concept on Design and Discovery of Potent Opioid Receptor Modulators. |
Virginia Commonwealth University |
8691442 |
52 |
Effects of modifications of residues in position 3 of dynorphin A(1-11)-NH2 on kappa receptor selectivity and potency. |
University of Arizona |
26611918 |
45 |
Enkephalin analogues with N-phenyl-N-(piperidin-2-ylmethyl)propionamide derivatives: Synthesis and biological evaluations. |
University of Arizona |
8576920 |
34 |
Design and synthesis of 1-aminocycloalkane-1-carboxylic acid-substituted deltorphin analogues: unique delta and mu opioid activity in modified peptides. |
University of Ferrara |
26465170 |
87 |
Discovery of Novel Multifunctional Ligands with ?/? Opioid Agonist/Neurokinin-1 (NK1) Antagonist Activities for the Treatment of Pain. |
University of Arizona |
26212775 |
77 |
Discovery of tripeptide-derived multifunctional ligands possessing delta/mu opioid receptor agonist and neurokinin 1 receptor antagonist activities. |
University of Arizona |
8384662 |
20 |
A topochemical approach to explain morphiceptin bioactivity. |
University of California |
8289187 |
47 |
Design of cyclic deltorphins and dermenkephalins with a disulfide bridge leads to analogues with high selectivity for delta-opioid receptors. |
University of Arizona |
24262888 |
105 |
The most effective influence of 17-(3-ethoxypropyl) substituent on the binding affinity and the agonistic activity in KNT-127 derivatives, ? opioid receptor agonists. |
Kitasato University |
24095014 |
52 |
N-Alkyl dien- and trienamides from the roots of Otanthus maritimus with binding affinity for opioid and cannabinoid receptors. |
Uos of Cagliari |
8096246 |
70 |
Design and synthesis of highly potent and selective cyclic dynorphin A analogs. 2. New analogs. |
University of Arizona |
24103580 |
36 |
Novel 6?-acylaminomorphinans with analgesic activity. |
Semmelweis University |
24090913 |
42 |
Synthesis and biological evaluation of novel delta (?) opioid receptor ligands with diazatricyclodecane skeletons. |
C.N.R. Istituto Di Farmacologia Traslazionale |
23988352 |
9 |
Systematic replacement of amides by 1,4-disubstituted[1,2,3]triazoles in Leu-enkephalin and the impact on the delta opioid receptor activity. |
Universit£ |
8057274 |
18 |
Discovery of a potent, peripherally selective trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonist for the treatment of gastrointestinal motility disorders. |
Eli Lilly |
23948248 |
52 |
Structure activity relationship studies of 17-cyclopropylmethyl-3,14?-dihydroxy-4,5?-epoxy-6?-(isoquinoline-3'-carboxamido)morphinan (NAQ) analogues as potent opioid receptor ligands: preliminary results on the role of electronic characteristics for affinity and function. |
Virginia Commonwealth University |
23932788 |
60 |
N-terminal guanidinylation of TIPP (Tyr-Tic-Phe-Phe) peptides results in major changes of the opioid activity profile. |
Clinical Research Institute of Montreal |
7996550 |
12 |
Development of a model for the delta opioid receptor pharmacophore. 2. Conformationally restricted Phe3 replacements in the cyclic delta receptor selective tetrapeptide Tyr-c[D-Cys-Phe-D-Pen]OH (JOM-13). |
University of Michigan |
7996549 |
40 |
Development of a model for the delta opioid receptor pharmacophore. 1. Conformationally restricted Tyr1 replacements in the cyclic delta receptor selective tetrapeptide Tyr-c[D-Cys-Phe-D-Pen]OH (JOM-13). |
University of Michigan |
24648867 |
58 |
Chiral Effect of a Phe Residue in Position 3 of the Dmt |
University of Arizona |
23822516 |
142 |
Cyclic enkephalins with a diversely substituted guanidine bridge or a thiourea bridge: synthesis, biological and structural evaluations. |
Universit£ |
7932577 |
24 |
Selective kappa-opioid agonists: synthesis and structure-activity relationships of piperidines incorporating on oxo-containing acyl group. |
Smithkline Beecham Farmaceutici |
23623711 |
82 |
Design and synthesis of novel opioid ligands with an azabicyclo[2.2.2]octane skeleton having a 7-amide side chain and their pharmacologies. |
Kitasato University |
23623418 |
140 |
Effect of anchoring 4-anilidopiperidines to opioid peptides. |
University of Arizona |
7658453 |
16 |
Stereoisomers of N-[1-hydroxy-(2-phenylethyl)-3-methyl-4-piperidyl]- N-phenylpropanamide: synthesis, stereochemistry, analgesic activity, and opioid receptor binding characteristics. |
Institute of Materia Medica |
17555306 |
6 |
o-Naphthalenedicarboxaldehyde derivative of 7'-aminonaltrindole as a selective delta-opioid receptor affinity label. |
University of Minnesota |
2822930 |
48 |
Structure-activity relationships of cyclic opioid peptide analogues containing a phenylalanine residue in the 3-position. |
Clinical Research Institute of Montreal |
29152051 |
40 |
?-Space Screening of Dermorphin-Based Tetrapeptides through Use of Constrained Arylazepinone and Quinolinone Scaffolds. |
Vrije Universiteit Brussel |
29853330 |
106 |
Chemical space screening around Phe |
Vrije Universiteit Brussel |
1967312 |
91 |
Synthesis and structure-activity relationships of dynorphin A-(1-8) amide analogues. |
Eisai |
28522254 |
42 |
Novel delta opioid receptor agonists with oxazatricyclodecane structure showing potent agonistic activities. |
Kitasato University |
1331451 |
68 |
Conformationally restricted deltorphin analogues. |
Clinical Research Institute of Montreal |
1320122 |
55 |
Ring substituted and other conformationally constrained tyrosine analogues of [D-Pen2,D-Pen5]enkephalin with delta opioid receptor selectivity. |
University of Arizona |
26496515 |
11 |
Iminothiazoline-Sulfonamide Hybrids as Jack Bean Urease Inhibitors; Synthesis, Kinetic Mechanism and Computational Molecular Modeling. |
Quaid-I-Azam University |
26520885 |
21 |
Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents. |
Hazara University |