Page last updated: 2024-09-03

pre 084 and somatostatin

pre 084 has been researched along with somatostatin in 1 studies

Compound Research Comparison

Studies
(pre 084)
Trials
(pre 084)
Recent Studies (post-2010)
(pre 084)
Studies
(somatostatin)
Trials
(somatostatin)
Recent Studies (post-2010) (somatostatin)
11607329011

Protein Interaction Comparison

ProteinTaxonomypre 084 (IC50)somatostatin (IC50)
Somatostatin receptor type 5Mus musculus (house mouse)0.0001
Protein-lysine 6-oxidaseHomo sapiens (human)0.01
Somatostatin receptor type 1Homo sapiens (human)0.0012
Somatostatin receptor type 1Mus musculus (house mouse)0.0001
Somatostatin receptor type 2Homo sapiens (human)0.0007
Somatostatin receptor type 2Mus musculus (house mouse)0.0002
Somatostatin receptor type 3Mus musculus (house mouse)0.0001
Somatostatin receptor type 5Rattus norvegicus (Norway rat)0.0009
Somatostatin receptor type 4Homo sapiens (human)0.0012
Somatostatin receptor type 3Homo sapiens (human)0.002
Delta-type opioid receptorRattus norvegicus (Norway rat)2
Mu-type opioid receptorRattus norvegicus (Norway rat)0.006
Somatostatin receptor type 5Homo sapiens (human)0.003
Somatostatin receptor type 4 Mus musculus (house mouse)0.0001

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Belyakov, S; Dambrova, M; Kazoka, H; Kuznecovs, J; Lebedev, A; Liepinsh, E; Mishnev, A; Orlova, N; Ponomaryov, Y; Vavers, E; Veinberg, G; Vikainis, S; Vilskersts, R; Vorona, M; Zvejniece, L1

Other Studies

1 other study(ies) available for pre 084 and somatostatin

ArticleYear
Synthesis and biological evaluation of 2-(5-methyl-4-phenyl-2-oxopyrrolidin-1-yl)-acetamide stereoisomers as novel positive allosteric modulators of sigma-1 receptor.
    Bioorganic & medicinal chemistry, 2013, May-15, Volume: 21, Issue:10

    Topics: Acetamides; Allosteric Regulation; Animals; Rats; Rats, Wistar; Receptors, sigma; Sigma-1 Receptor; Stereoisomerism; Structure-Activity Relationship

2013