substance p (6-11), orn(6)- has been researched along with substance p in 4 studies
| Studies (substance p (6-11), orn(6)-) | Trials (substance p (6-11), orn(6)-) | Recent Studies (post-2010) (substance p (6-11), orn(6)-) | Studies (substance p) | Trials (substance p) | Recent Studies (post-2010) (substance p) |
|---|---|---|---|---|---|
| 5 | 0 | 0 | 17,289 | 277 | 2,010 |
| Protein | Taxonomy | substance p (6-11), orn(6)- (IC50) | substance p (IC50) |
|---|---|---|---|
| Substance-P receptor | Rattus norvegicus (Norway rat) | 0.0005 | |
| Substance-K receptor | Rattus norvegicus (Norway rat) | 0.2 | |
| Substance-K receptor | Homo sapiens (human) | 0.2455 | |
| Substance-P receptor | Homo sapiens (human) | 0.0011 | |
| Neuromedin-K receptor | Homo sapiens (human) | 0.125 | |
| Substance-K receptor | Mesocricetus auratus (golden hamster) | 0.148 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Antoniou, M; Poulos, C; Tsegenidis, T | 1 |
| Hagan, RM; Jordan, CC; Karagiannis, K; Poulos, C; Stavropoulos, G | 1 |
| Antoniou, M; Maggi, CA; Patacchini, R; Poulos, C; Rovero, P | 1 |
| Hagan, RM; Jordan, CC; Karagiannis, K; Manolopoulou, A; Poulos, C; Stavropoulos, G | 1 |
4 other study(ies) available for substance p (6-11), orn(6)- and substance p
| Article | Year |
|---|---|
Synthesis and biological activity of analogues of the C-terminal hexapeptide of substance P with modifications at glutaminyl and methioninyl residues. Structure-activity studies.
Topics: Amino Acid Sequence; Animals; Colon; Glutamine; Guinea Pigs; Ileum; Methionine; Molecular Sequence Data; Muscle, Smooth; Peptide Fragments; Portal Vein; Rats; Receptors, Neurokinin-2; Receptors, Neurotransmitter; Structure-Activity Relationship; Substance P | 1992 |
Synthesis of a potent antagonist of substance P by replacing the CH2SCH3 and the alpha-carboxamide groups of the methionine at [Orn6]-SP6-11 by benzyl ester groups.
Topics: Amino Acid Sequence; Animals; Aspartic Acid; Guinea Pigs; Ileum; Methionine; Molecular Sequence Data; Muscle Contraction; Peptide Fragments; Portal Vein; Rats; Receptors, Tachykinin; Substance P | 1993 |
Synthesis and biological activity of NK1 tachykinin antagonists not containing D-residues.
Topics: Amino Acid Sequence; Animals; Drug Design; Guinea Pigs; Ileum; Molecular Sequence Data; Molecular Structure; Neurokinin-1 Receptor Antagonists; Peptide Fragments; Pulmonary Artery; Rabbits; Receptors, Neurokinin-1; Structure-Activity Relationship; Substance P | 1994 |
Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acids.
Topics: Amino Acid Sequence; Amino Acids; Animals; Colon; Glutamates; Glutamic Acid; Guinea Pigs; Ileum; In Vitro Techniques; Methionine; Molecular Sequence Data; Oligopeptides; Peptide Fragments; Portal Vein; Rats; Receptors, Neurotransmitter; Receptors, Tachykinin; Structure-Activity Relationship; Substance P | 1993 |