PYX 2: neuropeptide Y receptor antagonist
ID Source | ID |
---|---|
PubMed CID | 16132128 |
MeSH ID | M0212109 |
Synonym |
---|
l-tyrosine, n-(n2-(n2-(n2-(n-(n-(n-(n2-(n-(n-acetyl-3-((2,6-dichlorophenyl)methyl)-l-tyrosyl)-l-isoleucyl)-l-asparaginyl)-l-leucyl)-l-isoleucyl)-d-threonyl)-l-arginyl)-l-glutaminyl)-l-arginyl)-3-((2,6-dichlorophenyl)methyl)- |
ac-tyr-3-(cl2-bzl)-ile-asn-leu-ile-d-thr-arg-gln-arg-tyr-3-(cl2bzl)-nh2 |
pyx-2 |
neuropeptide y (27-36) amide, ac-(3-(2,6-dichlorobenzyl)tyrosyl(27,36)-threonyl(32))- |
acetyl-27,36-(3-(2,6-dichlorobenzyl)tyr-32-thr)neuropeptide y (27-36) amide |
neuropeptide y (27-36) amide, acetyl-(3-(2,6-dichlorobenzyl)tyr(27,36)-thr(32))- |
146999-93-1 |
ac-(3-(2,6-dichlorobenzyl)tyr(27,36)-d-thr(32))-neuropeptide y (27-36) amide |
pyx 2 |
DTXSID50163558 |
Excerpt | Reference |
---|---|
" Furthermore, NPY was without effect on the dose-response curve to ATP in resting conditions." | ( Failure of the putative neuropeptide Y antagonists, benextramine and PYX-2, to inhibit Y2 receptors in rat isolated prostatic vas deferens. Corsi, M; Palea, S; Ratti, E; Rimland, JM; Trist, DG, 1995) |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 7 (87.50) | 18.2507 |
2000's | 1 (12.50) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |