Page last updated: 2024-12-11
rs 93427-007
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
RS 93427-007: PGI2 mimetic; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 6438966 |
MeSH ID | M0143170 |
Synonyms (11)
Synonym |
---|
rs-93520 |
4-[(1s,2r,3s,6r,7e)-2-[(3s)-3-cyclohexyl-3-hydroxyprop-1-yn-1-yl]-3-hydroxybicyclo[4.2.0]octan-7-ylidene]butanoic acid |
gtpl1886 |
rs 93520 |
rs 93427 |
105284-21-7 |
butanoic acid, 4-(2-(3-cyclohexyl-3-hydroxy-1-propynyl)-3-hydroxybicyclo(4.2.0)oct-7-ylidene)-, (1s-(1alpha,2alpha(r*),3beta,6alpha,7z))- |
rs-93427-007 |
rs 93427-007 |
(4e)-4-[(1s,2r,3s,6r)-2-[(3s)-3-cyclohexyl-3-hydroxyprop-1-ynyl]-3-hydroxy-7-bicyclo[4.2.0]octanylidene]butanoic acid |
Q27088639 |
Research Excerpts
Dosage Studied
Excerpt | Relevance | Reference |
---|---|---|
" In spontaneously hypertensive rats, the dose-response for the hypotensive response to bolus doses of RS93427 was not altered by concomitant steady state infusion of a threshold dose (1 micrograms kg-1 min-1) of GTN." | ( Selective anti-platelet aggregation synergism between a prostacyclin-mimetic, RS93427 and the nitrodilators sodium nitroprusside and glyceryl trinitrate. Fulks, J; Hedley, L; Lee, CH; Loveday, M; Smith, DL; VanAntwerp, D; Willis, AL, 1989) | 0.28 |
" Much work remains to be done, including examination of RS-93427 in chronic studies with various dosage forms, particularly in the study of atherosclerosis." | ( Orally active prostacyclin-mimetic RS-93427: therapeutic potential in vascular occlusive disease associated with atherosclerosis. Kertesz, D; Kluge, A; O'Yang, C; Smith, DL; Vigo, C; Willis, AL; Wu, H, 1987) | 0.27 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Bioassays (1)
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1346377 | Human DP1 receptor (Prostanoid receptors) | 2000 | The Journal of pharmacology and experimental therapeutics, May, Volume: 293, Issue:2 | Affinities, selectivities, potencies, and intrinsic activities of natural and synthetic prostanoids using endogenous receptors: focus on DP class prostanoids. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Research
Studies (6)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 4 (66.67) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 1 (16.67) | 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] |
Market Indicators
Research Demand Index: 12.41
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.41) All Compounds (24.57) |
Study Types
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 | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |