Ro 47-8634: structure in first source
ID Source | ID |
---|---|
PubMed CID | 6426756 |
CHEMBL ID | 3956076 |
SCHEMBL ID | 7796731 |
MeSH ID | M0331751 |
Synonym |
---|
ro 47-8634 |
4-tert-butyl-n-(6-(2-hydroxy-ethoxy)-5-(2-hydroxy-phenoxy)-2,2'-bipyrimidin-4-yl)-benzenesulfonamide |
4-tert-butyl-n-[6-(2-hydroxyethoxy)-5-(2-hydroxyphenoxy)-2-pyrimidin-2-ylpyrimidin-4-yl]benzenesulfonamide |
FT-0666091 |
desmethyl bosentan |
253688-61-8 |
SCHEMBL7796731 |
DTXSID10423786 |
CHEMBL3956076 , |
ro-47-8634 |
AKOS030240417 |
J-015961 |
unii-n373r7n42r |
n373r7n42r , |
4-(tert-butyl)-n-(6-(2-hydroxyethoxy)-5-(2-hydroxyphenoxy)-[2,2'-bipyrimidin]-4-yl)benzenesulfonamide |
4-(1,1-dimethylethyl)-n-[6-(2-hydroxyethoxy)-5-(2-hydroxyphenoxy)[2,2'-bipyrimidin]-4-yl]benzenesulfonamide |
bdbm50532572 |
benzenesulfonamide, 4-(1,1-dimethylethyl)-n-(6-(2-hydroxyethoxy)-5-(2-hydroxyphenoxy)(2,2'-bipyrimidin)-4-yl)- |
4-(1,1-dimethylethyl)-n-(6-(2-hydroxyethoxy)-5-(2-hydroxyphenoxy)(2,2'-bipyrimidin)-4-yl)benzenesulfonamide |
demethoxybosentan |
bosentan metabolite, ro 47-8634 |
Excerpt | Reference | Relevance |
---|---|---|
" The oral bioavailability of bosentan was 43% to 48%, with a small interindividual variability of 20%." | ( Multiple-dose pharmacokinetics, safety, and tolerability of bosentan, an endothelin receptor antagonist, in healthy male volunteers. Birnboeck, H; Eggers, H; Hopfgartner, G; Jonkman, JH; Meyer, J; Schmitt, R; van Marle, S; Viischer, HW; Weber, C, 1999) | 0.3 |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Endothelin-1 receptor | Homo sapiens (human) | IC50 (µMol) | 26.0000 | 0.0000 | 0.7647 | 9.9000 | AID1626367 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
phosphatidylinositol phospholipase C activity | Endothelin-1 receptor | Homo sapiens (human) |
endothelin receptor activity | Endothelin-1 receptor | Homo sapiens (human) |
protein binding | Endothelin-1 receptor | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
plasma membrane | Endothelin-1 receptor | Homo sapiens (human) |
plasma membrane | Endothelin-1 receptor | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1323149 | Drug level assessed as human recombinant CYP3A4-mediated compound formation treated with bosentan at 5 uM in presence of NADPH after 30 mins by LC-MS/MS analysis | 2016 | European journal of medicinal chemistry, Oct-04, Volume: 121 | Metabolism study and biological evaluation of bosentan derivatives. |
AID1323162 | Drug level in human liver microsomes treated with bosentan at 5 uM in presence of NADPH after 30 mins by LC-MS/MS analysis | 2016 | European journal of medicinal chemistry, Oct-04, Volume: 121 | Metabolism study and biological evaluation of bosentan derivatives. |
AID1323173 | Retention time of the compound | 2016 | European journal of medicinal chemistry, Oct-04, Volume: 121 | Metabolism study and biological evaluation of bosentan derivatives. |
AID1626367 | Displacement of radioligand from ETA receptor (unknown origin) expressed in fall armyworm sf9 cell membranes | 2016 | Bioorganic & medicinal chemistry letters, 08-01, Volume: 26, Issue:15 | From bosentan (Tracleer®) to macitentan (Opsumit®): The medicinal chemistry perspective. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 4 (80.00) | 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] |
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 (12.38) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (20.00%) | 5.53% |
Reviews | 1 (20.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 3 (60.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |