SKF-89,145: Difference between revisions

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Updating {{drugbox}} (no changed fields - added verified revid - updated 'ChemSpiderID_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wik
Importing Wikidata short description: "Chemical compound"
 
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{{Short description|Chemical compound}}
{{Drugbox| verifiedrevid = 447370634
{{Drugbox
|
| verifiedrevid = 449588965
|IUPAC_name = 4-(6-methyl-5,7-dihydro-4''H''-thieno[2,3-c]pyridin-4-yl)benzene-1,2-diol
| IUPAC_name = 4-(6-methyl-5,7-dihydro-4''H''-thieno[2,3-c]pyridin-4-yl)benzene-1,2-diol
| image=SKF-89145_structure.png
| image = SKF-89,145 Structure.svg
| CAS_number=

| ATC_prefix=
<!--Clinical data-->
| ATC_suffix=
| tradename =
| ATC_supplemental=
| licence_EU =
| PubChem= 10061214
| pregnancy_category =
| legal_UK =
| routes_of_administration =

<!--Pharmacokinetic data-->
| bioavailability =
| metabolism =
| elimination_half-life =
| excretion =

<!--Identifiers-->
| CAS_number =
| ATC_suffix =
| PubChem = 10061214
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| ChemSpiderID = 8236766
| DrugBank=
| ChEMBL = 1591046
| C = 14 | H = 15 | N = 1 | O = 2 | S = 1

| molecular_weight = 261.339 g/mol
<!--Chemical data-->
| C=14 | H=15 | N=1 | O=2 | S=1
| smiles = Oc1ccc(cc1O)C2CN(C)Cc3sccc23
| smiles = Oc1ccc(cc1O)C2CN(C)Cc3sccc23
| StdInChI = 1S/C14H15NO2S/c1-15-7-11(10-4-5-18-14(10)8-15)9-2-3-12(16)13(17)6-9/h2-6,11,16-17H,7-8H2,1H3
| bioavailability=
| StdInChIKey = SYHALWYYSDMSLE-UHFFFAOYSA-N
| protein_bound =
| metabolism =
| elimination_half-life=
| excretion =
| licence_EU =
| pregnancy_category =
| legal_UK =
| routes_of_administration=
}}
}}


'''SKF-89,145''' is a drug which acts as a [[dopamine agonist]] selective for the [[Dopamine receptor D1|D<sub>1</sub>]] subtype. The ''N''-desmethyl derivative SKF-89,626 is also a selective D<sub>1</sub> agonist with similar potency and selectivity to SKF 89,145.<ref name="pmid3501846">{{cite journal |author=O'Boyle KM, Waddington JL |title=New substituted 1-phenyl-3-benzazepine analogues of SK&F 38393 and N-methyl-thienopyridine analogues of dihydroxynomifensine with selective affinity for the D-1 dopamine receptor in human post-mortem brain |journal=Neuropharmacology |volume=26 |issue=12 |pages=1807–10 |year=1987 |month=December |pmid=3501846 |doi= 10.1016/0028-3908(87)90139-0|url=}}</ref>
'''SKF-89,145''' is a drug which acts as a [[dopamine agonist]] selective for the [[Dopamine receptor D1|D<sub>1</sub>]] subtype. The ''N''-desmethyl derivative SKF-89,626 is also a selective D<sub>1</sub> agonist with similar potency and selectivity to SKF 89,145.<ref name="pmid3501846">{{cite journal | vauthors = O'Boyle KM, Waddington JL | title = New substituted 1-phenyl-3-benzazepine analogues of SK&F 38393 and N-methyl-thienopyridine analogues of dihydroxynomifensine with selective affinity for the D-1 dopamine receptor in human post-mortem brain | journal = Neuropharmacology | volume = 26 | issue = 12 | pages = 1807–10 | date = December 1987 | pmid = 3501846 | doi = 10.1016/0028-3908(87)90139-0 | s2cid = 34415106 }}</ref>


==References==
== References ==
{{reflist}}
{{Reflist}}


{{Dopamine receptor modulators}}
{{Dopaminergics}}


[[Category:Dopamine agonists]]
[[Category:D1-receptor agonists]]
[[Category:Catechols]]
[[Category:Catechols]]
[[Category:Thienopyridines]]
[[Category:Thienopyridines]]



{{nervous-system-drug-stub}}
{{nervous-system-drug-stub}}