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Revision as of 00:04, 16 January 2012 editThe chemistds (talk | contribs)Extended confirmed users5,761 edits added CSID, (Std)InChI & (Std)InChIKey← Previous edit Latest revision as of 20:24, 7 November 2024 edit undoGraeme Bartlett (talk | contribs)Administrators249,731 editsm variable cols 
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{{short description|Chemical compound}}
{{Drugbox {{Drugbox
| drug_name = BSPP
| verifiedrevid = 428799225 | verifiedrevid = 471588151
| IUPAC_name = 2,6-di-tert-butyl-4-(3-hydroxy-2-spiropentylpropyl)-phenol | IUPAC_name =2,6-di-tert-butyl-4-<nowiki/>{methyl}phenol
| image = BSPP_structure.png
| image = Bspp.svg


<!--Clinical data--> <!--Clinical data-->
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<!--Identifiers--> <!--Identifiers-->
| CAS_number = | CAS_number = 938174-18-6
| CAS_number_Ref = {{Cascite|changed|GSRS}}
| ATC_prefix = none | ATC_prefix = none
| ATC_suffix = | ATC_suffix =
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = | DrugBank =
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 17238838 | ChemSpiderID = 17238838
| InChI = 1/C21H34O2/c1-19(2,3)16-11-15(12-17(18(16)23)20(4,5)6)13-21(14-22)9-7-8-10-21/h11-12,22-23H,7-10,13-14H2,1-6H3
| UNII = AN78SQ2WKC
| InChIKey = CTFKOMUXSHQLLL-UHFFFAOYAG
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C21H34O2/c1-19(2,3)16-11-15(12-17(18(16)23)20(4,5)6)13-21(14-22)9-7-8-10-21/h11-12,22-23H,7-10,13-14H2,1-6H3
| StdInChI = 1S/C21H34O2/c1-19(2,3)16-11-15(12-17(18(16)23)20(4,5)6)13-21(14-22)9-7-8-10-21/h11-12,22-23H,7-10,13-14H2,1-6H3
| StdInChIKey = CTFKOMUXSHQLLL-UHFFFAOYSA-N
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = CTFKOMUXSHQLLL-UHFFFAOYSA-N


<!--Chemical data--> <!--Chemical data-->
| chemical_formula = | chemical_formula =
| C=21 | H=34 | O=2 | C=21 | H=34 | O=2
| smiles =C(C)(C)(C)C1=C(C(=CC(=C1)CC1(CCCC1)CO)C(C)(C)C)O
| molecular_weight = 318.492 g/mol
| smiles = C2CCCC2(CO)Cc(cc(C(C)(C)C)c1O)cc1C(C)(C)C
}} }}


'''BSPP''' is a compound used in scientific research which acts as a ] at the ] ].<ref>Kerr DIB, Khalafy J, Ong J, Perkins MV, Prager RH, Puspawati NM, Rimaz M. Synthesis and Biological Activity of Allosteric Modulators of GABAB Receptors, Part 2. 3-(2,6-Bis-tert-butyl-4-hydroxyphenyl)propanols. ''Australian Journal of Chemistry''. 2006;59:457-462.</ref> It has a synergistic effect with GABA<sub>B</sub> agonists such as ] at GABA<sub>B</sub> autoreceptors but not heteroreceptors, suggesting it may be useful for distinguishing between these GABA<sub>B</sub> receptor subtypes.<ref>Parker DA, Marino V, Ong J, Puspawati NM, Prager RH. The CGP7930 analogue 2,6-di-tert-butyl-4-(3-hydroxy-2-spiropentylpropyl)-phenol (BSPP) potentiates baclofen action at GABA(B) autoreceptors. ''Clinical and Experimental Pharmacology and Physiology''. 2008 Sep;35(9):1113-5. PMID 18430050</ref> '''BSPP''' is a compound used in scientific research which acts as a ] at the ] ].<ref>{{cite journal | vauthors = Kerr DI, Khalafy J, Ong J, Perkins MV, Prager RH, Puspawati NM, Rimaz M | title = Synthesis and biological activity of allosteric modulators of GABAB receptors, part 2. 3-(2, 6-bis-tert-butyl-4-hydroxyphenyl) propanols. | journal = Australian Journal of Chemistry | date = September 2006 | volume = 59 | issue = 7 | pages = 457–62 | doi = 10.1071/CH06164 }}</ref> It has a synergistic effect with GABA<sub>B</sub> agonists such as ] at GABA<sub>B</sub> autoreceptors but not heteroreceptors, suggesting it may be useful for distinguishing between these GABA<sub>B</sub> receptor subtypes.<ref name="pmid18430050">{{cite journal | vauthors = Parker DA, Marino V, Ong J, Puspawati NM, Prager RH | title = The CGP7930 analogue 2,6-di-tert-butyl-4-(3-hydroxy-2-spiropentylpropyl)-phenol (BSPP) potentiates baclofen action at GABA(B) autoreceptors | journal = Clinical and Experimental Pharmacology & Physiology | volume = 35 | issue = 9 | pages = 1113–5 | date = September 2008 | pmid = 18430050 | doi = 10.1111/j.1440-1681.2008.04948.x | s2cid = 25608408 }}</ref>


==References==

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== References ==
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