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{{short description|Chemical compound}} |
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{{cs1 config|name-list-style=vanc|display-authors=6}} |
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{{drugbox |
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{{drugbox |
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| Watchedfields = changed |
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| verifiedrevid = 446393243 |
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| verifiedrevid = 451211295 |
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| IUPAC_name = ethyl 3,6a,11,14-tetrahydro-9-methoxy-2-propyl-3,5-dimethyl-(12H)-isoquinopyrrolobenzoxazine-1-carboxylate |
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| IUPAC_name = ethyl 3,6a,11,14-tetrahydro-9-methoxy-2-propyl-3,5-dimethyl-(12H)-isoquinopyrrolobenzoxazine-1-carboxylate |
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| image = PD0298029_structure.png |
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| image = PD0298029_structure.png |
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| CAS_number = |
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| ATC_prefix = |
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| index_label = |
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| ATC_suffix = |
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| index2_label = |
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| CAS_number = |
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| ATC_supplemental = |
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| PubChem = |
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| ATC_prefix = |
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| ATC_supplemental = |
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| PubChem = 60210050 |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 26233369 |
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| ChemSpiderID = 26233369 |
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| C=27 | H=32 | N=2 | O=4 |
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| chemical_formula = C<sub>27</sub>H<sub>32</sub>N<sub>2</sub>O<sub>4</sub> |
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| molecular_weight = 448.554 |
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| smiles = CCCc1c(c2c(n1C)cc(c3c2CN4CCc5cc(ccc5C4O3)OC)C)C(=O)OCC |
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| smiles = CCCc1c(c2c(n1C)cc(c3c2CN4CCc5cc(ccc5C4O3)OC)C)C(=O)OCC |
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| InChI = 1/C27H32N2O4/c1-6-8-21-24(27(30)32-7-2)23-20-15-29-12-11-17-14-18(31-5)9-10-19(17)26(29)33-25(20)16(3)13-22(23)28(21)4/h9-10,13-14,26H,6-8,11-12,15H2,1-5H3 |
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| InChIKey = MTMZSGQXRVRKSY-UHFFFAOYAV |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C27H32N2O4/c1-6-8-21-24(27(30)32-7-2)23-20-15-29-12-11-17-14-18(31-5)9-10-19(17)26(29)33-25(20)16(3)13-22(23)28(21)4/h9-10,13-14,26H,6-8,11-12,15H2,1-5H3 |
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| StdInChI = 1S/C27H32N2O4/c1-6-8-21-24(27(30)32-7-2)23-20-15-29-12-11-17-14-18(31-5)9-10-19(17)26(29)33-25(20)16(3)13-22(23)28(21)4/h9-10,13-14,26H,6-8,11-12,15H2,1-5H3 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = MTMZSGQXRVRKSY-UHFFFAOYSA-N |
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| StdInChIKey = MTMZSGQXRVRKSY-UHFFFAOYSA-N |
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| smiles2 = CCCc1n(C)c5cc(C)c3OC4c2ccc(OC)cc2CCN4Cc3c5c1C(=O)OCC |
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| C=27 | H=32 | N=2 | O=4 |
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| bioavailability = |
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| molecular_weight = 448.553 g/mol |
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| protein_bound = |
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| smiles = CCCc1n(C)c5cc(C)c3OC4c2ccc(OC)cc2CCN4Cc3c5c1C(=O)OCC |
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| metabolism = |
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}} |
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}} |
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'''PD-0298029''' is a drug which acts as a selective ] for the ]. It was developed for the treatment of ], but poor bioavailability and rapid metabolism in animal studies have meant its use is largely limited to ''in vitro'' research into the M<sub>4</sub> and other muscarinic receptors.<ref name="pmid12086495">{{cite journal |author=Böhme TM, Augelli-Szafran CE, Hallak H, Pugsley T, Serpa K, Schwarz RD |title=Synthesis and pharmacology of benzoxazines as highly selective antagonists at M(4) muscarinic receptors |journal=Journal of Medicinal Chemistry |volume=45 |issue=14 |pages=3094–102 |year=2002 |month=July |pmid=12086495 |doi= |url=}}</ref><ref>Boehme TM, Angelli-Szafran CE, Corinne E, Hallak H and Schwarz RD. Analogs of M4 selective synthetic muscarinic receptor antagonists: Synthesis, binding and pharmacokinetic properties. ''Medicinal Chemistry Research''. 2002; 11(8):423–433.</ref><ref>Progress in Medicinal Chemistry 43. (2005). Chapter 4, Muscarinic Receptor Subtype Pharmacology and Physiology, by Richard M Eglen. pp 128-129. ISBN 0444515720</ref> |
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'''PD-0298029''' is a drug which acts as a selective ] for the ]. It was developed for the treatment of ], but poor bioavailability and rapid metabolism in animal studies have meant its use is largely limited to ''in vitro'' research into the M<sub>4</sub> and other muscarinic receptors.<ref name="pmid12086495">{{cite journal | vauthors = Böhme TM, Augelli-Szafran CE, Hallak H, Pugsley T, Serpa K, Schwarz RD | title = Synthesis and pharmacology of benzoxazines as highly selective antagonists at M(4) muscarinic receptors | journal = Journal of Medicinal Chemistry | volume = 45 | issue = 14 | pages = 3094–3102 | date = July 2002 | pmid = 12086495 | doi = 10.1021/jm011116o }}</ref><ref>{{cite journal | vauthors = Boehme TM, Angelli-Szafran CE, Corinne E, Hallak H, Schwarz RD | title = Analogs of M4 selective synthetic muscarinic receptor antagonists: Synthesis, binding and pharmacokinetic properties. | journal = Medicinal Chemistry Research | date = January 2002 | volume = 11 | issue = 8 | pages = 423–433 }}</ref><ref name="Eglen_2005">{{cite journal | vauthors = Eglen RM | title = Muscarinic receptor subtype pharmacology and physiology | journal = Progress in Medicinal Chemistry |publisher=Elsevier Science |location=Amsterdam London | volume = 43 | issue = | pages = 105–136 (128) | date = 2005 | pmid = 15850824 | doi = 10.1016/S0079-6468(05)43004-0 |isbn=978-0-444-51572-8 }}</ref> |
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== See also == |
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==See also== |
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* ] |
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== References == |
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== References == |
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{{Reflist}} |
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{{Reflist}} |
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{{Muscarinic acetylcholine receptor modulators}} |
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{{Cholinergics}} |
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{{nervous-system-drug-stub}} |