Misplaced Pages

PD-0298029: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively
Page 1
Page 2
← Previous editContent deleted Content addedVisualWikitext
Revision as of 21:07, 18 September 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{drugbox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'DrugBank_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Misplaced Pages talk:WikiProject← Previous edit Latest revision as of 04:42, 26 October 2024 edit undo76.174.0.57 (talk) Cats. 
(27 intermediate revisions by 18 users not shown)
Line 1: Line 1:
{{short description|Chemical compound}}
{{cs1 config|name-list-style=vanc|display-authors=6}}
{{drugbox {{drugbox
| Watchedfields = changed
| verifiedrevid = 446393243 | verifiedrevid = 451211295
| IUPAC_name = ethyl 3,6a,11,14-tetrahydro-9-methoxy-2-propyl-3,5-dimethyl-(12H)-isoquinopyrrolobenzoxazine-1-carboxylate | IUPAC_name = ethyl 3,6a,11,14-tetrahydro-9-methoxy-2-propyl-3,5-dimethyl-(12H)-isoquinopyrrolobenzoxazine-1-carboxylate
| image = PD0298029_structure.png | image = PD0298029_structure.png

| CAS_number =
| ATC_prefix = | index_label =
| ATC_suffix = | index2_label =
| CAS_number =
| ATC_supplemental =
| PubChem = | ATC_prefix =
| ATC_suffix =
| ATC_supplemental =
| PubChem = 60210050
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 26233369 | ChemSpiderID = 26233369
| C=27 | H=32 | N=2 | O=4
| chemical_formula = C<sub>27</sub>H<sub>32</sub>N<sub>2</sub>O<sub>4</sub>
| molecular_weight = 448.554
| smiles = CCCc1c(c2c(n1C)cc(c3c2CN4CCc5cc(ccc5C4O3)OC)C)C(=O)OCC | smiles = CCCc1c(c2c(n1C)cc(c3c2CN4CCc5cc(ccc5C4O3)OC)C)C(=O)OCC
| 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
| InChIKey = MTMZSGQXRVRKSY-UHFFFAOYAV
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| 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 | 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
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = MTMZSGQXRVRKSY-UHFFFAOYSA-N | StdInChIKey = MTMZSGQXRVRKSY-UHFFFAOYSA-N
| smiles2 = CCCc1n(C)c5cc(C)c3OC4c2ccc(OC)cc2CCN4Cc3c5c1C(=O)OCC
| C=27 | H=32 | N=2 | O=4
| bioavailability =
| molecular_weight = 448.553 g/mol
| protein_bound =
| smiles = CCCc1n(C)c5cc(C)c3OC4c2ccc(OC)cc2CCN4Cc3c5c1C(=O)OCC
| metabolism =
| bioavailability =
| elimination_half-life =
| protein_bound =
| pregnancy_category =
| metabolism =
| legal_status =
| elimination_half-life =
| routes_of_administration =
| pregnancy_category =
| legal_status =
| routes_of_administration =
}} }}


'''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> '''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>


== See also ==

==See also==
* ] * ]
* ]


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


{{Muscarinic acetylcholine receptor modulators}}
{{Cholinergics}}



]
]
]
]
] ]

]

{{nervous-system-drug-stub}}