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SCH-442,416: Difference between revisions

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Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (report errors
 
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{{cs1 config|name-list-style=vanc}}
{{chembox
| Verifiedfields = changed
| verifiedrevid = 409169500464385200
|ImageFile=SCH442416_structure.png
| ImageFile=SCH-422,416 Structure.svg
| ImageSize=200px
|IUPACName PIN=2-(Furan-2-furylyl)-7-[3-(4-methoxyphenyl)propyl]-7''H''-pyrazolo[4,3-''e''][1,2,4]triazolo[1,5-''c'']pyrimidin-5-amine
| OtherNames=SCH-442,416
|Section1= {{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| IUPHAR_ligand = 3283
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 8843413
| InChI = 1/C20H19N7O2/c1-28-14-8-6-13(7-9-14)4-2-10-26-18-15(12-22-26)19-23-17(16-5-3-11-29-16)25-27(19)20(21)24-18/h3,5-9,11-12H,2,4,10H2,1H3,(H2,21,24)
| InChIKey = AEULVFLPCJOBCE-UHFFFAOYAA
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = ZMC4G1W59S
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 136689
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = AEULVFLPCJOBCE-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|changed|??}}
| CASNo=316173-57-6
| PubChem = 10668061
| SMILES = n1n3c(nc4c(c3nc1c2occc2)cnn4CCCc5ccc(OC)cc5)N
}}
|Section2= {{Chembox Properties
| Formula=C<sub>20</sub>H<sub>19</sub>N<sub>7</sub>O<sub>2</sub>
| MolarMass=389.410
| Appearance=
| Density=
| MeltingPt=
| BoilingPt=
| Solubility=
}}
|Section3= {{Chembox Hazards
| MainHazards=
| FlashPt=
| AutoignitionPt =
| Autoignition=
}}
}}
 
'''SCH-442,416''' is a highly selective [[adenosine]] [[Adenosine A2a receptor|A<sub>2a</sub>]] subtype receptor [[Antagonist (pharmacology)|antagonist]]. It is widely used in its <sup>11</sup>C [[isotopic labelling|radiolabelled]] form to map the distribution of A<sub>2a</sub> receptors in the brain, where they are mainly found in the [[striatum]], [[nucleus accumbens]], and [[olfactory tubercle]].<ref>{{cite journal | vauthors = Moresco RM, Todde S, Belloli S, Simonelli P, Panzacchi A, Rigamonti M, Galli-Kienle M, Fazio F. | display-authors = 6 | title = In vivo imaging of adenosine A2A receptors in rat and primate brain using [11C]SCH442416. ''| journal = European Journal of Nuclear Medicine and Molecular Imaging''. 2005| volume = Apr;32( | issue = 4):405-13. PMID| pages = 405–13 | date = April 2005 | pmid = 15549298 | doi = 10.1007/s00259-004-1688-5 | s2cid = 20909406 }}</ref> Given its distribution in the brain, A<sub>2a</sub> receptors have been investigated for the treatment of various neurological disorders, and SCH-442,416 has shown promise in treatment of [[depression (mood)|depression]],<ref>{{cite journal | vauthors = El Yacoubi M, Costentin J, Vaugeois JM. | title = Adenosine A2A receptors and depression. ''| journal = Neurology''. 2003| Decvolume = 9;61( | issue = 11 Suppl 6): | pages = S82-7. PMID| date = December 2003 | pmid = 14663017 | doi = 10.1212/01.wnl.0000095220.87550.f6 | s2cid = 36219448 }}</ref> [[Parkinson's disease]],<ref>{{cite journal | vauthors = Matsuya T, Takuma K, Sato K, Asai M, Murakami Y, Miyoshi S, Noda A, Nagai T, Mizoguchi H, Nishimura S, Yamada K. | display-authors = 6 | title = Synergistic effects of adenosine A2A antagonist and L-DOPA on rotational behaviors in 6-hydroxydopamine-induced hemi-Parkinsonian mouse model. ''| journal = Journal of Pharmacological Sciences''. 2007| volume = Mar;103( | issue = 3):329-32. PMID| pages = 329–32 | date = March 2007 | pmid = 17341841 | doi = 10.1254/jphs.scz070058 | doi-access = free }}</ref> and [[catalepsy]].<ref>{{cite journal | vauthors = Mihara T, Noda A, Arai H, Mihara K, Iwashita A, Murakami Y, Matsuya T, Miyoshi S, Nishimura S, Matsuoka N. | display-authors = 6 | title = Brain adenosine A2A receptor occupancy by a novel A1/A2A receptor antagonist, ASP5854, in rhesus monkeys: relationship to anticataleptic effect. ''| journal = Journal of Nuclear Medicine''. 2008| volume = Jul;49( | issue = 7):1183-8. PMID| pages = 1183–8 | date = July 2008 | pmid = 18552135 | doi = 10.2967/jnumed.108.051474 | doi-access = free }}</ref>
 
== References ==
{{pharm-stub}}
{{reflistReflist|2}}
 
== External links ==
==References==
* [httphttps://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=micad.chapter.SCH442416-11C Molecular Imaging and Contrast Agent Database: SCH-442,416]
{{reflist|2}}
 
==External links==
* [http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=micad.chapter.SCH442416-11C Molecular Imaging and Contrast Agent Database: SCH-442,416]
 
{{Adenosinergics}}
 
[[Category:Phenol4-Methoxyphenyl etherscompounds]]
[[Category:Furans2-Furyl compounds]]
[[Category:Adenosine receptor antagonists]]
 
{{nervous-system-drug-stub}}