Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H16N8 |
Molecular Weight | 272.309 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC1=NC(N)=C2N=C(N(C)C2=N1)N3N=CC=N3
InChI
InChIKey=CYYQMAWUIRPCNW-UHFFFAOYSA-N
InChI=1S/C12H16N8/c1-3-4-5-8-16-10(13)9-11(17-8)19(2)12(18-9)20-14-6-7-15-20/h6-7H,3-5H2,1-2H3,(H2,13,16,17)
Molecular Formula | C12H16N8 |
Molecular Weight | 272.309 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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2-n-Butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization. | 2005 Nov 3 |
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ST 1535: a preferential A2A adenosine receptor antagonist. | 2006 Oct |
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The novel adenosine A2a receptor antagonist ST1535 potentiates the effects of a threshold dose of L-DOPA in MPTP treated common marmosets. | 2006 Sep 28 |
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Adenosine A2A receptor antagonists improve deficits in initiation of movement and sensory motor integration in the unilateral 6-hydroxydopamine rat model of Parkinson's disease. | 2007 Aug |
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The novel adenosine A2a antagonist ST1535 potentiates the effects of a threshold dose of l-dopa in unilaterally 6-OHDA-lesioned rats. | 2007 Feb 16 |
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Characterization of the antiparkinsonian effects of the new adenosine A2A receptor antagonist ST1535: acute and subchronic studies in rats. | 2007 Jul 2 |
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Interaction of A2A adenosine and D2 dopamine receptors modulates corticostriatal glutamatergic transmission. | 2007 Nov |
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Behavioural and neurochemical characterization of the adenosine A2A receptor antagonist ST1535. | 2008 Jan 28 |
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A2A adenosine receptor antagonists protect the striatum against rotenone-induced neurotoxicity. | 2009 May |
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Novel investigational adenosine A2A receptor antagonists for Parkinson's disease. | 2009 Nov |
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Direct B-alkyl Suzuki-Miyaura cross-coupling of 2-halopurines. Practical synthesis of ST1535, a potent adenosine A2A receptor antagonist. | 2010 Aug 6 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 15:32:30 UTC 2023
by
admin
on
Sat Dec 16 15:32:30 UTC 2023
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Record UNII |
NTK8WWM73W
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Record Status |
Validated (UNII)
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Record Version |
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FDA ORPHAN DRUG |
811021
Created by
admin on Sat Dec 16 15:32:30 UTC 2023 , Edited by admin on Sat Dec 16 15:32:30 UTC 2023
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9860294
Created by
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496955-42-1
Created by
admin on Sat Dec 16 15:32:30 UTC 2023 , Edited by admin on Sat Dec 16 15:32:30 UTC 2023
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NTK8WWM73W
Created by
admin on Sat Dec 16 15:32:30 UTC 2023 , Edited by admin on Sat Dec 16 15:32:30 UTC 2023
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DTXSID60432000
Created by
admin on Sat Dec 16 15:32:30 UTC 2023 , Edited by admin on Sat Dec 16 15:32:30 UTC 2023
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PRIMARY |
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