An adenosine A2A receptor antagonist
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ST1535

Item No. 10611

Technical Information
Formal Name
2-butyl-9-methyl-8-(2H-1,2,3-triazol-2-yl)-9H-purin-6-amine
CAS Number
496955-42-1
Molecular Formula
C12H16N8
Formula Weight
Purity
≥98%
Formulation
A solid
DMF: 5mg/mLDMSO: 5mg/mLDMSO:PBS (pH 7.2) (1:9): 0.1mg/mL
λmax
233, 290 nm
SMILES
CCCCC1=NC(N)=C2C(N(C)C(N3N=CC=N3)=N2)=N1
InChi Code
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)
InChi Key
CYYQMAWUIRPCNW-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ST1535 is an adenosine A2A receptor antagonist.1 It is selective for adenosine A2A over A1 receptors (Kis = 2.3 and 107 nM, respectively, in radioligand binding assays). ST1535 inhibits agonist-induced production of cAMP in CHO cells expressing adenosine A2A receptors (IC50 = 353 nM). In vivo, ST1535 (10 and 20 mg/kg) reduces haloperidol-induced catalepsy in mice. It reduces the number of jaw tremors in a rat model of Parkinsonian jaw tremors induced by tacrine (Item No. 70240).2 ST1535 (20 and 40 mg/kg) increases locomotor activity and reverses motor disabilities in a marmoset model of MPTP-induced Parkinson’s disease.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Stasi, M.A., Borsini, F., Varani, K., et alST 1535: a preferential A2A adenosine receptor antagonist. Int. J. Neuropsychopharmacol. 9(5), 575-584 (2006).

    2. Tronci, E., Simola, N., Borsini, F., et alCharacterization of the antiparkinsonian effects of the new adenosine A2A receptor antagonist ST1535: acute and subchronic studies in rats. Eur. J. Pharmacol. 566(1-3), 94-102 (2007).

    3. Rose, S., Jackson, M.J., Smith, L.A., et alThe novel adenosine A2a receptor antagonist ST1535 potentiates the effects of a threshold dose of L-DOPA in MPTP treated common marmosets. Eur. J. Pharmacol. 546(1-3), 82-87 (2006).