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AZD-4635

SKU: orb1226546

Description

AZD-4635 (HTL 1071) is a potent, selective and orally available adenosine 2A receptor (A2AR) inhibitor with Ki of 1.7 nM, > 30-fold selectivity over other adenosine receptors; reverses the inhibitory effects of different concentrations of adenosine in CHO cells stably expressing human A2AR with IC50 of 0.1 nM (incubated with 0.1 uM adenosine); reverses suppression and restores IFNγ secretion in cells incubated with NECA in ex vivo CD8+ T cell assay; reduces tumor burden and enhances antitumor immunity in vivo.Lung Cancer Phase 2 Clinical(In Vitro):In the presence of 0.1, 1 and 10 μM adenosine, the IC50s of AZD4635 for inhibition of cAMP production are 0.79, 10.0 and 142.9 nM, respectively.

Images & Validation

Key Properties

CAS Number1321514-06-0
MW315.736
Purity>98% (HPLC)
FormulaC15H11ClFN5
SMILESNC1=NC(C2=CC=C(F)C=C2)=C(C3=CC(C)=NC(Cl)=C3)N=N1
TargetAdenosine Receptor
SolubilityDMSO: Soluble ( < 1 mg/ml refers to the product slightly soluble or insoluble )

Bioactivity

In Vitro
In the presence of 0.1, 1 and 10 μM adenosine, the IC50s of AZD4635 for inhibition of cAMP production are 0.79, 10.0 and 142.9 nM, respectively.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

HTL 1071

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Protocol Information

AZD-4635 (orb1226546)

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Available Sizes

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2 mg
$ 90.00
5 mg
$ 130.00
10 mg
$ 180.00
25 mg
$ 290.00
50 mg
$ 430.00
100 mg
$ 640.00
500 mg
$ 1,380.00