GLPBio

AZD4635

Catalog No.: GC19049Purity:>99.50%Synonyms: HTL-1071, Imaradenant
AZD4635 is a potent, selective, and oral adenosine 2A receptor (A2AR) inhibitor, with a Ki value of 1.7nM.

Products are for research use only. Not for human use. We do not sell to patients.


AZD4635
Cas No.: 1321514-06-0
10mM (in 1mL DMSO)In Stock
$52.00
1
1mgIn Stock
$28.00
1
5mgIn Stock
$76.00
1
10mgIn Stock
$111.00
1
25mgIn Stock
$173.00
1
50mgIn Stock
$266.00
1
100mgIn Stock
$401.00
1

Citations

No citations are currently available for this product. Below are selected publications citing GlpBio products.
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

Description

AZD4635 is a potent, selective, and oral adenosine 2A receptor (A2AR) inhibitor, with a Ki value of 1.7nM [1]. AZD4635 can increase the expression of CD25 (IL2Ra), an activation marker on CD8 T cells, and increase the expression of granzyme B on CD4 and CD8 T cells to improve immune activation[2]. AZD4635 has been widely used in different animal models to reduce tumor burden and enhance antitumor immunity [3].

In vitro, AZD4635 treatment at 3µM for 30min significantly reversed the immunosuppressive effect of 5µM 5 '-(N-ethylcarboxamide) adenosine (NECA) on dendritic cells, and increased the expression of ovalbumin (OVA)[4]. After stimulation with anti-CD3 and anti-28 monoclonal antibodies, combined treatment with anti-PD-L1 antibody (10µg/ml) and AZD4635 (0.2 µM) for 6 hours enhanced CD8+ T cell function and increased IL-2 and IFN-γ secretion[5].

In vivo, AZD4635 (25mg/kg) administered by gavage once daily for 15 days in combination with sodium polyoxotungstate (POM-1) and anti-CD73 antibody treatment resulted in enhanced T cell activation in the spleen and increased IFN-γ and monocyte levels in the spleen and bone marrow in a mouse model of myeloma[6].

References:
[1] Borodovsky A, Wang Y, Ye M, et al. Preclinical pharmacodynamics and antitumor activity of AZD4635, a novel adenosine 2A receptor inhibitor that reverses adenosine mediated T cell suppression[J]. Cancer Research, 2017, 77(13_Supplement): 5580-5580.
[2] Budhu S, Mane M, Bah M A, et al. Optimizing breast cancer therapy by inhibiting the adenosine receptor and oxygen consumption[J]. Cancer Research, 2023, 83(7_Supplement): 2517-2517.
[3] Borodovsky A, Wang Y, Ye M, et al. Inhibition of A2AR by AZD4635 induces anti-tumor immunity alone and in combination with anti-PD-L1 in preclinical models[J]. Cancer Research, 2018, 78(13_Supplement): 3751-3751.
[4] Borodovsky A, Barbon C M, Wang Y, et al. Small molecule AZD4635 inhibitor of A2AR signaling rescues immune cell function including CD103+ dendritic cells enhancing anti-tumor immunity[J]. Journal for Immunotherapy of Cancer, 2020, 8(2): e000417.
[5] Li J, Huang H H, Tu B, et al. Reversal of the CD8+ T-Cell exhaustion induced by chronic HIV-1 infection through combined blockade of the adenosine and PD-1 pathways[J]. Frontiers in Immunology, 2021, 12: 687296.
[6] Yang R, Elsaadi S, Misund K, et al. Conversion of ATP to adenosine by CD39 and CD73 in multiple myeloma can be successfully targeted together with adenosine receptor A2A blockade[J]. Journal for immunotherapy of cancer, 2020, 8(1): e000610.

Protocol

Cell experiment [1]:

Cell lines

Mouse bone marrow-derived progenitor cells

Preparation Method

Mouse bone marrow-derived precursor cells were cultured for 16 days in complete T cell medium supplemented with 200ng/ml rmFLT3L and 5ng/ml rmGM-CSF. After initial incubation with growth cytokines for 10 days, 3µM AZD4635 or DMSO (as a control) was added, and after 30 minutes of incubation, 5µM NECA was added. After that, the culture with growth cytokines was continued for 6 days before the cells were harvested for analysis.

Reaction Conditions

3µM; 30min

Applications

AZD4635 treatment rescued the immunosuppressive effects of mouse bone marrow-derived progenitor cells and promoted the generation of bone marrow-derived precursors into CD103+ dendritic cell.
Animal experiment [2]:

Animal models

C57BL/KalwRij mice

Preparation Method

C57BL/KalwRij mice were raised in a standard sterile environment and injected intravenously with 2×105 5T33 multiple myeloma (MM) cells on day 0 and intraperitoneally with 10mg/kg monoclonal anti-CD73 antibody on days 2, 4, 8, 11, and 15. AZD4635 (25mg/kg) was administered by gavage once a day from day 0, and mice were sacrificed on day 15, and spleen tissues were collected for analysis.

Dosage form

25mg/kg/day for 15 days; p.o.

Applications

AZD4635 treatment resulted in a significant decrease in the number of CD138 MM cells in the spleen of mice, an increase in the number of monocytes, and enhanced T cell activation.

References:
[1] Borodovsky A, Barbon C M, Wang Y, et al. Small molecule AZD4635 inhibitor of A2AR signaling rescues immune cell function including CD103+ dendritic cells enhancing anti-tumor immunity[J]. Journal for Immunotherapy of Cancer, 2020, 8(2): e000417.
[2] Yang R, Elsaadi S, Misund K, et al. Conversion of ATP to adenosine by CD39 and CD73 in multiple myeloma can be successfully targeted together with adenosine receptor A2A blockade[J]. Journal for immunotherapy of cancer, 2020, 8(1): e000610.

Product Documents

Purity:>99.50%Appearance:A solid

Chemical Properties

CAS No.
1321514-06-0
Synonyms
HTL-1071, Imaradenant
SMILES
NC1=NC(C2=CC=C(F)C=C2)=C(C3=CC(Cl)=NC(C)=C3)N=N1
Molecular Formula
C15H11ClFN5
Molecular Weight
315.73
Solubility
DMSO : ≥ 83.3 mg/mL (263.83 mM);Water : < 0.1 mg/mL (insoluble)
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

Reviews

Review for AZD4635

Rating: 5
  • 5 Star100%
  • 4 Star0%
  • 3 Star0%
  • 2 Star0%
  • 1 Star0%