Imaradenant (AZD4635) - 98%, high purity , Adenosine A2a receptor antagonist, CAS No.1321514-06-0, Adenosine A2a receptor antagonist

Item Number
I414133
Grouped product items
SKUSizeAvailabilityPrice Qty
I414133-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90
I414133-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$114.90
I414133-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$194.90
I414133-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$289.90
I414133-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$449.90

Adenosine Receptor Antagonists

Basic Description

SynonymsC72299 | S8720 | AZD4635 (HTL1071) | HTL1071 | HTL-1071 | 1321514-06-0 | AKOS037515559 | IMARADENANT [WHO-DD] | 5-(4-fluorophenyl)-6-(2-chloro-6-methyl-pyridin-4-yl)-1,2,4-triazin-3-amine | CS-0022379 | NCWQLHHDGDXIJN-UHFFFAOYSA-N | HY-101980 | BS-15183 |
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsImaradenant (AZD4635, HTL1071) is an oral A2AR antagonist that binds to human A2AR with a Ki of 1.7 nM and with > 30-fold selectivity over other adenosine receptors.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAdenosine A2a receptor antagonist
Product Description

Information

Imaradenant (AZD4635) Imaradenant (AZD4635, HTL1071) is an oral A2AR antagonist that binds to human A2AR with a Ki of 1.7 nM and with > 30-fold selectivity over other adenosine receptors.


Targets

A2AR (Cell-free) 1.7 nM(Ki)


In vitro

In CHO cells stably expressing human A2AR, the IC50s of AZD4635 for inhibition of cAMP production are 0.79, 10.0 and 142.9 nM in the presense of 0.1, 1 and 10 μM adenosine, respectively.


In vivo

Blockade of A2AR signaling with AZD4635 could reduce tumor burden and enhance antitumor immunity.

AI Insight

Product Properties

ALogP2.6

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 6-(2-chloro-6-methylpyridin-4-yl)-5-(4-fluorophenyl)-1,2,4-triazin-3-amine
INCHI InChI=1S/C15H11ClFN5/c1-8-6-10(7-12(16)19-8)14-13(20-15(18)22-21-14)9-2-4-11(17)5-3-9/h2-7H,1H3,(H2,18,20,22)
InChi Key NCWQLHHDGDXIJN-UHFFFAOYSA-N
Canonical SMILES CC1=CC(=CC(=N1)Cl)C2=C(N=C(N=N2)N)C3=CC=C(C=C3)F
Isomeric SMILES CC1=CC(=CC(=N1)Cl)C2=C(N=C(N=N2)N)C3=CC=C(C=C3)F
PubChem CID 86676119
Molecular Weight 315.73

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeDateItem
L2313374Certificate of AnalysisNov 27, 2023 I414133
L2314344Certificate of AnalysisNov 27, 2023 I414133
L2314345Certificate of AnalysisNov 27, 2023 I414133
L2314346Certificate of AnalysisNov 27, 2023 I414133
L2314347Certificate of AnalysisNov 27, 2023 I414133
L2314348Certificate of AnalysisNov 27, 2023 I414133
L2314373Certificate of AnalysisNov 27, 2023 I414133
L2314375Certificate of AnalysisNov 27, 2023 I414133

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References

1. Borodovsky A, Barbon CM, Wang Y, Ye M, Prickett L, Chandra D, Shaw J, Deng N, Sachsenmeier K, Clarke JD et al..  (2020)  Small molecule AZD4635 inhibitor of A 2A R signaling rescues immune cell function including CD103 + dendritic cells enhancing anti-tumor immunity.  J Immunother Cancer,  (2): (e000417).  [PMID:32727810] [10.1136/jitc-2019-000417]
2. A-González N, Castrillo A.  (2011)  Liver X receptors as regulators of macrophage inflammatory and metabolic pathways..  Biochim Biophys Acta,  1812  (8): (982-94).  [PMID:21193033] [10.1021/op500134e]

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