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GPCR/G Protein
Adenosine Receptor
ANR 94 - 98%, high purity , CAS No.634924-89-3

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ANR 94 - 98%, high purity , CAS No.634924-89-3

COA

Grade & Purity:

≥98%

Cas Number: 634924-89-3
Molecular Weight: 207.23
PubChem CID: 11805896
PubChem SID: 488197750

In stock

Item Number

A286839

Grouped product items
SKU	Size	Availability	Price
A286839-5mg	5mg	3	$116.90
A286839-10mg	10mg	3	$179.90
A286839-25mg	25mg	3	$403.90
A286839-50mg	50mg	3	$706.90
A286839-100mg	100mg	5	$1,272.90

Adenosine A2Aantagonist

View related series

Adenosine Receptor (113) Class A GPCR (4138) GPCR/G Protein (3172)

Basic Description

Synonyms	9H-Purin-6-amine, 8-ethoxy-9-ethyl- \| SCHEMBL15689328 \| ANR94 \| ANR-94 \| HY-103162 \| MS-23133 \| 8-Ethoxy-9-ethyl-9H-purin-6-amine \| A918056 \| NCGC00387128-01 \| DTXSID30473127 \| 8-ETHOXY-9-ETHYLPURIN-6-AMINE \| 8-ethoxy-9-ethyladenine \| 9H-Purin-6-amine,8-e
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Adenosine A2Areceptor (AA2AR) antagonist (Kivalues are 643 and 46 nM for rat and human AA2ARs respectively). Most active AA2AR antagonist for human receptors. Displays activity in the treatment of Parkinson's diseasein vivo; improves parkinsonian motor de
Storage Temp	Room temperature
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Imidazopyrimidines
    - Subclass Purines and purine derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Imidazopyrimidines
Subclass	Purines and purine derivatives
Intermediate Tree Nodes	Not available
Direct Parent	6-aminopurines
Alternative Parents	Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	6-aminopurine - Alkyl aryl ether - Aminopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Azacycle - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Amine - Organic oxygen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488197750
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488197750
IUPAC Name	8-ethoxy-9-ethylpurin-6-amine
INCHI	InChI=1S/C9H13N5O/c1-3-14-8-6(7(10)11-5-12-8)13-9(14)15-4-2/h5H,3-4H2,1-2H3,(H2,10,11,12)
InChIKey	QUGDTMONBLMLLD-UHFFFAOYSA-N
Smiles	CCN1C2=NC=NC(=C2N=C1OCC)N
Isomeric SMILES	CCN1C2=NC=NC(=C2N=C1OCC)N
Molecular Weight	207.23
Reaxy-Rn	9556468
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9556468&ln=

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

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

Analytical Chart:

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6 results found

Lot Number	Certificate Type	Date	Item
B2328493	Certificate of Analysis	Feb 20, 2023	A286839
B2328500	Certificate of Analysis	Feb 20, 2023	A286839
C2503390	Certificate of Analysis	Feb 20, 2023	A286839
B2328490	Certificate of Analysis	Feb 20, 2023	A286839
B2328503	Certificate of Analysis	Feb 20, 2023	A286839
B2328504	Certificate of Analysis	Feb 20, 2023	A286839

Chemical and Physical Properties

Solubility	Solvent:DMSO, Max Conc. mg/mL: 10.36, Max Conc. mM: 50; Solvent:ethanol, Max Conc. mg/mL: 20.72, Max Conc. mM: 100
Molecular Weight	207.230 g/mol
XLogP3	0.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	3
Exact Mass	207.112 Da
Monoisotopic Mass	207.112 Da
Topological Polar Surface Area	78.900 Å²
Heavy Atom Count	15
Formal Charge	0
Complexity	215.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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