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ChemicalBook--->CAS DataBase List--->104615-18-1

104615-18-1

104615-18-1 Structure

104615-18-1 Structure
IdentificationBack Directory
[Name]

CGS 15943
[CAS]

104615-18-1
[Synonyms]

CGS 15943
CGS-15943A
CGS-15943 solid
CGS-15943 ADENOSINE A1 RECEPTOR
9-CHLORO-2-(2-FURYL)(1,2,4)TRIAZOLO(1,5-C)QUINAZOLIN-5-AMINE
9-chloro-2-(2-furyl)-(1,2,4)triazolo(1,5-c)quinazolin-5-imine
9-Chloro-2-(furan-2-yl)[1,2,4]triazolo[1,5-c]quinazolin-5-amine
9-CHLORO-2-(2-FURANYL)-[1,2,4]TRIAZOLO[1,5-C]QUINAZOLIN-5-AMINE
[1,2,4]Triazolo[1,5-c]quinazolin-5-amine,9-chloro-2-(2-furanyl)-
9-Chloro-5,6-dihydro-2-(furan-2-yl)[1,2,4]triazolo[1,5-c]quinazolin-5-imine
[Molecular Formula]

C13H8ClN5O
[MDL Number]

MFCD01529897
[MOL File]

104615-18-1.mol
[Molecular Weight]

285.69
Chemical PropertiesBack Directory
[Melting point ]

278-279 °C
[density ]

1.72±0.1 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

DMSO: >16 mg/mL
[form ]

solid
[pka]

1.23±0.30(Predicted)
[color ]

white
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Potent adenosine receptor antagonist
[Definition]

ChEBI: A member of the class of triazoloquinazolines that is [1,2,4]triazolo[1,5-c]quinazoline substited at positions 2, 5 and 9 by furan-2-yl, amino and chloro groups respectively. A potent antagonist at adenosine A1 and adenosi e A2A receptors.
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 27, p. 1549, 1990 DOI: 10.1002/jhet.5570270605
[Biological Activity]

Potent adenosine receptor antagonist (K i values are 3.5, 4.2, 16 and 51 nM for human A 1 , A 2A , A 2B and A 3 receptors respectively). Orally active in vivo .
[Biochem/physiol Actions]

CGS-15943 is a potent and non-selective adenosine receptor antagonist. It exhibits anti-carcinogenic and anti-apoptotic activity.
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

CGS 15943(104615-18-1)1HNMR
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