CAS 490-59-5: Alloxazine
Formula:C10H6N4O2
InChI:InChI=1S/C10H6N4O2/c15-9-7-8(13-10(16)14-9)12-6-4-2-1-3-5(6)11-7/h1-4H,(H2,12,13,14,15,16)
InChI key:InChIKey=HAUGRYOERYOXHX-UHFFFAOYSA-N
SMILES:O=C1C=2C(NC=3C(N2)=CC=CC3)=NC(=O)N1
Synonyms:- 1,2,3,4-Tetrahydrobenzopteridine-2,4-Dione
- 10H-Benzo[g]pteridine-2,4-dione
- 1H,2H,3H,4H-Benzo[g]pteridine-2,4-dione
- 1H-benzo[g]pteridine-2,4-dione
- 2,4-Dioxobenzo[g]pteridine
- 6,7-Benzolumazine
- Benzo[g]pteridine-2,4(1H,3H)-dione
- Benzo[g]pteridine-2,4(3H,10H)-dione
- Flavoquinone
- Isoalloxazine
- NSC 203056
- See more synonyms
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Found 6 products.
Alloxazine
CAS:Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor.Formula:C10H6N4O2Purity:99.75%Color and Shape:SolidMolecular weight:214.18Alloxazine
CAS:Alloxazine is a redox potential molecule that can form stable complexes with proton, nitrogen atoms, and oxidation catalysts. It is used as a sample preparation reagent for the isolation of dna duplexes. Alloxazine has shown to have biochemical properties of DNA duplexes, such as stability and photochemical properties. The magnesium salt of alloxazine has been shown to act as an oxidation catalyst in organic synthesis reactions. Alloxazine has been studied as a model system for steric interactions with the electron donor and acceptor moieties in biological systems.Formula:C10H6N4O2Purity:Min. 95%Molecular weight:214.18 g/molBenzo[g]pteridine-2,4(1H,3H)-dione
CAS:Formula:C10H6N4O2Purity:95%Color and Shape:SolidMolecular weight:214.1802
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