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A28651

Sigma-Aldrich

Alloxazine

96%

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Synonym(s):
Benzo[g]pteridine-2,4(1H,3H)-dione, Isoalloxazine
Empirical Formula (Hill Notation):
C10H6N4O2
CAS Number:
Molecular Weight:
214.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

form

powder

SMILES string

O=C1NC(=O)c2nc3ccccc3nc2N1

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

HAUGRYOERYOXHX-UHFFFAOYSA-N

Gene Information

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WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Su Ma et al.
Microbial cell factories, 16(1), 37-37 (2017-03-02)
Cellobiose dehydrogenase (CDH) is an extracellular enzyme produced by lignocellulolytic fungi. cdh gene expression is high in cellulose containing media, but relatively low CDH concentrations are found in the supernatant of fungal cultures due to strong binding to cellulose. Therefore
Hideaki Takahashi et al.
The Journal of chemical physics, 129(20), 205103-205103 (2008-12-03)
The isoalloxazine ring (flavin ring) is a part of the coenzyme flavin adenine dinucleotide and acts as an active site in the oxidation of a substrate. We have computed the free energy change Deltamicro(red) associated with one-electron reduction of the
Olayinka O Ogunro et al.
Nano letters, 9(3), 1034-1038 (2009-02-25)
We have studied the structural and electronic stability of a helical ribbon of flavin mononucleotide wrapping around single-walled carbon nanotubes using first-principles density-functional calculations. The helical ribbon is formed through hydrogen bonding between adjacent uracil moieties of the isoalloxazine ring
Sammeta V Raju et al.
PloS one, 7(3), e32112-e32112 (2012-03-24)
Alcohol abuse is associated with increased lung infections. Molecular understanding of the underlying mechanisms is not complete. Airway epithelial ion transport regulates the homeostasis of airway surface liquid, essential for airway mucosal immunity and lung host defense. Here, air-liquid interface
Allen M Orville et al.
Biochemistry, 48(4), 720-728 (2009-01-13)
Flavin C4a-OO(H) and C4a-OH adducts are critical intermediates proposed in many flavoenzyme reaction mechanisms, but they are rarely detected even by rapid transient kinetics methods. We observe a trapped flavin C4a-OH or C4a-OO(H) adduct by single-crystal spectroscopic methods and in

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