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Dokumente

A28651

Sigma-Aldrich

Alloxazin

96%

Synonym(e):

Benzo[g]pteridin-2,4(1H,3H)-dion, Isoalloxazin

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About This Item

Empirische Formel (Hill-System):
C10H6N4O2
CAS-Nummer:
490-59-5
Molekulargewicht:
214.18
EG-Nummer:
207-714-3
MDL-Nummer:
MFCD00005020
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24890699
NACRES:
NA.22

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)

InChIKey

HAUGRYOERYOXHX-UHFFFAOYSA-N

Angaben zum Gen

human ... ADORA1(134) , ADORA2A(135) , ADORA2B(136)

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Riboflavin Impurity A Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1936

Riboflavin Impurity A

VISNAGIN AldrichCPR

T341649

VISNAGIN

SCH 58261 ≥98% (HPLC), solid

Sigma-Aldrich

S4568

SCH 58261

N-(5-Hexinyl)phthalimid ≥95%

Sigma-Aldrich

543993

N-(5-Hexinyl)phthalimid

8-Cyclopentyl-1,3-dipropylxanthine solid

Sigma-Aldrich

C101

8-Cyclopentyl-1,3-dipropylxanthine

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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
Limor Radoszkowicz et al.
Physical chemistry chemical physics : PCCP, 13(25), 12058-12066 (2011-06-01)
Time-resolved fluorescence decay of flavin adenine dinucleotide (FAD) was studied at room temperature in water and water-methanol mixtures by a fluorescence upconversion technique. The observations were focused on the most initial decay phase (200 ps), before the residual fluorescence assumes
Tzong-Yuan Lin et al.
The Journal of biological chemistry, 287(45), 38338-38346 (2012-09-21)
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Amanda B Witte et al.
Biomacromolecules, 13(2), 507-516 (2011-12-24)
The present study describes the biophysical characterization of generation-five poly(amidoamine) (PAMAM) dendrimers conjugated with riboflavin (RF) as a cancer-targeting platform. Two new series of dendrimers were designed, each presenting the riboflavin ligand attached at a different site (isoalloxazine at N-3
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