Skip to Content
Merck
CN

L3307

Lumazine

97%

Synonym(s):

2,4(1H,3H)-Pteridinedione, 2,4-Dihydroxypteridine, 2,4-Pteridinediol

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C6H4N4O2
CAS Number:
Molecular Weight:
164.12
EC Number:
207-652-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
157503
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


assay

97%

SMILES string

Oc1nc(O)c2nccnc2n1

InChI

1S/C6H4N4O2/c11-5-3-4(8-2-1-7-3)9-6(12)10-5/h1-2H,(H2,8,9,10,11,12)

InChI key

UYEUUXMDVNYCAM-UHFFFAOYSA-N



Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Xiaofeng Zhang et al.
Journal of molecular biology, 328(1), 167-182 (2003-04-10)
6,7-Dimethyl-8-ribityllumazine is the biosynthetic precursor of riboflavin, which, as a coenzyme, plays a vital role in the electron transfer process for energy production in all cellular organisms. The enzymes involved in lumazine biosynthesis have been studied in considerable detail. However
M S Ibrahim et al.
Journal of pharmaceutical and biomedical analysis, 28(2), 217-225 (2002-04-04)
The interaction of lumazine, an antibacterial drug, with alpha-, beta-cyclodextrins and DNA in aqueous solution was studied by differential pulse stripping voltammetry and cyclic voltammetry as well as UV-vis spectroscopy. The electrochemical and absorption spectral data indicated a 1:1 complex
Cosima D Calvano et al.
Analytical and bioanalytical chemistry, 398(1), 499-507 (2010-07-02)
Nowadays, matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry represents an emerging and versatile tool for analysis of lipids. However, direct (i.e., with no previous separation of lipid classes) analysis of crude extracts containing a complex mixture of lipids (a problem