50635-52-4 Usage
Chemical compound
A derivative of the flavin molecule.
Structure
Produced by the addition of a carboxymethyl group to the N(3) position of the 1,5-dihydro form of lumiflavin.
Role
Often used as a cofactor in enzymatic reactions.
Enzyme types
Primarily involved in oxidoreductase or dehydrogenase enzymes.
Function
Involved in electron transfer processes.
Specific role
Acts as an electron carrier to facilitate the conversion of substrates.
Role variation
The specific role can vary depending on the particular enzyme and its substrate.
Importance
An important target for study and potential applications in biotechnology and medical research.
Check Digit Verification of cas no
The CAS Registry Mumber 50635-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50635-52:
(7*5)+(6*0)+(5*6)+(4*3)+(3*5)+(2*5)+(1*2)=104
104 % 10 = 4
So 50635-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N4O4/c1-7-4-9-10(5-8(7)2)18(3)13-12(16-9)14(22)19(6-11(20)21)15(23)17-13/h4-5,16H,6H2,1-3H3,(H,17,23)(H,20,21)
50635-52-4Relevant academic research and scientific papers
Heelis, Paul F.,Hartman, Rosemarie F.,Rose, Seth D.
, p. 6053 - 6056 (1994)
Alcohols and ethers that do not normally photoadd to flavins do so in the presence of EDTA to produce covalent attachment of an alkyl group at C(4a).Thus, irradiation of an aerated solution containing both EDTA and t-butanol resulted in rapid formation of an air-stable, reduced flavin, FIH-C(4a)CH2C(CH3)2OH.Similar results were also obtained with ethanol, 1-propanol, 2-propanol, pinacol, poly(ethylene glycol), and dioxane, but not with methanol or acetone.
