642-75-1 Usage
Description
Adrenolutin, also known as 1-Methyl-1H-indole-3,5,6-triol, is a chemical compound with potential applications in various fields. It is derived from the indole family and has a unique chemical structure that allows it to interact with specific biological systems.
Uses
Used in Pharmaceutical Industry:
Adrenolutin is used as a research compound for studying the effects of amlodipine on neurohormones and oxidative stress in nonischemic cardiomyopathy. This application is crucial for understanding the underlying mechanisms of the disease and developing potential therapeutic strategies.
Used in Biological Studies:
Adrenolutin serves as a valuable tool in biological research, particularly in the study of amlodipine's impact on neurohormones and oxidative stress. This knowledge can contribute to the development of new treatments and interventions for nonischemic cardiomyopathy, a condition that affects the heart's ability to pump blood effectively.
Check Digit Verification of cas no
The CAS Registry Mumber 642-75-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 642-75:
(5*6)+(4*4)+(3*2)+(2*7)+(1*5)=71
71 % 10 = 1
So 642-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO3/c1-10-4-9(13)5-2-7(11)8(12)3-6(5)10/h2-3,11-12H,4H2,1H3
642-75-1Relevant articles and documents
The participation of Singlet Oxygen in Dye-Sensitized Photooxidation Reaction of Catecholamines
Kruk, I.
, p. 607 - 613 (2007/10/02)
The photooxidation of catecholamines (adrenaline, noradrenaline and dopamine) sensitized by methylene blue (MB), rose bengal (RB) and fluoresceine (FL) proceed via aminochromes and an indolic pathway.In D2O rate constants of sensitized photooxidation are increased for about 2,7 times over rates in water. 1,3-diphenylisobenzofuran (DPBF), 1,4-diazobicyclooctane (DABCO) and azide anion were more effective inhibitors of the reaction in D2O than in H2O.Superoxide dismutase markedly decreases the rates of photooxidation in H2O and in D2O.Isotope effects and 1O2-quenchers sensitivities indicate that singlet oxygen participates on photooxidation processes of catecholamines.
