2389-86-8 Usage
Uses
Used in Pharmaceutical Industry:
Nalpha-Acetyl-D-arginine dihydrate is used as a building block for the synthesis of various drugs and compounds. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Cardiovascular and Metabolic Disorders Treatment:
Nalpha-Acetyl-D-arginine dihydrate is used as a therapeutic agent for the treatment of cardiovascular and metabolic disorders. Its potential benefits in these areas are attributed to its ability to modulate key physiological processes and pathways involved in these conditions.
Used in Cognitive Function Improvement:
Nalpha-Acetyl-D-arginine dihydrate is used as a cognitive enhancer, with research suggesting that it may improve cognitive function by modulating neurotransmitter levels and promoting neuronal health.
Used in Antioxidant and Anti-Inflammatory Applications:
Nalpha-Acetyl-D-arginine dihydrate is used for its antioxidant and anti-inflammatory properties, which may help protect cells from oxidative stress and reduce inflammation, contributing to overall health and well-being.
Used in Research for Therapeutic Agents:
In research, Nalpha-Acetyl-D-arginine dihydrate is used as a potential therapeutic agent for conditions such as diabetes, hypertension, and neurodegenerative diseases. Its multifaceted properties make it a promising candidate for further investigation and development in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 2389-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2389-86:
(6*2)+(5*3)+(4*8)+(3*9)+(2*8)+(1*6)=108
108 % 10 = 8
So 2389-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N4O3/c1-5(13)12-6(7(14)15)3-2-4-11-8(9)10/h6H,2-4H2,1H3,(H,12,13)(H,14,15)(H4,9,10,11)
2389-86-8Relevant articles and documents
Product-substrate engineering by bacteria: Studies on clavaminate synthase, a trifunctional dioxygenase
Lloyd, Matthew D.,Merritt, Kirsten D.,Lee, Victor,Sewell, Timothy J.,Wha-Son, Byeng,Baldwin, Jack E.,Schofield, Christopher J.,Elson, Steve W.,Baggaley, Keith H.,Nicholson, Neville H.
, p. 10201 - 10220 (2007/10/03)
Evidence is presented that clavaminate synthase (CS) catalyses three oxidative reactions in the clavulanic acid biosynthetic pathway. The first CS catalysed step (hydroxylation) is separated from the latter two (oxidative cyclisation and desaturation) by the action of a hydrolytic enzyme, proclavaminate amidinohydrolase, which modifies (or 'mutates') the sidechain of the product of the first reaction thereby converting it into a substrate for the second CS catalysed reaction.
