3558-32-5 Usage
Uses
Used in Sports Nutrition:
(R/S)-2-AMINO-5-METHYLHEXANOIC ACID is used as a dietary supplement for athletes and fitness enthusiasts to support muscle growth, enhance recovery after exercise, and maintain muscle mass. Its role in protein synthesis and muscle repair makes it an essential component of sports nutrition regimens.
Used in Medical Applications:
Leucine is used as a therapeutic agent in medical applications for patients with conditions that affect muscle mass and function, such as muscle wasting diseases, sarcopenia, and cachexia. Its ability to promote muscle protein synthesis and support muscle repair can help improve muscle strength and overall physical performance in these patients.
Used in Food and Beverage Industry:
(R/S)-2-AMINO-5-METHYLHEXANOIC ACID is used as a functional ingredient in food and beverage products, particularly those targeting athletes, bodybuilders, and individuals seeking to improve their muscle health and performance. It can be incorporated into protein shakes, bars, and other supplements to provide a concentrated source of leucine and support muscle growth and recovery.
Used in Research and Development:
Leucine is utilized in research and development for its potential role in various biological processes, including the regulation of gene expression, cell signaling, and metabolism. Its involvement in the growth and repair of muscle tissue makes it a valuable subject for studies aimed at understanding the molecular mechanisms underlying muscle health and function.
Used in Pharmaceutical Industry:
(R/S)-2-AMINO-5-METHYLHEXANOIC ACID is used as an active pharmaceutical ingredient in the development of drugs targeting muscle-related disorders and conditions. Its role in muscle protein synthesis and repair makes it a promising candidate for the treatment of muscle wasting diseases, sarcopenia, and other muscle-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 3558-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3558-32:
(6*3)+(5*5)+(4*5)+(3*8)+(2*3)+(1*2)=95
95 % 10 = 5
So 3558-32-5 is a valid CAS Registry Number.
3558-32-5Relevant academic research and scientific papers
Studies on Angiotensin Converting Enzyme Inhibitors. 4. Synthesis and Angiotensin Converting Enzyme Inhibitory Activities of 3-Acyl-1-alkyl-2-oxoimidazolidine-4-carboxylic Acid Derivatives
Hayashi, Kimiaki,Nunami, Ken-ichi,Kato, Jyoji,Yoneda, Naoto,Kubo, Masami,et al.
, p. 289 - 297 (2007/10/02)
(4S)-1-Alkyl-3-acyl>-2-oxoimidazolidine-4-carboxylic acid derivatives (3) were prepared by two methods.Their angiotensin converting enzyme (ACE) inhibitory activities and antihypertensive effects were evaluated, and the structure-activity relationships were discussed.The dicarboxylic acids 3a-n possessing S,S,S configuration showed potent in vitro ACE inhibitory activities with IC 50 values of 1.1x10-8-1.5x10-9 M.The most potent compound in this series, monoester 3p, had an ID 50 value of 0.24 mg/kg, po for inhibition of angiotensin I induced pressor response in normotensive rats and produced a dose-dependent decrease in systolic blood pressure of spontaneously hypertensive rats (SHRs) at doses of 1-10 mg/kg, po.
Biosynthesis of the Cephalotaxus Alkaloids. Investigations of the Biosynthesis of Deoxyharringtonine, Isoharringtonine, and Harringtonine
Gitterman, Amy,Parry, Ronald J.,Dufresne, Richard F.,Sternbach, Daniel D.,Cabelli, Michael D.
, p. 2074 - 2081 (2007/10/02)
Precursor incorporation experiments have been used to investigate the biosynthesis of the antitumor Cephalotaxus alkaloids deoxyharringtonine (2), isoharringtonine (3), and harringtonine (4).It has been established that the acyl portion of deoxyharrington
