53602-74-7 Usage
Description
(2S)-2-(acetyl-nitroso-amino)-3-(1H-indol-3-yl)propanoic acid, also known as ANAP, is an amino acid derivative with a unique molecular structure featuring an acetyl-nitroso-amino group attached to a 1H-indol-3-yl propanoic acid backbone. (2S)-2-(acetyl-nitroso-amino)-3-(1H-indol-3-yl)propanoic acid can be found in certain food sources and has potential implications in pharmaceuticals and medicine due to its distinctive chemical properties and possible biological activities.
Uses
Used in Pharmaceutical and Medicinal Applications:
(2S)-2-(acetyl-nitroso-amino)-3-(1H-indol-3-yl)propanoic acid is used as a pharmaceutical and medicinal compound for its potential biological activities. Its unique chemical structure may contribute to various therapeutic effects, although further research is required to fully understand its properties and applications in this field.
Used in Research and Development:
(2S)-2-(acetyl-nitroso-amino)-3-(1H-indol-3-yl)propanoic acid serves as a subject of research and development in the scientific community. Its presence in food sources and potential biological activities make it an interesting candidate for exploring new applications and understanding its role in health and disease.
Check Digit Verification of cas no
The CAS Registry Mumber 53602-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53602-74:
(7*5)+(6*3)+(5*6)+(4*0)+(3*2)+(2*7)+(1*4)=107
107 % 10 = 7
So 53602-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N3O4/c1-8(17)16(15-20)12(13(18)19)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,18,19)/t12-/m0/s1
53602-74-7Relevant articles and documents
Comparison of HNO reactivity with tryptophan and cysteine in small peptides
Keceli, Gizem,Moore, Cathy D.,Toscano, John P.
supporting information, p. 3710 - 3713 (2014/12/09)
Recent discoveries of important pharmacological properties have drawn attention to the reactivity of HNO (azanone, nitroxyl) with biologically relevant substrates. Apart from its role in thiol oxidation, HNO has been reported to have nitrosative properties, for example, with tryptophan resulting in N-nitrosotryptophan formation. We have investigated the reactivity of HNO with tryptophan and small peptides containing either tryptophan or both a tryptophan and a cysteine residue. Our results point to the more reactive nature of cysteine towards HNO compared with tryptophan.
