57105-53-0 Usage
Description
Tryptophan, N-indol-3-ylacetyl(6CI), also known as Indole-3-acetyl-L-tryptophan, is an indole-3-acetyl-amino acid conjugate that plays a significant role in various biological processes. It is involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses, making it a crucial component in the study of cellular and molecular biology.
Uses
Used in Pharmaceutical Industry:
Tryptophan, N-indol-3-ylacetyl(6CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds, such as β-D-galactosidase and β-D-glucosidase inhibitors. These inhibitors have potential applications in the treatment of various diseases and conditions, including lysosomal storage disorders and certain types of cancer.
Used in Agricultural Industry:
In the agricultural industry, Tryptophan, N-indol-3-ylacetyl(6CI) is utilized in the development of bioactive compounds that can help regulate plant growth and development. Its involvement in the control of auxin activity makes it a valuable tool for understanding and manipulating plant responses to various environmental stimuli, which can lead to improved crop yields and resistance to diseases.
Used in Research and Development:
Tryptophan, N-indol-3-ylacetyl(6CI) is also used as a research tool in the field of molecular biology and biochemistry. It can be employed in the study of protein-protein interactions, enzyme inhibition, and other cellular processes, contributing to the advancement of scientific knowledge and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 57105-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57105-53:
(7*5)+(6*7)+(5*1)+(4*0)+(3*5)+(2*5)+(1*3)=110
110 % 10 = 0
So 57105-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H19N3O3/c25-20(10-14-12-23-18-8-4-2-6-16(14)18)24-19(21(26)27)9-13-11-22-17-7-3-1-5-15(13)17/h1-8,11-12,19,22-23H,9-10H2,(H,24,25)(H,26,27)/t19-/m0/s1
57105-53-0Relevant articles and documents
Preparation of synthetic auxin-amino acid conjugates
Revelou, Panagiota-Kyriaki,Constantinou-Kokotou, Violetta
, p. 1708 - 1712 (2019/05/15)
Auxin amide conjugates are regulators of the most important auxin, indole-3-acetic acid (IAA), which is considered responsible for many important processes within the plants. Herein, amide conjugates of IAA were synthesized employing a simple and efficient coupling method with WSCI·HCl, a water-soluble condensing reagent, in the presence of 1-hydroxybenzotriazole. IAA conjugates with 10 amino acids along with their corresponding methyl esters were prepared in excellent yields, up to 95%, aiming to facilitate their identification in plant species. Eight IAA-amino acid methyl ester conjugates are characterized here for the first time.
Syntheses of IAA- and IPA-amino acid conjugates
Katritzky, Alan R.,Khelashvili, Levan,Munawar, Ali
supporting information; experimental part, p. 9171 - 9173 (2009/04/11)
(Chemical Equation Presented) Amino acid derivatives of IAA and IPA are prepared conveniently and efficiently by coupling of readily available 2a-b with diverse free amino acids 3a-g and (3c+3c′) to give compounds 4a-j, (4c+4c′) and (4h+4h′) in 38-70% yie
