57105-48-3 Usage
Description
INDOLE-3-ACETYL-L-GLUTAMIC ACID (IAGlu) is an indole-3-acetyl-amino acid conjugate that plays a significant role in the regulatory mechanisms controlling auxin activity. INDOLE-3-ACETYL-L-GLUTAMIC ACID (IAGlu) is involved in various physiological and pathophysiological responses, making it a crucial component in the study of plant growth and development.
Uses
Used in Plant Biology Research:
INDOLE-3-ACETYL-L-GLUTAMIC ACID (IAGlu) is used as a research compound for understanding the regulatory mechanisms of auxin activity. Its role in controlling plant growth and development is essential for studying various physiological and pathophysiological responses in plants.
Used in Agricultural Applications:
IAGlu is used as a growth regulator in agriculture to enhance crop yield and quality. By modulating auxin activity, it can potentially improve plant resistance to stressors and optimize growth conditions.
Used in Pharmaceutical Development:
INDOLE-3-ACETYL-L-GLUTAMIC ACID (IAGlu) is used as a potential therapeutic agent for developing treatments targeting auxin-related conditions. Its role in controlling auxin activity could lead to the development of new drugs for various medical applications.
Used in Environmental Science:
IAGlu is used as a tool in environmental science to study the effects of auxin activity on ecosystems and the environment. Understanding its role in plant growth and development can help in developing strategies for sustainable agriculture and ecosystem management.
Check Digit Verification of cas no
The CAS Registry Mumber 57105-48-3 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, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57105-48:
(7*5)+(6*7)+(5*1)+(4*0)+(3*5)+(2*4)+(1*8)=113
113 % 10 = 3
So 57105-48-3 is a valid CAS Registry Number.
57105-48-3Relevant 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.
Stable-isotope labeled metabolites of the phytohormone, indole-3-acetic acid
Illic, Nebojsa,Magnus, Volker,Oestin, Anders,Sandberg, Goeran
, p. 433 - 440 (2007/10/03)
1,3-Dicyclohexylcarbodiimide-mediated condensation of [3a,4,5,6,7,7a-13C6]indole-3-acetic acid with the bis(tert-butyl) esters of L-aspartic or L-glutamic acids, followed by removal of the ester groups by dilute alkali, afforded N-([3a,4,5,6,7,7a-13C6]indol-3-ylacetyl)-L-aspartic and N-([3a,4,5,6,7,7a-13C6]indol-3-ylacetyl)-L-glutamic acids, labeled forms of compounds involved in the regulation of plant growth and development. The corresponding conjugates of (R,S)-2,3-dihydro-2-oxoindole-3-acetic acid, which are likewise of physiological significance, were labeled with 15N in the amino acid moieties and were synthesized via the N-hydroxysuccinimide ester.
