41863-47-2 Usage
Uses
Used in Pharmaceutical Industry:
O-PHOSPHO-DL-TYROSINE is used as a key compound for the development of pharmaceuticals targeting various diseases. Its unique phosphorylated structure allows it to interact with specific enzymes and receptors, making it a promising candidate for drug discovery and design.
Used in Research and Development:
In the field of research, O-PHOSPHO-DL-TYROSINE serves as an important tool for studying the role of tyrosine phosphorylation in cellular processes. It can be used to investigate the effects of phosphorylation on protein function, signal transduction pathways, and the regulation of cellular activities.
Used in Diagnostic Applications:
O-PHOSPHO-DL-TYROSINE can be employed in the development of diagnostic tests and assays to detect the presence of specific phosphorylated proteins or to monitor the activity of certain enzymes. This can be particularly useful in the early detection and monitoring of diseases associated with abnormal tyrosine phosphorylation.
Used in Biochemical Studies:
As a phosphorylated amino acid, O-PHOSPHO-DL-TYROSINE can be utilized in biochemical studies to understand the mechanisms of protein phosphorylation and dephosphorylation. This knowledge can contribute to the development of targeted therapies for diseases involving dysregulated tyrosine kinase or phosphatase activity.
Check Digit Verification of cas no
The CAS Registry Mumber 41863-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,6 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41863-47:
(7*4)+(6*1)+(5*8)+(4*6)+(3*3)+(2*4)+(1*7)=122
122 % 10 = 2
So 41863-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12NO6P/c11-7-3-1-6(2-4-7)5-8(9(12)13)10-17(14,15)16/h1-4,8,11H,5H2,(H,12,13)(H3,10,14,15,16)/t8-/m0/s1
41863-47-2Relevant academic research and scientific papers
The herbicide glyphosate and related molecules: Physicochemical and structural factors determining their mobility in phloem
Bromilow, Richard H.,Chamberlain, Keith
, p. 368 - 373 (2007/10/03)
The herbicide glyphosate shows excellent symplastic distribution to roots and new growth when applied to the foliage of plants. Though the phloem transport of non-ionised and of monobasic weak acids can be understood in terms of the intermediate permeability theory, the multiple ionisable functionality of glyphosate, which has three acid groups and a strong amine base, precludes simple interpretation of its systemicity. Accordingly, the behaviour of an analogue of glyphosate based on a phenyl ring and carrying the same ionisable functionalities has been examined in castor bean (Ricinus communis L) plants, together with that of related compounds in which the number of ionisable groups has been sequentially reduced. The close glyphosate analogue was symplastically transported almost as efficiently as glyphosate itself, whereas its monoethyl phosphonate ester, together with simpler analogues such as phenylphosphonic acids and phenylalanine, were less well translocated. It is thus the unique combination of ionisable functionality that confers good symplastic mobility, and loss of one or more of these ionisable functionalities leads to decreased movement in phloem. The reasons for such functional requirements for effective transport via phloem are not understood, though there is no evidence for recognition by specific carriers; the accumulation of glyphosate in phloem vessels is good but not exceptional, but once transported to roots and rhizomes it is exceptionally well retained. (C) 2000 Society of Chemical Industry.
