7479-20-1 Usage
Description
3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID, also known as 1-methyltryptophan, is a chemical compound that belongs to the class of indole derivatives. It is a derivative of tryptophan and is characterized by its potential as a pharmaceutical precursor and its involvement in the synthesis of various biologically active compounds. 3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID holds promise for its anti-inflammatory and immunosuppressive properties, making it a valuable candidate for the development of new drugs targeting a range of diseases.
Uses
Used in Pharmaceutical Synthesis:
3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with diverse therapeutic applications.
Used in Anti-Inflammatory and Immunosuppressive Applications:
In the medical field, 3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID is used as an anti-inflammatory and immunosuppressive agent, leveraging its potential to modulate immune responses and reduce inflammation, which is crucial for treating conditions characterized by excessive immune activity or chronic inflammation.
Used in Research and Development of Neurodegenerative Disorders:
3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID is utilized as a research compound in the study of neurodegenerative disorders, given its potential therapeutic effects and the need to understand its impact on neurological conditions.
Used in Cancer Research:
In oncology, 3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID is used as a research tool to explore its role in cancer treatment, with the aim of identifying its potential as a therapeutic agent against various types of cancer.
Used in Autoimmune Disease Research:
3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID is employed in the investigation of autoimmune diseases, focusing on its capacity to regulate immune responses and potentially mitigate the effects of these conditions.
Each application underscores the versatility and significance of 3-(1-METHYL-1H-INDOL-3-YL)-PROPIONIC ACID in advancing medical science and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 7479-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7479-20:
(6*7)+(5*4)+(4*7)+(3*9)+(2*2)+(1*0)=121
121 % 10 = 1
So 7479-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c1-13-8-9(6-7-12(14)15)10-4-2-3-5-11(10)13/h2-5,8H,6-7H2,1H3,(H,14,15)
7479-20-1Relevant articles and documents
-
Hart,Potts
, p. 2940 (1962)
-
Sodium Iodide/Hydrogen Peroxide-Mediated Oxidation/Lactonization for the Construction of Spirocyclic Oxindole-Lactones
Li, Guofeng,Huang, Liwu,Xu, Jiecheng,Sun, Wangsheng,Xie, Junqiu,Hong, Liang,Wang, Rui
supporting information, p. 2873 - 2877 (2016/09/16)
The sodium iodide/hydrogen peroxide-mediated oxidation/lactonization of indolepropionic acids was achieved, affording the corresponding spirocyclic oxindole-lactones in moderate to high yields. This metal-free procedure features mild reaction conditions, non-toxicity and easy handling, with hydrogen peroxide (H2O2) as a clean oxidant. (Figure presented.).
Thee-component, one-pot synthesis of hexahydroazepino[3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity
Reddy, B.V. Subba,Venkata Ganesh,Vani,Ramalinga Murthy,Kalivendi, Shasi V,Yadav
supporting information, p. 4501 - 4503 (2015/02/06)
A three-component, four-center Ugi reaction has been developed to produce a novel class of 2-aryl-3-oxo-hexahydroazepino[3,4-b]indole and 2-aryl-3-oxo-tetrahydro-1H-pyrido[3,4-b]indole derivatives in good to high yields. A few of them exhibit moderate cyt
