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82333-52-6

N-γ-L-glutamyl-2-aminophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82333-52-6 Structure

  • Basic information

    1. Product Name: N-γ-L-glutamyl-2-aminophenol
    2. Synonyms:
    3. CAS NO:82333-52-6
    4. Molecular Formula:
    5. Molecular Weight: 238.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82333-52-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-γ-L-glutamyl-2-aminophenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-γ-L-glutamyl-2-aminophenol(82333-52-6)
    11. EPA Substance Registry System: N-γ-L-glutamyl-2-aminophenol(82333-52-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 82333-52-6(Hazardous Substances Data)

82333-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82333-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,3 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82333-52:
(7*8)+(6*2)+(5*3)+(4*3)+(3*3)+(2*5)+(1*2)=116
116 % 10 = 6
So 82333-52-6 is a valid CAS Registry Number.

82333-52-6Downstream Products

82333-52-6Relevant articles and documents

Design, synthesis and biological evaluation of glutamic acid derivatives as anti-oxidant and anti-inflammatory agents

Pagire, Suvarna H.,Lee, Eunhye,Pagire, Haushabhau S.,Bae, Eun Jung,Ryu, Soo Jung,Lee, Dahye,Kim, Min Hee,Kim, Geum Ran,Hwang, Kyu-Seok,Ahn, Sukyung,Maeng, Jin Hee,Song, Jin Sook,Bae, Myung Ae,Lee, Don Hang,Ahn, Jin Hee

, p. 529 - 532 (2018)

A series of glutamic acid derivatives was synthesized and evaluated for their antioxidant activity and stability. We found several potent and stable glutamic acid derivatives. Among them, compound 12b exhibited good in vitro activity, chemical stability and cytotoxicity. A prototype compound 12b showed an anti-inflammatory effect in LPS-stimulated RAW 264.7 cell lines and in a zebrafish model.

Drug Latentiation by γ-Glutamyl Transpeptidase

Magnan, Sanne D. J.,Shirota, Frances N.,Nagasawa, Herbert T.

, p. 1018 - 1021 (2007/10/02)

The N-γ-glutamyl derivatives of L-thiazolidine-4-carboxylic acid, 4-aminobutyric acid, 1-aminocyclopentanecarboxylic acid, 2-aminophenol, and p-fluoro-L-phenylalanine (compounds 6, 8, 9, 10, and 12 respectively) were synthesized using the synthom phthaloylglutamic anhydride.Their relative rates of cleavage by the enzyme γ-glutamyl transpeptidase (γ-GT) were determined in order to evaluate the possibility for their selective release by this enzyme which is elevated in certain pathological conditions.Compounds 6, 8, and 9 were not readily solvolyzed by γ-GT, but compounds 10 and 12, as well as the N-γ-glutamylated derivatives of 3- and 4-aminophenol, were readily cleaved.

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