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Tetramic acid is a class of organic compounds characterized by a four-membered ring structure with a carbonyl group and an acidic proton. Found in natural products such as fungal and bacterial metabolites, these compounds exhibit a broad spectrum of biological activities, including antimicrobial, antiviral, and antitumor properties. Their versatile structure and potential as lead compounds for drug development make tetramic acids attractive targets for the synthesis of new pharmaceuticals and agrochemicals.

503-83-3

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503-83-3 Usage

Uses

Used in Pharmaceutical Industry:
Tetramic acid is used as a lead compound for drug development due to its wide range of biological activities and potential in creating new pharmaceuticals.
Used in Agrochemical Industry:
Tetramic acid is used as a precursor in the synthesis of new agrochemicals, such as insecticides and herbicides, owing to its versatile structure and biological properties.
Used in Dye Industry:
Tetramic acid is used in the development of synthetic dyes, leveraging its chemical properties for color production and application in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 503-83-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 503-83:
(5*5)+(4*0)+(3*3)+(2*8)+(1*3)=53
53 % 10 = 3
So 503-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H5NO2/c6-3-1-4(7)5-2-3/h1,5,7H,2H2

503-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-1,2-dihydropyrrol-5-one

1.2 Other means of identification

Product number -
Other names Tetraminsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:503-83-3 SDS

503-83-3Downstream Products

503-83-3Relevant academic research and scientific papers

Synthesis of a leopolic acid-inspired tetramic acid with antimicrobial activity against multidrug-resistant bacteria

Mattio, Luce,Musso, Loana,Scaglioni, Leonardo,Pinto, Andrea,Martino, Piera Anna,Dallavalle, Sabrina

supporting information, p. 2482 - 2487 (2018/10/04)

The increasing emergence of multidrug-resistant pathogens is one of the biggest threats to human health and food security. The discovery of new antibacterials, and in particular the finding of new scaffolds, is an imperative goal to stay ahead of the evolution of antibiotic resistance. Herein we report the synthesis of a 3-decyltetramic acid analogue of the ureido dipeptide natural antibiotic leopolic acid A. The key step in the synthetic strategy is an intramolecular Lacey-Dieckmann cyclization reaction of a linear precursor to obtain the desired 3-alkyl-substituted tetramic acid core. The synthesized analogue is more effective than the parent leopolic acid A against Gram-positive (Staphylococcus pseudintermedius) and Gram-negative (E. coli) bacteria (MIC 8 μg/mL and 64 μg/mL, respectively). Interestingly, the compound shows a significant activity against Staphylococcus pseudintermedius strains expressing a multidrug-resistant phenotype (average MIC 32 μg/mL on 30 strains tested). These results suggest that this molecule can be considered a promising starting point for the development of a novel class of antibacterial agents active also against resistant strains.

REMEDY FOR DIABETES

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Page/Page column 22, (2010/04/23)

A method of screening a compound having a hypoglycemic effect (hereinafter referred to as "hypoglycemic compound"), a remedy for diabetes which contains a compound having a novel function mechanism, etc. More specifically speaking, a method of screening a hypoglycemic compound capable of binding to the β subunit of a trimeric GTP-binding protein, a remedy for diabetes comprising a hypoglycemic compound, which is characterized by being capable of binding to the β subunit of a trimeric GTP-binding protein, as the active ingredient, etc.

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