2134-29-4
2134-29-4
Chemical Structure
Reuterin
Synonym(s): 3-Hydroxypropionaldehyde; 3-Hydroxypropanal
- No. CAS: 2134-29-4
- Formula:C3H6O2
- Molecular Weight:74.08
IUPAC Name: 3-hydroxypropanal
InChIKey: AKXKFZDCRYJKTF-UHFFFAOYSA-N
SMILES: O=CCCO
Biological Activity: Reuterin is a broad-spectrum antimicrobial agent active against Gram positive and Gram negative bacteria, as well as yeasts, moulds and protozoa. Reuterin is produced by specific strains of Lactobacillus reuteri during anaerobic metabolism of glycerol. Reuterin also demonstrates potent antimicrobial activity against a broad panel of human and poultry meat campylobacter spp. Isolates[1][2].
| Referencia número | Nombre del producto | Pureza | Descripciòn | Pricing | |||||||||||||||||||
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Reuterin | 98.45% | Reuterin is a broad-spectrum antimicrobial agent active against Gram positive and Gram negative bacteria, as well as yeasts, moulds and protozoa. Reuterin is produced by specific strains of Lactobacillus reuteri during anaerobic metabolism of glycerol. Reuterin also demonstrates potent antimicrobial activity against a broad panel of human and poultry meat campylobacter spp. Isolates. | ||||||||||||||||||||
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Succinaldehydic acid | 97.26% | Succinaldehydic acid is a catabolite of GABA. | ||||||||||||||||||||
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Glycolaldehyde-1-13C | 99.0% | Glycolaldehyde-1-13C is the 13C labeled Glycolaldehyde. | ||||||||||||||||||||
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Glycolaldehyde-2-13C | 99.30% | Glycolaldehyde-2-13C is the 13C labeled Glycolaldehyde. | ||||||||||||||||||||
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2-Hydroxyacetaldehyde | 2-Hydroxyacetaldehyde acts as a ribonucleotide synthesis precursor and a LDL modifier. 2-Hydroxyacetaldehyde specifically targets lysine residues of high-affinity LDL receptors and their apolipoproteins. By blocking the ε-amino groups of apolipoproteins, 2-Hydroxyacetaldehyde prevents receptor recognition, thereby reducing LDL degradation by macrophages. 2-Hydroxyacetaldehyde generates modified LDL, which serves as a probe for investigating non-receptor-dependent catabolic pathways. | |||||||||||||||||||||
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4-Penten-1-ol | 99.99% | 4-Penten-1-ol is commonly used as a flavor ingredient in various products, including food, beverages, and perfumes, and can also be used as a starting material for the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. In addition, 4-Penten -1-ol has been investigated for its potential use as a biobased solvent due to its low toxicity and biodegradability, and its antimicrobial properties against certain bacteria and fungi, which may make it useful for developing new Antibacterial agents. | ||||||||||||||||||||
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4-Chlorobutanal | 96.76% | 4-Chlorobutanal is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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Pent-4-ynal | 97.63% | Pent-4-ynal is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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4-Hydroxybutanal | 4-Hydroxybutanal is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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2-Hydroxyacetaldehyde-13C2 | 2-Hydroxyacetaldehyde-13C2 is the 13C-labeled 2-Hydroxyacetaldehyde (HY-28911). | |||||||||||||||||||||
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5-Oxopentanoic acid | 5-Oxopentanoic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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References
- [1]. Schaefer L, et al. The antimicrobial compound reuterin (3-hydroxypropionaldehyde) induces oxidative stress via interaction with thiol groups. Microbiology (Reading). 2010;156(Pt 6):1589-1599. [Content Brief]
- [2]. Asare PT, et al. Reuterin Demonstrates Potent Antimicrobial Activity Against a Broad Panel of Human and Poultry Meat Campylobacter spp. Isolates. Microorganisms. 2020;8(1):78. Published 2020 Jan 6. [Content Brief]
