142-18-7
142-18-7
Chemical Structure
Monolaurin
Synonym(s): 1-Monolaurin
- CAS No.: 142-18-7
- Formula:C15H30O4
- Molecular Weight:274.40
IUPAC Name: 2,3-dihydroxypropyl dodecanoate
InChIKey: ARIWANIATODDMH-UHFFFAOYSA-N
SMILES: CCCCCCCCCCCC(OCC(CO)O)=O
Biological Activity: Monolaurin (1-Monolaurin) is an orally active antibiotic with antiviral and antibacterial properties[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Monolaurin | 98.97% | Monolaurin (1-Monolaurin) is an orally active antibiotic with antiviral and antibacterial properties. | ||||||||||||||||||||
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Monolaurin (Standard) | ≥98% | Monolaurin (Standard) is the analytical standard of Monolaurin. This product is intended for research and analytical applications. Monolaurin (1-Monolaurin) is an orally active antibiotic with antiviral and antibacterial properties. | ||||||||||||||||||||
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Monolaurin-d23 | Monolaurin-d23 is the deuterium labeled Monolaurin. Monolaurin (1-Monolaurin) possesses anti-viral and anti-bacterial activity. | |||||||||||||||||||||
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1-Undecanoylglycerol | 98.0% | 1-Undecanoylglycerol is a monoacylglycerol with antibacterial activity, which can be used in food additives research. | ||||||||||||||||||||
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(2R)-Monolaurin | (2R)-Monolaurin ((2R)-1-Monolaurin) ((2r)-2,3-Dihydroxypropyl Dodecanoate) is the R-enantiomer of Monolaurin (HY-121620). (2R)-Monolaurin is significantly up-regulated in the rectal contents of weaned yaks after the addition of traditional Chinese medicine compound. | |||||||||||||||||||||
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(2S)-Monolaurin | (2S)-Monolaurin ((2S)-1-Monolaurin) is the S-enantiomer of Monolaurin (HY-121620) and is mirror-symmetrical to (2R)-Monolaurin (HY-187069). | |||||||||||||||||||||
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1-Monononanoin | 1-Monononanoin is an acylglycerol. | |||||||||||||||||||||
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1-Monomyristin | 98.0% | 1-Monomyristin acts as an insecticide, enzyme inhibitor, antibacterial and antifungal agent, with an IC50 of 18 μM against rat FAAH and an IC50 of 32 μM against rat MAGL. 1-Monomyristin inhibits 2-oleoylglycerol hydrolysis via MAGL. 1-Monomyristin suppresses the growth of Staphylococcus aureus, Aggregatibacter actinomycetemcomitans and Candida albicans. 1-Monomyristin is lethal to brine shrimp. 1-Monomyristin exhibits marginal cytotoxicity against prostate cancer cells. 1-Monomyristin is applicable to research related to bacterial infections, fungal infections, renal cancer, prostate adenocarcinoma and pancreatic cancer. | ||||||||||||||||||||
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1-Monopalmitin | 99.89% | 1-Monopalmitin (Glyceryl palmitate) is an activator of the PI3K/Akt pathway and an inhibitor of P-glycoprotein (P-gp). 1-Monopalmitin can induce G2/M arrest and caspase-dependent apoptosis in cancer cells, while inhibiting IAPs protein expression. 1-Monopalmitin can increase drug accumulation by inhibiting P-gp activity in intestinal Caco-2 cells. 1-Monopalmitin has the ability to induce protective autophagy and apoptosis of lung cancer cells (IC50=50-58 μg/mL), with low toxicity to normal cells. | ||||||||||||||||||||
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2,3-Dihydroxypropyl decanoate | 99.92% | 2,3-Dihydroxypropyl decanoate (1-Decanoyl-rac-glycerol) is a derivative of Decanoic acid (HY-W015309) and a non-ionic surfactant, with an IC50 > 100 μM against Shp2-PTP, VHR and HePTP. 2,3-Dihydroxypropyl decanoate is found in the roots of Angelica dahurica (Baizhi). 2,3-Dihydroxypropyl decanoate acts as a component of reverse micelle systems for the encapsulation of proteins and nucleic acids. | ||||||||||||||||||||
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1-Palmitoyl-sn-glycerol | 99.99% | 1-Palmitoyl-sn-glycerol is a biochemical assay reagent. | ||||||||||||||||||||
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2,3-Dihydroxypropyl tridecanoate | 2,3-Dihydroxypropyl tridecanoate is an acylglycerol. | |||||||||||||||||||||
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2,3-Dihydroxypropyl pentadecanoate | 99.83% | 2,3-Dihydroxypropyl pentadecanoate is a monoacylglycerol that is found in wheat bran extracts. 2,3-Dihydroxypropyl pentadecanoate levels are increased in a HepaRG cell-based model of hepatic steatosis induced by BSA-conjugated palmitate. | ||||||||||||||||||||
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References
- [1]. Harry G Preuss, et al. Minimum inhibitory concentrations of herbal essential oils and monolaurin for gram-positive and gram-negative bacteria. Mol Cell Biochem. 2005 Apr;272(1-2):29-34. [Content Brief]
- [2]. Edy Subroto, et al. Bioactive monolaurin as an antimicrobial and its potential to improve the immune system and against COVID-19: a review. Food Research 4(6):2355-2365.
- [3]. Manohar V, et al. In vitro and in vivo effects of two coconut oils in comparison to monolaurin on Staphylococcus aureus: rodent studies. J Med Food. 2013 Jun;16(6):499-503. [Content Brief]
