111-03-5
Chemical Structure
Monoolein
Synonym(s): MG (18:1)
- CAS No.: 111-03-5
- Formula:C21H40O4
- Molecular Weight:356.54
IUPAC Name: 2,3-dihydroxypropyl oleate
InChIKey: RZRNAYUHWVFMIP-KTKRTIGZSA-N
SMILES: CCCCCCCC/C=C\CCCCCCCC(OCC(O)CO)=O
Biological Activity: Monoolein is a biocompatible lipid molecule that can be used as a carrier for bone repair. Monoolein exhibits anti-inflammatory activity by inhibiting the immune response induced by LPS (HY-D1056). It exerts its anti-inflammatory effects by reducing the production of immune response factors such as IL-12 p40, IL-6, and TNF-α, and inhibiting the generation of NO. Monoolein can be used in drug delivery and research in the field of inflammatory diseases [1][2].
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Monoolein | 99.9% | Monoolein is a biocompatible lipid molecule that can be used as a carrier for bone repair. Monoolein exhibits anti-inflammatory activity by inhibiting the immune response induced by LPS (HY-D1056). It exerts its anti-inflammatory effects by reducing the production of immune response factors such as IL-12 p40, IL-6, and TNF-α, and inhibiting the generation of NO. Monoolein can be used in drug delivery and research in the field of inflammatory diseases . | ||||||||||||||||||||
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Monoolein (Standard) | ≥98% | Monoolein is a biocompatible lipid molecule that can be used as a carrier for bone repair. Monoolein exhibits anti-inflammatory activity by inhibiting the immune response induced by LPS (HY-D1056). It exerts its anti-inflammatory effects by reducing the production of immune response factors such as IL-12 p40, IL-6, and TNF-α, and inhibiting the generation of NO. Monoolein can be used in drug delivery and research in the field of inflammatory diseases . | ||||||||||||||||||||
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Monoolein-d7 | 99.0% | Monoolein-d7 is deuterium labeled Monoolein. Monoolein is an endogenous metabolite. | ||||||||||||||||||||
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Monoolein-d5 | 99.94% | Monoolein-d5 is the deuterium labeled Monoolein. Monoolein is an endogenous metabolite. | ||||||||||||||||||||
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References
- [1]. Ali I, et al. Monoolein, isolated from Ishige sinicola, inhibits lipopolysaccharide-induced inflammatory response by attenuating mitogen-activated protein kinase and NF-κB pathways. Food Sci Biotechnol. 2017 Apr 30;26(2):507-511. [Content Brief]
- [2]. Issa JP, et al. Monoolein and chitosan gels as potential carriers of the rhBMP-2, using decortication surgical technique in Wistar rats as experimental model. Micron. 2008 Oct;39(7):952-9. [Content Brief]
