Molecular structure of 1-Oleoyl-sn-glycero-3-phosphocholine, CAS Number: 19420-56-5
1-Oleoyl-sn-glycero-3-phosphocholine (CAS 19420-56-5)
Alternate Names:
1-(9Z-Octadecenoyl)-sn-glycero-3-phosphocholine, 1-cis-9-Octadecenoyl-sn-glycero-3-phosphocholine, 1-Oleoyl-2-hydroxy-sn-glycerol-3-phosphocholine
Application:
1-Oleoyl-sn-glycero-3-phosphocholine is a reference for the analysis of lysolecithins
CAS Number:
19420-56-5
Molecular Weight:
521.67
Molecular Formula:
C26H52NO7P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
1-Oleoyl-sn-glycero-3-phosphocholine a reactive molecule that belongs to the group of phospholipids. It is a reference for the analysis of lysolecithins extracted from tissues and cell membranes. It can be found in the cell membrane or extracellular space and modulates voltage-dependent calcium channels, enzyme activities, and hydrophilic interaction chromatography.
1-Oleoyl-sn-glycero-3-phosphocholine (CAS 19420-56-5) References
- What makes the bioactive lipids phosphatidic acid and lysophosphatidic acid so special? | Kooijman, EE., et al. 2005. Biochemistry. 44: 17007-15. PMID: 16363814
- Molecular identification of lyso-glycerophosphocholines as endogenous immunosuppressives in bovine and rat gonadal fluids. | Foulds, LM., et al. 2008. Biol Reprod. 79: 525-36. PMID: 18509166
- Transbilayer distribution of bromine in fluid bilayers containing a specifically brominated analogue of dioleoylphosphatidylcholine. | Wiener, MC. and White, SH. 1991. Biochemistry. 30: 6997-7008. PMID: 2069956
- Acyl transfer from phosphocholine lipids to melittin. | Pridmore, CJ., et al. 2011. Chem Commun (Camb). 47: 1422-4. PMID: 21170466
- Bioactive lysophospholipids generated by hepatic lipase degradation of lipoproteins lead to complement activation via the classical pathway. | Ma, W., et al. 2014. Invest Ophthalmol Vis Sci. 55: 6187-93. PMID: 25205869
- Lysophosphatidylcholine acts in the constitutive immune defence against American foulbrood in adult honeybees. | Riessberger-Gallé, U., et al. 2016. Sci Rep. 6: 30699. PMID: 27480379
- In vivo microsampling to capture the elusive exposome. | Bessonneau, V., et al. 2017. Sci Rep. 7: 44038. PMID: 28266605
- Fluoride exposure altered metabolomic profile in rat serum. | Yue, B., et al. 2020. Chemosphere. 258: 127387. PMID: 32947680
- Glycerophospholipid metabolism is involved in rheumatoid arthritis pathogenesis by regulating the IL-6/JAK signaling pathway. | Su, J., et al. 2022. Biochem Biophys Res Commun. 600: 130-135. PMID: 35219101
- Multi-omics analysis of biomarkers and molecular mechanism of rheumatoid arthritis with bone destruction. | Huang, Q., et al. 2022. Joint Bone Spine. 89: 105438. PMID: 35820599
- Synthesis of a fluorescent analogue of phosphatidylcholine. | Schmidt, N. and Gercken, G. 1985. Chem Phys Lipids. 38: 309-14. PMID: 4085088
- Interaction of enantiomeric alkylacyl and diacylglycero-phosphocholines with cholesterol in bilayer membranes. | Hermetter, A. and Paltauf, F. 1982. Chem Phys Lipids. 31: 283-9. PMID: 7172344
- Critical analysis of phospholipid hydrolyzing activities in ripening tomato fruits. Study by spectrofluorimetry and high-performance liquid chromatography. | Rouet-Mayer, MA., et al. 1995. Lipids. 30: 739-46. PMID: 7475990
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Oleoyl-sn-glycero-3-phosphocholine, 5 mg | sc-213397 | 5 mg | $64.00 | |||
1-Oleoyl-sn-glycero-3-phosphocholine, 25 mg | sc-213397A | 25 mg | $257.00 | |||
1-Oleoyl-sn-glycero-3-phosphocholine, 100 mg | sc-213397B | 100 mg | $408.00 | |||
1-Oleoyl-sn-glycero-3-phosphocholine, 500 mg | sc-213397C | 500 mg | $663.00 | |||
1-Oleoyl-sn-glycero-3-phosphocholine, 1 g | sc-213397D | 1 g | $918.00 | |||
1-Oleoyl-sn-glycero-3-phosphocholine, 5 g | sc-213397E | 5 g | $2448.00 |