Product Information
- (2R)-3-(dodecanoyloxy)-2-hydroxypropyl 2-(trimethylammonio)ethyl phosphate
- 1-Dodecanoyl-sn-glycero-3-phosphocholine
- 1-Dodecanoyl-sn-glycerol-3-phosphorylcholine
- 1-Dodecanoyllysolecithin
- 1-Lauroyl-2-hydroxy-sn-glycero-3-phosphocholine
- 1-Lauroyl-<span class="text-smallcaps">L</span>-α-phosphorylcholine
- 3,5,9-Trioxa-4-phosphaheneicosan-1-aminium, 4,7-dihydroxy-N,N,N-trimethyl-10-oxo-, inner salt, 4-oxide, (7R)-
- 3,5,9-Trioxa-4-phosphaheneicosan-1-aminium, 4,7-dihydroxy-N,N,N-trimethyl-10-oxo-, inner salt, 4-oxide, (R)-
- C12-Lysophosphatidylcholine
- Choline, hydroxide, dihydrogen phosphate, inner salt, 3-ester with 1-monolaurin, <span class="text-smallcaps">L</span>-
- See more synonyms
- L-alpha-Lysophosphatidylcholine, lauroyl
- Laurin, 1-mono-, 3-(dihydrogen phosphate), monoester with choline hydroxide, inner salt, <span class="text-smallcaps">L</span>-
- LysoPC 12
- alpha-L-Lysophosphatidylcholine dodecyl
1-Lauroyl-2-Hydroxy-sn-Glycero-3-Phosphatidylcholine is a synthetic compound that has been shown to inhibit the growth of viruses, such as HIV and herpes simplex virus. It also inhibits the replication of hepatitis C virus in cell culture. This compound has been used to study the biochemical properties of phospholipids, including their function in gene expression and lipid metabolism, as well as their role in viral replication. 1-Lauroyl-2-Hydroxy-sn-Glycero-3-Phosphatidylcholine is not active against bacteria and fungi. This compound interacts with cellular membranes by binding with hydroxyl groups on glycerol molecules, which are part of the phospholipid bilayer structure, forming hydrogen bonds with other hydroxyl groups on adjacent molecules. The molecule can then be cleaved by an enzyme or oxidized by an organic acid to form a fatty
Chemical properties
Technical inquiry about: 3D-VAA55918 1-Lauroyl-2-Hydroxy-sn-Glycero-3-Phosphatidylcholine
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