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. 2014 May 6;11(94):20131062. doi: 10.1098/rsif.2013.1062

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© 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.

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Figure 2. — The structures of 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC), 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC), 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1,2-palmitoyl-sn-glycerol-3-phosphocholine (DPPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1,2-tridecanoyl-sn-glycero-3-phosphatidylcholine (C₁₃ PC) and 1-stearoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (SOPC). Carbon chain lengths and melting transition temperatures given in parentheses. (Online version in colour.)