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. 2013 Jul 23;8(7):e70025. doi: 10.1371/journal.pone.0070025

Table 1. BH-forming ability and the physical properties of phospholipids.

Phospholipids Acyl groups T m (°C)a MWb Total net charge No. of anion charge logP c logD c (pH 5.5) Hydrogen bond acceptorsc Hydrogen bonddonorsc Freely rotating bondsc Polar surface area (angstrom2)c Polarizabilityc (×10−24) BH induction (EC20 values, mM)d
dilauroyl-PC 12∶0 0 621.8 0 1 6.62 7.23 9 1 32 118.17 1 6
dimyristoyl-PC 14∶0 23 677.9 0 1 8.05 8.65 9 1 36 121 1 12
dipalmitoyl-PC 16∶0 42 734.0 0 1 10.09 10.69 9 1 40 121 1 ND
distearoyl-PC 18∶0 55 790.1 0 1 12.12 12.73 9 1 44 121 1 ND
dioleoyl-PC 18∶1 −22 788.1 0 1 11.96 12.57 9 1 42 121 1 5
dimyristoyl-PE 14∶0 48 635.8 0 1 11.00 8.51 9 3 36 144.190 68.93 ND
dipalmitoyl-PE 16∶0 63 691.9 0 1 13.70 11.20 9 3 40 144.19 76.276 ND
dipalmitoyl-PS 16∶0 51 735.9 −1 2 13.04 9.55 11 4 41 181.49 78.717 ND
a

Tm: Phase transition temperature was derived from Cevc et al (1993) in Phospholipids Handbook (Cevc, G., ed.), pp. 939–956, Marcel Dekker, New York.

b

given by supplier.

c

Values were retrieved from ChemSpider (www.chemspider.com), predicted by Advanced Chemistry Development (ACD/Laboratories) software.

d

performed by this study.