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- W2006641337 abstract "Abstract Unlike the parent diacid, the dimethyl ester of (αR,α'R)-dimethylmeso-bilirubin-XIIIα exhibits only a weak bisignate circular dichroism (CD) spectrum in a wide variety of solvents. This implies a loss of conformation stabilization afforded (in the diacid) by intramolecular hydrogen bonding, and with it the loss of an allosteric effect that forces the parent acid into the P-helicity conformational enantiomer." @default.
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- W2006641337 date "1991-08-01" @default.
- W2006641337 modified "2023-10-17" @default.
- W2006641337 title "On the Conformation of Bilirubin Dimethyl Ester from Circular Dichroism Spectroscopy" @default.
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- W2006641337 doi "https://doi.org/10.1080/00387019108020677" @default.
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