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. 2014 Apr 10;9(4):e94780. doi: 10.1371/journal.pone.0094780

Figure 1. Chemical structure and stereo-configuration of the stereoisomers of diadenosine 5′,5″″-P1,P4-dithio-P2,P3-chloromethylenetetraphosphate (compound 1), and of adenosine 5′-(P1-thio-P2,P3-chloromethylenetriphosphate), (compound 2).

Figure 1

RP and SP designate the absolute configuration of chiral P1- and P4-phosphorothioates; r and s, the absolute configuration of the pseudo-asymmetric carbon of the P2,P3-chloromethylene group in compound 1; R and S, the absolute configuration of the chloromethylene group in compound 2. Ade, 5′-adenosyl; N.A., Not Asymmetric.