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. 2020 Apr 30;63(18):10170–10187. doi: 10.1021/acs.jmedchem.0c00415

Table 2. Chirality Profile of EMs.

  all organic EMs (n = 345)
  all, n (%) de novo, n (n = 143) nature-inspired, n (n = 132) natural, n (n = 70)
achiral compounds 126 (37a) 84 29 13
chiral compounds 219 (63a) 59 103 57
1 stereocenter 50 (23b) 28 15 7
>1 stereocenter 169 (77b) 31 88 50
mixture of stereoisomers 18 (8b) 11 5 2
single stereoisomer 201 (92b) 48 98 55
a

% of compounds on a total of 345 active principles included in the EML.

b

% of compounds on a total of 219 chiral compounds.