Relative configuration of tetrahedral stereo centers

In the case of stereogenic centers absolute and relative stereo configurations are both supported. Both the MDL stereo representations ( chiral flag and enhanced stereo representation ) and the Daylight stereo representation are supported. All molecules originating from Daylight SMILES represent absolute stereo configuration, as SMILES does not support relative configuration.

MDL Enhanced Stereo Representation

In MDL's enhanced stereo representation all stereo center atoms are labeled with one of the following:

1. ABS

2. *OR *n **

3. *AND *n **

They define a grouping of the stereogenic centers.

Stereogenic centers belonging to ABS represent absolute stereochemistry, i.e. chirality. (All unlabeled stereo centers are also thought to belong to the ABS group by default.)

Stereogenic centers belonging to an *OR *n ** group (e.g. OR1) represents one stereoisomer that is either the structure as drawn (R, S) OR the epimer in which the stereogenic centers have the opposite configuration (S, R).

Stereogenic centers belonging to an **AND *n * ** group (e.g. AND1) represents a mixture of two enantiomers: the structure as drawn AND the epimer in which the stereogenic centers have the opposite configuration. (e.g. racemic mixture.)

For example:

Molecule	Interpretation
	A pure sample of one stereoisomer:
	A pure sample of one of these enantiomers:or
	A pure sample of one of these enantiomers:or
	A sample that is a mixture of the two enantiomers:and
	A pure sample of one of these diastereomers:or oror