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A new system for the designation of chemical compounds. 2. Coding of cyclic compounds
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Do chemical graphs have a natural order? some regularities of a “compacted maximal adjacency code”
inferred← citeshttps://doi.org/10.1016/0166-1280(92)85063-qopenalex-snapshot
Coding system for quasi-polycyclic structures
inferred← citeshttps://doi.org/10.1016/0166-218x(88)90004-2openalex-snapshot
Determining structural similarity of chemicals using graph-theoretic indices
inferred← citeshttps://doi.org/10.1016/0166-218x(95)00022-jopenalex-snapshot
Chemistry and discrete mathematics
inferred← citeshttps://doi.org/10.1016/0898-5529(90)90105-hopenalex-snapshot
A language for acyclic groups
inferred← citeshttps://doi.org/10.1021/ci00025a001openalex-snapshot
Chemical Graphs: Looking Back and Glimpsing Ahead
inferred← citeshttps://doi.org/10.1021/ci050352vopenalex-snapshot
Assessing the Scaffold Diversity of Screening Libraries
inferred← citeshttps://doi.org/10.1021/ci990422wopenalex-snapshot
SMILES Extensions for Pattern Matching and Molecular Transformations: Applications in Chemoinformatics
inferred← citeshttps://doi.org/10.1109/csb.2003.1227324openalex-snapshot
Experimental studies of the universal chemical key (UCK) algorithm on the NCI database of chemical compounds
inferred← citeshttps://doi.org/10.1142/s021972000400051xopenalex-snapshot
AN EMPIRICAL STUDY OF THE UNIVERSAL CHEMICAL KEY ALGORITHM FOR ASSIGNING UNIQUE KEYS TO CHEMICAL COMPOUNDS
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