Abstract
A newly formulated information-theoretic topological index, structural information content (SIC), was applied to quantitative structure-activity relationship (QSAR) studies with N-alkylnorketobemidones and triazinones. Results show that SIC encodes sufficient molecular structural information to correlate significantly with the physical as well as biological properties of both the groups of congeners.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 322-325 |
| Number of pages | 4 |
| Journal | Arzneimittel-Forschung/Drug Research |
| Volume | 32 |
| Issue number | 4 |
| State | Published - 1982 |