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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Basak, Subhash C | - |
| dc.contributor.author | Mills, Denise | - |
| dc.contributor.author | Mumtaz, Moiz M | - |
| dc.contributor.author | Balasubramanian, Krishnan | - |
| dc.date.accessioned | 2013-08-20T09:45:59Z | - |
| dc.date.available | 2013-08-20T09:45:59Z | - |
| dc.date.issued | 2003-06 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/20670 | - |
| dc.description | 1385-1391 | en_US |
| dc.description.abstract | Topostructural (TS) and topochemical (TC) indices, geometrical descriptors, and ab initio (STO-3G) quantum chemical indices have been employed either alone or hierarchically in the development of quantitative structure-activity relationship (QSAR) models of the aryl hydrocarbon (Ah) receptor binding potency of a set of 34 dibenzofurans. Results show that, for the full set, the TS and TC indices explain most of the variance in the data. The addition of 3-D and quantum chemical indices makes only slight improvement in the predictive capability of QSAR models. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.42A(06) [June 2003] | en_US |
| dc.title | Use of topological indices in predicting aryl hydrocarbon receptor binding potency of dibenzofurans: A hierarchical QSAR approach | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.42A(06) [June 2003] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 42A(6) 1385-1391.pdf | 1.62 MB | Adobe PDF | View/Open |
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