## Abstract The disposition of diphenhydramine (I) and four of its ring substituted analogues, 4‐bromodiphenhydramine (II), 4‐methyldiphenhydramine (III), 2‐methyldiphen‐hydramine (IV), and 4‐__t__‐butyldiphenhydramine (V), was investigated in the rabbit, during and after intravenous infusion. The
The concept of molecular structure in structure–activity relationship studies and drug design
✍ Scribed by Bernard Testa; Lemont B. Kier
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 859 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0198-6325
No coin nor oath required. For personal study only.
✦ Synopsis
We can justify the use of any model, method, or algorithm if we clearly state our goals, understand the basis of our procedures, and fully appreciate the true nature and limitations of the results. As we have illustrated here, the creation of new wisdom may appear to be a consequence of our labors. There are cases, however, where this creation may be only an illusion. In any analysis of structure-activity, property-activity, or structure-property relationships, the degree of understanding of the nature of the starting data therefore determines the level of confidence ascribable to any result and prediction. This is, in essence, the message of our inquisitive meditations on the deep nature of structure-activity relationships.
📜 SIMILAR VOLUMES
## Abstract Organophosphate pesticides (OPPs; e.g. chlorpyrifos, diazinon, paraoxon) are a wide and heterogeneous group of organophosphorus compounds. Their biological activity of inhibiting acetylcholinesterase (AChE) or butyrylcholinesterase (BChE) ranks them as life endangering agents. The neces