In silico development of anesthetics based on barbiturate and thiobarbiturate inhibition of GABAA.
Comput Biol Chem
; 88: 107318, 2020 Oct.
Article
in En
| MEDLINE
| ID: mdl-32622179
ABSTRACT
The inhibition of GABAA can be used in general anesthesia. Although, barbiturates and thiobarbiturates are used in anesthesia, the mechanism of their action hasn't been established. QSAR modeling is a wieldy used technique in these cases and this study presents the QSAR modeling for a group of barbiturates and thiobarbiturates with determined anesthetic activity. Developed QSAR models were based on conformation independent and 2D descriptors as well as field contribution. As descriptors used for developing conformation independent QSAR models, (SMILES) notation and local invariants of the molecular graph were used. Monte Carlo optimization method was applied for building QSAR models for two defined activities. Methodology for developing QSAR models capable of dealing with the small dataset that integrates dataset curation, "exhaustive" double cross-validation and a set of optimal model selection techniques including consensus predictions was used. Two-dimensional descriptors with definite physicochemical meaning were used and modeling was done with the application of both partial least squares and multiple linear regression models with three latent variables related to simple and interpretable 2D descriptors. Different statistical methods, including novel method - the index of ideality of correlation, were used to test the quality of the developed models, especially robustness and predictability and all obtained results were good. In this study, obtained results indicate that there is a very good correlation between all developed models. Molecular fragments that account for the increase/decrease of a studied activity were defined and further used for the computer-aided design of new compounds as potential anesthetics.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thiobarbiturates
/
Barbiturates
/
Receptors, GABA-A
/
Quantitative Structure-Activity Relationship
/
GABA-A Receptor Antagonists
/
Anesthetics
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Comput Biol Chem
Journal subject:
BIOLOGIA
/
INFORMATICA MEDICA
/
QUIMICA
Year:
2020
Type:
Article