Id |
Subject |
Object |
Predicate |
Lexical cue |
T165 |
0-4 |
Sentence |
denotes |
3.2. |
T166 |
6-19 |
Sentence |
denotes |
Lipophilicity |
T167 |
20-156 |
Sentence |
denotes |
Lipophilicity or fat friendliness of a molecule defines the dissolving capability in fat, oil or any non-polar solvent (Lindsley, 2010). |
T168 |
157-280 |
Sentence |
denotes |
The water n-octanol partition coefficient (log Po/w) is used as the measure of lipophilicity (Constantinescu et al., 2019). |
T169 |
281-409 |
Sentence |
denotes |
Various computational methods are developed for the estimation of log Po/w for diverse performance upon different chemical sets. |
T170 |
410-745 |
Sentence |
denotes |
The SwissADME provides five different predictive models such as XLOGP3 (Cheng et al., 2007), WLOGP (Wildman & Crippen, 1999), MLOGP (Moriguchi et al., 1992), SILICOS-IT (http://silicos-it.be.s3-website-eu-west-1.amazonaws.com/software/filter-it/1.0.2/filter-it.html, 2016) and iLOGP (Daina et al., 2014) for better prediction accuracy. |
T171 |
746-873 |
Sentence |
denotes |
Predicted lipophilicity (Log P) values of the spice molecules obtained from different calculation models are shown in Figure 1. |
T172 |
874-1107 |
Sentence |
denotes |
All the molecules subjected to lipophilicity test lie in the range of +1.2 to +4.19 of consensus value that obeys the Lipinski’s limit of log p < 5, which suggests they can be used for further clinical trials (Arnott & Planey, 2012). |
T173 |
1108-1218 |
Sentence |
denotes |
The lowest lipophilicity is observed for Vanillin and the highest for Nerolidol, among the screened molecules. |
T174 |
1219-1310 |
Sentence |
denotes |
From Figure 1, it is found that all the ligand molecules have positive lipophilicity value. |
T175 |
1311-1386 |
Sentence |
denotes |
Hence, these molecules satisfy the essential criteria to be drug molecules. |