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Molecular Modeling of Quinoline-Based Compounds as Potential Dual Inhibitors of Reverse Transcriptase and Integrase of HIV

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DOI: 10.4236/cmb.2018.83007    221 Downloads   405 Views  

ABSTRACT

As follow-up of our past publication [1], we propose that quinolones (as part of the pyridinone family) are capable to increase the number of interactions with HIV reverse transcriptase (RT) or integrase (IN) by adding a halogen in position C-8 of aromatic portion of the quinolones. This addition could help with the activity of dual inhibitors of RT and IN. In this work, we add a chlorine atom with the rationale to identify in the docking simulations a halogen interaction with the oxygen in the near aminoacids in the binding pockets of RT and IN enzymes. Our docking studies started with RT and 320 structures. Later, we took 73 structures with good results in docking with RT. The structures that we choose contain ester or acids groups in C-3 due the structural similarity with groups in charge to interact with the Mg++ ions in Elvitegravir. In conclusion, we obtained 14 structures that could occupy the allosteric pocket of RT and could inhibit the catalytic activity of IN, for this reason could be dual inhibitors. A major perspective of this work is the synthesis and testing of the potential dual inhibitors designed.

1. Introduction

In our research group we were working with pyridinone derivates as antiretroviral against HIV-1 [1] [2] . This kind of compounds belongs to a family of non-nucleoside reverse transcriptase inhibitors (NNRTI) [3] . In our last publication we could observe that quinolones have big possibilities to be inhibitors of RT and IN [1] . The structures of pyridinone derivates have the possibility to interact with conserved aminoacids in RT to inhibit the activity of the enzyme [4] [5] . Also, the substituents in the pyridinone derivates could interact with Mg++ ions located in a small space between DNA and IN in the nucleus of the cell. This is to avoid that the enzyme IN blocks the action of DNA as proposed by Wang et al. [6] . The quinolone ring has an aromatic portion facilitating the making of analogues or adding substituents that could contribute to the activity of the compounds. Based on this rationale, here we designed compounds that have in common a chlorine substituent in C-8 of the quinolones and have the basic structure of the pharmacophore published by Freeman et al. [7] . The new structures were designed according with the matrix in Figure 1. Some structures have ester and acid substituent that could give to the compounds the possibility to be dual inhibitors [6] [8] . Some structures contain a hydroxyl substituent in N-1 in a similar way as is published by Wang et al. [5] . As we can see, the structures show one to three halogens in total but two of the halogens in some of the structures remain in positions C-6 and C-8 of the aromatic ring. It’s possible that the chlorine in C-8 position could contribute in the activity of the molecule of quinolone as RT or IN inhibitor due a halogen bond with other aminoacids [9] .

Actually, multi-halogenated compounds belong to the HAART therapy against HIV infection because they are bioactive. As an example of halogenated drugs

Figure 1. Chemical structures of the quinolone derivatives considered in this work.

against HIV Figure 2 shows six drugs. These drugs have been authorized by the Food and Drug Administration (FDA) of the USA. Doravirine is in Phase III of its development. Figure 2 shows halogenated and multihalogenated compounds against RT and IN. The RT inhibitors halogenated are Efavirenz, Doravirine and Etravirine; and the IN inhibitors are Raltegravir, Elvitegravir and Dolutegravir [10] [11] .

The objective of this work is to propose new compounds with dual activity against RT and IN which contains halogens that contribute to the activity against HIV-1 and that could reduce the quantity of drugs to be taken orally. The infected persons have to take several pills in a treatment called HAART that have secondary effects. If the quantity of drugs is reduced, the secondary effects will be reduced and will be a benefit to the treated patients [12] .

2. Methods

Based on the scheme of structures analyzed in our previous publication [1] we propose 320 chemical structures that are synthetically accessible. The goal is to maintain the main structural characteristics of the hybrid pyridinone-UC781 molecule [4] but using the quinolone scaffold according to the matrix of substituent in Figure 2. In general, the design was constituted by a polar group at C-3 and an unsaturated aliphatic chain in C-4 of the scaffold of quinolone. The scaffold of quinolone in all the schemes has a chlorine in C-8 with the goal of increasing the interactions with the binding sites of RT and IN and, overall, improving its activity as potential dual inhibitors. The design of some quinolones

Figure 2. Drugs halogenated and multihalogenated inhibitors of RT and IN of HIV.

was inspired in the compounds developed by Wang et al. [6] because contain an N-OH substitution.

For the docking studies described below, the crystallographic structures of the biomolecular targets were retrieved from the Protein Data Bank (PDB) (http://www.rcsb.org) [13] . Table 1 summarizes the information of the two structures of RT [14] and one for IN [15] used in this work. The Table 1 includes the information of the co-crystallized ligand in each structure. All computational studies were conducted with Molecular Operating Environment (MOE) software, version 2014 [16] to make the results comparable with the previous published study [1] .

2.1. Structure Preparation

This study is a continuation of our previous results published [1] . The same structures were used. The full details of the preparation of the structures are published in Cabrera et al. [1] .

2.2. Validation of Docking Protocol

Similar to the previous work [1] before docking of the halogenated structures of the Figure 1, the docking protocol was validated by re-docking of the co-crystal ligands in their corresponding crystallographic structure. As reference, Table 1 shows the ligands and their respective enzymes used in validation. For this validation were considered semi-flexible the three co-crystal ligands (R165481, R157208 and GS9137) and was done with the MMFF94x force field with the

Table 1. Summary of the crystallographic structures of RT and IN used in this work.

default settings of MOE [16] (e.g., 500 iterations in total with 30 consecutive attempts to select the best result). The binding pocket was defined as the set of amino acids within of 4.5 Å of the co-crystal ligand.

2.3. 3D flexible Alignment of Pyridinone Structures

The flexible alignment of the new quinolones structures was performed to explore if these new structures could adopt similar conformation as the co-crystalized pyridinone analogues. Similar to our previous work, we selected a sample of 10% (32 structures) and each was aligned flexibly to the co-crystal coordinates of R157208 and R165481. For this study, the structure of the co-crystal compound was kept rigid. The docking was conducted with MOE maintaining the default settings (500 iterations in total with 30 consecutive attempts to find the best result) with the MMFF94x force field.

2.4. Docking

2.4.1. Docking with RT

For this study, 320 quinolone structures were docked with the crystallographic structures PDB ID: 2BAN and 2B5J [13] and the same settings of the validation were maintained. As result of the docking with the two crystallographic structures, 73 structures were selected to further analysis with IN. In the process of analysis, the protein ligand interaction fingerprints (PLIFs) were important to select the 73 structures. PLIFs were generated with MOE ligand.

2.4.2. Docking with IN

For73 structures were selected based on the similarity with the functional groups and binding poses with known dual inhibitors of RT and IN. The 73 structures were docked with the crystallographic structure PDB ID: 3L2U with the same parameters used in the docking of the crystal ligand (Elvitegravir, GS9137) [15] .

2.5. Calculation of Drug-Like Properties

In order to explore the potential oral bioavailability of the structures proposed, we calculated the pharmaceutical properties molecular weight (MW), the partition coefficient octanol/water (Log P) as a measure of lipophilicity, topological polar surface area (TPSA), number of hydrogen bond donors (HBD), number of hydrogen bond acceptors (HBA), and number of rotatable bonds (RB) [17] [18] .

3. Results and Discussion

3.1. Alignment of Crystallographic Structures of RT

The coordinates obtained in our previous work [1] of the structures aligned and superposed were used to run the docking using 320 structures of pyridinone derivates. The structures selected for this study were PDB ID: 2BAN and 2B5J [13] .

3.2. Validation of the Docking Protocol with RT

Before docking the newly structures proposed in this work (Figure 1), the docking protocol was validated as described in the Methods section. The root-mean square deviation (RMSD) values between the co-crustal and predicted positions were low: the RMSD values were 0.8222 and 0.7393 for 2BAN and 2B5J, respectively. The relative docking scores obtained were −9.1224 and −8.6151 for 2BAN and 2B5J, respectively. These results indicate that the settings used in the docking are correct to reproduce the binding modes shown in the crystal structure.

3.3. Alignment with Co-Crystalized Pyridinone Derivatives

A sample of 10% of the data (32 structures) was taken of the 320 structures in a scheme of stratified random sampling. The structures were aligned flexibly with the position of crystallographic structures of R157208 and R165481 (Table 1). In the analysis of the results, the best values were obtained for the structures aligned with R165481. The results were not so different to those obtained in the previous work [1] . In this study, the values of alignment of the new structures with R157208 were less negative than the values of the alignment of the same structures but with R165481. The 32 structures with R157208 had an average of alignment energy of −80.05 Kcal/mol with a standard deviation of ±9.58 Kcal/mol. The average of alignment energy for R165481 was −83.40 Kcal/mol and standard deviation of ±11.14 Kcal/mol (Table of 3D alignment results in supplementary material as Table S1). As an example of the alignment, Figure 3 shows the 3D alignment of structures 180 and 270 with R157208 and R165481, respectively. The results of the alignments of structures 180 and 270 are close to the average values and are possible to observe the good overlap with reference structures.

Figure 3. Alignment of the structures 180 and 270 with R157208 and R165481.

3.4. Binding Modes with RT, PDB ID: 2BAN

After the docking assay performed with MOE for 320 new molecules using PDB ID: 2BAN, we select 72 structures maintaining interaction with important aminoacids for this investigation. The contacts of interest observed were between the substituent in C-4 of each molecule with Tyr188 and the conserved aminoacids Trp229; and the interaction of substituent in C-3 with conserved aminoacid Pro236 due to a 180˚ rotation of the molecule but always maintaining the characteristic interaction of pyridinones and other non-nucleoside RT inhibitors [19] [20] [21] between hydrogen in N-1 and the oxygen of Lys101 (Figure 4). Pro236 was the aminoacid with most contacts with the ligand. Another common interaction observed with the docked molecules was with the chlorine atom in C-8 and the oxygen of the carbonyl group in Pro236. The distances shown for the structures that have halogen bond are between 2.9 and 3.5 Å.

Also, is important to indicate that as result of docking we could identify some structures with double interaction with aminoacids of interest because at the same time show the possibility to have contacts with Pro236 and Tyr188 (structures 152 and 181); and contacts with Pro236 and Trp229 observed in the structures 123 and 158 (Figure 5). The structures mentioned have good results of score as we can see in the Table 2.

In general, Table 2 highlights seven structures with the best results and 10 structures with less favorable results. This distinction is based on the relation of average and standard deviation in the docking assay with PDB ID: 2BAN.

Structures with multiple interactions with aminoacids of interest have better possibilities as inhibitors according with the docking with 2BAN.

3.5. Binding Modes with RT, PDB ID: 2B5J

The results of docking of 320 structures with PDB ID: 2B5J helped us to identify

Figure 4. Docking model of molecule 146 with the structure of RT PDB ID: 2BAN. The model shows interaction characteristic between NOH and the oxygen of the carbonyl group of Lys101; and interaction between substituent in C-3 and Pro236.

Figure 5. Docking model of structures 152 and 123 showing double interaction with aminoacids in the structure of RT PDB ID: 2BAN. There are contacts with Pro236 and Tyr188 for Structure 152; and contacts Pro236 and Trp229 for structure 123.

64 structures with contact with aminoacids of interest as Trp229, Pro236, Tyr181 and Tyr188. The average of score as result of the docking was −7.0418 with a standard deviation of 0.897 in this study. Taking in count the average and the standard deviation, there are 10 outstanding molecules and seven molecules with lower priority (Table 3). In general, the most common contact of the ligands is with Trp229.

Docking with the structure PDB ID: 2B5J revealed that compounds 7 and 33 have the possibility to interact with two aminoacids simultaneously with the substituent in C-4 that can confer to the ligands maintain activity against RT. Figure 6 shows that the substituent in C-4 of compound 7 interacts with Trp229 and Tyr188 at same time while a related substituent at the equivalent position of compound 33 interacts with Tyr181 and Tyr 188.

Another interesting interaction that we observed in docking with quinolones 266 and 270 was a halogen interaction between Iodine and Pro236 as is shown in Figure 7 for quinolone 270. The conformation adopted by the ligand enables to contact with Lys101 that is the characteristic interaction of pyridinone.

In the docking performed with PDB ID: 2B5J we could observe less halogen interactions than the docking with PDB ID: 2BAN. The contacts with chlorine in position C-8 are with Lys103. This kind of contact helps to fix the quinolone to

Table 2. Docking results with RT PDB ID: 2BAN. Aminoacid Pro236 without indication of halogen interaction means that the interaction is between substituent in C-3 with Pro236.

Table 3. Docking results with RT PDB ID: 2B5J.

Figure 6. Binding modes of structures 7 and 123 with double interaction with aminoacids in RT PDB ID: 2B5J. There are contacts with Trp229 and Tyr188 for Structure 7; and contacts Tyr181 and Tyr188 for structure 33.

Figure 7. Docking model of structure 270 in the allosteric pocket of RT PDB ID: 2B5J showing an interaction of iodine in C-3 with Pro236.

the allosteric site and the flexibility of the substituent in C-4 let the ligand to make contact with Tyr181 or Trp229 (Figure 8). As example of this, we show docking of 58.

Another interesting result was observed with the docking of 143 (Figure 9),

Figure 8. Binding mode of structure 58 in the allosteric pocket of RT PDB ID: 2B5J where is possible to observe interactions between hydrogen of NOH and Lys101; chlorine in C-8 with Lys103 and substituent in C-4 with Trp229.

Figure 9. Docking model of structure 143 in the allosteric site of RT PDB ID: 2B5J showing interaction with aminoacids Lys101, Leu100, Pro236 and Tyr188.

which at same time show interaction with Tyr188 and pro236 with C-4 and C-3 substituents respectively. So, if the interaction with Tyr188 is lost because a mutation the compound could maintain activity against RT because Pro236, which is an aminoacid, conserved.

We found 21 structures that coincide in Table 2 and Table 3; this could mean that they have a better probability to be RT inhibitors. Some structures have contact with conserved aminoacids, as Trp229 and Pro236 mentioned by Li et al. [5] which is favorable because this evidence give more probability to think that this contacts could help in the activity of the compounds. In the Table 4 are

Table 4. Structures that are matching in Table 2 and Table 3.

shown the 21 structures and the aminoacid of contact depending of PDB structure of RT.

3.6. Validation of the Docking Protocol with IN

In order to validate the docking with IN, we re-docked the co-crystal ligand in PDB ID: 3L2U (Figure 10), Elvitegravir. The binding mode was reproducible by MOE with a RMSD value of 1.3 Å (similar to our previous work [1] ).

3.7. Docking with IN

We docked 73 selected quinolone structures that showed key interactions in the docking models with PDB ID: 2BAN and 2B5J, respectively. The docking with IN was done with the structure of IN PDB ID: 3L2U (Structures of quinolones in supplementary material as Figure S1). The quinolones have ester or carboxylic acid groups at C-3 and carbonyl group in C-2. Similar to the quinolones, Elvitegravir has a carboxylic acid at C-3 and a carbonyl group at C-4. In Table 5 is

Figure 10. Re-docking of co-crystal (Elvitegravir) with the crystallographic structure of IN, PDB ID: 3L2U. The predicted binding pose is in green and the observed position in the crystallographic structure is in yellow. The RMSD value was 1.3 Å.

Table 5. Docking results with RT PDB ID: 3L2U.

summarized the results of 14 structures with potential to be dual inhibitors of RT and IN.

In Table 5 we can see how quinolone 138 have the best result of score docking (−6.686) with PDB ID: 3L2U and have similar interaction to Elvitegravir with the two Mg++ ions (Figure 11). In the Figure 11, we can see in yellow color the quinolone overlapped on Elvitegravir (green color). The distances and the space IN-DNA between the Mg++ ions and the oxygens of quinolone has an average of 2.5 Å according with MOE. The distances between Mg++ ions and Elvitegravir in MOE are near to 2 Å.

The less favorable result in docking with 3L2U is for quinolone 82 because have a score of −4.031. The distances between oxygens in quinolone and the Mg++ ions have an average of 2.6 Å. The Figure 12 show the interactions of quinolone and Mg++ in the space between IN and DNA.

Figure 11. Docking of structure 138 showing interactions with Mg++ ions. In yellow quinolone 138 and in green Elvitegravir structure.

Figure 12. Docking of structure 82 showing interactions with Mg++ ions and distances between oxygen and Mg++ ions.

3.8. Quinolones Potential Dual Inhibitors of RT and IN

As result of the entire analysis of docking with RT and IN we got 14 quinolones that could act like dual inhibitors. In Figure 13 is showing the five best structures that could be dual inhibitors. The first five structures are recommended to be synthetized according with the score results and the contact with Mg++ ions and aminoacids of interest in the space between IN-DNA and the allosteric space in RT, respectively.

3.9. Drug-Like Properties

The structures identified as potential compounds with activity against RT and IN were evaluated in base to the rules of Lipinski and Veber, which comprise six pharmacological properties of interest. The pharmacological properties calculated to 73 structures were MW, Log P, HBD and HBA, RB and TPSA. The results are included in supplementary material (Table S2).

4. Conclusions and Perspective

The results of docking with RT reveal in MOE that chlorine in C-8 of the quinolone could has the capacity to interact with Pro236 or Lys103 forming a halogen bond. The most important halogen interaction is with an oxygen atom of the carbonyl group of Pro236. Pro236 is a conserved aminoacid that could contribute to the inhibition activity of RT even help to preserve the activity with

Figure 13. Chemical structures of the most promising quinoline-based compounds as potential dual inhibitors reverse transcriptase and integrase of HIV.

mutant strains of HIV. After analysis of the docking results of 320 quinolone structures with PDB ID: 2BAN, 2B5J and 3L2U, 14 structures were identified with possible dual activity in inhibition of RT and IN. There was not any halogen interaction between the 14 structures and IN. The most promising compounds to be synthetized are the quinolones 138, 111, 46, 83 and 151 (Figure 13). The structure 151 shown halogen interaction with Pro236 in RT. The binding mode adopted by molecules 111, 46 and 151 is like molecule 138 in Figure 11, while molecule 83 adopted a binding mode like quinolone 82 in Figure 12.

The main perspective of this work is synthetizing the structures proposed in this work and perform their biological evaluation (assays of cytotoxicity and inhibition of the activity of RT and IN) with the purpose of verifying the computational results.

Acknowledgements

A.C.V. is grateful to CONACyT and UNAM for the postdoctoral scholarship #291222. This work was supported by the Instituto de Investigaciones Biomédicas, UNAM through the program Nuevas Alternativas de Tratamiento para Enfermedades Infecciosas (Novel Alternatives for the Treatment of Infection Diseases) (NUATEI-IIB-UNAM), and Programa de Apoyo a la Investigación y el Posgrado (PAIP) grant 5000-9163, Facultad de Química, UNAM.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

Supplementary Material

Table S1. 3D alignment scores (kcal/mol) calculated with MOE of 32 selected compound with the structure of two co-crystallized pyridinones.

Table S2. Drug-like properties of newly designed compounds as potentially inhibitors of RT an IN.

Figure S1. 73 structures docked with RT.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

Cabrera, A. , Hernández, L. , Chávez, D. and Medina-Franco, J. (2018) Molecular Modeling of Quinoline-Based Compounds as Potential Dual Inhibitors of Reverse Transcriptase and Integrase of HIV. Computational Molecular Bioscience, 8, 122-148. doi: 10.4236/cmb.2018.83007.

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