Identification of a 3-aminoimidazo[1,2-a]pyridine inhibitor of HIV-1 reverse transcriptase
© Elleder et al.; licensee BioMed Central Ltd. 2012
Received: 11 July 2012
Accepted: 28 November 2012
Published: 11 December 2012
Despite the effectiveness of highly active antiretroviral therapy (HAART), there remains an urgent need to develop new human immunodeficiency virus type 1 (HIV-1) inhibitors with better pharmacokinetic properties that are well tolerated, and that block common drug resistant virus strains.
Here we screened an in-house small molecule library for novel inhibitors of HIV-1 replication.
An active compound containing a 3-aminoimidazo[1,2-a]pyridine scaffold was identified and quantitatively characterized as a non-nucleoside reverse transcriptase inhibitor (NNRTI).
The potency of this compound coupled with its inexpensive chemical synthesis and tractability for downstream SAR analysis make this inhibitor a suitable lead candidate for further development as an antiviral drug.
Despite more than 25 years of research, drug treatment of HIV infection remains a major therapeutic challenge. The most effective regimen for treating HIV-1 infection is highly active antiretroviral therapy (HAART) that usually consists of a non-nucleoside reverse transcriptase inhibitor (NNRTI) or protease inhibitor together with two nucleoside (or nucleotide) reverse transcriptase inhibitors (NRTIs).
Over 50 NNRTIs have been described to date. Five of these NNRTIs have been approved by the United States FDA for the clinical treatment of HIV infection and AIDS. The first generation NNRTIs used are efavirenz, nevirapine and delavirdine. However, the rapid emergence of virus drug-resistant virus limited the effectiveness of these drugs. The second-generation NNRTIs, etravirine and rilpivirine, are more active against both drug-sensitive and resistant virus strains. However, despite this progress there is a continued need for the development of novel NNRTIs which have better pharmacokinetic properties and inhibit common drug-resistant virus strains.
Here we screened a chemical library to identify novel inhibitors of HIV-1 replication. We report the identification of a lead compound containing a 3-aminoimidazo[1,2-a]pyridine scaffold that acts as an NNRTI, with inherent features that render it attractive for further development as an antiviral drug.
The Salk Institute in-house small molecule collection is a chemically diverse set of synthetic compounds based on divergent design principles. Fundamental to this compound collection is a Diversity-Oriented Synthesis (DOS) approach that is pharmacophore or scaffold-centric, with emphasis on the use of multi-component synthetic reactions (MCRs) and a variety of post-MCR transformations or reaction cascades. The diversity criteria are biased by Lipinski’s ‘Rule of 5’, ADME-Tox filtering, exclusion of reactive substituents and incorporation of masked functional groups within scaffold side chains to enable additional chemical manipulations via forward or reverse chemical genetic screening methodologies. The synthetic economy realized by such a library design permits the inclusion of rare and exotic building blocks, which further enhances the chemical diversity of the library and mitigates the limitations of library size, scope, and scale. An additional attribute of the library design, due in large part to the economics of syntheses, is the ability to rapidly determine structure-to-activity relationships (SAR) early in the evaluation of lead compounds. Each pharmacophore-based library subset can be readily expanded to further explore the relevant target space, enabling both lead optimization and lead evolution (or scaffold hopping) to proceed in parallel.
Four hundred and eighty compounds, constituting a cross-section of the Salk library, were screened in a plate-based assay to identify small molecules that inhibit a single cycle of replication by a VSVg-pseudotyped HIV-1 vector (pNL4-3LucR+E-) encoding firefly luciferase. This vector is competent for only the early steps of retroviral replication leading up to viral DNA integration and gene expression. Human 293T cells were pretreated for 1 hr with 1 μM final concentration of the individual compounds and then challenged with the VSVg pseudotyped HIV-1 vector in the continued presence of that compound. After 24 hrs, the luciferase activity of each sample was determined.
Because the initial screen was performed by scoring firefly luciferase reporter gene expression from a VSVg pseudotyped virus vector, it was possible that the F2 compound inhibited either an early step of HIV-1 replication, VSVg-mediated cellular entry, or firefly luciferase reporter activity. To exclude possible effects on VSVg-specific cellular entry and firefly luciferase activity, F2 was tested for its ability to block infection of CEM-GFP lymphocytic indicator cells by a replication-competent HIV-1 vector with a wild-type CXCR4-tropic HIV-1 envelope glycoprotein. In this assay, infection by the wild-type virus leads to the expression of a GFP reporter gene in a Tat-deficient HIV-1 provirus that is resident in the CEM-GFP cell line. The measured EC50 in these experiments (0.862 ± 0.088 μM; n = 2) (Figure 1C), was similar to the value obtained with the VSVg-pseudotyped virus. The CC50 value obtained with the CEM-GFP cells was 25.4 ± 2.1 μM (n = 2), selectivity index = 29.5. Similarly, F2 inhibited infection of primary human peripheral blood mononuclear cells (PBMCs) by a replication-competent HIV-1 vector (NL4-3 Nef + IRES rluc) with a measured EC50 of 0.865 ± 0.222 μM (Figure 1D) in the absence of cell toxicity, up to 10μM of compound tested (data not shown, selectivity index > 11.6). Taken together, these results suggested that F2 blocks an early step of HIV-1 replication.
Resistance profile against wild type and RT mutant VSV-G pseudotyped HIV-1 vectors
Antiviral EC50 (μM)a, b
0.165 ± 0.039
1.676 ± 0.271
1.275 ± 0.357
3.233 ± 0.127
34.1 ± 2.4
0.019 ± 0.002
2.879 ± 0.006
1.260 ± 0.159
0.841 ± 0.049
0.014 ± 0.003
0.011 ± 0.005
0.006 ± 0.0
0.015 ± 0.001
0.014 ± 0.002
In this report we describe a new lead candidate NNRTI inhibitor that has activity against wild-type and some of the common drug-resistant variants of HIV-1 reverse transcriptase. Serendipitously, this new lead scaffold is structurally isosteric with THR-50, a benzimidazole-based NNRTI (Figure 3B). The imidazo[1,2-a]pyridine pharmacophore of F2 can be realized by three instances of bioistosteric replacement on the benzimidazole scaffold; (1) N1 nitrogen is converted to carbon, (2) bridgehead carbon adjacent to C7 is converted to nitrogen, and (3) benzylic methylene (CH2) is converted to NH. These subtle changes in the inhibitor core slightly enhance the physical properties, create an additional H-bond donor interaction, and greatly simplify the synthesis of analogs for optimization studies.
While the THR-50 compound is the more potent inhibitor against wild-type and drug-resistant variants of HIV-1 reverse transcriptase, the F2 compound has several distinct advantages for downstream drug development. Specifically, F2 features an imidazo[1,2-a]pyridine core scaffold that is generated in a simple, inexpensive, single chemical transformation that belongs to a special class of diversity generating chemistries known as Multi-Component Reactions (MCR), leading to high product yield and purity. By contrast, the benzimidazole core scaffold of the NNRTI THR-50 results from a three-step chemical process (Figure 3B) resulting in an overall yield of 40% and requiring purification operations after each reaction step. Furthermore, the number of possible analogs to F2, based on commercially available building blocks, is on the order of 106 compounds, versus 103 for THR-50. These two molecular structures are further distinguished by the addition of an H-donating group (NH) for additional binding interactions as well as lowering clog P and improving the pharmacological properties. Therefore, the lead F2 compound is an excellent candidate for further development as an antiviral drug through small molecule SAR and structure-guided design.
The Salk Small Molecule Screening Collection was designed and synthesized in-house using known methods. The imidazo[1,2-a]pyridines were prepared in a 96 well microplate (Eppendorf, 2.2 ml deepwell, polypropylene) as a combinatorial matrix where 2-amino pyridine were dispensed to all wells, aromatic aldehydes were dispensed as row reagents, isonitriles were dispensed as column reagents, and lewis acid catalyst scadium (III) triflate was dispensed to all wells. The amine and isonitriles were prepared as 0.5 M stock solutions in 1,2 dichloroethane (DCE), and the aldehydes and lewis acid were prepared as 0.5 M and 0.025 M (respectively) stock solutions in 2,2,2-trifluorothanol (TFE). For a given well: 200 μl of 0.5M 2-amino pyridine in DCE, 200 μl of 0.5 M aromatic aldehyde in TFE and 200 μl of 0.025 M scandium (III) triflate in TFE were added and mixed on a plate shaker for 15 minutes at room temperature. To this solution was added 200 μl of 0.5 M isonitrile in TFE and 200 μl of (1:1 v/v) DCE-TFE solvent. Final reaction volume was 1.0 ml and theoretical concentration was 0.1 M. The plate was sealed (heat seal, foil) and allowed to shake for 5 days at room temperature. After 5 days, the crude reaction mixture was evaporated to dryness and resuspended in 1.0 ml dichloromethane (DCM). This crude reaction mixture was transferred to a filter plate charged with a cocktail of scavenging resins (PS-Trisamine, PS-NCO, PS-TsNHNH2) and silica gel and allowed to gravity filter after 2 hr. Each well was rinsed with 2.0ml DCM, the fractions combined and were concentrated to dryness. Resultant purity-enriched compound was resuspended in 1.0 ml DMSO (100%) for a theoretical stock solution of 100 mM. From the 100 mM master (or mother) plate, 10 mM compound in DMSO daughter plates were generated and distributed for assays. Analytical quality control was performed via high-throughput LCMS on an Agilent 1100 HPLC-LC/MSD Trap XCT MS employing ballistic gradients on Synergi Fusion RP C18 (Phenomenex) columns and acetronitrile-water solvent system. Hits were resynthesized on a 1.0 mmol scale, purified by preparative liquid chromatography and characterized by NMR and LCMS.
DNA constructs and virus production
The VSVg-pseudotyped HIV-1 vector was generated by transient transfection of human 293T cells (American Type Culture Collection No. CRL-11268), with plasmid pNL4-3LucR+E- and pMD.G plasmid that expresses the VSVg glycoprotein. The titer was determined by antibody staining for Gag (p24) expressing cells following infection. The LAI-based replication-competent HIV-1 vector was generated by transient transfection of human 293T cells with plasmid pLai3Luc2. The NL4-3 Nef+ IRES rluc vector encoding renilla luciferase was derived from NL4-3 Nef+ IRES eGFP vector by replacement of the eGFP open reading frame with renilla luciferase (kindly provided by the Chanda laboratory, Sanford-Burnham Medical Institute, La Jolla). The set of vectors harboring the RT mutations and corresponding wild type form (pNLNgoMIV R+E-.luc) were based on the HIV-1 NL4-3 strain; the RT region of these vectors was derived from the BH10 isolate. The vectors were pseudotyped with VSVg by cotransfection with pMD.G plasmid in 293T cells. To generate the cells that express luciferase from established HIV proviral DNA, 293T cells were infected with the VSVG pseudotyped HIV-1 pNL4-3LucR+E- vector and passaged for two weeks to remove any remaining unintegrated viral DNA.
Tissue culture-based infectivity assays
Ten thousand human 293T cells were plated in 80 μl medium in each well of 96-well tissue culture plate. Next day, 10 μl of each diluted compound was added to reach the desired concentration and incubated at 37°C for 1 hour. A 10 μl aliquot of medium containing the VSVG pseudotyped HIV-1 vector (multiplicity of infection of 0.1-0.5) was then added to each well. Twenty-four hours after viral challenge, the medium was carefully removed and 60 μl of the Bright-Glo reagent (Promega, Madison, WI) diluted 1:1 in PBS was added to lyse the cells and provide the luciferin substrate for virus-encoded firefly luciferase. After several minutes the luminescence associated with each sample was measured, and served as readout to quantify virus infectivity in each well. The best fitted curves and EC50 values were calculated using Prism 4 software (GraphPad Software, San Diego). The degree of synergism between screen compounds and AZT (Sigma, St. Louis, MO) were determined by testing the compounds in the infectivity assay individually and in combinations at a fixed molar ratio over a range of serial dilutions. The data were then analyzed by the isobologram technique, which evaluates the compound interactions by a dose-oriented geometric method[13, 14]. Cytotoxicity of the compounds was measured 24 hours after treatment of mock-infected cells by adding an equal volume of CellTiter-Glo (Promega, Madison, WI) and reading luminescence.
In the assays employing the replication-competent pLai3Luc2 HIV-1 vector, CEM-GFP lymphocytic indicator cells were pretreated with F2 for 1 hr in 24-well plates, challenged with the virus by spinoculation at 1,200 × g for 1 hr and the number of GFP positive cells was determined by flow cytometry two days later using FACScan (Becton-Dickinson, Franklin Lakes, NJ).
Human PBMCs from an uninfected individual were obtained from the UCSD Center for AIDS Research. Samples were collected with written informed consent under Salk Institutional Review Board Protocol # 10–004. PBMCs were activated in PBMC Growth Medium (RPMI 1640 with 15% FBS, Pen/Strep, 25 mM HEPES, 100 U/ml IL-2) supplemented with 5 μg/ml PHA-P. Two days after activation, the PBMC’s were maintained in the same medium (without PHA-P) for 3 more days. Aliquots of 2x104 PBMCs were then plated in 80 μl PBMC Growth Medium in each well of white 96 well plates (CoStar) and returned to the incubator overnight. Serial 3-fold dilutions of compound F2, ranging from 100 μM to 1.37 μM in concentration, were made up in 10% DMSO. Eight replicate samples were then set up, with 10 μl aliquots of the serially-diluted compounds added to the cells, and preincubated at 37°C for one hour prior to virus challenge. The cells were then challenged with 10 μl per well of the NL4-3 Nef+ IRES rluc virus vector bringing the total volume in each well to 100 μl final. The plates were incubated at 37°C for five days and then viral infection was monitored by adding 100 μl per well of Renilla-Glo Luciferase Reagent (Promega) and measuring the resultant luciferase activities using a Topcount-HTS (PerkinElmer). Cell toxicity was assessed on a duplicate plate of samples by adding 100 μl Cell-Titer Glo Reagent (Promega) and reading on a Topcount-HTS.
Real-time PCR quantitation of viral DNA
Total cellular DNA was harvested 24 hours post infection with the AccuPrep genomic DNA extraction kit (Bioneer Life Science Corp., Rockville, MD). The amount of viral DNA products was quantified by real-time PCR on ABI Prism 7900 Sequence Detection System (Applied Biosystems, Foster City, CA) with the following primers and probes: early HIV-1 reverse transcripts with primers ert2f, ert2r, probe ERT2, late HIV-1 reverse transcripts with primers MH531, MH532, probe LRT-P. To normalize for the number of cellular DNA equivalents in the samples, a single-copy locus in the PBGD gene was amplified with primers PBGD1 (5’-AAGGGATTCACTCAGGCTCTTTC), PBGD2 (5’-GGCATGTTCAAGCTCCTTGG) and probe PBGD-P (5’-VIC-CCGGCAGATTGGAGAGAAAAGCCTGT-MGBNFQ).
HIV-1 RT in vitro enzyme assay
The assay was adapted from references[14, 19]. HIV-1 RT (0.5 units; Ambion, Austin, TX) was incubated with different concentrations of the F2 compound for 5 minutes at room temperature. A template-primer mixture was then added to a final concentration of 5 μg/ml oligo(dT)20, 10 μg/ml poly(rA), 1.25 μM [α-32P]dTTP and 10 μM dTTP. The sample was incubated at 37°C for 60 minutes. Aliquots of the reaction were spotted on DEAE paper, washed twice with 2xSSC buffer (300 mM NaCl, 30 mM sodium citrate) and once with 95% ethanol, dried and exposed to a PhosporImager screen (Molecular Dynamics, Sunnyvale, CA). The screens were scanned by a FLA-5100 instrument (Fujifilm Life Science, Stamford, CT) and the amount of incorporated labeled phosphate was used to quantify the RT activity. The best fitted curves and IC50 values were calculated using Prism 4 software (GraphPad Software, San Diego).
This work was supported by the Nomis Foundation, the James B. Pendleton Charitable Trust (JATY) and NIH Grant P30 CA014195-38 (JATY and JPN). JPN is an investigator with the Howard Hughes Medical Institute. This research was supported [in part] by the Intramural Research Program of NIH, National Cancer Institute (SH). We thank members of the Noel and Young labs for helpful discussions. We thank Justin Ramsey for assistance in preparing the Salk in-house library and Kevin Olivieri, Lars Pache, and Sumit Chanda (Sanford-Burnham Medical Research Institute) for providing the NL4-3 Nef+ IRES rluc virus construct.We thank Dr. David Smith and the UCSD Center for AIDS Research for providing PBMC samples.
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