Functionalized Congeners of 2H-Chromene P2Y6 Receptor Antagonists

The P2Y6 receptor (P2Y6R), a Gq-coupled receptor, is a potential drug discovery target for various inflammatory and degenerative conditions. Antagonists have been shown to attenuate colitis, acute lung injury, etc. In the search for competitive antagonists, we have investigated the SAR of 3-nitro-2-(trifluoromethyl)-2H-chromene derivatives, although high affinity is lacking. We now reveal that long-chain amino-functionalized congeners display greatly enhanced affinity in the antagonism of UDP-induced Ca2+ mobilization in human (h) P2Y6R-transfected 1321N1 astrocytoma cells. A 6-(Boc-amino-n-heptylethynyl) analogue 30 (MRS4940) had an IC50 of 162 nM, which was a 123-fold greater affinity than the corresponding unprotected primary alkylamine, 107-fold greater than the corresponding pivaloyl derivative 30, and 132-fold selective compared to the P2Y14R. However, similar Boc-amino chains attached at the 8-position produced weak µM affinity. Thus, the P2Y6R affinity depended on the chain length, attachment point, and terminal functionality. Off-target activities, at 45 sites, were tested for acylamino derivatives 20, 24, 26, 30, 31, and 37, which showed multiple interactions, particularly at the biogenic amine receptors. The more potent analogues may be suitable for evaluation in inflammation and cancer models, which will be performed in future studies.

We have also explored in detail the structure-activity relationship (SAR) of UDP and CDP derivatives as P2Y 6 R agonists and separated their ability to activate the P2Y 6 R from activity at the G i -coupled P2Y 14 R, which is also UDP-activated [19].However, the discovery of potent and selective P2Y 6 R antagonists has lagged behind other purinergic GPCRs, although numerous studies have suggested their potential utility as a drug discovery target [1,[4][5][6]8,[20][21][22][23][24][25][26][27][28].Only a few classes of P2Y 6 R antagonists have been explored.The first selective antagonists were in a series of di-arylisothiocyanates, among which MRS2578 (Figure 1) is the most widely used.This compound does not bind in or near the orthosteric binding site but rather binds covalently to a Cys residue in the intracellular receptor region [6].This binding induces a mechanism called "redox-induced degradation" by which the receptor is driven to the proteasome for degradation.Another class of P2Y 6 R antagonists was identified through library screening to discover a 2H-chromene derivative 2a as a reversible P2Y 6 R antagonist of µM affinity, and its SAR was initially explored by Ito et al. [29].We have further mapped the SAR, focusing on 6-and 8-position substitutions, e.g., 6,8-difluoro 2b [30,31].These antagonists contain an alkyl nitro group and are racemic, characteristics that are considered less than optimal for drug development.Nevertheless, we have gradually improved this series' affinity, including in this work.Machine learning is an alternative approach that was used to identify ABBV-744 3 as a non-surmountable P2Y 6 R antagonist [32].Recently, a 2-(1H-pyrazol-3-yl)-1H-benzo[d]imidazole derivative 4 was described as a potent P2Y 6 R antagonist that attenuated colitis and acute lung injury [33].
Cells 2024, 13, x FOR PEER REVIEW 2 of 14 discovery of potent and selective P2Y6R antagonists has lagged behind other purinergic GPCRs, although numerous studies have suggested their potential utility as a drug discovery target [1,[4][5][6]8,[20][21][22][23][24][25][26][27][28].Only a few classes of P2Y6R antagonists have been explored.The first selective antagonists were in a series of di-arylisothiocyanates, among which MRS2578 (Figure 1) is the most widely used.This compound does not bind in or near the orthosteric binding site but rather binds covalently to a Cys residue in the intracellular receptor region [6].This binding induces a mechanism called "redox-induced degradation" by which the receptor is driven to the proteasome for degradation.Another class of P2Y6R antagonists was identified through library screening to discover a 2H-chromene derivative 2a as a reversible P2Y6R antagonist of µM affinity, and its SAR was initially explored by Ito et al. [29].We have further mapped the SAR, focusing on 6-and 8-position substitutions, e.g., 6,8-difluoro 2b [30,31].These antagonists contain an alkyl nitro group and are racemic, characteristics that are considered less than optimal for drug development.Nevertheless, we have gradually improved this series' affinity, including in this work.Machine learning is an alternative approach that was used to identify ABBV-744 3 as a non-surmountable P2Y6R antagonist [32].Recently, a 2-(1H-pyrazol-3-yl)-1Hbenzo[d]imidazole derivative 4 was described as a potent P2Y6R antagonist that attenuated colitis and acute lung injury [33].This SAR study of the 2H-chromene class of P2Y6R antagonists applies a functionalized congener design approach [34].Homologous ω-aminoalkyl-functionalized congeners, and their acylated derivatives, of adenosine receptor (AR) ligands were first reported by Jacobson et al. in 1985 as a model for other GPCRs [35].Strategically chain-extended orthosteric AR agonists and antagonists had enhanced affinity when a terminal amine was present [35].A later X-ray structure of the A 2A AR complex with a xanthine amine congener (XAC) featured its aminoalkyl chain facing outward from the orthosteric binding site and interacting with polar residues [36], as envisioned in an earlier design [35].A series of aminoalkyl congeners of the M1 muscarinic acetylcholine receptor antagonist telenzepine showed an affinity optimum with a 10-methylene length [37].We now empirically apply a similar strategy for the P2Y6R, for which there is no experimental structure, as a means of indirectly probing the binding site environment.We considered that the functionalized This SAR study of the 2H-chromene class of P2Y 6 R antagonists applies a functionalized congener design approach [34].Homologous ω-aminoalkyl-functionalized congeners, and their acylated derivatives, of adenosine receptor (AR) ligands were first reported by Jacobson et al. in 1985 as a model for other GPCRs [35].Strategically chain-extended orthosteric AR agonists and antagonists had enhanced affinity when a terminal amine was present [35].A later X-ray structure of the A 2A AR complex with a xanthine amine congener (XAC) featured its aminoalkyl chain facing outward from the orthosteric binding site and interacting with polar residues [36], as envisioned in an earlier design [35].A series of aminoalkyl congeners of the M 1 muscarinic acetylcholine receptor antagonist telenzepine showed an affinity optimum with a 10-methylene length [37].We now empirically apply a similar strategy for the P2Y 6 R, for which there is no experimental structure, as a means of indirectly probing the binding site environment.We considered that the functionalized chains appended might extend into the phospholipid bilayer, as was shown for the A 3 AR [38].
The list of 2H-chromene analogues compared here for human (h) P2Y 6 R functional inhibition is shown in Table 1, including reference compounds 2 and 4-18.The primary pharmacological assay consisted of the calcium mobilization measurement in hP2Y 6 R-expressing Cells 2024, 13, 1366 3 of 14 1321N1 astrocytoma cells using a fixed UDP (agonist) concentration of 100 nM [30,31].The newly prepared derivatives  were synthesized as shown in Figure 2, with the full synthetic procedures and spectral characterization in the Supplementary Materials.The derivatization concentrated on the 6 and 8 positions of original hit compound 2a using 6-I and 8-I intermediates (10 and 11, respectively) subjected to Sonogashira reactions to install various extended alkyne chains, including those bearing a Boc-amino terminal group.The Boc protection was removed using TFA to yield the corresponding alkyl amines.Table 1.The inhibition of UDP (100 nM)-induced Ca 2+ mobilization in hP2Y 6 R stably transfected 1321N1 human astrocytoma cells.a The structure of compound 4 appears in Figure 1.
Cells 2024, 13, x FOR PEER REVIEW 3 of 14 chains appended might extend into the phospholipid bilayer, as was shown for the A3AR [38].
The list of 2H-chromene analogues compared here for human (h) P2Y6R functional inhibition is shown in Table 1, including reference compounds 2 and 4-18.The primary pharmacological assay consisted of the calcium mobilization measurement in hP2Y6R-expressing 1321N1 astrocytoma cells using a fixed UDP (agonist) concentration of 100 nM [30,31].The newly prepared derivatives  were synthesized as shown in Figure 2, with the full synthetic procedures and spectral characterization in the Supplementary Materials.The derivatization concentrated on the 6 and 8 positions of original hit compound 2a using 6-I and 8-I intermediates (10 and 11, respectively) subjected to Sonogashira reactions to install various extended alkyne chains, including those bearing a Boc-amino terminal group.The Boc protection was removed using TFA to yield the corresponding alkyl amines.
Table 1.The inhibition of UDP (100 nM)-induced Ca 2+ mobilization in hP2Y6R stably transfected 1321N1 human astrocytoma cells.a The structure of compound 4 appears in Figure 1.

2, 5-41
Compound R with the full synthetic procedures and spectral characterization in the Supplementary Materials.The derivatization concentrated on the 6 and 8 positions of original hit compound 2a using 6-I and 8-I intermediates (10 and 11, respectively) subjected to Sonogashira reactions to install various extended alkyne chains, including those bearing a Boc-amino terminal group.The Boc protection was removed using TFA to yield the corresponding alkyl amines.
Table 1.The inhibition of UDP (100 nM)-induced Ca 2+ mobilization in hP2Y6R stably transfected 1321N1 human astrocytoma cells.a The structure of compound 4 appears in Figure 1.

2, 5-41
Compound R   with the full synthetic procedures and spectral characterization in the Supplementary Materials.The derivatization concentrated on the 6 and 8 positions of original hit compound 2a using 6-I and 8-I intermediates (10 and 11, respectively) subjected to Sonogashira reactions to install various extended alkyne chains, including those bearing a Boc-amino terminal group.The Boc protection was removed using TFA to yield the corresponding alkyl amines.
Table 1.The inhibition of UDP (100 nM)-induced Ca 2+ mobilization in hP2Y6R stably transfected 1321N1 human astrocytoma cells.a The structure of compound 4 appears in Figure 1.

Materials and Methods
The representation synthetic methods for compounds 24, 30, and 36 are presented here (Figure 2), and the methods for the other compounds are found in the Supplementary Materials (Figure S1).

Materials
Unless noted, the reagents and solvents were purchased from Sigma-Aldrich (St. Louis, MO, USA).The anhydrous solvents were obtained directly from commercial sources.The Boc-amino-alkynes and other alkynes were obtained from Ambeed (Arlington Heights, IL, USA), except for N-Boc-non-8-yn-1-amine, N-Boc-9-decyn-1-amine, and 10-Br-1-decyne, which were purchased from Acrotein (Hoover, AL, USA).All the reactions were performed using anhydrous solvents and under dry nitrogen.Room temperature or rt refers to 25 ± 2 • C. The 1 H-NMR spectra were obtained with a Bruker 400 MHz spectrometer in CDCl 3 (7.26ppm) and MeOD (3.31 ppm).The chemical shifts are expressed as ppm downfield and coupling constants (J) are given in Hz.The TLC analysis utilized glass sheets precoated with silica gel F254 (0.2 mm) from Aldrich.The purity of the final compounds (19-41) was checked using a Hewlett−Packard 1100 HPLC (Agilent Technologies Inc., Palo Alto, CA, USA) equipped with an Agilent Eclipse 5 µm XDB-C18 analytical column (50 × 4.6 mm); the mobile phase: a linear gradient solvent system, 10 mM EAA (triethylammonium acetate):CH 3 CN from 95:5 to 0:100 in 20 min; and the flow rate was 1.0 mL/min.UV absorption peaks (230, 254, and 280 nm) were detected using a diode array detector.All the derivatives later evaluated pharmacologically showed >95% purity by analytical HPLC.Low-resolution mass spectrometry was performed with a JEOL SX102 spectrometer with 6 kV Xe atoms following desorption from a glycerol matrix or on an Agilent LC/MS 1100 MSD, with an Atlantis C18 column (Waters, Milford, MA, USA).High-resolution mass spectroscopic (HRMS) measurements were carried out on a proteomics-optimized Q-TOF-2 (Micromass-Waters) using external polyalanine calibration and observation of mass accuracies.

Assay of hP2Y 6 R-Induced Ca 2+ Transients
To screen for P2Y 6 R antagonist activity, PLC-mediated calcium mobilization assays were carried out using the recombinant human P2Y 6 R stably expressed in 1321N1 astrocytoma cells (hP2Y 6 R-1321N1) according to the previously published method [30].Briefly, the hP2Y 6 R-1321N1 cells were seeded on 96-well black plates and incubated overnight.The antagonists were pretreated along with the FLIPR dye (Calcium 6 assay kit, Molecular Devices, San Jose, CA, USA) containing 5 mM probenecid for 45 min, prior to agonist addition followed by an immediate intracellular Ca 2+ measurement.UDP was used as a P2Y 6 R agonist (final concentration 100 nM, EC 50 13 nM in PLC activation).Here, probenecid was used as an organic anion transporter inhibitor to prevent the efflux of the dye into the extracellular environment.During incubation, the membrane permeable dye enters the cytoplasm and cleaves the acetoxymethyl protection to enable Ca 2+ binding.When the P2Y 6 R was activated by UDP, the increased calcium concentration was directly measured by intracellular changes in the fluorescence intensity with a Fluorescent Imaging Plate Reader (FLIPR TETRA , Molecular Devices, San Jose, CA, USA).

Assay of hP2Y 14 R Binding
The affinity of three P2Y 6 R antagonists was tested at the hP2Y 14 R using whole-cell binding of a specific fluorescent antagonist MRS4174 [31] in CHO cells stably overexpressing the hP2Y 14 R (CHO-hP2Y 14 R).Briefly, 1 × 10 4 cells were seeded on a 96-well plate for 24 h prior to the assay and incubated at 37 • C and 5% CO 2 in Dulbecco's modified Eagle's medium/nutrient mixture F-12 (DMEM/F12) supplemented with 10% fetal bovine serum, 100 units/mL penicillin, 100 µg/mL streptomycin, and 0.5 mg/mL selective antibiotic G418 sulfate.On the day of the assay, three unlabeled P2Y 6 R antagonists (24, 30, and 37) were diluted separately in the serum-free media with a 10-fold serial dilution (1 nM-100 µM).The cells were first incubated with unlabeled ligands for 30 min at 37 • C and 5% CO 2 followed by another 30 min of incubation with 20 nM fluorescent antagonist (MRS 4174).After the incubation, the cells were washed three times with Dulbecco's phosphate-buffered saline (1X DPBS) without Ca 2+ /Mg 2+ to remove the residual unlabeled and labeled fluorescent ligands.The cells were detached using Cellstripper and resuspended in 1X DPBS for a flow cytometry analysis.The competitive binding assays were performed on a CytoFLEX flow cytometer (Beckman Coulter, CA, USA).

Cell Culture and Cell Viability
The 1321N1 astrocytoma (hP2Y 6 R-overexpressing) and HeLa (non-transfected) cell lines were cultured in Dulbecco's modified Eagle's medium (DMEM, HyClone, Logan, UT, USA) supplemented with 5% heat-inactivated fetal bovine serum (FBS, HyClone, UT, USA), 100 U/mL penicillin, and 100 µg/mL streptomycin in 5% CO 2 at 37 • C. The cell viability was determined using an MTT kit (Sigma, St. Louis, MO, USA) according to the manufacturer's instructions.Briefly, 1 × 10 4 cells were seeded in triplicate in 96-well plates.The hP2Y 6 R-astrocytoma and HeLa cells were treated with a P2Y 6 R agonist and antagonists at a range of concentrations and incubated for 12 h.The cell viability was measured at 490 nm using a SpectraMax-M5 Spectrometer (Molecular Devices, San Jose, CA, USA).

Statistical Analysis
The pharmacological parameters were determined using the Prism 10.2.2 software (GraphPad, San Diego, CA, USA).The values are expressed as the mean ± standard error mean.The data were analyzed by analysis of variance (ANOVA) followed by post hoc analysis to check the statistical difference among the groups with p < 0.05 being considered significant.

Functional Antagonism
As reported in our previous studies [30,40], the mono-halo substitution of the core 3nitro-2-(trifluoromethyl)-2H-chromene heterocycle in 5-11 indicates a preference for 8-and 6-position substitution, compared to the 5 and 7 positions (Table 1).A comparison of the triethylsilyl-alkynyl groups placed at the 5, 6, and 8 positions (12)(13)(14) is consistent with the substitution preference at the 8 and 6 positions, with sub-µM affinity in derivatives 13 and 14.Furthermore, the presence of a p-substituted phenyl ring with various terminal groups in derivatives 15-18 indicated the relative freedom of substitution at the 6 position, suggesting that it is located in a region on the receptor with no strict steric constraints.Previously, both hydrophilic (e.g., 16 and 17) and hydrophobic terminal groups are tolerated, although none were found to greatly enhance the affinity.
Table 1 shows the structures and P2Y 6 R inhibitory affinity of newly synthesized (19-41) compounds, as well as their lipophilicity and aqueous solubility predictions.Sigmoidal inhibition curves for selected derivatives appear in Figure 3.There is no indication of P2Y 6 R agonist activity for any tested antagonists.The high affinity reported for compound 4, in the reduction of IP 3 production in response to 10 µM UDP in hP2Y 6 R-HEK cells [33], was not confirmed in our assay (Ca 2+ mobilization in response to 100 nM UDP in hP2Y 6 R-1321N1 cells).Compound 4 appeared to be only a weak hP2Y 6 R antagonist (18.9 ± 8.5% inhibition at 100 µM).   1.
Given the unknown receptor binding site location for this series, we expanded the SAR by probing the distal changes while maintaining the CF3 and NO2 groups as constant.Instead of a rigid phenyl ring, we introduced flexible alkyl or oxyalkyl (PEG) groups on the anchoring ethynyl moiety.Varying both the length and the terminal functionality of these groups had characteristic effects on the hP2Y6R affinity.The 6 position (19-35) was more extensively modified than the 8 position (36)(37)(38)(39)(40)(41).A progression from a chain length of 3 to 8 methylenes extending the ethynyl moiety was examined, and the affinity values are also shown graphically, comparing the terminal primary amines and terminal Boc-  1.
Given the unknown receptor binding site location for this series, we expanded the SAR by probing the distal changes while maintaining the CF 3 and NO 2 groups as constant.Instead of a rigid phenyl ring, we introduced flexible alkyl or oxyalkyl (PEG) groups on the anchoring ethynyl moiety.Varying both the length and the terminal functionality of these Cells 2024, 13, 1366 9 of 14 groups had characteristic effects on the hP2Y 6 R affinity.The 6 position (19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31)(32)(33)(34)(35) was more extensively modified than the 8 position (36)(37)(38)(39)(40)(41).A progression from a chain length of 3 to 8 methylenes extending the ethynyl moiety was examined, and the affinity values are also shown graphically, comparing the terminal primary amines and terminal Boc-amines (Figure S2, Supplementary Materials).The pattern of Boc-amino at the chain terminus (6 position) being more potent than unblocked amino was consistent for different chain lengths (except for 8 methylenes).The progression of affinity with increasing chain length was not smooth (7 > 4 > 3 > 6 > 8 methylenes), which probably indicates specific interactions with groups on the receptor rather than tethering away from the receptor.Thus, there was no clear definition of the environment around the appended chains or evidence that they reach polar head groups of the phospholipid bilayer [38], as was our original hypothesis.
A terminal Br group in 19 and 36 was associated with moderate µM affinity.At the 6 position, the Boc-amino derivatives tended to have greater antagonist potency than the corresponding amino derivatives.The presence of the Boc-amino-protecting group in the 6-position-derivatized 30 enhanced the affinity by 17-fold compared to the primary amino derivative 29.However, removing the Boc-amino-protecting group in the 8-positionderivatized 40 did not affect the affinity, which was weak in both cases (IC 50 20-30 µM).Curiously, the extension of Boc derivative 30 by one single carbon in 33 reduced it by 160-fold.At both the 6 and 8 positions, the introduction of a hydrophilic PEG chain terminating in a carboxylic acid greatly reduced the affinity, which is consistent with a mainly hydrophobic environment.
Prediction of the physicochemical and pharmacokinetic properties was performed using the Stardrop Software (Version 7.4.0,Table 1 and Table S1, Supplementary Materials) [41].Among the reference compounds, nonpolar compounds 2 and 5-14 were predicted to cross the BBB.Among the newly synthesized analogues, only the two ω-bromo-alkyl analogues 19 and 36, both lacking H-bond donors, were predicted to cross the blood-brain barrier (BBB), and all except the carboxylate analogues 35 and 41 were predicted to have intestinal bioavailability.Most other compounds had only one H-bond donor, which contributed to human intestinal permeability and high flexibility.However, the potent compound 30 had low predicted aqueous solubility (0.86 mg/mL), while the ω-aminoalkyl analogues had a predicted aqueous solubility of ~100 mg/mL and pKa of 8.7-9.Although a nitro group is unusual in pharmaceuticals, there are examples of approved drugs containing this functionality [41].
The original lead compound 2a was shown to be P2Y 6 R-selective compared to all the other P2YRs [29].The antagonistic affinity at one other P2YR, i.e., hP2Y 14 R, was determined here for the selected compounds (Figure 4) using a previously reported fluorescent binding assay in whole cells [31].The P2Y 14 R affinity was generally weak.Broader off-target binding interactions at 45 different membrane-bound proteins were assayed by the NIMH Psychoactive Drug Screening Program (PDSP) [42] for acylamino derivatives 20, 24, 26, 30, 31, and 37 (Tables 2 and S2).Curiously, while the highest affinity P2Y 6 R antagonist 30 displayed seven off-target interactions, including relatively potent interactions at the α 2Aand α 2B -adrenergic receptors, the corresponding pivaloyl derivative 31 (only one O atom different) had only two weak interactions (K i , µM): α 2A , 3.5; σ 2 , 3.3.In contrast, 6,8-difluoro analogue 2b had no off-target interactions.analogues 19 and 36, both lacking H-bond donors, were predicted to cross the blood-brain barrier (BBB), and all except the carboxylate analogues 35 and 41 were predicted to have intestinal bioavailability.Most other compounds had only one H-bond donor, which con tributed to human intestinal permeability and high flexibility.However, the potent com pound 30 had low predicted aqueous solubility (0.86 mg/mL), while the ω-aminoalky analogues had a predicted aqueous solubility of ~100 mg/mL and pKa of 8.7-9.Although a nitro group is unusual in pharmaceuticals, there are examples of approved drugs con taining this functionality [41].
Potent P2Y 6 R agonist 5-iodouridine-5 ′ -O-diphosphate (MRS2693, EC 50 15 nM in PLC activation) and three antagonists were tested for effects on cell viability using a 3-(4,5dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay [44] in two cell lines, hP2Y 6 R-1321N1 human astrocytoma cells and HeLa cells (Figure 5, Table S3).The minor effects, following 12 h exposure, were slightly greater in the HeLa cells than in the astrocytoma cells.The agonist (≤10 µM) had no significant effect in the astrocytoma cells, but there was a modest increased (4-6%) viability at ≥1 µM in the HeLa cells.The antagonist MRS4841 2b [43] had only minor inhibition of viability at 10 µM (22% in the HeLa cells and 12% in the hP2Y 6 R-1321N1 cells).However, MRS4940 30 at 1 µM inhibited viability by 29% in the HeLa cells and 23% in the hP2Y 6 R-1321N1 cells.The minor cell viability inhibition by 2b and 30 at concentrations higher than their receptor affinity appeared to be dose-dependent, but there was no indication of P2Y 6 R-dependent effects on proliferation.Thus, we expect that this series of antagonists will be useful as pharmacological tool compounds.
to be dose-dependent, but there was no indication of P2Y6R-dependent effects on proliferation.Thus, we expect that this series of antagonists will be useful as pharmacological tool compounds.astrocytoma, (E-H)) treated with antagonists MRS4830 (6-fluoro-3-nitro-2-(trifluoromethyl)-2H-chromene), 2b, and 30 and with agonist MRS2693 at a range of concentrations up to 10 µM, following exposure for 12 h.Viability was determined using the MTT assay [44], showing mean ± SEM as a percentage of control.* p< 0.05.Percent data are in Supplementary Materials.(E-H)) treated with antagonists MRS4830 (6-fluoro-3-nitro-2-(trifluoromethyl)-2H-chromene), 2b, and 30 and with agonist MRS2693 at a range of concentrations up to 10 µM, following exposure for 12 h.Viability was determined using the MTT assay [44], showing mean ± SEM as a percentage of control.* p < 0.05.Percent data are in Supplementary Materials.

Discussion
In conclusion, we followed our previous results that the 2H-chromenes could be derivatized most effectively, with respect to receptor affinity, at the 6 and 8 positions.Further SAR exploration of 2H-chromene derivatives as P2Y 6 R antagonists has led to the identification of potent analogues containing an extended alkyl chain terminating in various functional groups, either charged or protected with a Boc-amino group.Curiously, the Boc-protected analogues were consistently more potent than the free amines, suggesting a hydrophobic environment around the extended chains, unlike earlier studies of GPCRfunctionalized congeners.Consistently, carboxylates on extended polar PEG chains greatly reduced the affinity.The affinity was not dependent on the methylene chain length.The highest affinity was observed for the 6-(Boc-aminoheptyl) analogue MRS4940 30 (IC 50 162 nM) and 4-(Boc-aminobutyl) analogue MRS4944 24 (IC 50 568 nM).Compound 30 was 132-fold selective compared to the P2Y 14 R.When the identical chain found in 30 was placed at the 8 position in 37, the affinity was 31-fold lower.However, 30 also slightly inhibited the cell viability at 2.5 µM (15-fold higher than the IC 50 ) and displayed offtarget interactions with two adrenergic receptors.The µM (or in some cases with greater affinity) off-target inhibition of binding at various receptors by multiple analogues, mainly α-adrenergic and dopamine receptors, is also a limitation of the use of these compounds.Multiple compounds at 10 µM displayed a small reduction in the cell viability in two cancer cell lines.

Conclusions
We have improved the affinity of previous 3-nitro-2-(trifluoromethyl)-2H-chromene derivatives as P2Y 6 R antagonists.The addition of a favored 6-ethynyl-linked chain indicated a hydrophobic receptor environment surrounding the pharmacophore.Although the P2Y 6 R affinity depended on the chain length, attachment point, and terminal functionality of the added chain, there was not a smooth progression of affinity with increased length.Nevertheless, some patterns were evident, such as the high affinity of Boc-protected amines.Thus, despite the limitations of this 2H-chromene series, and given the difficulty of discovery of new chemotypes as antagonists, some of these analogues may now be evaluated further to probe the applicability of P2Y 6 R antagonists for potential treatment of neurodegeneration, cancer, and inflammatory and other conditions.

Table 2 .
Cont.MRS4956.c If no value is given, the affinity at all other receptors, channels, and transporters examined, as shown in the Supplementary Materials file, are >10 µM.