Synthesis and Characterization of Edaravone Analogues as Remyelinating Agents and Putative Mechanistic Probes

Edaravone (EDA), an antioxidant drug approved for the treatment of ischemic stroke and amyotrophic lateral sclerosis, was recently proposed as a remyelinating candidate for the treatment of multiple sclerosis. Here, we synthesized twelve EDA analogues 2b–4c showing three substitution patterns A–C, searching for improved remyelinating agents and putative molecular targets responsible for their regenerative activity. We profiled them in three primary assays to determine their stimulation of oligodendrocyte progenitor cell metabolism (tetrazolium MTT assay), their antioxidant potential (2,2-diphenyl-1-picrylhydrazyl-DPPH assay) and to predict their bioavailability (virtual ADME profile). Active 4′-carboxylate 2b, 4′-ester 2c and N1-carbamate-4′-ester 4a were further characterized, justifying their in vitro effects and selecting 4a as a putative EDA 1 prodrug suitable for in vivo testing.


Introduction
Multiple sclerosis (MS) is a chronic, inflammatory, demyelinating and neurodegenerative disease of the central nervous system (CNS) [1].Current treatments for MS are effective in controlling the inflammatory component of the disease but fail in preventing the continuous loss of axons and neurons that leads to a permanent neurological disability [2].The repair of damage to the myelin sheaths that surround axons and allow the propagation of nerve signals is inadequate in MS, particularly in the more advanced stages of the disease.The generation of new myelin-forming oligodendrocytes involves the differentiation of a population of glial cells, the oligodendrocyte progenitor cells (OPCs).The identification of drugs capable of inducing differentiation of OPCs present within damaged areas into remyelinating oligodendrocytes is an opportunity for MS treatment aimed to promote tissue repair [3].
We [4] and others [5,6] determined the remyelinating activity of the radical scavenger edaravone (EDA) 1a, a neuroprotective agent for the treatment of ischemic stroke and/or amyotrophic lateral sclerosis (ALS) in Japan, USA and Canada [7].We also identified two positions (A and B, Figure 1) whose limited substitutions (2a and 3a, Figure 1) were compatible with remyelination in different in vitro and ex vivo disease models [4].Here, we designed and assessed synthetic strategies to provide twelve EDA analogues, including seven A, two B and three C substitutions (respectively, 2b-h, 3b,c and 4a-c, Figure 1); the C pattern was introduced to protect the redox-sensitive EDA nucleus and provide access to alcohol 2g and azide 2h.We also inserted four photoactivatable probes [8] (azides 2f, 2g and 2j, and aryldiazirine 2h, Figure 1) for covalent binding and mass spectrometry-proteomics identification of any unknown protein target responsible for remyelination.
Molecules 2023, 28, x FOR PEER REVIEW 2 of 14 We [4] and others [5,6] determined the remyelinating activity of the radical scavenger edaravone (EDA) 1a, a neuroprotective agent for the treatment of ischemic stroke and/or amyotrophic lateral sclerosis (ALS) in Japan, USA and Canada [7].We also identified two positions (A and B, Figure 1) whose limited substitutions (2a and 3a, Figure 1) were compatible with remyelination in different in vitro and ex vivo disease models [4].Here, we designed and assessed synthetic strategies to provide twelve EDA analogues, including seven A, two B and three C substitutions (respectively, 2b-h, 3b,c and 4a-c, Figure 1); the C pattern was introduced to protect the redox-sensitive EDA nucleus and provide access to alcohol 2g and azide 2h.We also inserted four photoactivatable probes [8] (azides 2f, 2g and 2j, and aryldiazirine 2h, Figure 1) for covalent binding and mass spectrometryproteomics identification of any unknown protein target responsible for remyelination.We determined the biological activity and physicochemical properties of twelve EDA analogues in a primary biological/ADME profiling cascade, and further tested three active analogues to rationalize their in vitro activity, to select an early lead for future studies.
Scheme 1. Synthesis of 4′-EDA ester 2c and photoactivatable 4′-amide EDAs 2d-f.We determined the biological activity and physicochemical properties of twelve EDA analogues in a primary biological/ADME profiling cascade, and further tested three active analogues to rationalize their in vitro activity, to select an early lead for future studies.
Molecules 2023, 28, x FOR PEER REVIEW 2 of 14 We [4] and others [5,6] determined the remyelinating activity of the radical scavenger edaravone (EDA) 1a, a neuroprotective agent for the treatment of ischemic stroke and/or amyotrophic lateral sclerosis (ALS) in Japan, USA and Canada [7].We also identified two positions (A and B, Figure 1) whose limited substitutions (2a and 3a, Figure 1) were compatible with remyelination in different in vitro and ex vivo disease models [4].Here, we designed and assessed synthetic strategies to provide twelve EDA analogues, including seven A, two B and three C substitutions (respectively, 2b-h, 3b,c and 4a-c, Figure 1); the C pattern was introduced to protect the redox-sensitive EDA nucleus and provide access to alcohol 2g and azide 2h.We also inserted four photoactivatable probes [8] (azides 2f, 2g and 2j, and aryldiazirine 2h, Figure 1) for covalent binding and mass spectrometryproteomics identification of any unknown protein target responsible for remyelination.We determined the biological activity and physicochemical properties of twelve EDA analogues in a primary biological/ADME profiling cascade, and further tested three active analogues to rationalize their in vitro activity, to select an early lead for future studies.
Molecules 2023, 28, x FOR PEER REVIEW 3 of 14 We obtained 4′-EDA amides bearing azides 2d, 2e and diazirine 2f through amidation of carboxylate 2b (step b, Scheme 1); the latter was obtained with a poor, unoptimized yield due to the limited diazirine stability.
We obtained 4′-EDA amides bearing azides 2d, 2e and diazirine 2f through amidation of carboxylate 2b (step b, Scheme 1); the latter was obtained with a poor, unoptimized yield due to the limited diazirine stability.
Purified mouse OPCs were grown for 24 h and treated with EDA 1 and analogues 2b-4c (10 μM) for 44 h; then, MTT was added and OPCs were incubated for 4 h.As shown in Figure 3, 4′-ester EDA 2c (pattern A) and N 1 -carbamate EDA 4′-ester 4a (pattern C) stimulated OPC metabolism comparably to EDA 1. EDA aryldiazirine 2f and alcohol 3a were cytotoxic at this concentration and inactive at lower dosages (not shown).Other EDA analogues, including putative photoactivatable azides 2d, 2e and 2h, did not stimulate OPC development compared to DMSO controls.A DPPH assay was carried out after 30 min of incubation with EDA 1 and its analogues in reported conditions [14] to determine their radical scavenging ability.Results, expressed as % inhibition, are shown in Figure 4.A DPPH assay was carried out after 30 min of incubation with EDA 1 and its analogues in reported conditions [14] to determine their radical scavenging ability.Results, expressed as % inhibition, are shown in Figure 4. We observed limited antioxidant activity, with 4′-carboxy EDA 2b being significantly more potent than EDA 1; we hypothesize that the moderately electron-donating effect of carboxylate in 2b, due to its negative charge at physiological pH, could better stabilize the radical formed after hydrogen donation to DPPH.Most A-B analogues showed comparable antioxidant activity to EDA 1 (ester 2c, azides 2d and h, alcohols 2g and 3b, and ether 3a).N 1 -Boc EDAs 4a-c (C) could not act as radical scavengers because a tautomeric EDA equilibrium [10] is prevented by their substitutions.
We used the QikProp tool [15] to predict the ADME properties of EDA analogues 1-4c; the full panel is provided in the Supplementary Materials (Table S1).Here, we focus on lipophilicity and cell permeability in the CNS, showing the partition between n-octanol and water (LogP), intestinal absorption (Caco-2 permeability), partition between blood and brain (LogBB), CNS absorption (Madin-Darby canine kidney-MDCK permeability) and predicted CNS access.These values are reported in Table 1, columns 2 to 6, with a general "druggability" indication (Lipinski Rule of Five violations, column 7).We observed limited antioxidant activity, with 4 -carboxy EDA 2b being significantly more potent than EDA 1; we hypothesize that the moderately electron-donating effect of carboxylate in 2b, due to its negative charge at physiological pH, could better stabilize the radical formed after hydrogen donation to DPPH.Most A-B analogues showed comparable antioxidant activity to EDA 1 (ester 2c, azides 2d and h, alcohols 2g and 3b, and ether 3a).N 1 -Boc EDAs 4a-c (C) could not act as radical scavengers because a tautomeric EDA equilibrium [10] is prevented by their substitutions.
We used the QikProp tool [15] to predict the ADME properties of EDA analogues 1-4c; the full panel is provided in the Supplementary Materials (Table S1).Here, we focus on lipophilicity and cell permeability in the CNS, showing the partition between n-octanol and water (LogP), intestinal absorption (Caco-2 permeability), partition between blood and brain (LogBB), CNS absorption (Madin-Darby canine kidney-MDCK permeability) and predicted CNS access.These values are reported in Table 1, columns 2 to 6, with a general "druggability" indication (Lipinski Rule of Five violations, column 7).EDA 1 was predicted as permeable in Caco-2 (oral) and MDCK (blood-brain barrier-BBB) models; its LogP and LogBB values indicated an acceptable lipo-vs.hydrophilicity ratio.MTT-active 4 -ester 2c and N 1 -Boc 4 -ester EDA 4a were characterized as orally bioavailable, with limited CNS access.Conversely, poor bioavailability was predicted for strong antioxidant carboxylate 2b; photoactivatable azides 2f, 2g and 2j; and diazirine 2h.EDA analogues 2b-4c showed no major violations of Lipinski's Rule of Five (molecular weight, rotatable bonds, hydrogen bond donor and acceptor groups).

Detailed Characterization-EDA Analogues 2b, 2c, 4a
Primary profiling identified three active EDA analogues, none endowed with both OPC stimulation and antioxidant properties as EDA 1.We focused on strong antioxidant 4-carboxy EDA 2b (DPPH assay) on moderately remyelinating 4 -ester EDA 2c and N 1 -Boc 4 -ester EDA 4a (MTT assay) to better characterize their biological activity.EDA 1 was also tested, as a positive standard.
We experimentally confirmed their predicted poor to medium-good permeability profile by measuring their LogD at physiological pH through a known procedure [14], and by determining their percentage bound to model lipid bilayers after incubation, as a measure of their affinity for cell-membrane-like liposomes.Results are shown in Table 2 (LogD 7 .4 , column 2; interaction with liposomes at 20 • C and 37 • C, columns 3 and 4, respectively).N 1 -Boc 4 -ester 4a showed a better LogD 7 .4 value than EDA 1 and 4 -ester EDA 2c (column 2); 4 -carboxy EDA 2b showed poor affinity for lipophilic environments.A similar pattern was observed with pre-formed liposomes at 20 • C, showing strong permeation/partition into liposomes for lipophilic 4a, medium for 4 -ester 2c and moderate for EDA 1 and 4 -carboxy EDA 2b (column 3); partition into liposomes increased with temperature (column 4, 37 • C), with the exception of N 1 -carbamate 4 -ester EDA 4a.
Density functional theory (DFT) methods were used to rationalize the experimental antioxidant activity of EDA analogues using Jaguar TM software [16], and optimizing structures at the 6-311++G(d,p) level for all atoms, as described in detail in the Material and Methods section.Predicted Molecular Electrostatic Potentials (MEPs) and Average Local Ionization Energies (ALIEs) are shown in the Supplementary Materials (Figure S1) and tabulated as energy values in Table S2.
The HOMO (Highest Occupied Molecular Orbitals) and LUMO (Lowest Unoccupied Molecular Orbitals) representation, and the ∆E energy gap for EDA analogues are tabulated in Table 3 (second to fourth column, respectively); their images are shown in the Supplementary Materials (Figure S2).The HOMO-LUMO ∆Es calculated for EDA 1 and analogues 2b, 2c and 4a predicted a trend to donate electrons, as their ionization potential (IP = −E HOMO , fifth column, Table 3) is higher than their electron affinity (EA = −E LUMO , sixth column).4 -Carboxy EDA 2b and its ester 2c exhibited the lowest ∆Es, predicting higher antioxidant potency [17]; these and N 1 -carbamate 4 -ester EDA 4a showed the highest EAs (sixth column), hinting to single electron transfer reactions (hydrogen free radical donation).HOMOs were delocalized on the phenyl and pyrazolone carbon atoms, while LUMOs were delocalized to the phenyl ring except for EDA 1, whose LUMO was delocalized to the pyrazolone ring (Figure S2).

Stability Studies-EDA Analogues 2c and 4a
We investigated the stability of 4 -ester EDA 2c and N 1 -carbamate 4 EDA 4a (respectively, black and grey bars, Figure 5) in biological media, checking both ester and N 1 -carbamate stability in 4a both by thin-layer chromatography (TLC) and by checking the DPPH radical scavenging activity of 2c and 4a after incubation.
FOR PEER REVIEW 8 of 14 Namely, 2c and 4a were incubated in PBS and in standard medium at 20 °C and 37 °C for 20 min; then, DPPH was added and the radical scavenging activity was measured in all media [14].The expected radical scavenging activity by 4′-ester EDA 2c was observed (dark bars, Figure 5), and its stability in biological media was confirmed by TLC.DPPHinactive N 1 -carbamate 4′-ester EDA 4a did not scavenge DPPH in both media at 20 °C (first and third light bars), and its stability was confirmed by TLC.Conversely, significant antioxidant activity was detected at 37 °C (second and last light bars, Figure 5) due to loss of t-Boc and conversion into DPPH-active 4′-ester EDA 2c; TLC confirmed N 1 -carbamate hydrolysis and 2c formation at 37 °C.

Discussion and Conclusions
Potent, safe myelin-repair-promoting treatments could be an effective therapy for MS and, possibly, for other demyelinating diseases [18].EDA 1 is a promising scaffold to build potent and selective remyelinating agents through a structural optimization program; importantly, its repurposing to treat MS could rapidly provide, after clinical evaluation, a well-tolerated and effective drug [4][5][6].
Twelve EDA analogues 2b-4c were synthesized, and small substituents were intro- Namely, 2c and 4a were incubated in PBS and in standard medium at 20 • C and 37 • C for 20 min; then, DPPH was added and the radical scavenging activity was measured in all media [14].The expected radical scavenging activity by 4 -ester EDA 2c was observed (dark bars, Figure 5), and its stability in biological media was confirmed by TLC.DPPH-inactive N 1 -carbamate 4 -ester EDA 4a did not scavenge DPPH in both media at 20 • C (first and third light bars), and its stability was confirmed by TLC.Conversely, significant antioxidant activity was detected at 37 • C (second and last light bars, Figure 5) due to loss of t-Boc and conversion into DPPH-active 4 -ester EDA 2c; TLC confirmed N 1 -carbamate hydrolysis and 2c formation at 37 • C.

Discussion and Conclusions
Potent, safe myelin-repair-promoting treatments could be an effective therapy for MS and, possibly, for other demyelinating diseases [18].EDA 1 is a promising scaffold to build potent and selective remyelinating agents through a structural optimization program; importantly, its repurposing to treat MS could rapidly provide, after clinical evaluation, a well-tolerated and effective drug [4][5][6].
Twelve EDA analogues 2b-4c were synthesized, and small substituents were introduced on A-C substitution patterns (Figure 2).Most of them were predicted by computational methods to be drug-like, BBB-permeable compounds.
Poorly bioavailable 4 -carboxy EDA 2b showed significantly higher antioxidant activity than parent EDA 1, while lipophilic N-aryl-and 5-substituted EDA analogues (ester 2c, azides 2d and 2h, alcohols 2g and 3a, and ether 3b) were comparable to EDA 1.We confirm a known, positive effect of lipophilicity on radical scavenging, and the compatibility of N 2 aryl substitutions with antioxidant activity [19].Unfortunately, lack of activity on OPCs prevented the use of putative photoactivatable EDA azides 2d, 2e and 2h, and diazirine 2f as tools for drug-target identification.
4 -Ester EDA 2c and N 1 -Boc 4 -ester EDA 4a showed comparable stimulation of OPC metabolism, and possibly of remyelination, to EDA 1.The activity for 4a was particularly intriguing, as N 1 -functionalization of EDA 1 prevents tautomeric equilibria and should cancel antioxidant activity.
Primary profiling could not exclude the antioxidant effects of EDA 1 being responsible for OPC prodifferentiating/remyelinating activity in cells.ADME profiling indicated that 4 -ester EDA 2c is bioavailable and should be hydrolyzed in vitro/in vivo by esterases to the potent antioxidant 4 -acid ETA 2b, possibly leading to remyelination.We hypothesize that at least part of the OPC stimulatory activity of 4 -ester 2c in the MTT assay could be due to in situ hydrolysis to 4 -acid ETA 2b; conversely, the poor bioavailability of 2b may preclude its access to the intracellular space, thus preventing OPC stimulation and remyelination after its direct in vitro/in vivo administration.
The metabolic OPC stimulation-remyelinating efficacy of DPPH-inactive N 1 -carbamate 4 -ester EDA 4a was surprising, as was its decreased permeation into lipophilic liposomes at 37 • C, until we observed the instability of its N 1 -carbamate, which was fully removed after 20 min' incubation at 37 • C in either PBS or standard culture medium.We suggest that 4a may act as a prodrug of 4 -ester EDA 2c in suitable conditions; we also suggest that both 4 -ester EDA 2c and N 1 -carbamate 4 -ester EDA 4a may act as prodrugs of the potent antioxidant, poorly bioavailable 4 -carboxy EDA 2b, through esterase-promoted ester hydrolysis.Please note that a long, 48 h incubation time at room temperature (rt) in the MTT assay should allow both 2c and 4a to be converted into 4 -acid EDA 2b in OPCs and that a short 30 min incubation at rt in the DPPH assay could not lead to carbamate hydrolysis for DPPH-inactive 4a, while raising the temperature at 37 • C enabled the formation of DPPH-active 2c.Consequently, the conversion of N 1 -carbamate 4 -ester 4a into 4 -ester 2c at 37 • C in the liposomal interaction explains the observed reduction in liposomal affinity/permeability vs. testing at 20 • C (no N 1 -carbamate hydrolysis).Our efforts to validate this prodrug hypothesis, and to modulate the structure and the stability of N 1 -EDA carbamates 4 through other substitutions, will be reported in due time.
The identification of a molecular target responsible for the remyelinating activity of EDA 1 through synthetic efforts could not be accomplished due to the lack of evidence for an alternative mechanism of action with respect to radical scavenging.Further studies, focused on biology-centered approaches to target identification and validation, are currently ongoing and will be reported in due time.

Synthesis 4.1.1. General
Chemical reactions were carried out in oven-dried glassware, using dry solvents under a nitrogen atmosphere.Dry and normal solvents were purchased (Sigma-Aldrich SRL., Milan, Italy) and directly used in chemical reactions.Commercial reagents were purchased from Sigma-Aldrich, and analytically examined for integrity before handling.Direct phase flash chromatography columns for products' purification were filled with commercial silica gel (240-400 mesh, Merck, Darmstadt, Germany).Thin-layer chromatography (TLC) was employed to monitor reactions using Merck-precoated 60F 254 silica gel plates.UV light at 254 nm was used as a detection method for chromophore-bearing compounds; alternatively, plate charring was carried out either with 50% aqueous H 2 SO 4 or 1% aqueous permanganate. 1H-and 13 C-nuclear magnetic resonance (NMR) spectra were recorded on Bruker DRX-400 and Bruker DRX-300 instruments in the most appropriate deuterated solvent (CDCl 3 , CD 3 OD or DMSO-d 6 ) depending on the solubility of intermediates and target compounds.Tetramethylsilane (TMS) was used as an internal standard to report chemical shift values (δ) for proton and carbon signals, expressed in parts per million (ppm).Electrospray ionization (ESI) mass spectrometry (MS) spectra were recorded on a Waters Micromass Q-Tof micro mass apparatus, while high-resolution (HR)-ESI MS spectra were recorded on an FT-ICR APEX II spectrometer (Bruker Daltonics, Billerica, MA, USA).
4 -Carboxy EDA 2b was purchased (Sigma-Aldrich SRL., Milan, Italy) and used as such.The synthesis of ETA ester 2c and N 1 -carbamate ester 4a are described here.The synthesis of any other EDA analogue is provided in the Supporting Information.NMR spectra and proton assignments are reported for EDA analogues 2c-4c in the Supplementary Materials.Thionyl chloride (0.99 mL, 14.0 mmol) was added to a stirred solution of carboxylate 2b (500 mg, 2.34 mmol) in MeOH (30 mL) at 0 • C. The reaction was left stirring at rt for 5 h.Reaction monitoring (TLC, eluent mixture: 7:3 n-hexane/AcOEt) showed the formation of a reaction product and the disappearance of 2. The solvent was then evaporated under reduced pressure, and the crude was dissolved in CH 2 Cl 2 (15 mL).Saturated aqueous NaHCO 3 (15 mL) was added to the organic layer, and the aqueous layer was extracted with CH 2 Cl 2 (3 × 15 mL).The organic extracts were dried with Na 2 SO 4 and evaporated under reduced pressure to obtain pure 2c (459 mg, 2.01 mmol, 86% yield) as a white solid.Analytical characterization-2c: A solution of di-tert-butyl dicarbonate (197 mg, 0.91 mmol) in dry CH 2 Cl 2 (2.5 mL) was added under nitrogen atmosphere to a stirred solution of ester 2c (150 mg, 0.646 mmol) in dry CH 2 Cl 2 (2.5 mL) at 0 • C.Then, a solution of DMAP (0.7 mg, 0.0646 mmol) in dry CH 2 Cl 2 (1 mL) was added at 0 • C, and the reaction mixture was gently warmed and stirred at rt for 6 h.The reaction was monitored with TLC (eluent mixture 8:2 n-hexane/AcOEt) until disappearance of 2c.The reaction mixture was washed with saturated aq.NH 4 Cl (7 mL).The organic extracts were dried with Na 2 SO 4 and evaporated under reduced pressure to a crude, which was purified with flash chromatography (silica gel, eluent mixture 8:2 n-hexane/AcOEt).Pure title compound 4a was obtained as a white solid (79.2 mg, 0.238 mol, 67% yield).Analytical characterization-4a:

OPC Cultures
Primary cultures of purified OPC (>99%) were obtained from the cerebral hemispheres of newborn CD1 Swiss mice [4] according to the authorization for the care and use of laboratory animals mentioned in Section 4.2.1.OPCs were grown in a defined serum-free Dulbecco's Modified Eagle Medium (DMEM) without thyroid hormones at 1 × 10 5 cells/cm 2 into poly-L-lysine-coated 96-well microtiter plates for 3 days.One day after plating, purified OPCs were incubated with or without EDA analogues (10 µM) in DMSO (0.001% vehicle) for 48 h.MTT reduction to formazan was carried out as previously described [4].MTT (Sigma-Aldrich, Milan, Italy) was added to the culture medium at a final 0.25 mg/mL concentration during the last 4 h of incubation.

2,2-Diphenyl-1-picrylhydrazyl (DPPH) Radical Scavenging Assay
The DPPH free radical scavenging activity of EDA analogues was determined using a previously described method [14].Appropriate aliquots of putative antioxidants 1-13c were mixed with DPPH in methanol (25 µM EDA analogue, 100 µM DPPH, final concentration); the reaction mixtures were shaken and then incubated for 30 min in the dark.Their absorbances, and the absorbance of a DPPH solution as a negative control, were then measured at 517 nm with a BioTek SynergyHT MicroPlate Reader spectrophotometer (Marshall Scientific, Hampton, NH, USA) against methanol as blank.The scavenging percentage of each EDA analogue was calculated according to the following equation: where A control is the control absorbance obtained by adding a methanol aliquot equal to the EDA analogue solution volume added to the methanolic DPPH solution and A sample is the absorbance of each test solution after 30 min incubation.All experiments were repeated at least three times, and measurements were run in triplicate.

Chemical Stability-DPPH Radical Scavenging Assay
4 -Ester 2c and N 1 -carbamate ester 4a were incubated in PBS and in a standard cell culture medium supplemented with FBS 10% at 20 • C and 37 • C.After 20 min, appropriate aliquots of the solutions were mixed with DPPH in methanol (25 µM, DPPH 100 µM, final concentration) and the DPPH radical scavenging assay was carried out as described above.Assay media after incubation were also monitored by TLC (eluent mixture: 1:1 cyclohexane/AcOEt).4.2.6.Determination of Distribution Coefficient (Log D 7 .4 ) LogD 7 .4 values were determined by slightly modifying a reported procedure [20].Namely, an 80 mM solution of each selected EDA analogue in DMSO was diluted in 1-octanol at a final 800 µM concentration.UV-vis spectra were acquired to determine λmax and the necessary dilutions to obtain absorption values for each tested analogue; between 0.5 and 1. 5 mL of each solution were placed in 15 mL conical centrifuge tubes, PBS was added (5 mL, pH 7.4) and the biphasic system was vigorously mixed using a vortex mixer (VELP Scientifica, Usmate Velate, MB, Italy) for 4 min.After centrifugation (2000× g, 30 min), the 1-octanol phase absorption was measured at each compound' λmax; the procedure was repeated to acquire data in triplicate.The distribution coefficient logD 7 .4 was calculated according to the following equation: where A i is the pre-extraction measured absorbance in 1-octanol and A f is the post-extraction final measured absorbance in 1-octanol.

Interaction Studies with Liposome Cell Membrane Models
EDA analogues dissolved in MeOH (0.1 mL) were added to 0.9 mL of large unilamellar phosphatidylcholine vesicles (PC LUVs) in PBS (3 mM lipid final concentration; 0.6 mM EDA analogue final concentration) and incubated at 37 • C for 20 min.Then, any remaining free EDA analogue was separated from liposomes by size-exclusion chromatography.
A disposable syringe (2.5 mL) packed with hydrated Sephadex G-50 resin was placed in a 15 mL plastic test tube and preconditioned with PBS; then, the liposomal suspension (1 mL) was gently added on the top of the syringe and centrifuged at 500× g for 10 min.The eluate was collected at the bottom of the test tube and lysed by addition of Triton X-100 (final concentration 1% v/v).The concentration of each EDA analogue in each solution was estimated with the Folin-Ciocalteu assay [21].Namely, 50% Folin-Ciocalteu reagent (150 µL) was added to test samples (50 µL) into a 96-well microplate and shaken.After 10 min, a 7.5% sodium carbonate solution (0.1 mL) was added; the mixtures were incubated in the dark for 1 h at rt; and, finally, the absorbance was measured at 765 nm on a BioTek SynergyHT MicroPlate Reader spectrophotometer (Marshall Scientific, Hampton, NH, USA) using an appropriate blank.Reference calibration curves were plotted for every sample.The ratio (%) of the drug incorporated into the lipid bilayer was then calculated according to the following equation: % ratio of incorporated antioxidant = 100 × [incorporated amount]/[added amount] (3) Experiments were repeated at least three times, and measurements were run in triplicate.

Computational Studies 4.3.1. In Silico ADME Predictions
The Schrodinger QikProp TM tool (Small-Molecule Drug Discovery Suite 2021-1, Schrodinger, LLC, New York, NY, USA) was used to forecast the absorption, distribution, metabolism and excretion (ADME) profile of the compounds under investigation.This tool employs an algorithm that relies on establishing a correlation between experimentally determined properties and Monte Carlo statistical mechanics simulations involving organic solutes placed within a periodic box containing explicit water molecules.QikProp exploits multiple indicators to gauge the putative central nervous system (CNS) activity of a small molecule, thereby assessing its ability to access the brain compartment by crossing the blood-brain barrier (BBB).The main indicators include the following: (i) the LogBB, i.e., the blood-brain partition coefficient; (ii) the apparent Madin-Darby canine kidney (MDCK) permeability, i.e., forecasting a small molecule's ability to permeate an MDCK layer, measured in nanometers per second (nm/sec); (iii) a CNS activity predictor, guessing the likelihood of a given compound to be CNS-active; and (iv) the apparent permeability through human colon carcinoma Caco-2 cell lines for compounds 2b-4c, estimated so as to predict oral bioavailability and assess drug efflux.Finally, violations of Lipinski's Rule of 5 (≤500 Daltons (Da) as molecular, ≤5 hydrogen bond donors, ≤10 hydrogen bond acceptors and LogP values ranging from 0 to 5) were recorded.

Quantum Chemical Simulations
The Jaguar TM tool (Small-Molecule Drug Discovery Suite 2021-1, Schrodinger, LLC, New York, NY, USA) was employed for electronic calculations such as Molecular Electrostatic Potential (MEP), Average Local Ionization Energy (ALIE), HOMO (Highest Occupied

Figure 3 .
Figure 3.Effect on metabolic activity of OPCs by EDA 1 and its analogues 2b-4c in the MTT assay (96-well plates, 48 h incubation).The histogram shows the rate of tetrazolium salt reduction into

Figure 2 .
Figure 2. Structure of twelve EDA analogues 2b-4c submitted to primary activity profiling.Purified mouse OPCs were grown for 24 h and treated with EDA 1 and analogues 2b-4c (10 µM) for 44 h; then, MTT was added and OPCs were incubated for 4 h.As shown in Figure3, 4 -ester EDA 2c (pattern A) and N 1 -carbamate EDA 4 -ester 4a (pattern C) stimulated OPC metabolism comparably to EDA 1. EDA aryldiazirine 2f and alcohol 3a were cytotoxic at this concentration and inactive at lower dosages (not shown).Other EDA analogues, including putative photoactivatable azides 2d, 2e and 2h, did not stimulate OPC development compared to DMSO controls.

Figure 3 . 3 .
Figure 3.Effect on metabolic activity of OPCs by EDA 1 and its analogues 2b-4c in the MTT assay (96-well plates, 48 h incubation).The histogram shows the rate of tetrazolium salt reduction into Figure 3.Effect on metabolic activity of OPCs by EDA 1 and its analogues 2b-4c in the MTT assay (96-well plates, 48 h incubation).The histogram shows the rate of tetrazolium salt reduction into formazan.Values represent the mean ± SEM of three experiments run in triplicate (** = p ≤ 0.001; *** = p ≤ 0.0001).

Table 1 .
In silico CNS bioavailability parameters for EDA 1
were purchased from Harlan Laboratories (San Pietro Al Natisone, Udine, Italy).All experimental procedures involving the use of CD1 Swiss mice were conducted in accordance with Directive 2010/63/EU of the European Parliament and of the Council concerning the protection of animals used for scientific purposes.The experiments received official authorization from the "Istituto Superiore di Sanità"-Service for Biotechnology and Animal Welfare and were also approved by the Italian Ministry of Health (Authorization n. 87/2017-PR-09/23/2018).