Targeted Library of Phosphonic-Type Inhibitors of Human Neutrophil Elastase

Despite many years of research, human neutrophil elastase (HNE) still remains an area of interest for many researchers. This multifunctional representative of neutrophil serine proteases is one of the most destructive enzymes found in the human body which can degrade most of the extracellular matrix. Overexpression or dysregulation of HNE may lead to the development of several inflammatory diseases. Previously, we presented the HNE inhibitor with kinact/KI value over 2,000,000 [M−1s−1]. In order to optimize its structure, over 100 novel tripeptidyl derivatives of α-aminoalkylphosphonate diaryl esters were synthesized, and their activity toward HNE was checked. To confirm the selectivity of the resultant compounds, several of the most active were additionally checked against the two other neutrophil proteases: proteinase 3 and cathepsin G. The developed modifications allowed us to obtain a compound with significantly increased inhibitory activity against human neutrophil elastase with high selectivity toward cathepsin G, but none toward proteinase 3.


Introduction
Neutrophils are phagocytic granulocytes which are part of the innate immune system and constitute the first line of defence against pathogenic microorganisms.Inflammatory stimulation by bacteria or fungi induces the recruitment of these granulocytes to the inflammation sites [1].Neutrophils attack an invading pathogen with an oxidative burst mainly based on the production of reactive oxygen species (ROS).In addition, they can also release antimicrobial peptides and a set of structurally related serine proteases, namely cathepsin G (CatG), neutrophil elastase (NE), proteinase 3 (PR3), and neutrophil serine proteinase 4 (NSP4).Release of antimicrobial peptides and neutrophil serine proteinases (NSPs) constitutes a non-oxidative mechanism of action [2,3].Human neutrophil elastase (HNE, EC 3.4.21.37), also known as human leukocyte elastase (HLE), was first described by Janoff and Scherer in 1968 [4].This enzyme is stored in azurophil (primary) granules of neutrophils.HNE belongs to the chymotrypsin-like serine protease superfamily.Next to other NSPs, it is also one of the most destructive enzymes found in the human body.It can degrade almost every element of the extracellular matrix (ECM), including elastin, proteoglycans, collagen, fibronectin, and laminin [4][5][6][7][8].The activity of neutrophil elastase is not only degradative or antibacterial.It plays also an important role in the regulation of local inflammatory response [9].Under normal physiological conditions, the heightened activity of neutrophil elastase is strictly regulated to avoid tissue degradation.Serpins, such as α1-antitrypsin (α1-AT), secretory leukocyte peptidase inhibitor (SLPI), and α2macroglobulin (α2-MG) are natural endogenous serine protease inhibitors [10,11].The unrestricted activity of elastase may lead to the development of the pathophysiological states including lung diseases such as chronic obstructive pulmonary disease (COPD), acute pathophysiological states including lung diseases such as chronic obstructive pulmonary disease (COPD), acute lung injury (ALI) and acute respiratory distress syndrome (ARDS), pulmonary emphysema, cystic fibrosis, or chronic bronchitis [12][13][14].
Diaryl esters of α-aminoalkylphosphonates and their peptidyl derivatives are known as highly specific and highly selective irreversible inhibitors of serine proteinases.The relatively easy synthetic approach to α-aminoalkylphosphonate diphenyl esters was described for the first time by Oleksyszyn et al. in 1979.Briefly, triphenyl phosphite undergoes an amidoalkylation reaction with benzyl carbamate and an appropriate aldehyde in acetic acid, affording α-aminophosphonate as a racemic mixture of both enantiomers [15].It was only in 1989 that their ability to irreversibly inactivate serine proteases by acting as the transition state analogues was confirmed.Interactions between the inhibitor and active site serine residue lead to the formation of a covalent protease-inhibitor complex [16].The most significant advantages of α-aminophosphonic-type inhibitors are their non-reactivity with cysteine, threonine, aspartyl, and metalloproteinases, along with their great stability in an aqueous solution including human plasma [17,18].Importantly, α-aminophosphonic inhibitors do not show toxicity in vivo [19].Therefore, many peptidyl derivatives of α-aminoalkylphosphonate diphenyl esters have been reported to act as effective irreversible inhibitors against several mammalian serine proteases, including trypsin, thrombin, uPA, granzymes, kallikreins, dipeptidyl peptidase IV, elastase, cathepsin G, and chymase, as well as bacterial (subtilisin, V8), and viral proteases (hepatitis C virus NS3/4A protease, West Nile virus NS2B/NS3 protease) [18,[20][21][22][23][24][25][26][27][28].
In our previous works, we checked the preferable group for P1 position for simple α -aminophosphonate diaryl esters as inhibitors of human neutrophil elastase and the most active substituent into the ester ring [24].As a result of these studies, we obtained the HNE inhibitor (Scheme 1), whose second-order rate constant of inhibition reaction (kinact/KI) is over 2,000,000 M −1 s −1 .We believe that further modifications of the previously described structure can improve kinetic parameters of designed peptydyl derivatives of 1-aminoalkylphosphonate diaryl esters toward HNE.The results presented by Kasperkiewicz et al. for the library of human neutrophil elastase coumarin substrates show that the introduction of unnatural amino acids could highly improve the potency of action [29].To create a diverse library of over a hundred new phosphonic-type inhibitors of human neutrophil elastase, we designed peptydyl derivatives containing diaryl ester of 1aminoalkylphosphonate as a warhead.Furthermore, we selected a group of proteinogenic and non-proteinogenic amino acids, both L and D configurations, and also a few amino acids with protective groups on the side chain (benzyl (Bzl) and benzyloxycarbonyl (Z)), as substrates for the synthesis of phosphonic tripeptides.We applied a classical solution chemical synthesis approach in the presence of O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate as a coupling reagent.The obtained library was then used in optimization studies to find the best sequence (positions P1-P3) showing the most potent inhibitory activity against human neutrophil elastase.The inhibitory potential was defined by enzyme kinetic studies, in the presence of a specific fluorogenic substrate for HNE (MeO-Suc-AAPV-AFC), and presented as the kinact/KI value which constitutes a crucial kinetic parameter to identify covalent inhibitors.To create a diverse library of over a hundred new phosphonic-type inhibitors of human neutrophil elastase, we designed peptydyl derivatives containing diaryl ester of 1-aminoalkylphosphonate as a warhead.Furthermore, we selected a group of proteinogenic and non-proteinogenic amino acids, both L and D configurations, and also a few amino acids with protective groups on the side chain (benzyl (Bzl) and benzyloxycarbonyl (Z)), as substrates for the synthesis of phosphonic tripeptides.We applied a classical solution chemical synthesis approach in the presence of O-(7-azabenzotriazol-1-yl)-N,N,N ′ ,N ′tetramethyluronium hexafluorophosphate as a coupling reagent.The obtained library was then used in optimization studies to find the best sequence (positions P1-P3) showing the most potent inhibitory activity against human neutrophil elastase.The inhibitory potential was defined by enzyme kinetic studies, in the presence of a specific fluorogenic substrate for HNE (MeO-Suc-AAPV-AFC), and presented as the k inact /K I value which constitutes a crucial kinetic parameter to identify covalent inhibitors.
Next, a few selected structures with the best potency toward HNE were tested in similar enzyme kinetic studies but in the presence of two other NSPs: proteinase 3 and cathepsin G, to determine their selectivity of action.The final step of our research included modifying the best candidate for a new peptydyl phosphonic-type inhibitor of HNE by introducing a hydroquinone moiety into the structure and separating the obtained racemic mixture into optically pure compounds.This division made it possible to compare the inhibitory potential against HNE, PR3, and CatG of individual diastereoisomers with configuration R or S at P1 position.

Results and Discussion
At the beginning, we decided to synthesize phosphonic tripeptides with the general formula Boc-(L)-Val-AA 1 -Val P (OC 6 H 4 -S-CH 3 ) 2 to check their influence on human neutrophil elastase inhibitory activity of different amino acid residue structures at P2 position.The inhibitory activity of 53 compounds was determined by enzyme kinetic studies in the presence of a MeO-Suc-AAPV-AFC as substrate for HNE and is presented in the table below as the k inact /K I ratio (Table 1).All values were then individually compared with the reference compound (27, Boc-(L)-Val-(L)-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 ) showing the highest inhibitory potential toward HNE, confirmed in our previous work [24].It was assumed that all compounds with higher values of the second-order rate constant of inhibition reaction (k inact /K I ) than the reference compound had better activity and inhibitory potential against HNE, whereas all compounds showing lower k inact /K I values were not good candidates for further optimization.Next, a few selected structures with the best potency toward HNE were tested in similar enzyme kinetic studies but in the presence of two other NSPs: proteinase 3 and cathepsin G, to determine their selectivity of action.The final step of our research included modifying the best candidate for a new peptydyl phosphonic-type inhibitor of HNE by introducing a hydroquinone moiety into the structure and separating the obtained racemic mixture into optically pure compounds.This division made it possible to compare the inhibitory potential against HNE, PR3, and CatG of individual diastereoisomers with configuration R or S at P1 position.

Results and Discussion
At the beginning, we decided to synthesize phosphonic tripeptides with the general formula Boc-(L)-Val-AA1-Val P (OC6H4-S-CH3)2 to check their influence on human neutrophil elastase inhibitory activity of different amino acid residue structures at P2 position.The inhibitory activity of 53 compounds was determined by enzyme kinetic studies in the presence of a MeO-Suc-AAPV-AFC as substrate for HNE and is presented in the table below as the kinact/KI ratio (Table 1).All values were then individually compared with the reference compound (27, Boc-(L)-Val-(L)-Pro-Val P (OC6H4-S-CH3)2) showing the highest inhibitory potential toward HNE, confirmed in our previous work [24].It was assumed that all compounds with higher values of the second-order rate constant of inhibition reaction (kinact/KI) than the reference compound had better activity and inhibitory potential against HNE, whereas all compounds showing lower kinact/KI values were not good candidates for further optimization.All structures containing amino acids with D configuration at the P2 position presented above showed inappreciable or no inhibitory activity against HNE.However, this result was not dependent on the relative configuration since no significant activity was observed for most of the L-amino acids used in this iteration.The presence of both aliphatic and aromatic residues as well as elongation of the aliphatic side chain of the P2 amino acid residue caused a decrease in inhibitory activity against HNE and lower k inact /K I values compared to the reference compound 27.Among all of the obtained peptides with the sequence Boc-L-Val-AA 1 -Val P (OC 6 H 4 -S-CH 3 ) 2 , compound 2 (Boc-L-Val-L-Ala-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ) displayed the highest potency (k inact /K I = 160,000 [M −1 s −1 ]) and was the most active HNE inhibitor in this series.Unfortunately, none of the tested modifications displayed higher activity than the reference compound 27 )) had significantly lower activity against HNE than the reference compound 27.Results for the library of human neutrophil elastase coumarin substrates presented by Kasperkiewicz et al. show that the substrate with L-Oic residue in the P2 position is around 60% more active than the substrate with L-Pro [29].Probably these differences between our results and the results for coumarin substrates are caused by the differences in the reactive group structure.We chose the valine residue in P1 position, which is more bulky than the alanine residue presented in P1 position in the mentioned coumarin substrate library.This valine residue could cause steric interaction with L-Oic residue, which reduces alignment to the active site of the enzyme and decreases the inhibitory activity of compound 29 against human neutrophil elastase.Taking into account the information from further studies on the optimization of the P3 position, it was decided to choose the L-Pro residue in the P2 position as the most promising structure.
Next, the 56 compounds with the general formula Boc-AA 2 -(L)-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 were synthesized using an approach analogous to that of the first iteration for optimization of the P2 position, and their activity against human neutrophil elastase was checked by the same enzyme kinetic assay for HNE.The inhibitory potential of all phosphonic peptides was presented as the k inact /K I [M −1 s −1 ] value (Table 2), and once again all results were compared to the reference compound (27).
Investigating the results from Table 2 for the L and D pair of the same amino acid, it can be seen that for most cases the presence of the D configuration at P3 position causes a decrease in activity of the inhibitors.The exceptions are five compounds with D-amino acids: D-Pip, D-Nip, D-HPhe, D-Cys(Bzl) and D-Lys(Z) at P3 position, for which slightly better activity was observed compared to their L counterparts.Despite this, it is worth emphasizing that for all compounds containing D-amino acids, the k inact /K I values were lower than those for the reference compound 27 (Boc-L-Val-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; The highest activity was observed for compound 80 ).These results clearly indicate that the human neutrophil elastase prefers L-amino acid residues at the P3 position, which coincides with the findings described above for the optimization of the P2 position.Secondly, the presence of protective groups, such as benzyl (Bzl) and benzyloxycarbonyl (Z), in the side chain had a negative effect and also reduced the inhibitory potential of peptidyl derivatives of α-aminoalkylphosphonate diphenyl esters toward HNE, compared to the reference 27.From this group, compound 100 (Boc-L-Thr(Bzl)-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 101,800 [M −1 s −1 ]) showed the highest potential, but it was still 2.2× lower than the potential of compound 27.Two other structures containing non-proteinogenic amino acids in P3 position, 62 (Boc-L-Abu-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 227,200 [M −1 s −1 ]) and 65 (Boc-L-Nva-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 209,000 [M −1 s −1 ]), had a level of inhibitory activity similar to that of 27.Finally, better results than with the reference 27 were obtained for two phosphonic peptides with proteinogenic amino acids (methionine or glutamine) in P3, compound 75 (Boc-L-Met-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 304,300 [M −1 s −1 ]) and 79 (Boc-L-Gln-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 743,300 [M −1 s −1 ]).Investigating the results from Table 2 for the L and D pair of the same amino acid, it can be seen that for most cases the presence of the D configuration at P3 position causes a decrease in activity of the inhibitors.The exceptions are five compounds with D-amino acids: D-Pip, D-Nip, D-HPhe, D-Cys(Bzl) and D-Lys(Z) at P3 position, for which slightly better activity was observed compared to their L counterparts.Despite this, it is worth emphasizing that for all compounds containing D-amino acids, the kinact/KI values were lower than those for the reference compound 27 (Boc-L-Val-L-Pro-Val P (OC6H4-4-S-CH3)2; kinact/KI = 229,000 [M −1 s −1 ]).
The highest activity was observed for compound 80 (Boc-D-Gln-L-Pro-Val P (OC6H4-4-S-CH3)2, kinact/KI = 81,780 [M −1 s −1 ]).These results clearly indicate that the human neutrophil elastase prefers L-amino acid residues at the P3 position, which coincides with the findings described above for the optimization of the P2 position.Secondly, the presence of protective groups, such as benzyl (Bzl) and benzyloxycarbonyl (Z), in the side chain had a negative effect and also reduced the inhibitory potential of peptidyl derivatives of α-   ) is also interesting due to the very similar structure of both inhibitors in that they have a sulfur atom instead of a CH 2 group.Despite this similarity, there is a significant difference in inhibition: compound 75 shows 2.4× better activity against HNE than 70.The gradual oxidation of the sulfur atom from the methionine side chain resulted in a 3.4× (Boc-L-Met(O)-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 773,400 [M −1 s −1 ]) and 7.1× (Boc-L-Met(O 2 )-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 1,626,200 [M −1 s −1 ]) increase in potency of action against HNE compared to the reference compound (k inact /K I = 229,000 [M −1 s −1 ]).It is worth noting a similar activity towards HNE of compounds 77 (Boc-L-Met(O)-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 773,400 [M −1 s −1 ]) and 79 (Boc-L-Gln-L-Pro-Val P (OC 6 H 4 -4-S-CH 3 ) 2 ; k inact /K I = 743,300 [M −1 s −1 ]), for which we can find significant similarities in the structure of the P3 residue.This shows how important the presence of an oxygen atom in this specific position of the side chain is for the interaction with the P3 pocket of HNE.
In order to verify the selectivity of the most active compounds of both groups, measurements of inhibitory activity against two other serine proteases, proteinase 3 and cathepsin G, were made.These enzymes are major representatives of neutrophil serine proteases (NSPs) which are closely related to human neutrophil elastase.Proteinase 3 is known as a close homologue of HNE with a very similar substrate specificity to small aliphatic residues, whereas cathepsin G presents a slightly different predisposition to binding hydrophobic (Phe or Leu) and basic (Lys or Arg) side chains at the S1 pocket [30].From the created library of phosphonic-type inhibitors of human neutrophil elastase, the best candidates with the highest value of second-order rate constant of inhibition reaction were selected: five from the first iteration (compounds 1, 2, 6, 8 and 29) and five from the second iteration (compounds 62, 75, 77, 78 and 79).The inhibitory potential of these compounds was tested in analogous enzymatic assays in the presence of PR3 or CatG instead of HNE, and their activity (k inact /K I [M −1 s −1 ]) toward all three NSPs was compared to the reference compound 27 (Tables 3 and 4).For all compounds, a complete lack of inhibition or nonsignificant inhibitory effect (k inact /K I < 50 M −1 s −1 ) on the proteolytic activity of cathepsin G was observed (Tables 3 and 4).Newly developed phosphonic-type inhibitors showed high selectivity toward CatG, so they can be successfully used to selectively inhibit only HNE, without any interaction with CatG present in the analysed sample.This result is probably caused by differences in the structure of active sites and dissimilar substrate specificity of HNE and CatG.
Unfortunately, an absolutely opposite effect was observed in the presence of proteinase 3.In this case, all of the tested inhibitors were recognized by the PR3 and specifically bound in its active site.Depending on the compound used, the observed inhibition of proteolysis was at various levels, as reflected by k inact /K I values from almost 43,000 to more than 2,300,000 M −1 s −1 (Tables 3 and 4).Comparing the inhibitory potential towards HNE and PR3 for almost all selected inhibitors, except compounds 2 and 6, showed higher specificity against proteinase 3. The high structural similarity of HNE and PR3 indicated a possible lack of selectivity of action, but such a relevant preference for PR3 was surprising.The three most potent phosphonic-type inhibitors of human neutrophil elastase (79, 77 and 78) were approximately twice as powerful inhibitors of proteinase 3.
As the last part of the inhibitor structure optimization, we decided to introduce the hydroquinone moiety, used in previous research, on the N-terminal of compound 78.It is important to note that all of the tested compounds were mixtures of two diastereoisomers, whereas the leading structure was tested as a single diastereoisomer.For this reason, an attempt was made to separate compound 111 into pure diastereoisomers.It was possible to obtain both diastereoisomers in pure form (112, 113).The previous studies led us to assume that the more active compound 113 has the R configuration at the P1 position, and the less active compound 112 has the S configuration [31][32][33].The activity toward HNE, PR3 and CatG was inspected for all three compounds.The results are summarized in Table 5.
they can be successfully used to selectively inhibit only HNE, without any interaction with CatG present in the analysed sample.This result is probably caused by differences in the structure of active sites and dissimilar substrate specificity of HNE and CatG.
Unfortunately, an absolutely opposite effect was observed in the presence of proteinase 3.In this case, all of the tested inhibitors were recognized by the PR3 and specifically bound in its active site.Depending on the compound used, the observed inhibition of proteolysis was at various levels, as reflected by kinact/KI values from almost 43,000 to more than 2,300,000 M −1 s −1 (Tables 3 and 4).Comparing the inhibitory potential towards HNE and PR3 for almost all selected inhibitors, except compounds 2 and 6, showed higher specificity against proteinase 3. The high structural similarity of HNE and PR3 indicated a possible lack of selectivity of action, but such a relevant preference for PR3 was surprising.The three most potent phosphonic-type inhibitors of human neutrophil elastase (79, 77 and 78) were approximately twice as powerful inhibitors of proteinase 3.
As the last part of the inhibitor structure optimization, we decided to introduce the hydroquinone moiety, used in previous research, on the N-terminal of compound 78.It is important to note that all of the tested compounds were mixtures of two diastereoisomers, whereas the leading structure was tested as a single diastereoisomer.For this reason, an attempt was made to separate compound 111 into pure diastereoisomers.It was possible to obtain both diastereoisomers in pure form (112, 113).The previous studies led us to assume that the more active compound 113 has the R configuration at the P1 position, and the less active compound 112 has the S configuration [31][32][33].The activity toward HNE, PR3 and CatG was inspected for all three compounds.The results are summarized in Table 5.As we expected, the introduction of hydroquinone moiety to the structure of compound 78 (Boc-L-Met(O) 2 -L-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 ) resulted in a significant increase in the inhibitory potential of the peptidyl derivatives of α-aminoalkylphosphonate diaryl esters 111 towards HNE (k inact /K I = 2,319,700 [M −1 s −1 ]) and PR3 (k inact /K I = 4,105,900 [M −1 s −1 ]), with a simultaneous lack of activity against CatG (k inact /K I < 50 [M −1 s −1 ]).The results confirm the established higher inhibition of a single diastereoisomer, with the R configuration at the P1 position.The isolation of an optically pure compound 113 led to an increase in inhibitory activity against both proteases, human neutrophil elastase (k inact /K I = 4,236,800 [M −1 s −1 ]) and proteinase 3 (k inact /K I = 8,951,600 [M −1 s −1 ]), compared to the mixture (S,R) 111.Similarly to the previous results, it was also noticed that these compounds showed definitely higher specificity towards PR3 than HNE.The chemical modification used in the described studies did not increase the selectivity of the action against human neutrophil elastase.Nevertheless, the remarkably high inhibitory activity confirmed by enzymatic kinetic assays makes these structures serious candidates for further structure-activity relationship studies in the discovery of new, highly specific and selective neutrophil serine protease inhibitors.
We presented a library of over 100 new phosphonic-type inhibitors of the human neutrophil elastase containing different proteinogenic and non-proteinogenic amino acid residues at P2 and P3 positions.The peptidyl derivatives of α-aminoalkylphosphonate diaryl esters show high specificity and great potential to act as human neutrophil elastase inhibitors, which was confirmed in kinetic studies.The top three most potent structures of all phosphonic tripeptides were 78 (Boc-L-Met(O) 2 -L-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 ; and 79 (Boc-L-Gln-L-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 ; k inact /K I = 743,300 [M −1 s −1 ]).A small modification of the best structure 78 led to the creation of new hydroquinone derivatives 111 and 113 showing, respectively, 1.4× (k inact /K I = 2,319,700 [M −1 s −1 ]) and 2.6× (k inact /K I = 4,236,800 [M −1 s −1 ]) higher inhibitory activity against HNE than the initial compound.
Although these inhibitors do not show activity against cathepsin G, they have an excellent ability to inhibit the activity of proteinase 3. The lack of selectivity of action directed towards only one neutrophil serine protease does not exclude the possible use of these inhibitors in further research or therapy.The presented phosphonic-type compounds can be successfully applied as dual inhibitors of human neutrophil elastase and proteinase 3 in some chronic neutrophilic inflammatory diseases when it is required to stop the activity of both proteases [34].The latest literature reports affirm that structures 111 and 113 can be some of the most powerful irreversible inhibitors which bind covalently to the active site of proteinase 3, with k inact /K I values of 4,105,900 [M −1 s −1 ] and 8,951,600 [M −1 s −1 ], respectively [35].

Materials and Methods
All chemical reagents and solvents were taken from commercial sources and used without purification.High-performance liquid chromatography analyses were carried out on a Waters Binary Module System (Waters, Milford, MA, USA) with a dual λ absorbance detector system fitted with a Supelco Ascentis C8 HPLC column (250 mm × 4.6 mm, 5 µm, Supelco, Bellefonte, PA, USA) with a 1 mL/min flow rate operating on a linear gradient from 5 to 95% B within 20 min (solvent A: H 2 O with 0.05% trifluoroacetic acid, solvent B: MeCN with 0.05% trifluoroacetic acid).High-performance liquid chromatography purification was carried out in a Varian ProStar system (Varian, Australia) with a dual λ absorbance detector system with the application of a Supelco Ascentis C8 HPLC column (250 mm × 21.2 mm, 5 µm) with a 15 mL/min flow rate and a linear gradient from 20 to 100% B within 20 min or 40 to 100% B within 20 min (depending on compound solubility), solvent A: H 2 O with 0.05% trifluoroacetic acid, solvent B: MeCN with 0.05% trifluoroacetic acid.The nuclear magnetic resonance spectra ( 1 H and 31 P) were recorded on a 400 MHz NMR Jeol PCZ 400S or Bruker Avance 600 MHz (Bruker, Billerica, MA, USA).High resolution mass spectra were recorded with a Brucker micro TOF-Q II (Bruker, Billerica, MA, USA).

Chemistry
The first step in producing tripeptide derivatives of diaryl esters of α-aminoalkanephosphonic acids with the sequence Boc-(L)-Val-AA 1 -Val P (O-C 6 H 4 -4-SCH 3 ) 2 was the reaction between 4-(methylmercapto)phenol and phosphorus (III) chloride in boiling acetonitrile (Scheme 2).The resultant tri-(4-methylsulfidophenyl) phosphite was subjected to an αamidoalkylation reaction with the aid of benzyl carbamate and isobutyraldehyde in acetic acid.The Cbz protecting group was then removed with a 33% HBr solution in acetic acid.The product was crystallized in methanol/diethyl ether and then subjected to a coupling reaction with appropriate Boc amino acid (AA 1 ) using O-(7-Azabenzotriazol-1yl)-N,N,N ′ ,N ′ -tetramethyluronium hexafluorophosphate (HATU) as a coupling reagent.Washing (5% NaHCO 3 , 5% citric acid, brine) and purification in HPLC yielded pure phosphonic dipeptide.Next, the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the product was paired with the Boc-(L)-Val-OH, also employing HATU as a coupling reagent.After extraction and purification in HPLC, pure phosphonic tripeptide was obtained.
N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) as a coupling reagent.Washing (5% NaHCO3, 5% citric acid, brine) and purification in HPLC yielded pure phosphonic dipeptide.Next, the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the product was paired with the Boc-(L)-Val-OH, also employing HATU as a coupling reagent.After extraction and purification in HPLC, pure phosphonic tripeptide was obtained.A similar approach (Scheme 3) produced tripeptides with the Boc-AA2-(L)-Pro-Val P (OC6H4-S-CH3)2 sequences.Briefly, after removing the Cbz group from Cbz-Val P (O-C6H4-SCH3)2, Boc-(L)-Pro-OH was attached, with HATU as a coupling reagent, to the resulting compound, and then the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the appropriate Boc amino acid (AA2) was attached with HATU as a coupling reagent.Extraction and purification in HPLC resulted in pure phosphonic tripeptide.A similar approach (Scheme 3) produced tripeptides with the Boc-AA 2 -(L)-Pro-Val P (OC 6 H 4 -S-CH 3 ) 2 sequences.Briefly, after removing the Cbz group from Cbz-Val P (O-C 6 H 4 -SCH 3 ) 2 , Boc-(L)-Pro-OH was attached, with HATU as a coupling reagent, to the resulting compound, and then the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the appropriate Boc amino acid (AA 2 ) was attached with HATU as a coupling reagent.Extraction and purification in HPLC resulted in pure phosphonic tripeptide.
N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) as a coupling reagent.Washing (5% NaHCO3, 5% citric acid, brine) and purification in HPLC yielded pure phosphonic dipeptide.Next, the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the product was paired with the Boc-(L)-Val-OH, also employing HATU as a coupling reagent.After extraction and purification in HPLC, pure phosphonic tripeptide was obtained.A similar approach (Scheme 3) produced tripeptides with the Boc-AA2-(L)-Pro-Val P (OC6H4-S-CH3)2 sequences.Briefly, after removing the Cbz group from Cbz-Val P (O-C6H4-SCH3)2, Boc-(L)-Pro-OH was attached, with HATU as a coupling reagent, to the resulting compound, and then the Boc protecting group was removed with a 33% solution of trifluoroacetic acid in dichloromethane, and the appropriate Boc amino acid (AA2) was attached with HATU as a coupling reagent.Extraction and purification in HPLC resulted in pure phosphonic tripeptide.For the synthesis of peptidyl derivatives of α-aminoalkylphosphonate diphenyl esters containing a hydroquinone moiety (Scheme 4), first the Boc protecting group was removed from compound 78, and a hydroquinone moiety, synthesized as described previously, was attached with HATU as a coupling reagent [24].After extraction, the tert-butyl group was removed with a 33% solution of trifluoroacetic acid in dichloromethane.The crude product was purified in HPLC.
The HPLC method served the purpose of separating pure diastereoisomers of compound 111.The separation was carried out at constant concentration of acetonitrile (40%) in water.After freeze-drying, the purity was confirmed by 31 P NMR and analytical HPLC (Scheme 5).

Scheme 1 .
Scheme 1. Structure of most active compound obtained in previous work.

Scheme 1 .
Scheme 1. Structure of most active compound obtained in previous work.

Table 1 .
Influence of the amino acid structure at P2 position of phosphonic peptides with the general formula Boc-(L)-Val-AA 1 -Val P (OC 6 H 4 -S-CH 3 ) 2 on the inhibitory activity toward human neutrophil elastase.