Design and synthesis of some new benzoylthioureido phenyl derivatives targeting carbonic anhydrase enzymes

Abstract

The present study aimed to develop potent carbonic anhydrase inhibitors (CAIs). The design of the target compounds was based on modifying the structure of the ureido-based carbonic anhydrase inhibitor SLC-0111. Six series of a substituted benzoylthioureido core were prepared featuring different zinc-binding groups; the conventional sulphamoyl group 4a–d and 12a–c, its bioisosteric carboxylic acid group 5a–d and 13a–c or the ethyl carboxylate group 6a–d and 14a–c as potential prodrugs. All compounds were assessed for their carbonic anhydrase (CA) inhibitory activity against a panel of four physiologically relevant human CA isoforms hCA I and hCA II, and hCA IX, and hCA XII. Compounds 4a, 4b, 4c, 4d, 5d, 12a, and 12c revealed significant inhibitory activity against hCA I that would highlight these compounds as promising drug candidates for the treatment of glaucoma.

Keywords:

• Sulphonamides
• carbonic anhydrase
• SLC-0111
• benzoylthioureido derivatives

Introduction

Carbonic anhydrase (CA, EC 4.2.1.1) enzyme is a well-known protein that exists in humans as fifteen distinct isoforms of the α-genetic family¹. CAs enzymes are metalloproteins containing zinc that efficiently catalyses the reversible conversion of carbon dioxide to bicarbonate and release proton². CA enzyme has eight distinct classes (α, β, γ, δ, ζ, η, θ, and ι) that have no significant sequence identity and were discovered independently. As a result, the carbonic anhydrase classes are excellent examples of catalytic function of biological evolution³. CAs are involved in important physiological processes such as acid–base regulation, gluconeogenesis, biosynthetic reactions⁴, electrolyte secretion, bone resorption/calcification, and tumorigenicity⁵. Consequently, inhibition of CAs can be a target for the treatment of glaucoma, obesity, neuropathic pain, arthritis, Alzheimer’s disease and cancer^6,7. Some CA isoforms notably isoform IX are found in high concentrations in many solid cancers and in lower concentrations in a variety of normal tissues with strong correlation between its expression and hypoxia^8–10 and where high CA levels are associated with poor prognosis¹¹. Therefore, the design of CAIs have been a beneficial strategy for the treatment of many diseases since the late 1950s where the primary sulphonamides and their isosteres emerged as promising drugs for decades^12–14. Most of the potent CAIs have been correlated with the presence of suitable zinc binding group (ZBG) to establish the required interaction within the hCAs active sites¹⁵, nevertheless many non-zinc binding CAIs have been recently developed¹⁶.

Literature survey unveiled that many ureido and thioureido phenyl derivatives exhibit remarkable CA inhibition activity (Figure 1). Interestingly, the ureido-substituted benzenesulfonamide CA inhibitor SLC-0111 was developed with a highly effective hCA IX/XII inhibitory activity and it was progressed to phase I/II clinical trials for the treatment of advanced metastatic solid cancers^17,18. Many studies focussed on the development of various SLC-0111 analogues through replacement of the 4-fluorophenyl tail, with either substituted thiazole compound I¹⁹, 4-trifluoromethylbenzoyl compounds II and III (IC₅₀ = 1.90 and 2.48 µM) respectively against hCAII²⁰ or acetyl moiety compound IV (IC₅₀ = 2.14 µM) against hCAII²¹ where they showed significant carbonic anhydrase inhibitory activity.

Figure 1. Chemical structure of some ureido and thioureido CAIs.

Accordingly, built on the reported carbonic anhydrase inhibitory activity of SLC-0111 and substituted benzoylthioureido compounds II–IV, we planned to synthesise new benzoylthioureido derivatives with potential carbonic anhydrase inhibitory activity. This is attained via replacement of 4-fluorophenyl ureido moiety of SLC-0111 with un/substituted benzoylthioureido ones, where the substitution at the benzoyl moiety involves either 3-chloro, 3,4-dichloro or 3-bromo substituent while retaining sulphamoyl phenyl of SLC-0111 to produce compounds 4a–d, or bioisosteric replacement of the sulphamoyl phenyl with benzoic acid to obtain 5a–d, or with ethyl benzoate moiety as potential prodrugs to give 6a–d.

Further modification includes substitution of 4-fluorophenyl ureido of SLC-0111 with 2-methoxy-4-substituted benzamido moiety while keeping the same substitution pattern of the zinc binding groups (sulphamoyl phenyl or benzoic acid) to afford 12a–c and 13a–c, respectively, or via the prodrug moiety (ethyl benzoate) to obtain 14a–c (Table 1).

Table 1. Inhibition data (K_I, nM) of human CA isoforms hCA I, II, IX and XII with compounds 4a–d, 5a–d, 6a–d, 12a–c, 13a–c, and 14a–c against SLC-0111 and AAZ; by a stopped flow CO₂ hydrase assay.

				KI (nM)^a
Compound	R	R1	R2	hCA I	hCA II	hCA IX	hCA XII
4a	–	H	H	75.70	78.00	106.00	57.40
4b	–	Cl	H	58.50	58.10	115.40	>100,000
4c	–	Cl	Cl	40.40	90.00	>100,000	88.10
4d	–	Br	H	65.00	67.00	>100000	82.00
5a	–	H	H	1504.70	464.60	2932.00	>100,000
5b	–	Cl	H	8797.60	5535.80	>100,000	>100,000
5c	–	Cl	Cl	>100,000	6000.30	1741.00	>100,000
5d	–	Br	H	5556.20	>100,000	>100,000	>100,000
6a	–	H	H	>100,000	>100,000	1739.30	>100,000
6b	–	Cl	H	>100,000	>100,000	1403.60	>100,000
6c	–	Cl	Cl	809.10	>100,000	239.10	>100,000
6d	–	Br	H	85.38	31.00	>100,000	>100,000
12a	-CH3	–	–	67.60	15.50	32.20	83.00
12b	-CH(CH3)2	–	–	>100,000	2766.20	1784.30	>100,000
12c	-p-CH3-C6H4	–	–	91.00	94.20	144.00	225.70
13a	-CH3	–	–	1709.60	647.00	1092.60	>100,000
13b	-CH(CH3)2	–	–	>100,000	193.50	289.00	>100,000
13c	-p-CH3-C6H4	–	–	>100,000	504.00	802.10	>100,000
14a	-CH3	–	–	>100,000	>100,000	1146.20	>100,000
14b	-CH(CH3)2	–	–	>100,000	>100,000	1496.40	>100,000
14c	-p-CH3-C6H4	–	–	>100,000	2019.70	1367.30	>100,000
SLC-0111^23	–	–	–	5080.00	960.00	45.00	4.50
AAZ	–	–	–	250.00	12.1	25.70	5.70

^aMean from 3 different assays, by a stopped flow technique (errors were in the range of ± 5–10% of the reported values).

This amendment aimed to explore the effect of such modification on the potency and/or selectivity of the designed compounds. Meanwhile, a highly flexible carbonyl thioureido linker was retained in all compounds (Figure 2).

Figure 2. Design of the target compounds as analogues to SCL-0111.

Results and discussion

Chemistry

The synthetic routes adopted for the synthesis of the target compounds 4a–d, 5a–d, 6a–d, 12a–c, 13a–c, and 14a–c are depicted in Schemes 1 and 2, respectively.

The synthesis of compounds 4a–d, 5a–d, and 6a–d was carried out by conversion of the appropriate benzoic acid derivative 1a–d to the corresponding acid chloride 2a–d, followed by reaction with ammonium thiocyanate to give the key intermediate benzoyl isothiocyanates 3a–d that were treated similarly with sulphanilamide, 4-aminobenzoic acid or ethyl 4-aminobenzoate to furnish the target compounds (Scheme 1). IR spectra of compounds 4a–d showed the appearance of characteristic bands at 3360–3255 cm⁻¹corresponding to NH₂ and NH, in addition to two stretching vibration bands at 1330–1160 cm⁻¹ attributed to the characteristic SO₂ group. ¹H NMR spectra revealed the appearance of D₂O exchangeable signal in the aromatic region around 7.42 ppm corresponding to two NH₂ protons of the SO₂NH₂ group as a singlet.

Scheme 1. Reagents and reaction conditions: (i) SOCl_2, methylene chloride, reflux, 4–5 h, (ii) NH₄SCN, acetone, reflux, 1–3 h, (iii) sulphanilamide or 4-aminobenzoic acid or ethyl 4-aminobenzoate, acetone, reflux, 2–3 h.

IR spectrum of compound 5c showed the appearance of characteristic carboxylic OH stretching vibration band at 3402 cm⁻¹ and carbonyl band at 1654 cm⁻¹. IR spectra of compounds 6a–d displayed characteristic bands at 3380–3350 cm⁻¹ corresponding to the NHs groups in addition to carbonyl bands of the ester at range of 1745–1712 cm⁻¹. ¹H NMR spectra of 6a–d revealed the appearance of triplet signal at 1.30–1.42 ppm for protons of methyl group of esters (CH₃CH₂-) and quartette signal at 4.33 ppm corresponding to (CH₃CH₂-) protons. Further, ¹³C NMR spectra of 6b, 6c, and 6d displayed ethyl carbons CH₃CH₂ at 14.6 ppm, CH₃CH₂ carbon at 61.2 ppm along with carbonyl carbons at 165.7 ppm and CS carbon at 176.4–179.3 ppm.

Additionally, the synthesis of the target acetamido-benzoylureido derivatives 12a–c, 13a–c, and 14a–c was performed by acylation of 4-amino-2-methoxybenzoic acid 7 with different acyl chlorides 8a–c in dry acetonitrile in the presence of potassium hydroxide to afford compounds 9a–c. The key intermediates 10a–c and 11a–c were obtained in situ through the formation of the corresponding acid chlorides via the reaction of the acid derivatives with thionyl chloride followed by ammonium thiocyanate. The intermediates 11a–c were not isolated but rather used in the synthesis of the target compounds by reaction with sulphanilamide, 4-aminobenzoic acid or ethyl 4-aminobenzoate in dry acetone to afford the target compounds 12a–c, 13a–c, and 14a–c, respectively in high yields (Scheme 2). The IR spectra of these compounds declared the presence of the expected new functional groups. The characteristics of the ¹H NMR spectra of 10a–c revealed the appearance of exchangeable NH protons at 7.27–7.41 ppm due to the sulphamoyl group, whereas compounds 11a–c showed –COOH proton at 12.80–13.05 ppm. Also compounds 12a–c displayed triplet-quartette signals for the ethyl protons at 1.32–1.43 and 4.32–4.46, respectively. This is in addition to the signals characteristic of the methyl, isopropyl, tolyl protons of the amide group of compounds 12a–c, 13a–c, and 14a–c. On the other hand, ¹³C NMR spectra of 12a, 13a and 14a showed signal at 24.7 ppm corresponding to CH₃ of acetamido group. Also, ¹³C NMR spectra of 12b and 13b revealed the isopropyl carbons (CHCH₃)₂ at 19.7 ppm and (CHCH₃)₂ carbon at 35.6 ppm. In addition, ¹³C NMR spectra of 13c displayed a signal at 21.5 ppm attributed for CH₃ carbons of the tolyl moiety.

Scheme 2. Reagents and reaction conditions: (i) KOH, acetonitrile, R.T, 1–2 h, (ii), SOCl₂, methylene chloride, reflux, 4–5 h, (iii) NH₄SCN, acetone, reflux, 1–3 h, (iv) sulphanilamide or 4-aminobenzoic acid or ethyl 4-aminobenzoate, acetone, reflux, 2–3 h.

Biological evaluation

Carbonic anhydrase inhibitory activity

The CA inhibitory activities of all synthesised compounds 4a–d, 5a–d, 6a–d, 12a–c, 13a–c, and 14a–c, as well as acetazolamide (AAZ) as a standard inhibitor were screened against four CA isoforms: hCA I, hCA II, hCA IX, and hCA XII. The selection of these four isoforms was based on the fact that hCA II is an antiglaucoma medication target, hCA IX and XII are well established targets for the therapy and prognosis of hypoxic malignancies, whereas, hCA I is one of the most common off-target isoforms for antiglaucoma and anticancer CAIs therapeutic application²².

The results showed that the inhibitory activity of the tested compounds against the four CA isoforms were highly dependent on the nature of the ZBG. In this context, the sulphamoyl derivatives (4a–d and 12a–c) appeared as the most potent inhibitors among other derivatives, which revealed that the –COOH group failed to be a good ZBG. Interestingly, the ubiquitous cytosolic isoform hCA I, which is highly abundant in the gastrointestinal tract and red blood cells, was the most inhibited isoform among the others. The tested compound elicited mild activity against hCA II and hCA IX and a poor activity against hCA XII. A closer look on the results pointed out that seven compounds 4a, 4b, 4c, 4d, 6d, 12a and 12c exhibited the best inhibitory activity against hCA I with K_I values ranging from 40.40–91.00 nM and better than the reference drug AAZ (250 nM). All of these compounds, except 6d, featured a free sulphamoyl group which strongly supported the binding rational. Trying to figure out the effect of the tail substitution on the activity, it could be noticed that a small acetamido group as in compound 12a was correlated to the highest activity against all hCA isoforms. Unsubstituted phenyl ring (compound 4a) was associated with good to moderate activity, notably this compound was the most potent against hCA XII with K_I value = 57.40 nM. The presence of 3-chloro substitution (compound 4b) gave the best activity agasinst hCA I, hCA II and h CA IX among the halogenated derivatives. The 3,4-dichloro and the 3-bromo derivatives, 4c and 4d, respectively, demonstarted good to moderate activity against hCA I, hCA II and h CA XII, where compound 4c elicited the most potent inhibitory activity against hCA I (K_I = 40.40 nM). It is noteworthy that the 3-bromo ethylbenzoate derivative 6d showed good to moderate activity against hCA I and hCA II.

Since the tested compounds were designed as modified derivatives of the lead compound SLC-0111, it deemed of interest to explore the impact of such modifications on the activity and selectivity of the targeted compounds. The results revealed a great increase in potency of the new compounds against hCA I and hCA II, especially compounds 4a–d, 12a and 12c compared to SLC-0111. On the other hand, there was much reduction in potency against hCA IX and hCA XII in all compounds. Therefore, it could be claimed that the modifications performed on the structure of SLC-0111 in the present investigation led to a switch in selectivity of the compounds to the non-cancer related isoforms hCA I and hCA II.

Conclusions

Twenty-one target compounds bearing a sulphamoyl, carboxylic or ethyl carboxylate substitutions and a diversely substituted phenyl tail moiety were designed as analogues of SLC-0111 and were synthesised through simple chemical procedures. All target compounds were assessed for their CA inhibitory activity against four relevant isoforms, namely hCA I, hCA II, hCA IX and hCA XII. The study revealed that the sulphamoyl group was the most efficient ZBG. Modifications of the substitution on the tail moiety had only a minor effect on activity and/or selectivity. Seven compounds 4a, 4b, 4c, 4d, 6d, 12a and 12c were selective against hCA I (Kis = 40.40–91.00 nM) compared to AAZ (Ki = 250.00 nM) which might present them as potential antiglaucoma drug candidates. Compounds bearing 4-acetamido-2-methoxy benzamido 12a or 2-methoxy- (4-methylbenzamido) 12c displayed superior activity (Kis= 67.60 and 91.00 nM) against hCAI more than that expressed by AAZ. Unlike SLC-0111, the targeted compounds were more selective to hCA I and hCA II rather than to hCA IX and hCA XII which would highlight these compounds as promising drug candidates for the treatment of glaucoma.

Materials and methods

Chemistry

General

All chemicals and solvents, which purchased and used without further purification. The melting points were measured using the SMP30 melting point apparatus. Thermo Scientific Nicolet iS10 spectrometer was used to record FT-IR spectra. ¹HNMR spectra were run on a Bruker 400 MHz spectrophotometer. ¹³CNMR spectra were recorded in δ scale given in ppm on a Bruker 101 MHz spectrophotometer. Both types of spectra were performed in DMSO-d_6. Elemental analyses were performed on a Thermo Scientific Flash 2000 elemental analyser at the Regional Center for Mycology and Biotechnology, Al-Azhar University, Egypt. All reactions were monitored by silica gel 60 F254 TLC and visualised under UV light (254 nm). Compounds 2a–d²⁴, 3a–d²⁵, 4a,b²⁶, 5a,b,d, 6a^27–29, 9a–c²⁴, 10a–c²⁵, 11a–c²⁶ were prepared according to the reported procedures.

General procedure for the preparation of target compounds 4a–d, 5a–d, 6a–d, 12a–c, 13a–c and 14a–c

The freshly prepared benzoyl isothiocyanate derivative 3a–d or 11a–c (1 mmol) was treated with sulphanilamide, 4-aminobenzoic acid or ethyl 4-aminobenzoate (1 mmol) in refluxing anhydrous acetone (10 ml) for 2–3 h. The reaction mixture was cooled to room temperature and the formed precipitate was collected by filtration and recrystallized from ethanol to give the final target compounds in high yields²⁸.

N-[(4-Sulphamoylphenyl)carbamothioyl]benzamide (4a)

Yellow crystals, (yield: 85%), m.p. 237–242 °C³⁰.

4-Chloro-N-[(4-sulfamoylphenyl)carbamothioyl]benzamide (4b)

Yellow crystals, (yield: 76%), m.p. 226–234 °C³⁰.

3,4-Dichloro-N-[(4-sulphamoylphenyl)carbamothioyl]benzamide (4c)

Yellow crystals, (yield: 75%), m.p. 206–208 °C; IR (KBr, ν_max/cm⁻¹): 3360, 3255 (NHs), 1670 (C=O), 1531 (C=S), 1327, 1157 (SO₂); ¹H NMR (DMSO-d6) δ ppm: 7.41 (s, 2H, NH_2, D₂O exchangeable), 7.82 (d, 1H, J = 8.4 Hz, Ar-H), 7.85–7.94 (m, 5H, Ar-H), 8.25 (d, 1H, J = 2.0 Hz, Ar-H), 11.89 (s, 1H, NH, D₂O exchangeable), 12.53 (s, 1H, NH, D₂O exchangeable); MS (m/z): 404.20 [M]⁺, 406.47 [M + 2]⁺; Anal. Calcd. for C₁₄H₁₁Cl₂N₃O₃S₂ (404.28): C, 41.59; H, 2.74; N, 10.39; Found C, 41.78; H, 2.95; N, 10.57.

4-Bromo-N-[(4-sulfamoylphenyl)carbamothioyl]benzamide (4d)

Yellow crystals, (yield: 75%), m.p. 215–217 °C; IR (KBr, ν_max/cm⁻¹): 3350–3245 (NHs), 1665 (C = O), 1520 (C = S), 1330, 1160 (SO₂); ¹H NMR δ ppm: 7.43 (s, 2H, NH_2, D₂O exchangeable), 7.63 (d, 2H, J = 8.6 Hz, Ar-H), 7.83–7.87 (m, 4H, Ar-H), 8.02 (d, 2H, J = 8.6 Hz, Ar-H), 11.83 (s, 1H, NH, D₂O exchangeable), 12.63 (s, 1H, NH, D₂O exchangeable); Anal. Calcd. for C₁₄H₁₂BrN₃O₃S₂ (414.29): C, 40.59; H, 2.92; N, 10.14; Found C, 40.47; H, 2.67; N, 10.03.

4-(3-Benzoylthioureido)benzoic acid (5a)

Yellow crystals, (yield: 75%), m.p. 212–224 °C³¹.

4-[3-(4-Chlorobenzoyl)thioureido]benzoic acid (5b)

Yellow crystals, (yield: 72%), m.p. 232–240 °C³¹.

4-[3-(3,4-Dichlorobenzoyl)thioureido]benzoic acid (5c)

Yellow crystals, (yield: 67%), m.p. 216–218 °C; IR (KBr, ν_max/cm⁻¹): 3402 (OH), 3290 (br, NHs), 1678, 1654 (C = O), 1523 (C = S); ¹H NMR δ ppm: 7.84–7.89 (m, 2H, Ar-H), 7.90–7.98 (m, 4H, Ar-H), 8.26 (s, 1H, Ar-H), 11.91 (s, 1H, NH, D₂O exchangeable), 12.56 (s, 1H, NH, D₂O exchangeable), 12.97 (s, 1H, OH, D₂O exchangeable); Anal. Calcd. for C₁₅H₁₀Cl₂N₂O₃S (369.22): C, 48.80; H, 2.73; N, 7.59; Found C, 49.07; H, 2.89; N, 7.80.

4-[3-(4-Bromobenzoyl)thioureido]benzoic acid (5d)

Yellow crystals, (yield: 60%), m.p. 206–215 °C³¹.

Ethyl-4-(3-benzoylthioureido)benzoate (6a)

Yellow crystals, (yield: 67%), m.p. 223–235 °C³².

Ethyl 4-[3-(4-chlorobenzoyl)thioureido]benzoate (6b)

Yellow crystals, (yield: 75%), m.p. 219–221 °C; IR (KBr, ν_max/cm⁻¹): 3350–3360 (NHs), 1740, (C = O) ester, 1665, (C = O) amide, 1535 (C = S); ¹H NMR δ ppm: 1.42 (t, 3H, J = 1.6 Hz, CH₃), 4.33 (q, 2H, J = 6.0 Hz, CH₂), 7.29–7.36 (m, 4H, Ar-H), 7.94–8.00 (m, 4H, Ar-H), 8.97 (s, 2H, 2NH, D₂O exchangeable); ¹³C NMR δ ppm: 14.6, 61.3, 110.3, 129.4, 129.7, 130.02, 130.08, 131.3, 142.9, 145.9, 165.7, 176.4; Anal. Calcd. for C₁₇H₁₅ClN₂O₃S (362.83): C, 56.28; H, 4.17; N, 7.72; Found C, 56.43; H, 4.28; N, 7.94.

Ethyl 4-[3-(3,4-dichlorobenzoyl)thioureido]benzoate (6c)

Yellow crystals, (yield: 67%), m.p. 216–218 °C; IR (KBr, ν_max/cm⁻¹): 3186 (NHs), 1712, 1693 (C = O), 1535 (C = S); ¹H NMR δ ppm: 1.33 (t, 3H, J = 7.1 Hz, CH₃), 4.33 (q, 2H, J = 10.0 Hz, CH₂), 7.34 (d, 2H, J = 8.4 Hz, Ar-H), 7.48 (d, 2H, J = 8.6 Hz, Ar-H), 7.90–8.02 (m, 4H, Ar-H), 8.95 (s, 1H, Ar-H), 11.87 (s, 1H, NH, D₂O exchangeable), 12.58 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: 14.6, 61.2, 110.3, 124.0, 129.4, 129.7, 130.2, 131.7, 133.0, 136.3, 142.6, 145.9, 165.7, 176.4, 179.2; MS (m/z): 397.27 [M]⁺, 396.68 [M]⁺, 399.34 [M + 2]⁺; Anal. Calcd. for C₁₇H₁₄Cl₂N₂O₃S (397.27): C, 51.40; H, 3.55; N, 7.05; Found C, 51.67; H, 3.62; N, 7.19.

Ethyl-4-[3-(4-bromobenzoyl)thioureido]benzoate (6d)

Yellow crystals, (yield: 75%), m.p. 218–220 °C; IR (KBr, ν_max/cm⁻¹): 3360–3380 (NHs), 1745, (C = O) ester, 1660, (C = O) amide, 1535 (C = S); ¹H NMR δ ppm: 1.33 (t, 3H, J = 7.0 Hz, CH₃), 4.32 (q, 2H, J = 7.0 Hz, CH₂), 7.76 (d, 2H, J = 8.5 Hz, Ar-H), 7.91 (d, 4H, J = 8.6 Hz, Ar-H), 8.00 (d, 2H, J = 8.6 Hz, Ar-H), 11.77 (s, 1H, NH, D₂O exchangeable), 12.69 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: 14.6, 61.2, 123.9, 127.5, 127.6, 130.2, 131.2, 131.7, 131.9, 142.6, 165.5, 167.7, 179.3; Anal. Calcd. for C₁₇H₁₅BrN₂O₃S (407.28): C, 50.13; H, 3.71; N, 6.88; Found C, 50.39; H, 3.85; N, 7.12.

4-Acetamido-2-methoxy-N-[(4-sulfamoylphenyl)carbamothioyl]benzamide (12a)

Yellow crystals, (yield: 75%), m.p. 225–227 °C; IR (KBr, ν_max/cm⁻¹): 3340, 3302 (NHs), 1697, 1666 (C = O), 1519 (C = S), 1338, 1157 (SO₂); ¹H NMR δ ppm: 2.11 (s, 3H, CH₃), 3.90 (s, 3H, OCH₃), 7.35 (d, J = 8, 1H, Ar-H), 7.41 (s, 2H, NH_2,D₂O exchangeable), 7.65–7.87 (m, 3H, Ar-H), 7.95–7.98 (m, 3H, Ar-H), 10.41 (s, 1H, NH, D₂O exchangeable), 11.12 (s, 1H, NH, D₂O exchangeable), 12.78 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: 24.7, 57.0, 102.5, 112.1, 113.2, 124.6, 126.7, 133.0, 141.1, 141.8, 146.3, 159.0, 164.8, 169.8; MS (m/z): 422.66 [M]⁺; Anal. Calcd. for C₁₇H₁₈N₄O₅S₂ (422.47): C, 48.33; H, 4.29; N, 13.26; Found C, 48.61; H, 4.45; N, 13.50.

4-Isobutyramido-2-methoxy-N-[(4-sulfamoylphenyl)carbamothioyl] benzamide (12b)

White crystals, (yield: 79%), m.p. 248–250 °C; IR (KBr, ν_max/cm⁻¹): 3300–3310 (NHs), 1710, 1690, (C = O) amide, 1520 (C = S), 1336, 1135 (SO₂); ¹H NMR δ ppm: 1.13 (d, 6H, J = 6.8 Hz,-CH(CH₃)₂), 2.61–2.68 (m, 1H, -CH(CH₃)₂), 4.01 (s, 3H, OCH₃), 7.36 (d, 1H, J = 7.1 Hz, Ar-H), 7.40 (s, 2H, NH₂, D₂O exchangeable), 7.73 (s, 1H, Ar-H), 7.86 (d, 2H, J = 8.6 Hz, Ar-H), 7.92–7.99 (m, 3H, Ar-H), 10.32 (s, 1H, NH, D₂O exchangeable), 11.11 (s, 1H, NH, D₂O exchangeable), 12.77 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: 19.7, 35.6, 57.0, 102.6, 112.2, 113.1, 124.6, 126.7, 133.0, 141.1, 141.9, 146.5, 159.0, 164.7, 176.6, 178.7; Anal. Calcd. for C₁₉H₂₂N₄O₅S₂ (450.53): C, 50.65; H, 4.92; N, 12.44; Found C, 50.89; H, 4.81; N, 12.67.

2-Methoxy-4-(4-methylbenzamido)-N-[(4-sulfamoylphenyl)carbamothioyl] benzamide (12c)

Yellow crystals, (yield: 82%), m.p. 250–252 °C; IR (KBr, ν_max/cm⁻¹): 3350–3205 (NHs), 1680, 1650, (C = O) amide, 1530 (C = S), 1320, 1154 (SO₂); ¹H NMR δ ppm: 2.40 (s, 3H, CH₃), 3.82 (s, 3H, OCH₃), 7.27 (s, 2H, NH_2, D₂O exchangeable), 7.36 (d, 2H, J = 7.9, Ar-H), 7.40 (d, 1H, J = 8.4, Ar-H), 7.46–7.50 (m, 1H, Ar-H), 7.69–7.72 (m, 1H, Ar-H), 7.80 (d, 2H, J = 8.8, Ar-H), 7.90 (d, 2H, J = 8.0, Ar-H), 7.96 (d, 2H, J = 8.6, Ar-H), 10.38 (s, 1H, NH, D₂O exchangeable), 10.48 (s, 2H, 2NH, D₂O exchangeable); Anal. Calcd. for C₂₃H₂₂N₄O₅S₂ (498.57): C, 55.41; H, 4.45; N, 11.24; Found C, 55.63; H, 4.61; N, 11.48.

4-[3-(4-Acetamido-2-methoxybenzoyl)thioureido]benzoic acid (13a)

Brown crystals, (yield: 82%), m.p. 245–247 °C; ¹H NMR δ ppm: 2.10 (s, 3H, CH₃), 4.00 (s, 3H, OCH₃), 7.34 (d, 1H, J = 7.1, Ar-H), 7.64 (s, 1H, Ar-H), 7.90–8.00 (m, 5H, Ar-H), 10.42 (s, 1H, NH, D₂O exchangeable), 11.11 (s, 1H, NH, D₂O exchangeable), 12.85 (s, 1H, NH, D₂O exchangeable), 13.05 (s, 1H, OH, D₂O exchangeable). ¹³C NMR δ ppm: 24.7, 57.0, 102.5, 112.0, 113.1, 123.7, 128.6, 130.4, 131.5, 133.0, 142.1, 146.3, 159.0, 164.8, 167.1, 169.8, 178.2; Anal. Calcd. for C₁₈H₁₇N₃O₅S (387.41): C, 55.81; H, 4.42; N, 10.85; Found C, 56.08; H, 4.56; N, 11.07.

4-[3-(4-Isobutyramido-2-methoxybenzoyl)thioureid])benzoic acid (13b)

Brown crystals, (yield: 76%), m.p. 256–258 °C; IR (KBr, ν_max/cm⁻¹): 3313 (br NHs, OH), 1689, 1670 (C = O), 1516 (C = S); ¹H NMR δ ppm: 1.12 (d, 6H, J = 6.8 Hz, CH(CH₃)₂), 2.60–2.67 (m, 1H, CH(CH₃)₂), 4.00 (s, 3H, OCH₃), 7.35 (d, 1H, J = 7.5 Hz, Ar-H), 7.72 (s, 1H, Ar-H), 7.92 (t, 3H, J = 8.2 Hz, Ar-H), 7.97 (t, 2H, J = 6.7 Hz, Ar-H), 10.30 (s, 1H, NH, D₂O exchangeable), 11.09 (s, 1H, NH, D₂O exchangeable), 12.86 (s, 1H, NH, D₂O exchangeable), 12.97 (s, 1H, OH, D₂O exchangeable). ¹³C NMR δ ppm: 19.7, 35.6, 56.9, 102.5, 112.1, 112.7, 123.4, 128.5, 130.4, 133.0, 142.0, 146.6, 158.9, 164.6, 167.1, 176.6, 178.1; MS (m/z): 416.32 [M + 1]⁺; Anal. Calcd. For C₂₀H₂₁N₃O₅S (415.46): C, 57.82; H, 5.10; N, 10.11; Found C, 57.95; H, 5.23; N, 10.40.

4-(3-(2-Methoxy-4-(4-methylbenzamido)benzoyl)thioureido]benzoic acid (13c)

Yellow crystals, (yield: 78%), m.p. 281–283 °C; IR (KBr, ν_max/cm⁻¹): 3353 (NHs), 3286 (OH) acide, 1687 (C = O) acide, 1670, 1650 (C = O) amide, 1553 (C = S); ¹H NMR δ ppm: 2.09 (s, 3H, CH₃), 4.05 (s, 3H, OCH₃), 7.36 (d, 2H, J = 10.0 Hz, Ar-H), 7.67–7.95 (m, 7H, Ar-H), 8.00 (d, 2H, J = 8.6 Hz, Ar-H), 10.46 (s, 1H, NH, D₂O exchangeable), 10.85 (s, 1H, NH, D₂O exchangeable), 11.15 (s, 1H, NH, D₂O exchangeable), 12.80 (s, 1H, OH, D₂O exchangeable). ¹³C NMR δ ppm: 21.5, 57.1, 113.6, 119.9, 123.7, 125.8, 128.6, 129.4, 129.5, 130.4, 130.6, 132.1, 142.4, 143.8, 146.4, 158.8, 164.8, 166.2, 167.4, 178.3; Anal. Calcd. for C₂₄H₂₁N₃O₅S (463.51): C, 62.19; H, 4.57; N, 9.07; Found C, 61.97; H, 4.73; N, 9.34.

Ethyl-4-[3-(4-acetamido-2-methoxybenzoyl)thioureido]benzoate (14a)

Brown crystals, (yield: 68%), m.p. 237–239 °C; IR (KBr, ν_max/cm⁻¹): 3487, 3205 (NHs), 1700 (C = O) ester, 1675, 1635 (C = O) amide, 1531 (C = S); ¹H NMR δ ppm: 1.32 (t, 3H, J = 7.1 Hz, CH₂CH₃), 2.09 (s, 3H, CH₃), 4.01 (s, 3H, OCH₃), 4.33 (q, 2H, J = 7.1 Hz, CH₂CH₃), 7.34 (d, 1H, J = 8.6, Ar-H), 7.65 (s, 1H, Ar-H), 7.96 (d, J = 8.5 Hz, 3H, Ar-H), 7.98–8.02 (m, 2H, Ar-H), 10.42 (s, 1H, NH, D₂O exchangeable), 11.12 (s, 1H, NH, D₂O exchangeable), 12.88 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: δ 14.6, 24.7, 57.0, 61.2, 102.5, 112.0, 113.1, 123.8, 127.6, 130.2, 133.0, 142.4, 146.3, 159.0, 164.8, 165.5, 169.8, 178.3; Anal. Calcd. for C₂₀H₂₁N₃O₅S (415.46): C, 57.82; H, 5.10; N, 10.11; Found C, 58.04; H, 5.19; N, 10.37.

Ethyl-4-[3-(4-isobutyramido-2-methoxybenzoyl)thioureido]benzoate (14b)

White crystals, (yield: 75%), m.p. 245–247 °C; IR (KBr, ν_max/cm⁻¹): 3302, 3186 (NHs), 1712, 1693,1666 (C = O), 1512 (C = S); ¹H NMR δ ppm: 1.13 (d, J = 6.8 Hz, 6H, CH(CH₃)₂), 1.33 (t, 3H, J = 7.1 Hz, -CH₂CH₃), 2.58–2.67 (m, 1H, CH(CH₃)₂), 4.01 (s, 3H, OCH₃), 4.32 (q, 2H, J = 4.1 Hz, -CH₂CH₃), 7.33–7.37 (m, 2H, Ar-H), 7.73 (s, 1H, Ar-H), 7.93–8.01 (m, 4H, Ar-H), 10.31 (s, 1H, NH, D₂O exchangeable), 11.10 (s, 1H, NH, D₂O exchangeable), 12.88 (s, 1H, NH, D₂O exchangeable); ¹³C NMR δ ppm: 14.6, 19.7, 31.0, 57.0, 61.3, 102.6, 110.7, 112.2, 123.6, 127.6, 129.4, 133.0, 142.4, 146.5, 159.0, 164.7, 165.5, 165.7, 178.2. MS (m/z): 444.25 [M + 1]⁺; Anal. Calcd. for C₂₂H₂₅N₃O₅S (443.52): C, 59.58; H, 5.68; N, 9.47; Found C, 59.79; H, 5.80; N, 9.71.

Ethyl-4-[3-(2-methoxy-4-(4-methylbenzamido)benzoyl)thioureido]benzoate (14c)

White crystals, (yield: 80%), m.p. 257–259 °C; IR (KBr, ν_max/cm⁻¹): 3205 (br, NHs), 1712 1693,1633 (C = O), 1531 (C = S); ¹H NMR δ ppm: 1.43 (t, 3H, J = 6.3 Hz, CH₂CH₃), 2.44 (s, 3H, CH₃), 4.02 (s, 3H, OCH₃), 4.46 (q, 2H, J = 7.0 Hz, -CH₂CH₃), 7.38 (s, 1H, Ar-H), 7.55 (d, J = 7.9 Hz, 2H, Ar-H), 7.71 (d, J = 7.4 Hz, 1H, Ar-H), 8.01–8.08 (m, 7H, Ar-H), 10.57 (s, 1H, s, 1H, NH. D₂O exchangeable), 11.82 (s, 1H, NH, D₂O exchangeable), 12.90 (s, 1H, NH, D₂O exchangeable); Anal. Calcd. for C₂₆H₂₅N₃O₅S (491.56): C, 63.53; H, 5.13; N, 8.55; Found C, 63.39; H, 5.31; N, 8.79.

Biological evaluation

Carbonic anhydrase inhibitory activity

A stopped flow CO₂ hydrase assay was adopted using an SX.18 MV-R Applied Photophysics (Oxford, UK) stopped-flow instrument to assess the inhibition against the various CA isozymes³³. Phenol red(at a concentration of 0.2 mM has been used as an indicator, working at the absorbance maximum of 557 nm, with 20 Mm Hepes (pH 7.5) as buffer, and 20 mM Na₂SO_4. The initial rates of the CA-catalysed CO₂ hydration reaction was run for a period of 10–100 s then completing as the reported protocol. The inhibition constants were obtained by non-linear least-squares methods using PRISM 3 and the Cheng–Prusoff equation, and represent the mean for at least three different determinations^34–36. All CA isofoms were recombinant ones obtained in-house as previously reported^37–42.

Disclosure statement

C. T. Supuran is Editor-in-Chief of the Journal of Enzyme Inhibition and Medicinal Chemistry and he was not involved in the assessment, peer review, or decision-making process of this paper. The authors have no relevant affiliations of financial involvement with any organisation or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript.

Additional information

Funding

This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties. C. T. Supuran and D. Vullo thank the Italian Ministry for University and Research (MIUR), for the project FISR2019_04819 BacCAD with which this research was funded.