Digalloyl Glycoside: A Potential Inhibitor of Trypanosomal PFK

Digalloyl Glycoside: A Potential Inhibitor of Trypanosomal PFK: Comparison

Please note this is a comparison between Version 1 by Elham Amin and Version 2 by Vivi Li.

Human African trypanosomiasis is an endemic infectious disease caused by Trypanosoma brucei via the bite of tsetse-fly. Most of the drugs used for the treatment, e.g., Suramin, have shown several problems, including the high level of toxicity. A In our previous study on the anti-trypanosomal potential of Euphorbia species, Euphorbia abyssinica displayed significant anti-trypanosomal activity. Therefore, a phytochemical investigation of the methanolic extract of E. abyssinica was carried out. Twelve compounds, including two triterpenes (1, 2); one sterol-glucoside (4); three ellagic acid derivatives (3, 9, 11); three gallic acid derivatives (5, 6, 10); and three flavonoids (7, 8, 12), were isolated. Compound (10) was obtained for the first time from genus Euphorbia while all other compounds except compound (4), were firstly reported in E. abyssinica. Consequently, an in silico study was used to estimate the anti-trypanosomal activity of the isolated compounds. Several compounds displayed interesting activity where 1,6-di-O-galloyl-d-glucose (10) appeared as the most potent inhibitor of trypanosomal phosphofructokinase (PFK). Moreover, molecular dynamics (MD) simulations and ADMET calculations were performed for 1,6-di-O-galloyl-d-glucose. In conclusion, 1,6-di-O-galloyl-d-glucose revealed high binding free energy, desirable molecular dynamics, and pharmacokinetic properties; therefore, it could be suggested for further in vitro and in vivo studies for trypanosomiasis.

Trypanosoma brucei
Euphorbia abyssinica
in silico
6-di-O-galloyl-d-glucose
molecular dynamics
ADMET

1. Introduction

Trypanosoma brucei is the causative agent of human African trypanosomiasis (HAT), sleeping sickness, via the bite of the tsetse fly. One of the most druggable target enzymes for the treatment of HAT is the trypanosomal phosphofructokinase (PFK) enzyme ^[1]. Suramin, a classic PFK inhibitor, is known to exhibit significant side effects such as hypersensitivity, agranulocytosis, and nephrotoxicity ^[2].

E. abyssinica J.F. Gmel latex was reported to yield ingenol esters and lathyrane derivatives as minor components besides euphol, euphorbol, lupeol, oleanolic acid, β-sitosterol, and β-sitosterol-3-O-glucoside. Also, it has shown significant antifungal activity against Aspergillus flavus, Aspergillus niger, and Candida albicans ^[3]. Furthermore, E. abyssinica has exhibited cytotoxic activity against Caco2 (IC₅₀ 11.3 µg/mL) ^[4]. Moreover, the root of E. abyssinica has shown potent chemosuppressive antimalarial activity against Plasmodium berghei infection in mice ^[5].

Recently, molecular docking is important in the estimation of the bioactivity of chemical compounds against a target and has shown great progress ^[6]. The evaluation of drug design depends on the identification and characterization of small-molecule binding sites on the target proteins ^[7].

In our previous research, the anti-trypanosomal activity of the methanolic extract of E. abyssinica against T. brucei brucei strain TC221 was investigated, and IC₅₀ values were determined as 17.3 and 19.4 μg/mL after 48 and 72 h incubation, respectively ^[8]. Consequently, the current study discusses the molecular modeling study of the compounds isolated from E. abyssinica J.F. Gmel. against the target proteins (PFK) of T. brucei. Furthermore, the molecular dynamics and pharmacokinetic properties of the most active compound are also presented in order to conclude the compound activity.

2. Investigation of Methylene Chloride Fraction of E. abyssinica J.F. Gmel

Chromatographic investigation of methylene chloride fraction led to isolation of four compounds. The structure of the isolated compounds was elucidated using 1D NMR and LC-HRMS. Compound (1): White needle powder (15 mg), m.p. 208–212 °C, gave a positive Libermann–Burchard’s test indicating its steroidal or triterpenoidal nature. LC-HRMS [M + H]⁺ m/z: 427.3931, R_t: 26.12 calculated for C₃₀H₅₀O. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CD₃OD.

Compound (2): White crystal powder (25 mg), m.p. 282–285 °C, gave a positive Libermann–Burchard’s test indicating its steroidal or triterpenoidal nature. LC-HRMS [M + H]⁻ m/z: 425.3859, R_t: 28.97 calculated for C₃₀H₅₀O. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CDCl_3.

Compound (3): Yellowish white amorphous powder (50 mg), m.p. 289–291 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁺ m/z: 345.0602, R_t: 16.99 calculated for C₁₇H₁₂O₈. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in DMSO-d6_.

Compound (4): White amorphous powder (24 mg), m.p. 290 °C; the color of the spot was invisible in TLC and under UV but after spraying with p-anisaldehyde, it was violet. It gave a positive Libermann–Burchard’s test indicating its steroidal or triterpenoidal nature and gave a positive with Molish’s test indicating its glycosidic nature. LC-HRMS [M + H]⁻ m/z: 575.3155, R_t: 25.82 calculated for C₃₅H₆₀O₆. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in DMSO-d6_.

3. Investigation of Ethyl Acetate Fraction of E. abyssinica J.F. Gmel

Chromatographic investigation of ethyl acetate fraction led to the isolation of seven compounds. The structure of the isolated compounds was elucidated using 1D, 2D NMR, and LC-HRMS. Compound (5): White crystalline powder (17 mg), m.p. 198–200 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁻ m/z: 183.0301, R_t: 8.37 calculated for C₈H₈O₅. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in (CD₃OD).

Compound (6): White crystalline powder (14 mg), m.p. 258–263 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁻ m/z: 169.0143, R_t: 5.01 calculated for C₇H₆O₅. ¹H-NMR (400 MHz) in CD₃OD and DEPT-Q NMR (100 MHz) in (CD₃OD).

Compound (7): Yellow powder (10 mg), m.p. 172–174 °C, LC-HRMS [M + H]⁺ m/z: 433.1125, R_t: 12.70 calculated for C₂₁H₂₀O₁₀. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CD₃OD.

Compound (8): Yellow amorphous powder (12 mg), m.p. 179–183 °C, LC-HRMS [M + H]⁺ m/z: 449.1074, R_t: 11.87 calculated for C₂₁H₂₀O₁₁. TLC investigation revealed an orange spot while it showed a deep purple spot under UV light, which became yellow–green when fumed with ammonia vapor but showed dark orange color with p-anisaldehde indicating its flavonoid-3-O-substituted nature. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CD₃OD.

Compound (9): Yellowish white amorphous powder (25 mg), m.p. 297 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁺ m/z: 493.0970, R_t: 9.57 calculated for C₂₂H₂₀O₁₃. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in DMSO-d_6.

Compound (10): Off-white amorphous powder (16 mg), m.p. 180–182 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁺ m/z: 485.0921, R_t: 8.29 calculated for C₂₀H₂₀O₁₄. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CD₃OD.

Compound (11): Yellowish white amorphous powder (45 mg), m.p. 267–268 °C, produced a positive reaction to FeCl₃ reagent. LC-HRMS [M + H]⁺ m/z: 653.1704, R_t: 11.93 calculated for C₂₉H₃₂O₁₇. ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in DMSO-d₆.

4. Investigation of n-Butanol Fraction of E. abyssinica J.F. Gmel

Chromatographic investigation of n-butanol fraction led to the isolation of one compound. The structure of the isolated compound was elucidated using ¹H-NMR, and LC-HRMS. Compound (12): Yellow amorphous powder (6 mg), m.p. 320–330 °C. UV λ_max (MeOH) nm: 225, 258, 347.5, (AlCl₃) 272.5, 297, 331, 421. LC-HRMS [M + H]⁺ m/z: 449.1074, R_t: 11.87 calculated for (C₂₁H₂₀O₁₁). ¹H-NMR (400 MHz) and DEPT-Q NMR (100 MHz) in CD₃OD. All isolated compounds are represented in (Figure 1).

Figure 1.

Structure of the isolated compounds from

E. abyssinica

5. Docking Study for Anti-Trypanosomal Activity

The results of docking procedures contained binding free energies Kcal/mol, binding affinity constant (ki in nm), distances (in Å) from the main residues, and type of interactions. Notably compounds 10, 7, 11, 8, and 12 in order, showed good binding affinity energies (from −18.9900 to −23.0767 Kcal/mol) when compared to the co-docked ligand suramin as a positive control (Figure 2). The main residues involved in the interaction between compounds and T. brucei PFK enzyme were Arg173, Ser341, Asn343, Lys226, Thr201, and Gly107 residues as well as Mg Atom (MG1002) that mark them as good candidates for T. brucei PFK inhibition, that could be used for the treatment of trypanosomiasis. Hydrogen acceptor and metal interactions were found to be the main formed interactions between compounds and the enzyme. 3D figures of the most active compounds via PyMOL 2.4 software were represented in (Figure 3).

Figure 2. Binding free energy score of the most active isolated compounds and suramin with T. brucei PFK enzyme (PDB ID:3F5M).

Figure 3.

3D interaction caption of the top docking pose of the most active isolated compounds.

6. Molecular Dynamics Simulations

With the aim of proofing the reliability of molecular docking results, further computational validation was achieved through a number of MDS experiments and binding free energy (ΔG) calculations on compound 10 (1,6-di-O-galloyl-d-glucose), as well as suramin. As seen in Figure 4, compound 10 was able to achieve stable binding inside the enzyme′s (i.e., phosphofructokinase, PDB ID:3F5M) active site with an average RMSD from the initial docking pose of 3.1 Å; however, it showed higher fluctuation in comparison with the standard drug suramin. Accordingly, it obtained a binding free energy value (ΔG) of −7.1 kcal/mol (ΔG of suramin was −8.8 kcal/mol).

Figure 4. The RMSD curve from the molecular dynamics simulations of compound 10. The X-axis represents the simulation time (in ps), while the y-axis represents the RMSD value (in nm).

7. Prediction of the Pharmacokinetic Properties and Toxicological Properties Using ADMET

After the molecular docking studies of 12 isolated compounds, the absorption, distribution, metabolism, elimination, and toxicity (ADMET) of the best dock scored compound along with suramin were evaluated (Table 1).

Table 1.

ADMET properties of compound

and suramin.

Properties		Compound 10	Suramin
Absorption	Caco-2 permeability (log Papp in 10⁻⁶ cm/s)	−1.682	−3.097
	HIA (% Absorbed)	15.64%	0
	P-glycoprotein substrate	Yes	Non
	P-glycoprotein I inhibitor	Non	Non
	P-glycoprotein II inhibitor	Non	Non
	Pure water solubility (log mol/L)	−2.895	−2.892
	Skin Permeability (log Kp)	−2.735	−2.735
Distribution	BBB Permeability (log BB)	−2.435	−4.438
	CNS permeability (log PS)	−4.668	−4.991
	VDss human (log L/kg)	1.614	−0.007
	Fraction unbound human (Fu)	0.347	0.379
Metabolism	CYP 2C19 inhibitor	Non	Non
	CYP 2C9 inhibitor	Non	Non
	CYP 2D6 inhibitor	Non	Non
	CYP 2D6 substrate	Non	Non
	CYP 3A4 inhibitor	Non	Non
	CYP 3A4 substrate	Non	Non
	CYP 1A2 inhibitor	Non	Non
Excretion	Total Clearance (log mL/min/kg)	0.47	−4.065
Excretion	Renal OCT2 substrate	Non	Non
Toxicity	Ames test	non-mutagen	non-mutagen
	Max. tolerated dose human (log mg/kg/day)	0.49	0.438
	Oral Rat Acute Toxicity LD₅₀ (mol/kg)	2.515	2.482
	Oral Rat Chronic Toxicity LOAEL (log mg/kg-bw/day)	3.491	6.817
	hERG I inhibitor	Non	Non
	hERG II inhibitor	Yes	Yes
	T. pyriformis toxicity (log μg/L)	0.285	0.285
	minnow toxicity (log mM)	5.837	6.162

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