PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF DISEASES CAUSED BY SARS-COV-2

Abstract

The present invention relates to a pharmaceutical composition for preventing or treating COVID-19 diseases, comprising an organic solvent extract of Justicia procumbens as an effective ingredient, a pharmaceutical composition for preventing or treating COVID-19 diseases, comprising justicidin-A as an effective ingredient, a pharmaceutical composition for preventing or treating COVID-19 diseases, comprising justicidin-B as an effective ingredient, or a pharmaceutical composition for preventing or treating COVID-19 diseases, comprising 6′ hydroxyl justicidin-B as an effective ingredient, and a food composition thereof for preventing or ameliorating COVID-19 diseases. According to the present invention, an anhydrous ethanol extract of Justicia procumbens, justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B effectively inhibit SARS-CoV-2 virus, and thus may effectively prevent, treat, or ameliorate diseases caused by SARS-CoV-2 virus.

Claims

1. A method for preventing, ameliorating or treating diseases caused by SARS-CoV-2, comprising administering a pharmaceutical composition comprising an organic solvent extract of Justicia procumbens into a subject in need thereof.

2. The method according to claim 1, wherein the organic solvent is an alcohol having 1 or more and 4 or less carbon atoms.

3. The method according to claim 1, wherein the organic solvent is at least one selected from methanol, ethanol, isopropanol, butanol, hexane, ethyl acetate, dichloromethane, ether, chloroform, and acetone.

4. The method according to claim 1, wherein the organic solvent is anhydrous ethanol.

5. The method according to claim 1, wherein the disease caused by said SARS-CoV-2 comprises coronavirus disease-19.

6. The method according to claim 5, wherein a symptom of the coronavirus disease-19 is at least one of fever, feebleness, cough, dyspnea, pneumonia, phlegm, sore throat, headache, hemoptysis, nausea, and diarrhea.

7. The method according to claim 1, wherein the disease caused by said SARS-CoV-2 is a respiratory disease.

8. The method according to claim 7, wherein the respiratory disease is pneumonia.

9. A method for preventing, ameliorating or treating diseases caused by SARS-CoV-2, comprising administering a pharmaceutical composition comprising justicidin-A into a subject in need thereof.

10. A method for preventing, ameliorating or treating diseases caused by SARS-CoV-2, comprising administering a pharmaceutical composition comprising justicidin-B into a subject in need thereof.

11. A method for preventing, ameliorating or treating diseases caused by SARS-CoV-2, comprising administering a pharmaceutical composition comprising 6′ hydroxyl justicidin-B into a subject in need thereof.

12. A method for preventing, ameliorating or treating diseases caused by SARS-CoV-2, comprising administering a pharmaceutical composition comprising an extract of Justicia procumbens into a subject in need thereof.

13. An anti-viral method against SARS-CoV-2, comprising administering a composition comprising justicidin-A into a subject in need thereof.

14. An anti-viral method against SARS-CoV-2, comprising administering a composition comprising justicidin-B into a subject in need thereof.

15. An anti-viral method against SARS-CoV-2, comprising administering a composition comprising 6′ hydroxyl Justicidin-B into a subject in need thereof.

16-35. (canceled)

Description

DESCRIPTION OF DRAWINGS

[0047] FIG. 1 shows a chemical structure of justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B according to the present invention.

[0048] FIG. 2 shows a position of justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B from the HPLC results of the anhydrous ethanol extract of Justicia procumbens according to the present invention.

[0049] FIG. 3 shows a SARS-CoV-2 virus inhibitory effect and cell viability of Justicia procumbens anhydrous ethanol extract, justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B according to the present invention.

MODE FOR INVENTION

[0050] Hereinafter, the present invention will be described in detail through preferred Preparing Examples, Examples, and Formulation Examples for better understanding of the present invention. However, the following Preparing Examples, Examples, and Formulation Examples are provided only for the purpose of illustrating the present invention, and thus the present invention is not limited thereto.

PREPARING EXAMPLE 1

Preparation of Anhydrous Ethanol Extract of Justicia procumbens

[0051] An anhydrous ethanol extract of Justicia procumbens used in an experiment was prepared by using Justicia procumbens (voucher specimen No: NIBRVP0000642884 in 2017) which was cultivated and collected in Jecheon, Chungbuk, and of which origin of the plant has been identified by the National Institute of Biological Resources, Ministry of Environment, Korea.

[0052] The dried Justicia procumbens was regularly cut, after which anhydrous ethanol was added 10 times the amount of the Justicia procumbens, immersed and extracted at room temperature for 24 hours, filtered to prepare a first extract, and then concentrated under reduced pressure. Then, anhydrous ethanol was added again eight times the amount of the Justicia procumbens, immersed and extracted again at room temperature for 24 hours, filtered to prepare a second extract, and then concentrated under reduced pressure. The resulting concentrates were combined to prepare an anhydrous ethanol extract of Justicia procumbens having a final solid content by about 10%, and then colloidal silicon dioxide was uniformly mixed so as to be 1:1 compared to the solid content of the extract. The resulting mixture was dried under reduced pressure at 60° C., and then uniformly pulverized to prepare a final anhydrous ethanol extract of Justicia procumbens in powder form.

Preparing Example 2

Preparation of Justicidin-A Through an Organic Synthesis Method

[0053] Justicidin-A (9-benzo[1,3]dioxol-5-yl-4,6,7-trimethoxy-3H -naphtho[2,3-c]furan-1-one) was prepared through a previously known method (Gunaganti Naresh, et al., 2015) and identified as follows.

[0054] .sup.1H-NMR (CDCl.sub.3, 500 MHz) δ 7.54(s, 1H), 7.06(s, 1H), 6.95(d, 1H, J=7.9 Hz), 6.82(d, 1H, J=1.5 Hz), 6.79(dd, 1H, J=1.6, 7.875 Hz), 6.04, 6.08(dd, 2H, J=1.45, 22.775 Hz), 5.54(s, 2H), 4.13(s, 3H), 4.07(s, 3H), 3.80(s, 3H). 13C-NMR (CDCl.sub.3, 125 MHz) δ 169.6, 151.7, 150.4, 147.9, 147.6, .sup.147.5, 134.5, 130.7, 128.6, 126.1, 124.6, 123.7, 119.4, 110.9, 108.3, 106.2, 101.3, 100.7, 66.7, 59.7, 56.2, 55.9. The purity of Justicidin-A was 99.52%.

PREPARING EXAMPLE 3

Preparation of Justicidin-B Through an Organic Synthesis Method

[0055] Justicidin-B (9-benzo[1,3]dioxol-5-yl-6,7-dimethoxy-3H-naphtho[2,3-c]furan one) was prepared through a previously known method (David C. Harrowven, et al., 2001) and identified as follows.

[0056] .sup.1H-NMR (CDCl.sub.3, 500 MHz) δ 7.70(s, 1H), 7.18(s, 1H), 7.11(s, 1H), 6.97(d, 1H, J=7.7 Hz), 6.86(d, 1H, J=1.45 Hz), 6.83(dd, 1H, J=1.7, 8.025 Hz), 6.07(d, 2H, J=22.6 Hz), 5.37(s, 2H), 4.05(s, 3H), 3.81(s, 3H). 13C-NMR (CDCl.sub.3, 125 MHz) δ 170.0, 151.9, 150.2, 147.7, 147.6, 139.7, 139.6, 133.3, 128.9, 128.5, 123.6, 118.6, 118.4, 110.7, 108.3, 106.1, 105.9, 101.3, 68.1, 56.2, 55.9. The purity of Justicidin-B was 98.55%.

PREPARING EXAMPLE 4

Preparation of 6′ Hydroxyl Justicidin-B Through an Organic Synthesis Method

[0057] 6′ hydroxyl justicidin-B was synthesized through the following process.

##STR00001##

[0058] Process 1: 6,7-dimethoxy-3-oxo-1,3-dihydronaphtho[2,3-c]furan-4-yl trifluoromethanesulfonate (3.0 g, 7.65 mmol) was dissolved in dioxane solvent (90 ml), and then 5-methoxymethoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzo[1,3]dioxol (2.83 g, 9.18 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (1.12 g, 1.53 mmol), lithium hydroxide monohydrate (642 mg, 15.3 mmol) were subsequently added under a nitrogen atmosphere. A temperature was raised up to 60° C. and reacted for four hours. After cooling down to room temperature, water was added to terminate the reaction, and then an extraction was performed with dichloromethane. An organic layer was dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated. A residue was purified by silica gel column chromatography so as to obtain the title compound of 6,7-dimethoxy-9-(6-methoxymethoxy-benzo[1,3]dioxol-5-yl)-3H-naphtho[2,3-c]furan-1-one (9 g, 21.2 mmol).

[0059] .sup.1H NMR: (DMSO-d.sub.6, 400 MHz) 87.92 (s, 1H), 7.48 (s, 1H), 6.95 (s, 1H), 6.87 (s, 1H), 6.73 (s, 1H), 6.08 (d, 2H, J=2.8 Hz), 5.38-5.49 (m, 2H), 4.90 (d, 1H, J=6.8 Hz), 4.81 (d, 1H, J=6.8 Hz), 3.93 (s, 3H), 3.65 (s, 3H), 2.93 (s, 3H).

[0060] Process 2: 6,7-dimethoxy-9-(6-methoxymethoxy-benzo[1,3]dioxol-5-yl)-3H-naphtho[2,3-c]furan-1-one (8 g, 18.9 mmol) was dissolved in ethanol (80 ml), and 44 ml of 12M HCl was added dropwise thereto, and the above reacted at 50° C. for 12 hours. After the reaction was completed, 100 ml of water was added, and then an extraction was performed with dichloromethane (200 ml, 100 ml, 50 ml). An obtained organic layer was washed with water (150 ml) and brine (100 ml), dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated. A residue was purified by silica gel column chromatography so as to obtain the title compound of 9-(6-hydroxy-benzo[1,3]dioxol-5-yl)-6,7-dimethoxy-3H-naphtho[2,3-c]furan-1-one (6′-HJB, 5.20 g, 13.7 mmol, 72.5%). The purity of 6′ hydroxyl justicidin-B was 98.76%.

[0061] .sup.1H NMR: (DMSO-d.sub.6, 400 MHz) δ 9.01 (s, 1H), 7.88 (s, 1H), 7.46 (s, 1H), 6.95 (s, 1H), 6.63 (s, 1H), 6.57 (s, 1H), 6.00 (d, 2H, J=2.00 Hz), 5.41 (s, 2H), 3.93 (s, 3H), 3.66 (s, 3H).

[0062] A structure of justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B are shown in FIG. 1.

PREPARING EXAMPLE 5

Preparation of Hydrous Ethanol Extract and Organic Solvent Extract of Justicia procumbens

[0063] An anhydrous ethanol extract of Justicia procumbens used in an experiment was prepared by using Justicia procumbens (voucher specimen No: NIBRVP0000590019 in 2016) which was cultivated and collected in Jecheon, Chungbuk, and of which origin of the plant has been identified by the National Institute of Biological Resources, Ministry of Environment, Korea.

[0064] After the dried Justicia procumbens was regularly cut and pulverized, which 10 g thereof was accurately taken and subjected to an extraction twice (two hours for a first extraction and one hour for a second extraction) in an amount of 100 ml under refluxing with ethanol, 95% hydrous ethanol, 60% hydrous ethanol, 30% hydrous ethanol, water, butanol, acetone, ethyl acetate, hexane, isopropanol, methanol, and dichloromethane as a solvent at 80 to 90° C., filtered, and concentrated under reduced pressure so as to obtain 0.2 to 1.9 g of the title compound (See Table 1).

TABLE-US-00001 TABLE 1 Extraction solvent Obtained amount (g) Yield rate (%) Ethanol 0.5 4.9 95% hydrous 0.8 8.1 ethanol 60% hydrous 1.5 15.1 ethanol 30% hydrous 1.8 18.4 ethanol Water 1.9 19.4 Butanol 0.4 4.1 Acetone 0.2 2.4 Ethyl acetate 0.3 3.3 Hexane 0.2 1.5 Isopropanol 0.4 3.6 Methanol 0.9 9.0 Dichloromethane 0.3 2.6

EXAMPLE 1

Pattern of High Speed Liquid Chromatography (HPLC) of Extract of Justicia procumbens and Identification of Justicidin-A, Justicidin-B, and 6′ Hydroxyl Justicidin-B

[0065] High-speed liquid chromatography (HPLC, Agilent 1260, USA) was performed under the conditions as shown in Table 2 below in order to identifyan active ingredient included in the anhydrous ethanol extract of Justicia procumbens prepared by the preparation method of above Preparing Example 1, and the results are shown in FIG. 2.

TABLE-US-00002 TABLE 2 Detector Ultraviolet absorption spectrophotometer Detection wavelength UV 256 nm Column Capcellpak C.sub.18 UG120 (4.6 × 250 mm, 5 μm) Column temperature 35° C. <Gradient program> Time % (minute) % Acetonitrile Water Mobile phase 0 15 85 5 15 85 40 46 54 60 55 45 70 60 40 75 40 60 76 15 85 Flux 0.8 mL/min Injection amount 10 μl

[0066] As a result of the HPLC test, justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B were detected from the anhydrous ethanol extract of Justicia procumbens. Specifically, the peak of justicidin-A was detected from the anhydrous ethanol extract of Justicia procumbens at a retention time (RT) of about 52 minutes, the peak of justicidin-B was detected at the RT of about 48 minutes, and the peak of 6′ hydroxyl justicidin-B was detected at the RT of about 38 minutes.

EXAMPLE 2

Experiment on Comparison of Inhibitory Effects In Vero Cell Lines Infected with SARS-CoV-2

[0067] To confirm a SARS-CoV-2 inhibitory effect of an anhydrous ethanol immersion extract of Justicia procumbens, main ingredients thereof such as justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B, a hydrous ethanol reflux extract of Justicia procumbens, and various organic solvent extracts of Justicia procumbens, the Vero cell lines were cultured for 24 hours, and dosed with the test drugs prepared in Preparing Examples 1 to 5 at 10 concentrations ranging from 0.1 micromolar (or microgram) to 50 micromolar (or microgram), while being infected with SARS-CoV-2 provided by the Korea Centers for Disease Control and Prevention (KCDC). Particularly, the Vero cells were seeded at 1.2×10.sup.4 per well into a 384-well tissue culture plate. On the following day, the compound at each concentration was subjected to a two-fold serial dilution and the Vero cells were treated therewith. Soon after, the cells treated with the compound were cultured at 37° C. for 24 hours to be infected with SARS-CoV-2 (COVID 19). Then, the cells were fixed, after which the cell membrane was subjected to permeabilization and treated with a primary antibody of anti-SARS-CoV-2 Nucleocapsid (N), and then also treated with a secondary antibody at 37° C. Cell nuclei were identified by staining with Hoechst 33342, and a fluorescence expression was subjected to imaging by using an Operetta high-content image analyzer (Perkin Elmer). Based on the resulting images, the proportion of infected cells was calculated and SARS-CoV-2 virus inhibitory efficacy of the drug was measured with Image Mining (IM) software, an internal analysis program. The SARS-CoV-2 virus inhibitory ability of drugs was summarized in Tables 3 to 5. In addition, the response curve and 50% inhibitory ability (IC.sub.50) values *?*according to a drug concentration were derived by using XLFit (IDBS) software, and the results were summarized in Tables 6 to 7 and FIG. 3. The cell viability for each of the test materials is shown in Tables 8 to 10 and FIG. 3.

TABLE-US-00003 TABLE 3 SARS-CoV-2 virus inhibitory ability (%, average ± standard deviation) Anhydrous ethanol immersion Chloroquine extract of Remdesivir Lopinavir (uM) Con- 6′ hydroxyl (uM) (uM) Positive cent Justicidin-B justicidin-B Positive Positive control ration (ug/mL) (uM) (uM) control group control group group 50 99.19 ± 0.26 100.28 ± 0.49  97.75 ± 2.47 94.38 ± 0.41 98.23 ± 2.11 99.37 ± 1.00 25 99.46 ± 0.11 100.00 ± 0.21  99.79 ± 0.60 84.62 ± 2.21 99.01 ± 0.02 98.93 ± 0.07 12.5 99.09 ± 0.82 100.01 ± 0.14  98.87 ± 1.49 63.58 ± 1.23 45.51 ± 8.72 99.31 ± 0.39 6.25 96.26 ± 2.78 98:73 ± 2.07 99.74 ± 0.24  10.79 ± 43.80  3.38 ± 5.94 97.70 ± 0.16 3.13 80.13 ± 7.59 100.03 ± 0.27  95.86 ± 0.86  5.89 ± 3.28  3.03 ± 0.67 61.07 ± 7.72 1.56 41.41 ± 7.30 99.61 ± 0.65 68.58 ± 3.12  0.65 ± 5.05  0.79 ± 3.76  3.52 ± 6.42 0.78 20.58 ± 3.88 99.26 ± 0.41 35.60 ± 0.69  3.03 ± 5.01  0.30 ± 2.05 −4.90 ± 2.07 0.39  4.84 ± 5.63 88.06 ± 0.59  3.39 ± 3.95 −1.29 ± 2.86 −0.60 ± 2.75 −2.86 ± 0.21 0.20  5.29 ± 0.24 48.73 ± 2.82 −1.71 ± 4.34  2.60 ± 1.90 −0.59 ± 1.18 −4.26 ± 0.03 0.10  4.46 ± 2.11 13.37 ± 6.72  1.45 ± 1.16 −2.24 ± 7.45  3.14 ± 0.24 −2.83 ± 2.09

TABLE-US-00004 TABLE 4 SARS-CoV-2 virus inhibitory ability (%, average ± standard deviation) 30% 60% 95% 100% Water ethanol ethanol ethanol ethanol Lopinavir extract of extract of extract of extract of extract of (uM) Con- Justicia Justicia Justicia Justicia Justicia Positive cent- Justicidin-A procumbens procumbens procumbens procumbens procumbens control ration (uM) (ug/mL.) (ug/mL) (ug/mL) (ug/mL) (ug/mL) group 50 93.3 ± 1.69 18.7 ± 2.84 98.9 ± 1.07 99.5 ± 0.16 99.6 ± 0.32 99.4 ± 0.35 99.6 ± 0.57 25 95.3 ± 0.61 10.5 ± 1.66 98.9 ± 0.88 99.1 ± 0.30 99.9 ± 0.35 99.3 ± 0.01 98.6 ± 0.28 12.5 98.1 ± 1.47  6.9 ± 3.00 96.5 ± 0.42 97.0 ± 0.73 99.4 ± 6.08 99.1 ± 0.26 22.6 ± 4.07 6.25 99.6 ± 0.16  7.2 ± 2.92 79.1 ± 1.91 90.3 ± 6.96 98.8 ± 0.45 99.1 ± 0.61 −0.1 ± 1.27 3.13 100.0 ± 0.36   0.7 ± 0.20 22.2 ± 5.15 73.4 ± 0.53 93.7 ± 2.41 98.5 ± 0.25  0.2 ± 6.78 1.56 99.0 ± 0.57  4.1 ± 5.49  8.0 ± 1.92 34.2 ± 6.43 58.5 ± 21.8 70.7 ± 7.31  1.7 ± 0.27 0.78 99.0 ± 1.58  1.5 ± 8.31 13.4 ± 6.95 26.4 ± 1.59 29.0 ± 0.74  53.9 ± 16.87  3.1 ± 3.84 0.39 95.2 ± 1.48  3.4 ± 8.96  7.2 ± 7.92 24.5 ± 6.57 22.0 ± 3.12 44.8 ± 4.59  1.2 ± 5.71 0.20 75.3 ± 4.37  3.4 ± 0.66  8.5 ± 6.36 14.8 ± 2.64 15.1 ± 0.80 23.2 ± 1.74  0.2 ± 2.44 0.10  25.7 ± 12.33  1.3 ± 2.74  12.1 ± 16.70  9.9 ± 8.26 11.2 ± 6.96  13.4 ± 10.56 −0.2 ± 4.23

TABLE-US-00005 TABLE 5 SARS-CoV-2 virus inhibitory ability (%, average ± standard deviation) Dichlorome- Ethyl Isopropanol Methanol Butanol Acetone thane acetate Remdesivir extract of extract of extractor extract of extract of extract of (uM)- Con- Justicia Justicia Justicia Justicia Justicia Justicia Positive cent- procumbens procumbens procumbens procumbens procumbens procumbens control ration (ug/mL) (ug/mL) (ug/mL) (ug/mL) (ug/mL) (ug/mL) group 50 99.0 ± 0.67 99.0 ± 0.39 99.3 ± 0.45 99.0 ± 0.05 99:2 ± 0.30 99.4 ± 0.27 93.5 ± 1.80 25 99.5 ± 0.07 99.4 ± 0.39 99.0 ± 0.03 99.4 ± 0.19 99.4 ± 0.28 98.9 ± 0.04 82.1 ± 1.40 12.5 99.3 ± 0.25 99.5 ± 0.06 99.6 ± 0.06 99.7 ± 0.04 99.6 ± 0.17 99.4 ± 0:08 47.9 ± 0.01 6.25 99.3 ± 0.86 96.7 ± 2.87 99.0 ± 0.71 99.3 ± 0.09 99.3 ± 0.41 99.4 ± 0.14 16.2 ± 2.56 3.13 98.8 ± 0.29 88.6 ± 1.65 98.9 ± 0.89 99.6 ± 0.28 98.9 ± 0:69 99.3 ± 0.02 11.8 ± 0.80 1.56 95.7 ± 0.53 54.7 ± 0.63 93.3 ± 2.76 99.0 ± 8.64 95.8 ± 1.53 95.4 ± 1.17  7.4 ± 1.96 0.78 67.1 ± 6.57  41.7 ± 10.09 78.2 ± 4.94 87.6 ± 3.34 81.8 ± 2.25 79.3 ± 5.63  7.1 ± 1.49 0.39  50.6 ± 27.00 28.5 ± 4.60  40.5 ± 12.72  64.4 ± 16.47 62.7 ± 2.84  46.6 ± 19.69  4.8 ± 4.21 0.20 20.46 ± 8.34  22.9 ± 0.40  23.6 ± 10.19  31.4 ± 11.15 21.0 ± 11.6 17.5 ± 6.73  7.2 ± 0.17 0.10  8.4 ± 2.08  12.1 ± 11.32 17.8 ± 1.31 23.2 ± 6.69  15.7 ± 16.13 11.1 ± 7.63  3.8 ± 5.51

TABLE-US-00006 TABLE 6 SARS-CoV-2 virus 50% inhibitory ability Test group (IC.sub.50 value) Anhydrous ethanol immersion 1.736 ug/mL extract of Justicia procumbens Justicidin-A 0.159 uM Justicidin-B 0.203 uM 6′ hydroxyl justicidin-B 1.060 uM Remdesivir (uM) - 10.776 uM Positive control group Lopinavir (uM) - 12.649 uM Positive control group Chloroquine (uM) - 8.781 uM Positive control group

TABLE-US-00007 TABLE 7 SARS-CoV-2 virus 50% inhibitory ability Test group (IC.sub.50 value) Water extract of Justicia procumbens >50 ug/mL 30% ethanol extract of Justicia procumbens 4.461 ug/mL 60% ethanol extract of Justicia procumbens 1.873 ug/mL 95% ethanol extract of Justicia procumbens 1.243 ug/mL 100% ethanol extract of Justicia procumbens 0.612 ug/mL Isopropanol extract of Justicia procumbens 0.409 ug/mL Methanol extract of Justicia procumbens 1.034 ug/mL Butanol extract of Justicia procumbens 0.465 ug/mL Acetone extract of Justicia procumbens 0.308 ug/mL Dichloromethane extract of 0.345 ug/mL Justicia procumbens Ethyl acetate extract of Justicia procumbens 0.429 ug/mL Lopinavir (uM) - Positive control group 14.475 uM Remdesivir (uM) - Positive control group 12.701 uM

TABLE-US-00008 TABLE 8 Cell viability (%, average ± standard deviation) Anhydrous ethanol immersion Remdesivir Lopinavir Chloroquine extract of (uM)- (uM)- (uM)- Con- Justicia 6′ hydroxyl Positive Positive Positive cent- procumbens Justicidin-B justicidin-B control control control ration (ug/mL) (uM) (uM) group group group 50  93.86 ± 0.24  78.67 ± 2.53  93.38 ± 0.72 102.40 ± 4.28  74.13 ± 1.69 59.69 ± 1.38 25  98.03 ± 6.58  83.49 ± 1.22  97.80 ± 1.29 107.95 ± 0.43  77.95 ± 1.50 71.29 ± 6.06 12.5 101.80 ± 6.36  90.01 ± 1.60 101.11 ± 0.36  104.4 ± 91.82 92.36 ± 2.16 83.63 ± 0.73 6.25 105.57 ± 7.31  94.60 ± 3.46 103.44 ± 1.31 98.92 ± 1.05 87.57 ± 7.72 90.84 ± 3.72 3.13 110.10 ± 3.31  98.69 ± 5.68 105.46 ± 0.38 94.32 ± 6.45 89.54 ± 1.11 97.41 ± 1.82 1.56 107.98 ± 8.24 102.83 ± 5.24 107.86 ± 0.60 97.46 ± 6.58 91.64 ± 6.21 89.11 ± 4.21 0.78 108.86 ± 6.82 108.21 ± 2.14 104.18 ± 3.43 92.43 ± 4.42 93.08 ± 6.02 91.66 ± 2.39 0.39 103.45 ± 7.55 107.70 ± 4.88 105.17 ± 0.85 95.76 ± 6.64 88.89 ± 3.07 83.14 ± 3.44 0.20 103.75 ± 3.25 110.62 ± 0.00 104.63 ± 0.44 88.32 ± 1.19 94.69 ± 5.45 87.70 ± 0.37 0.10 106.63 ± 1.14 107.08 ± 1.75 100.66 ± 0.73 98.25 ± 4.51 86.74 ± 0.49 83.10 ± 6.34

TABLE-US-00009 TABLE 9 Cell viability (%, average ± standard deviation) 30% 60% 95% 100% Lopinavir Water ethanol ethanol ethanol ethanol (uM) - Con- extract of extract of extract of extract of extract of Positive cent- Justicidin-A procumbens procumbens procumbens procumbens procumbens control ration (uM) (ug/mL) (ug/mL) (ug/mL) (ug/mL) (ug/mL) group 50 98.0 ± 3.04 94.5 ± 0.56 96.7 ± 0.93 92.0 ± 1.94  89.0 ± 1.73 85.0 ± 3.92 68.8 ± 2.30 25 99.5 ± 1.81 94.4 ± 0.07 96.9 ± 1.80 98.1 ± 0.63  93.4 ± 4.41 89.6 ± 1.83 87.0 ± 1.45 12.5 96.5 ± 0.20 94.4 ± 2.34 101.2 ± 1.89  98.8 ± 0.23  97.0 ± 1.73 93.4 ± 1.00 90.5 ± 0.75 6.25 96.9 ± 3.33 96.3 ± 2.68 101.3 ± 0.17  101.9 ± 0.30   99.8 ± 2.30 96.7 ± 2.43 92.0 ± 4.01 3.13 98.4 ± 1.93 94.9 ± 0.41 100.4 ± 0.66  101.0 ± 0.92  102.0 ± 0.15 98.6 ± 4.03 94.2 ± 3.17 1.56 97.4 ± 0.09 98.8 ± 2.61 98.8 ± 0.68 102.0 ± 2.15  104.6 ± 0.30 101.1 ± 0.44  93.3 ± 1.23 0.78 100.1 ± 1.00  94.7 ± 2.51 98.7 ± 2.00 98.4 ± 0.72 101.2 ± 1.76 100.3 ± 2.83  86.6 ± 8.13 0.39 101.3 ± 1.55  96.7 ± 2.79 99.9 ± 1.79 101.9 ± 0.93  101.6 ± 1.00 1004.3 ± 2.83   85.0 ± 13.65 0.20 97.6 ± 0.61 92.4 ± 0.25 94.2 ± 4.87 96.4 ± 0.89  95.3 ± 0.86 95.6 ± 0.45 91.8 ± 2.06 6.10 96.7 ± 2.19 95.7 ± 1.07 98.6 ± 2.58 96.9 ± 2.24  99.2 ± 2.46 99.0 ± 2.84 94.6 ± 1.80

TABLE-US-00010 TABLE 10 SARS-CoV-2 virus 50% inhibitory ability Test group (IC.sub.50 value) Anhydrous ethanol immersion 1.18 ug/mL extract of Justicia procumbens Justicidin-B 0.17 uM 6′ hydroxyl justicidin-B 0.05 uM Hydroxy-chloroquine (uM) - 9.33 uM Positive control group

[0068] As can be understood from above Tables 3 to 10 and FIG. 3, it was confirmed that the anhydrous ethanol extracts of Justicia procumbens prepared by Preparing Examples 1 to 4 and the active ingredients thereof, such as justicidin-A, justicidin-B, and 6′ hydroxyl justicidin-B show a SARS-CoV-2 inhibitory ability remarkably more excellent than that of Remdesivir, which is a positive control group, Lopinavir and Chloroquine, which are main ingredients of Kaletra, when being compared with each other at 50% inhibitory concentration (IC.sub.50) values. These test groups showed no particular cytotoxicity up to the highest concentration tested.

[0069] In addition, in case of the hydrous ethanol extract and organic solvent extract of Justicia procumbens, which were prepared by Preparing Example 5, it was confirmed that all the hydrous ethanol extracts excluding the water extract and organic solvent extracts show an excellent SARS-CoV-2 inhibitory ability, and all the extracts show at least 80% of cell viability even at 50 ug/mL with regard to cytotoxicity.

EXAMPLE 3

Experiment on Comparison of Therapeutic Effects In Vero Cell Lines Infected with SARS-CoV-2

[0070] To confirm a SARS-CoV-2 treatment effect of the anhydrous ethanol immersion extract of Justicia procumbens and main ingredients thereof such as justicidin-B and 6′ hydroxyl justicidin-B, the VERO cells were cultured (2×10.sup.4 cell/well), and then infected with SARS-CoV-2 virus at MOI 0.1 (2×10.sup.3 PFU/100 ul) in an incubator at 37° C. for one hour. The infected cells were washed with PBS, and the drugs prepared according to Preparing Examples 1, 3 and 4 were added to the cells for each concentration. And, a culture fluid was obtained after 48 hours, an RNA level present in the SARS-CoV-2 virus particles was measured by qRT-PCR, and comparative analysis was performed with a control group (a viral infected group without drug treatment). To measure the IC.sub.50 of the drug, the concentration started at 100 uM and diluted by two steps before use. In this case, the cell viability was confirmed by WST-1 assay.

TABLE-US-00011 TABLE 11 SARS-CoV-2 virus 50% inhibitory ability Test group (IC.sub.50 value) Anhydrous ethanol immersion 1.18 ug/mL extract of Justicia procumbens Justicidin-B 0.17 uM 6′ hydroxyl justicidin-B 0.05 uM Hydroxy-chloroquine (uM) - 9.33 uM Positive control group

TABLE-US-00012 TABLE 12 50% cell viability inhibitory concentration Test group (CC.sub.50 value) Anhydrous ethanol immersion 340 ug/mL extract of Justicia procumbens Justicidin-B >800 uM 6′ hydroxyl justicidin-B 314 uM Hydroxy-chloroquine (uM) - 160 uM Positive control group

[0071] As can be understood from above Table 11, when the VERO cells previously infected with SARS-CoV-2 virus one hour before are treated with the anhydrous ethanol immersion extract of Justicia procumbens and the active ingredients thereof, such as justicidin-B, and 6′ hydroxyl justicidin-B, it was confirm that this extract and those ingredients shows a SARS-CoV-2 inhibitory ability about 8 to 187 times higher than that of Hydroxychloroquine, a positive control group, when being compared with each other at 50% inhibitory concentration (IC.sub.50) values. It was just like the case of the VERO cells being simultaneously treated with the virus and the drug. Base on the results of 50% cell viability concentration in Table 12, the concentration showing cytotoxicity of these test groups was at least about 288 times higher compared to a concentration showing the drug efficacy, thereby it was confirm that the test drug is very safe.

[0072] In Formulation Examples 1 to 3 below, the examples of preparing drug medicines, foods, and beverages according to one example of the present invention will be described in detail. In Preparing Example below, the extract of Justicia procumbens may include at least one selected from the methanol, ethanol, isopropanol, butanol, hexane, ethyl acetate, dichloromethane, ether, chloroform, and acetone extracts of Justicia procumbens.

FORMULATION EXAMPLE 1

Preparation of Medicament

[0073] 1-1: Preparation of Powder

[0074] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0075] Lactose 100 mg

[0076] Talc 10 mg

[0077] The above ingredients were mixed and filled into an airtight pack to prepare powder.

[0078] 1-2 Preparation of Tablet

[0079] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0080] Maize starch 100 mg

[0081] Lactose 100 mg

[0082] Magnesium stearate 2 mg

[0083] The above ingredients were mixed and compressed to prepare a tablet according to a conventional method for preparing tablets.

[0084] 1-3 Preparation of Capsule

[0085] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0086] Maize starch 100 mg

[0087] Lactose 100 mg

[0088] Magnesium stearate 2 mg

[0089] The above ingredients were mixed and filled into a gelatin capsule to prepare a tablet according to a conventional method for preparing capsules.

[0090] 1-4 Preparation of Injection

[0091] 100 mg of extract of Justicia procumbens, justicidin-B, justicidin-A, or 6′ hydroxyl justicidin-B

[0092] Suitable amount of sterilized distilled water for injection

[0093] Suitable amount of pH adjusting agent

[0094] An injection was prepared with the above content of ingredients per ampoule (2 ml) according to a conventional method for preparing injections.

[0095] 1-5 Preparation of Liquid Medicine

[0096] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0097] Sugar 20 g

[0098] Isomerized glucose syrup 20 g

[0099] Suitable amount of lemony flavor

[0100] Distilled water was added to adjust the total amount to 1.00 ml. The above ingredients were mixed according to a conventional method for preparing liquid medicines, and then filled into a brown bottle, and sterilized to prepare a liquid medicine.

[0101] 1-6 Preparation of Inhalant

[0102] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0103] 1,1,1,2-tetrafluoroethane 15 g

[0104] Anhydrous ethanol 1.5 g

[0105] Citric acid (anhydride) 0.05 mg

[0106] Polyethylene glycol 500 mg

[0107] The above ingredients were mixed according to a conventional method for preparing inhalants, and then filled into a container.

FORMULATION EXAMPLE 2

Preparation of Food

[0108] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0109] Suitable amount of vitamin mixture

[0110] Vitamin A acetate 70 μg

[0111] Vitamin E 1.0 mg

[0112] Vitamin B1 0.13 mg

[0113] Vitamin B2 0.15 mg

[0114] Vitamin B6 0.5 mg

[0115] Vitamin B12 0.2 μg

[0116] Vitamin C 10 mg

[0117] Biotin 10 μg

[0118] Nicotinic acid amide 1.7 mg

[0119] Folic acid 50 μg

[0120] Calcium pantothenate 0.5 mg

[0121] Suitable amount of mineral mixture

[0122] Ferrous sulfate 1.75 mg

[0123] Zinc oxide 0.82 mg

[0124] Potassium phosphate monobasic 15 mg

[0125] Calcium phosphate dibasic 55 mg

[0126] Potassium citrate 90 mg

[0127] Calcium carbonate 100 mg

[0128] Magnesium chloride 24.8 mg

[0129] As for a composition ratio of the above vitamin and mineral mixtures, ingredients suitable for health functional foods were mixed according to a preferred example, but a mixing ratio thereof may be arbitrarily modified, and the above ingredients may be mixed according to a conventional method for preparing health functional foods, and then may be used in preparing a health functional food composition (e.g., nutritional candy, etc.) according to a conventional method.

FORMULATION EXAMPLE 3

Preparation of Beverage

[0130] 100 mg of extract of Justicia procumbens, justicidin-A, justicidin-B, or 6′ hydroxyl justicidin-B

[0131] Citric acid 1000 mg

[0132] Oligosaccharide 100 g

[0133] Plum concentrate 2 g

[0134] Taurine 1 g

[0135] Distilled water was added to adjust the total amount to 900 ml.

[0136] The above ingredients were mixed according to a conventional method for preparing health functional beverages, and then stirred and heated at 85° C. for about one hour, after which the resulting solution was filtered and collected into a sterilized 2 ontainer, sealed and sterilized, and then stored in a refrigerator. After that, the resulting product was used in preparing the health functional beverage composition of the present invention.

[0137] As for the above composition ratio, the ingredients relatively suitable for a preferred beverage were mixed according to a preferred example, but a mixing ratio thereof may be arbitrarily modified according to regional and ethnic preferences such as a class of demand, a country of demand, an intended use, etc.