N-acetyl-3-fluoroneuraminic acid as antiviral drug.

The present invention relates to an antiviral drug.

It is known that a sialic acid is positioned at an end of a glyco­chain of a glycoprotein or glycolipid and is greatly releated to the physiological activity of the sugar chain. For elucidating the function of the sialic acid, the production of sialic acid derivatives is thought important.

The fluorinated derivatives of N-acetyl neuraminic acid having a fluorine atom in 2-position (M. N. Shana and R. Eby, carbohydr. Res., Vol. 127, p. 201, 1984) or in 9-position (M. Sharma and W. Korytnyl, J. Carbohydr. Chem. Vol. 1, p. 311, 1982 to 1983) were already produced. However, the derivatives having a fluorine atom in 3-position, where steric structure is established, have not been produced, yet.

After intensive investigations made for the purpose of sterically and selectively introducing a fluorine atom into the 3-position of N-­acetylneuraminic acid, Mect Corporation found out a useful process for producing N-acetyl-3-fluoroneuraminic acid and filed Japanese Patent Application No. 62-52358.

After further investigations of the physiological activity, etc. of N-acetyl-3-fluoroneuraminic acid, the present inventors have found out that this compound remarkably inhibits the activity of sialidase which plays an important role in the viral or bacterial infection. The present invention has been completed on the basis of this finding.

An object of the present invention is to provide an antiviral drug comprising N-acetyl-3-fluoroneuraminic acid or a pharmacologically acceptable salt thereof.

The present invention relates to an antiviral drug comprising N-­acetyl-3-fluoroneuraminic acid of the following formula: <chemistry id="chem0001" num="0001"><img file="EP0341735A1_D0001.tif" /></chemistry> or a pharmacologically acceptable salt thereof.

Fig. 1 is a Dixon plot showing an inhibition pattern of N-acetyl-3-­fluoroneuraminic acid.

N-acetyl-3-fluoroneuraminic acid of the above formula (I) is produced by, for example, as follows: either (1) an inert gas containing fluorine or (2) acetyl hypofluorite produced by introducing an inert gas containing fluorine into a mixture of acetic acid and an acetic acid salt is introduced into an aqueous acetic acid solution or dichloromethane solution of an alkyl 5-acetamido-2, 6-anhydro-4,7,8,9-tetra-0-acetyl-2,3,5-trideoxy-D-glycero-D-galacto-2-­enonate of the following formula (II): <chemistry id="chem0002" num="0002"><img file="EP0341735A1_D0002.tif" /></chemistry> wherein R⁴ epresents a lower alkyl group and Ac represents an acetyl group, to conduct the addition reaction.

The compound of the above general formula II is producible by, for example, a process disclosed in "Dai-9-kai T shitsu Symposium K en Yoshi­sh (the 9th Glucide Sympsium) p. B11."

As the inert gas containing fluorine, an argon gas containing 1 to 2% of fluorine is used. The gas is introduced into the solution of the compound of the above general formula II in an aqueous acetic solution or in dichloromethane at a low temperature of around 7°C for 1 to 2 hr to form a difluorinated product having a fluorine atom at 2-position and 3-­position in cis form as well as two kinds of monofluorinated products having -OCOCH₃ at 2-position and a fluorine atom at 3-position in cis-­and trans-form. When acetyl hypofluorite is used, the monofluorinated product is mainly formed.

The monofluorinated product is separated from the reaction liquid and purified by distilling off the solvent under reduced pressure, subjecting the residue to a column chromatography with silica gel, eluting the product with, for example, an ethyl acetate/ether mixture and recrystallizing it.

The monofluorinated product thus formed is deacetylated to form N-­acetyl-3-fluoroneuraminic ester, and its ester group is then removed to produce the above-described N-acetyl-3-fluoroneuraminic acid.

N-acetyl-3-fluoroneuraminic acid is effective for various viral infections. This fact is proved by its effect of inhibiting the action of sialidase (neuramindase) [see "Tanpakushitsu Kakusan K so (Protein, Nucliec Acid and Enzyme)," Vol. 25, No. 1 (1980), pages 30 to 48].

The effective dose of N-acetyl-3-fluoroneuraminic acid is usually 1 µg to 10 mg.

N-acetyl-3-fluoroneuraminic acid is usable in various forms. It is administered by injection, inhalation or oral administration.

In order to prepare the antiviral drug of the present invention, various kinds of additives can be incorporated into the drug. Such additives include a diluent, a binder, a disintegrator, a lubricant, a film forming agent, etc.

The diluent includes glucose, starch, lactose, mannitol, sorbitol, sucrose, kaolin, dextrin, cyclodextrin, titanium oxide, anhydrous calcium phosphate, light anhydrous silicate, talc, natural hydrated magnesium silicate, precipitated calcium carbonate, magnesium metasilicate aluminate, crystalline cellulose, calcium carboxymethyl cellulose, and a mixture thereof.

The binder includes starch, dextrin, Traganth gum, gelatin, polyvinylpyrrolidone, polyvinyl alcohol, methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, hydroxypropyl starch, crystalline cellulose, pectine, polypectine, sodium polypectinate, polyhydroxyethyl methacrylate, carboxymethyl cellulose, sodium carboxymethyl cellulose, Acacia gum, sodium alginate, and a mixture thereof.

The disintegrator includes starch, crystalline cellulose, carboxymethyl cellulose, calcium carboxymethyl cellulose, carboxymethyl starch, hydroxypropyl starch, powdered agar, mannan, and a mixture thereof.

The lubricant includes talc, stearic acid, magnesium and calcium stearate, hydrogenated oil, sesame oil, paraffin, and a mixture thereof.

The film forming agent includes cellulose derivatives such as ethyl cellulose (EC), carboxymethyl cellulose (CMEC), cellulose acetate (CA), cellulose acetate phthalate (CAP), hydroxypropylmethyl cellulose (HPMC), hydroxypropylmethyl cellulose (HPMC), methyl cellulose (MC), hydroxypropyl cellulose (HPC); and polyvinyl derivalives such as polyvinyl acetal diethylamino acetate, methacrylic acid/ ethyl acrylate copolymer, methacrylic acid/ methyl acrylate copolymer, ethyl methacrylate/­ methacrylic acid trimethyl ammonium chloride ethyl copolymer, dimethylaminoethyl methacrylate/ methyl acrylate copolymer.

When the film forming agent is coated on the drug, a conventional coating aid such as a plasticizer as well as other various additives for preventing the medicines from adhering to each other when the coating is made, are added to the drug of the present invention, in order to improve the property of the film forming agent and to make easier the coating procedure.

Further, the following additives can be used for preparing the present drug in the form of inhalation or injection.

Calcium chloride, potassium chloride, sodium chloride, hydrochloric acid, citric acid, sodium citrate, succinic acid, acetic acid, potassium acetate, sodium acetate, tartaric acid, potassium hydroxide, sodium hydroxide, injection water, sodium chloride injection, sodium carbonate, sodium bicarbonate, lactic acid, sodium lactate, maleic acid, sulfuric acid, phosphoric acid, potassium phosphate, sodium phosphate, potassium hydrogen phosphate, calcium hydrogen phosphate, potassium dihydrogen phosphate, sodium hydrogen phosphate, sodium dihydrogen phosphate, sodium phosphite, sodium dihydrogen phosphite, potassium pyrophosphite, sodium pyrophoshite, ℓ-arginine, purified egg yolk lecithin, purified gelatin, gelatin, lactose, human serum albumin, polyethylene glycol 400, 1,500, 4,000 and 6,000, polyoxyethylene hydrogenated castor oil 60, and sodium ethylenediamine tetraacetate.

The following Reference Examples and Examples will further illustrate the present invention.

Reference Example 1

Argon gas containing 1.7% (6.1 mmol) of fluorine (Fe) was introduced, for 2 hr, into 25 ml (7°C) of an acetic acid solution of 2.3 g (4.8 mmol) of methyl 5-acetamido-2,6-anhydro-4,7,8,9-tetra-0-acetyl-2,3,5-trideoxy-­D-glycero-D-galacto-2-enonate of the following formula IIa: <chemistry id="chem0003" num="0003"><img file="EP0341735A1_D0003.tif" /></chemistry> wherein Ac represents an acetyl group (the same shall apply hereinafter).

Then, the solvent was distilled off under reduced pressure, to obtain 2.5 g of a syrup. The syrup was treated according to a column chromatography with silica gel (250 g of G 60; a product of Merck Co.), followed by the elution with a solvent mixture of ethyl acetate and ether (volume ratio: 3/1) and recrystallization from a solvent mixture of dichloromethane and isopropyl ether to form the following three products:

(1) Methyl 5-acetamido-4,7,8,9-tetra-0-acetyl-1,2,3,5-trideoxy-2,3-­difluoro-D-erythro-₂-L-gluco-2-nonulosonate:

[Molecular structure]

<chemistry id="chem0004" num="0004"><img file="EP0341735A1_D0004.tif" /></chemistry>

Yield: 900 mg (36%)

[Physical properties]

Melting point: 92°C [α] <maths id="math0001" num=""><math display="inline"><mrow><mfrac linethickness="0"><mrow><mtext>20</mtext></mrow><mrow><mtext>D</mtext></mrow></mfrac></mrow></math><img file="EP0341735A1_D0005.tif" /></maths> - 48.12° (C=0.55, chloroform) <tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col4" align="left">Elementary analysis: C₂₀H₂₇N₁O₁₁F₂</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Calculated:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:46.97;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.32;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:2.73</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Found:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:47.00;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.37;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:3.00</entry></row></tbody></tgroup></table></tables> Rf=0.54 (ethyl acetate) ¹ H-NMR δ (CDCl₃ ) 5.00(H-3, J _{3. 4} = 9.85 Hz) 5.39(H-4, J _{4. 5} =10.26 Hz) 4.40(H-5, J _{5. 6} =10.66 Hz) 4.27(H-6, J _{6. 7} = 2.38 Hz) 5,39(H-7, J _{7. 8} = 8.06 Hz) 5.16(H-8, J _{8. 9} = 5.68 Hz, J_{8. 9′} = 2.71 Hz) 4.01, 4.32(H-9, H-9′, J_{9. 9′} = 12.55 Hz) 5.49(NH, J_{NH, 5} = 10.20 Hz) 3.91(COO<u style="single">CH</u>₃ ) 1.91(NCO<u style="single">CH</u>₃ ) 2.05, 2.10, 2.11, 2.13(OAc)

(2) Methyl 5-acetamido-2,4,7,8,9-penta-0-acetyl-3,5-dideoxy-4-fluoro-D-­erythro-₂-L-gluco-2-nonulosonate:[Molecular structure]

<chemistry id="chem0005" num="0005"><img file="EP0341735A1_D0006.tif" /></chemistry>

Yield: 190 mg (7%)

[Physical properties]

Melting point: 119°C [α]<maths id="math0002" num=""><math display="inline"><mrow><mfrac linethickness="0"><mrow><mtext>20</mtext></mrow><mrow><mtext>D</mtext></mrow></mfrac></mrow></math><img file="EP0341735A1_D0007.tif" /></maths> - 56.5° (C=0.21, CHCl₃) <tables id="tabl0002" num="0002"><table frame="all"><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col4" align="left">Elementary analysis: C₂₂H ₃₀NO₁₄F</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Calculated:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:47.91;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.48;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:2.53</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Found:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:48.10;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.35;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:2.30</entry></row></tbody></tgroup></table></tables> Rf=0.26 ¹ H-NMR δ (CDCl₃ ) 4.62(H-3, J _{3. 4} = 9.60 Hz) 5.48(H-4, J _{4. 5} =10.05 Hz) 4.24(H-5, J _{5. 6} =10.54 Hz) 4.11(H-6, J _{6. 7} = 2.29 Hz) 5,35(H-7, J _{7. 8} = 4.66 Hz) 5.02(H-8, J _8.9 = 6.69 Hz, J_{8. 9′} = 2.44 Hz) 4.14, 4.51(H-9, H-9′, J_{9. 9′} = 12.46 Hz) 5.58(NH, J_{NH, 5} = 10.08 Hz) 3.85(COOCH₃ ) 1.89(NCOCH₃ ) 2.04, 2.06, 2.10, 2.15, 2.24(OAc)

(3) Methyl 5-acetamido-2,4,7,8,9-penta-0-acetyl-3,5-dideoxy-3-fluoro-D-­erythro-₂-L-manno-3-nonulosonate:[Molecular structure]

<chemistry id="chem0006" num="0006"><img file="EP0341735A1_D0008.tif" /></chemistry>

Yield: 30 mg, (7%)

[Physical properties]

Melting Point: 194°C [α]<maths id="math0003" num=""><math display="inline"><mrow><mfrac linethickness="0"><mrow><mtext>20</mtext></mrow><mrow><mtext>D</mtext></mrow></mfrac></mrow></math><img file="EP0341735A1_D0009.tif" /></maths> - 24.5° (C=0.19, chloroform) <tables id="tabl0003" num="0003"><img file="EP0341735A1_D0010.tif" /></tables> Rf=0.23 (ethylacetate) ¹ H-NMR δ (CDCl₃) 4.94(H-3, J _{3. 4} = 2.57 Hz) 5.50(H-4, J _{4. 5} =10.68 Hz) 4.14(H-5, J _{5. 6} =10.61 Hz) 4.25(H-6, J _{6. 7} = 1.84 Hz) 5.35(H-7, J _{7. 8} = 5.13 Hz) 5.13(H-8, J _8.9 = 6.60 Hz, J_{8. 9′} = 2.20 Hz) 4.57(H-9, J _9.9′ = 12.46 Hz) 5.43(NH, J_{NH, 5} = 8.79 Hz) 3.84(COO<u style="single">CH</u>₃ ) 1.92(NCO<u style="single">CH</u>₃ ) 2.04, 2.05, 2.11, 2.17, 2.18(OAc)

Reference Example 2

Argon gas containing 1.5% (10 mmol) of fluorine (F₂ ) was introduced into a cartridge containing a mixture of potassium acetate and acetic acid, to form acety l hypofluorite (AcOF). AcOF was introduced into 10 ml of an acetic acid solution of 480 mg (1.0 mmol) of methyl 5-acetamido-­2,6-anhydro-4,7,8,9-tetra-0-acetyl-2,3,5-trideoxy-D-glycero-D-galacto-2-­enonate (the same solution as that used in Example 1) at room temperature for 1 hr. Then, the solvent was distilled off at 60°C under reduced pressure, to obtain 520 mg a syrup.

The syrup was treated according to the column chromatography with silica gel (60 g of G 60; a product of Merck Co.), followed by the elution with a solvent mixture of ethyl acetate and ether (volume ratio: 3/1) and recrystallization from a solvent mixture of dichloromethane and isopropyl ether, to form the same products as those formed in Reference Example 1 as follows: <ul id="ul0001" list-style="none"><li>(1) Methyl 5-acetamido-4,7,8,9-tetra-0-acetyl-2,3,5-trideoxy-2,3-difluoro-­D-erythro-₂-L-gluco-2-nonulosonate [yield: 40 mg (7.7%)], and</li><li>(2) Methyl-5-acetamido-2,4,7,8,9-penta-0-acetyl-3,5-dideoxy-3-fluoro-D-­erythro-₂-L-gluco-2-nonulosonate [yield: 190 mg (34%)].</li></ul>

Reference Example 3

1 ml of methanol containing 2 mmol of sodium methoxide (NaOCH₃ ) was added to 3 ml of a solution of 55 mg of methyl 5-acetamido-2,4,7,8,9-­penta-0-acetyl-3,5-dideoxy-3-fluoro-D-erythro-₂-L-glucononulosonatre [(2) produced in Reference Example 1 or 2] in anhydrous methanol, and the mixture was stirred at room temperature for 30 min. A slightly excess amount of Dowex 50 [H⁺ ] was added to the reaction liquid and the mixture was stirred. The resin was taken by filtration, and then washed with 5 ml of methanol. The filtrate was concentrated under reduced pressure and recrystallized from a solvent mixture of methanol, ethyl acetate and petroleum ether, to obtain the following compound (6) [yield: 24 mg (75%)].

(6) Methyl 5-acetamido-3,5-dideoxy-3-fluoro-D-erythro-₂-L-gluco-2-­nonulosonate

[Molecular structure]

<chemistry id="chem0007" num="0007"><img file="EP0341735A1_D0011.tif" /></chemistry>

[Physical properties]

Melting point: 209°C (recrystallized from a solvent mixture of methanol, ethyl acetate and petroleum ether) [α]<maths id="math0004" num=""><math display="inline"><mrow><mfrac linethickness="0"><mrow><mtext>20</mtext></mrow><mrow><mtext>D</mtext></mrow></mfrac></mrow></math><img file="EP0341735A1_D0012.tif" /></maths> - 41.14° (C=0.86, H₂ O) <tables id="tabl0004" num="0004"><table frame="all"><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col4" align="left">Elementary analysis: C₁₂H ₂₀NO₉ F</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Calculated:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:42.23;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.9;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:4.1</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Found:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:42.37;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:6.0;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:4.3</entry></row></tbody></tgroup></table></tables> ¹H-NMR δ (D₂ O) 4.75(H-3, J _{3. 4} = 8.98 Hz) 4.09-4.18(3H, H-4, H-5, H-6) 3.56(H-7, J _{6. 7} = 1.10 Hz) 3.71(H-8, J _7.8 = 8.79 Hz J_{8. 9} = 6.05 Hz, J_{8. 9} = 3.43 Hz) 3.63, 3.8(H-9, H-9′, J _9.9′ =11.9 Hz)

Reference Example 4

20 mg (0.036 mmol) of methyl 5-acetamido-2,4,7,8,9-penta-0-acetyl-­3,5-dideoxy-3-fluoro-D-erythro-₂-L-gluco-nonulosonate produced in Reference Example 1 or 2 was added to 1ml of a methanol solution containing 20% of a 1 N aqueous NaOH solution, and the resultant mixture was stirred at room temperature for 1 h.

Then, 1 ml of a methanol solution containing 2 mmol of sodium methoxide (NaOCH₃ ) was added to the reaction liquid and the mixture was stirred at room temperature for 30 min. A slightly excess amount of Dowex 50 [H⁺ ] was added to the reaction liquid and the mixture was stirred. After filtration, the resin was washed with 10 ml of water. The filtrate was concentrated under reduced pressure. The residue was dissolved in water. A small amount of active carbon was added to the solution and the mixture was stirred. Then, the active carbon was filtered off and the filtrate was dried in vacuum, to obtain the following compound (7). [yield: 9 mg (76 %)].

(7) 5-Acetamido-3,5-dideoxy-3-fluoro-D-erythro-₂-L-gluco-2-nonulosonic acid

[Molecular structure]

<chemistry id="chem0008" num="0008"><img file="EP0341735A1_D0013.tif" /></chemistry>

[Physical properties]

Melting point: 205°C [α]<maths id="math0005" num=""><math display="inline"><mrow><mfrac linethickness="0"><mrow><mtext>20</mtext></mrow><mrow><mtext>D</mtext></mrow></mfrac></mrow></math><img file="EP0341735A1_D0014.tif" /></maths> - 40.02° (C=0.86, H₂ O) <tables id="tabl0005" num="0005"><table frame="all"><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col4" align="left">Elementary analysis: C₁₁H ₁₈NO₉ F</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Calculated:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:40.37;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.54;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:4.27</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Found:</entry><entry namest="col2" nameend="col2" align="char" char=".">C:40.07;</entry><entry namest="col3" nameend="col3" align="char" char=".">H:5.51;</entry><entry namest="col4" nameend="col4" align="char" char=".">N:4.21</entry></row></tbody></tgroup></table></tables> ¹H-NMR δ (D₂ O) 4.71(H-3, J _{3. 4} = 8.42 Hz) 4.10-4.15(3H, H-4, H-5, H-6) 3.54(H-7, J _{6. 7} = 0 Hz) 3.73(H-8, J _7.8 = 8.79 Hz J_{8. 9} = 6.05 Hz), J_{8, 9} = 2.75 Hz) 3.63, 3.83(H-9, H-9′, J _9,9′ = 11.91 Hz) 2.06(NCOCH₃ )

Example 1

100 µ ℓ of a 0.5 mM solution of 4-methylumbelliferyl-N-­acetylneuraminic acid (4-MU-NeuAc) (a product of Nakarai Kagaku Co., Ltd) of the following formula: <chemistry id="chem0009" num="0009"><img file="EP0341735A1_D0015.tif" /></chemistry>

100 µ ℓ of a 200 mM sodium acetate buffer (pH 4.2) and 100 µ ℓ of N-­acetyl-3-fluoroneuraminic acid (compound 1) 4 to 400 µM were added to an enzyme solution (100 m ℓ) (10 mU/ml) of sialidase (a product of Nakarai Kagaku Co., Ltd.) product from Arthrobacter ureafaciens in a test tube, and the reaction was conducted in a water bath at 37 °C for 15 min. Then, 3.6 ml of a 200 mM glycine/NaOH buffer (pH 10.4) was added to the reaction mixture in the test tube to terminate the reaction. the concentration of 4-methylumbelliferone formed in the reaction solution was determined from its fluorescence intensity at an excitation wave length of 360 nm and an emission wave length of 440 nm with a fluorescence spectrophotometer (a product of Hitachi, Ltd.). The amount of free sialic acid was determined from this value.

The sialidase inhibition rate was determined according to the following formula:<maths id="math0006" num=""><img file="EP0341735A1_D0016.tif" /></maths>

The results are shown in Table 1 and Fig. 1.

It is apparent from Table 1 that Compound 1 remarkably inhibits the activity of sialidase.

Fig. 1 is a Dixon plot showing the reaction rates obtained by using two different substrate concentrations in the presence of Compound 1. It is apparent from Fig. 1 that the inhibition of Compound 1 is competitive with the substrate. <tables id="tabl0006" num="0006"><table frame="all"><title>Table 1</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col3" align="left">Inhibiting effect on sialidase produced by Arthrobacter ureaffacients:</entry></row><row><entry namest="col1" nameend="col1" align="center"><u style="single">Compound 1 (mM)</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">NeuAc released (n mol)</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">Inhibition rate (%)</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">None</entry><entry namest="col2" nameend="col2" align="char" char=".">27.3</entry><entry namest="col3" nameend="col3" /></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.1</entry><entry namest="col2" nameend="col2" align="char" char=".">4.9</entry><entry namest="col3" nameend="col3" align="char" char=".">82.0</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.01</entry><entry namest="col2" nameend="col2" align="char" char=".">14.0</entry><entry namest="col3" nameend="col3" align="char" char=".">48.9</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="char" char=".">0.001</entry><entry namest="col2" nameend="col2" align="char" char=".">23.0</entry><entry namest="col3" nameend="col3" align="char" char=".">14.3</entry></row></tbody></tgroup></table></tables>

Examples 2 and 3

The same procedure as that of Example 1 was repeated except that sialidases produced by Vibrio colerae and Streptococcus sp. were used, and then the inhibition rate of Compound 1 was determined. The results are shown in the following Tables 2 and 3. <tables id="tabl0007" num="0007"><table frame="all"><title>Table 2</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col3" align="left">Inhibiting effect on sialidase produced by Vibrio colerae:</entry></row><row><entry namest="col1" nameend="col1" align="center"><u style="single">Compound 1 (mM)</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">NeuAc released (n mol)</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">Inhibition rate (%)</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">None</entry><entry namest="col2" nameend="col2" align="char" char=".">5.8</entry><entry namest="col3" nameend="col3" /></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.1</entry><entry namest="col2" nameend="col2" align="char" char=".">2.8</entry><entry namest="col3" nameend="col3" align="char" char=".">52.7</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.01</entry><entry namest="col2" nameend="col2" align="char" char=".">5.3</entry><entry namest="col3" nameend="col3" align="char" char=".">8.4</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="char" char=".">0.001</entry><entry namest="col2" nameend="col2" align="char" char=".">5.9</entry><entry namest="col3" nameend="col3" align="char" char=".">-0.2</entry></row></tbody></tgroup></table></tables><tables id="tabl0008" num="0008"><table frame="all"><title>Table 3</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col3" align="left">Inhibiting effect on sialidase produced by Streptococcus sp.</entry></row><row><entry namest="col1" nameend="col1" align="center"><u style="single">Compound 1 (mM)</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">NeuAc released (n mol)</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">Inhibition rate (%)</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">None</entry><entry namest="col2" nameend="col2" align="char" char=".">11.3</entry><entry namest="col3" nameend="col3" /></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.1</entry><entry namest="col2" nameend="col2" align="char" char=".">2.8</entry><entry namest="col3" nameend="col3" align="char" char=".">75.4</entry></row><row><entry namest="col1" nameend="col1" align="char" char=".">0.01</entry><entry namest="col2" nameend="col2" align="char" char=".">8.5</entry><entry namest="col3" nameend="col3" align="char" char=".">24.6</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="char" char=".">0.001</entry><entry namest="col2" nameend="col2" align="char" char=".">10.5</entry><entry namest="col3" nameend="col3" align="char" char=".">7.4</entry></row></tbody></tgroup></table></tables>

It is apparent from the above tables that Compound 1 had an inhibiting effect on sialidases produced by various microorganisms.

(Acute toxicity)

The acute toxicity test of Compound 1 was conducted by an intravenous injection in female mice.

Experiment conditions:

Animals used: Female ICR mice (6 week old) Medicine concentration: 13 to 15 W/V % in distilled water Number of mice for each level: 10 Observation period: 14 days.

Results:

The results are shown in Table 4. It is apparent that the toxicity of Compound 1 was quite low. <tables id="tabl0009" num="0009"><table frame="all"><title>Table 4</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Administration method</entry><entry namest="col2" nameend="col2" align="center">Dose (mg)</entry><entry namest="col3" nameend="col3" align="center">Number of deaths</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Intravenous injection</entry><entry namest="col2" nameend="col2" align="right">200</entry><entry namest="col3" nameend="col3" align="right">0</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="right">400</entry><entry namest="col3" nameend="col3" align="right">0</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="right">600</entry><entry namest="col3" nameend="col3" align="right">0</entry></row></tbody></tgroup></table></tables>