Novel antibiotic SF-2107 series substance and process for preparing the same
AssigneeMeiji Seika Kaisha, Ltd.
InventorsNorio Ezaki, Takashi Shomura, Shoichi Amano, Tomizo Niwa, Michio Kojima, Tatsuo Ito
Life of this patent
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Abstract
Disclosed is a novel antibiotic SF-2107 series substance consisting essentially of Substance SF-2107 A-1, Substance SF-2107 B and/or Substance SF-2107 C, each having the phisico-chemical properties as described in the specification, which substance exhibits an antibacterial activity against both gram-positive and gram-negative bacteria and is useful for pharmaceuticals, bactericides, disinfectants, etc. Also disclosed is a process for preparing the substance.
Claims7
An antibiotic Substance SF-2107 A-1 having the following physico-chemical properties:
- Elementary analysis:
- C, 58.39 wt %;
- H, 7.88 wt %;
- O, 33.73 wt % (balance) which does not contain any nitrogen, halogen, sulfur, phosphorus
- Molecular weight:
- 900-1100 (gel filtration method)
- Melting point:
- 170 .degree.-184.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.25 +20.degree. (c=0.2, Methanol)
- Ultraviolet absorption spectrum:
- Absorption maxima at 250 nm (E.sub.1 cm.sup.1% =72), 342 nm (206), (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3460, 2950, 1730, 1630, 1610, 1460, 1380, 1300, 1280, 1130, 1100, 1040, 910, 860, 820, 790, 750, 740, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Pale yellow powder Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.67 (chloroform:methanol=5:1)=0.56 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water
An antibiotic Substance SF-2107 B having the following physico-chemical properties:
- Elementary analysis:
- C, 53.66 wt %;
- H, 6.75 wt %;
- O, 39.59 wt % (balance) which does not contain any nitrogen, sulfur, phosphorus, or halogen
- Molecular weight:
- 900-1100 (gel filtration method)
- Melting point:
- 170.degree.-175.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.23 =-5.degree. (c=1, Methanol)
- Ultraviolet absorption spectrum:
- Absorption maxima at 242 nm (E.sub.1 cm.sup.1% =52), 343 (206), (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3450, 2970, 2930, 1720, 1600, 1440, 1370, 1270, 1170, 1130, 1040, 980, 790, 750, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Slightly yellowish powder
- Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.34 (chloroform:methanol=5:1)=0.51 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water
An antibiotic Substance SF-2107 C having the following physico-chemical properties:
- Elementary analysis:
- C, 57.50 wt %;
- H, 7.04 wt %;
- O, 34.46 wt % (balance) which does not contain any nitrogen, sulfur, phosphorus, or halogen
- Molecular weight:
- 900-1100 (gel filtration method)
- Melting point:
- 155.degree.-168.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.23 =+29.8.degree. (c=1, methanol)
- Ultraviolet absorption spectrum:
- Absorption maximum at 345 nm (E.sub.1 cm.sup.1% =258) (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3430, 2930, 1720, 1620, 1600, 1440, 1370, 1300, 1270, 1130, 1100, 1050, 900, 790, 750, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Slightly yellowish powder
- Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.27 (chloroform:methanol=5:1)=0.07 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water
An antibacterial composition which comprises as an active ingredient, an antibacterially effective amount of Substance SF-2107 A-1 having the following physico-chemical properties:
- Elementary analysis:
- C, 58.39 wt %, H, 7.88 wt %;
- O, 33.73 wt % (balance) which does not contain any nitrogen, sulfur, phosphorus, or halogen
- Molecular weight:
- 900-1100 (gel filtration method)
- Melting point:
- 170.degree.-184.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.25 =+20.degree. (c=0.2, Methanol)
- Ultraviolet absorption spectrum:
- Absorption maxima at 250 nm (E.sub.1 cm.sup.1% =72), 342 nm (206), (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3460, 2950, 1730, 1630, 1610, 1460, 1380, 1300, 1280, 1130, 1100, 1040, 910, 860, 820, 790, 750, 740, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Pale yellow powder
- Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.67 (chloroform:methanol=5:1)=0.56 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water, and a pharmaceutically acceptable carrier.
An antibacterial composition which comprises as an active ingredient, an antibacterially effective amount of Substance SF-2107 B having the following physico-chemical properties:
- Elementary analysis:
- C, 53.66 wt %;
- H, 6.75 wt %;
- O, 39.59 wt % (balance) which does not contain any nitrogen, sulfur, phosphorus, or halogen
- Molecular weight:
- 900-1100 (gel filtration method) PG,29
- Melting point:
- 170.degree.-175.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.23 =-5.degree. (c=1, Methanol)
- Ultraviolet absorption spectrum:
- Absorption maxima at 242 nm (E.sub.1 cm.sup.1% =52), 343 (206), (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3450, 2970, 2930, 1720, 1600, 1440, 1370, 1270, 1170, 1130, 1040, 980, 790, 750, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Slightly yellowish powder
- Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.34 (chloroform:methanol=5:1)=0.51 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water, and a pharmaceutically acceptable carrier.
An antibacterial composition which comprises as an active ingredient, an antibacterially effective amount of Substance SF-2107 C having the following physico-chemical properties:
- Elementary analysis:
- C, 57.50 wt %;
- H, 7.04 wt %;
- O, 35.46 wt % (ballance) which does not contain any nitrogen, sulfur, phosphorus, or halogen
- Molecular weight:
- 900-1100 (gel filtration method)
- Melting point:
- 155.degree.-168.degree. C. (slowly molten)
- Specific rotation:
- [.alpha]sub.D.sup.23 =+29.8.degree. (c=1, methanol)
- Ultraviolet absorption spectrum:
- Absorption maximum at 345 nm (E.sub.1 cm.sup.1% =258) (in methanol)
- Infrared absorption spectrum:
- Characteristic absorption bands at 3430, 2930, 1720, 1620, 1600, 1440, 1370, 1300, 1270, 1130, 1100, 1050, 900, 790, 750, 690 cm.sup.-1 (KBr tablet method)
- Color reaction:
- Iodine reaction, Lemieux reaction, positive Ninhydrin reaction, ferric chloride reaction, negative
- State:
- Slightly yellowish powder
- Neutrality, acidity or basicity:
- Acting as a neutral or weakly acidic substance (electrophoresis)
- Silica gel thin-layer chromatography:
- Rf=0.27 (chloroform:methanol=5:1)=0.07 (acetone:benzene=5:1)
- Solubility:
- Soluble in methanol, acetone. Sparingly soluble in benzene, chloroform, n-hexane, water, and a pharmaceutically acceptable carrier.
Dependencies are inferred from the claim text.