PL439095A1 - 4'-Methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone and method of production of 4'-methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone - Google Patents
4'-Methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone and method of production of 4'-methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavoneInfo
- Publication number
- PL439095A1 PL439095A1 PL439095A PL43909521A PL439095A1 PL 439095 A1 PL439095 A1 PL 439095A1 PL 439095 A PL439095 A PL 439095A PL 43909521 A PL43909521 A PL 43909521A PL 439095 A1 PL439095 A1 PL 439095A1
- Authority
- PL
- Poland
- Prior art keywords
- methylglucopyranosyl
- flavone
- methyl
- formula
- hours
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/06—Benzopyran radicals
- C07H17/065—Benzo[b]pyrans
- C07H17/07—Benzo[b]pyran-4-ones
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
- C12P19/60—Preparation of O-glycosides, e.g. glucosides having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/645—Fungi ; Processes using fungi
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Saccharide Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Przedmiotem zgłoszenia jest 4'-metylo-3-O-β-D-(4"-O-metyloglukopiranozylo)-flawon o wzorze 2 oraz sposób wytwarzania 4'-metylo-3-O-β-D-(4"-O-metyloglukopiranozylo)-flawonu, który polega na tym, że do podłoża odpowiedniego dla grzybów strzępkowych wprowadza się szczep Isaria fumosorosea KCH J2, następnie po upływie co najmniej 72 godzin do hodowli wprowadza się substrat, którym jest 4'-metyloflawon o wzorze 1, rozpuszczony w rozpuszczalniku organicznym mieszającym się z wodą, transformację prowadzi się w temperaturze od 20 do 30 stopni Celsjusza, przy ciągłym wstrząsaniu, co najmniej 96 godzin, po czym produkt ekstrahuje się rozpuszczalnikiem organicznym niemieszającym się z wodą i oczyszcza chromatograficznie, przy czym 4'-metylo-3-O-β-D-(4"-O-metyloglukopiranozylo)-flawon o wzorze 2 znajduje się we frakcji o pośredniej polarności, w piątym paśmie od linii startu.The subject of the application is 4'-methyl-3-O-β-D-(4"-O-methylglucopyranosyl)-flavone of the formula 2 and a method for producing 4'-methyl-3-O-β-D-(4"-O -methylglucopyranosyl)-flavone, which consists in introducing the Isaria fumosorosea KCH J2 strain into the substrate suitable for filamentous fungi, then, after at least 72 hours, the substrate is introduced into the culture, which is 4'-methylflavone of the formula 1, dissolved in a water-miscible organic solvent, transformation is carried out at a temperature of 20 to 30 degrees Celsius, with continuous shaking, for at least 96 hours, after which the product is extracted with a water-immiscible organic solvent and purified by chromatography, 4'-methyl -3-O-β-D-(4"-O-methylglucopyranosyl)-flavone of formula 2 is found in the fraction of intermediate polarity, in the fifth band from the starting line.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL439095A PL439095A1 (en) | 2021-09-30 | 2021-09-30 | 4'-Methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone and method of production of 4'-methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL439095A PL439095A1 (en) | 2021-09-30 | 2021-09-30 | 4'-Methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone and method of production of 4'-methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone |
Publications (1)
Publication Number | Publication Date |
---|---|
PL439095A1 true PL439095A1 (en) | 2023-04-03 |
Family
ID=85783962
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL439095A PL439095A1 (en) | 2021-09-30 | 2021-09-30 | 4'-Methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone and method of production of 4'-methyl-3-O-β-D-(4''-O-methylglucopyranosyl)-flavone |
Country Status (1)
Country | Link |
---|---|
PL (1) | PL439095A1 (en) |
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2021
- 2021-09-30 PL PL439095A patent/PL439095A1/en unknown
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