PL413954A1 - Method for producing optically pure (+)-(R)-7-hydroxyflavanone - Google Patents
Method for producing optically pure (+)-(R)-7-hydroxyflavanoneInfo
- Publication number
- PL413954A1 PL413954A1 PL413954A PL41395415A PL413954A1 PL 413954 A1 PL413954 A1 PL 413954A1 PL 413954 A PL413954 A PL 413954A PL 41395415 A PL41395415 A PL 41395415A PL 413954 A1 PL413954 A1 PL 413954A1
- Authority
- PL
- Poland
- Prior art keywords
- hydroxyflavanone
- optically pure
- hours
- producing optically
- organic solvent
- Prior art date
Links
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Sposób wytwarzania (+)-(R)-7-hydroksyflawanonu, polega na tym, że do podłoża odpowiedniego dla grzybów strzępkowych wprowadza się szczep Aspergillus niger 13/5, następnie po upływie co najmniej 48 godzin do hodowli wprowadza się substrat, którym jest mieszanina racemiczna 7-hydroksyflawanonu o wzorze 1, rozpuszczona w rozpuszczalniku organicznym mieszającym się z wodą. Transformację prowadzi się przy ciągłym wstrząsaniu, co najwyżej 30 godzin, po czym produkt ekstrahuje się rozpuszczalnikiem organicznym, niemieszającym się z wodą i oczyszcza chromatograficznie. Związek ten może znaleźć zastosowanie jako antyoksydant w przemyśle spożywczym oraz jako składnik preparatów farmaceutycznych i kosmetycznych.The method of producing (+) - (R) -7-hydroxyflavanone is that an Aspergillus niger 13/5 strain is introduced into a medium suitable for filamentous fungi, then after at least 48 hours the substrate which is a mixture is introduced into the culture. racemic 7-hydroxyflavanone of formula 1, dissolved in a water-miscible organic solvent. The transformation is carried out with continuous shaking, at most 30 hours, after which the product is extracted with an organic solvent immiscible with water and purified by chromatography. This compound can be used as an antioxidant in the food industry and as an ingredient in pharmaceutical and cosmetic preparations.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL413954A PL227311B1 (en) | 2015-09-14 | 2015-09-14 | Method for producing optically pure (+)-(R)-7-hydroxyflavanone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL413954A PL227311B1 (en) | 2015-09-14 | 2015-09-14 | Method for producing optically pure (+)-(R)-7-hydroxyflavanone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL413954A1 true PL413954A1 (en) | 2017-03-27 |
| PL227311B1 PL227311B1 (en) | 2017-11-30 |
Family
ID=58360236
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL413954A PL227311B1 (en) | 2015-09-14 | 2015-09-14 | Method for producing optically pure (+)-(R)-7-hydroxyflavanone |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL227311B1 (en) |
-
2015
- 2015-09-14 PL PL413954A patent/PL227311B1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL227311B1 (en) | 2017-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP4585270A3 (en) | Medium chain fatty acid esters of beta-hydroxybutyrate and butanediol and compositions and methods for using same | |
| MX385720B (en) | NEW HYDROXY ACID DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. | |
| AU2015205268A1 (en) | Pyridylaminoacetic acid compound and polyoxyethylene castor oil-containing pharmaceutical composition | |
| SG11201906688VA (en) | Novel ester compounds, method for the production thereof and use thereof | |
| PL407699A1 (en) | Method of obtaining 7-O-�-D-glucopyranosyl-5-hydroxy-4'-methoxyisoflavone and 5-O-�-D-glucopyranosyl-7-hydroxy-4'-methoxyisoflavone | |
| MA39468A (en) | ENERGY DRINKS AND OTHER NUTRITIONAL ADDICTS FROM AGAVE-BASED SPIRITS | |
| PL417788A1 (en) | 8-O-β-D-4"-methoxyglucopyranosyl-6-methylflavone and method for producing 8-O-β-D-4"-methoxyglucopyranosyl-6-methylflavone | |
| PL413954A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413955A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PE20180453A1 (en) | DERIVATIVES OF ACID (S) -2'-VINYL-ABSCISSIC | |
| PL413947A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413948A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413946A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413939A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| WO2016069542A3 (en) | Lactone compounds and methods of making and using same | |
| PL413945A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413949A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413953A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413950A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL413951A1 (en) | Method for producing optically pure (+)-(R)-7-hydroxyflavanone | |
| PL417881A1 (en) | Method for producing optically clean (+)-(R)-7-hydroxyflavanone | |
| PL418557A1 (en) | 4'-O-β-D-glucopyranosyl-4,2'-dihydroxy-3'-[3"-methylbutyl]-6'-methoxy-α,β-dihydrochalcone and method for obtaining 4'-O-β-D-glucopyranosyl-4,2'-dihydroxy-3'-[3"-methylbutyl]-6'-methoxy-α,β-dihydrochalcone | |
| PL417789A1 (en) | Method for producing 7-O--D-4"-methoxyglucopiranosil flavanone | |
| PL417882A1 (en) | Method for producing optically clean (+)-(R)-7-hydroxyflavanone | |
| PL417205A1 (en) | Method for producing 6β-hydroxyandrost-4-en-3,11,17-trione |