PL417198A1 - 3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione - Google Patents

3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione

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Publication number
PL417198A1
PL417198A1 PL417198A PL41719816A PL417198A1 PL 417198 A1 PL417198 A1 PL 417198A1 PL 417198 A PL417198 A PL 417198A PL 41719816 A PL41719816 A PL 41719816A PL 417198 A1 PL417198 A1 PL 417198A1
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PL
Poland
Prior art keywords
dihydroxyandrost
dione
carbon
hydroxylation
producing new
Prior art date
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PL417198A
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Polish (pl)
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PL232297B1 (en
Inventor
Ewa Kozłowska
Natalia Hoc
Monika Dymarska
Edyta Kostrzewa-Susłow
Jakub Grzeszczuk
Elżbieta Pląskowska
Monika Urbaniak
Łukasz Stępień
Tomasz Janeczko
Original Assignee
Uniwersytet Przyrodniczy we Wrocławiu
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Application filed by Uniwersytet Przyrodniczy we Wrocławiu filed Critical Uniwersytet Przyrodniczy we Wrocławiu
Priority to PL417198A priority Critical patent/PL232297B1/en
Publication of PL417198A1 publication Critical patent/PL417198A1/en
Publication of PL232297B1 publication Critical patent/PL232297B1/en

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Steroid Compounds (AREA)

Abstract

Zgłoszenie dotyczy sposobu wytwarzania 3ß,11?-dihydroksyandrost-5-en-7,17-dionu o wzorze 2. W wyniku działania układu enzymatycznego zawartego w komórkach szczepu Beauveria caledonica KCh J3.4 o sekwencji 1, następuje hydroksylacja przy atomie węgla C-7, utlenienie grupy hydroksylowej usytuowanej przy tym węglu do grupy karbonylowej oraz stereoselektywna hydroksylacja przy atomie węgla C-11. Uzyskany w ten sposób produkt wydziela się z wodnej kultury mikroorganizmu, znanym sposobem, przez ekstrakcję rozpuszczalnikiem organicznym niemieszającym się z wodą (chloroform).The application relates to a method for producing 3ß, 11'-dihydroxyandrost-5-ene-7,17-dione of formula 2. As a result of the enzyme system contained in the cells of the strain Beauveria caledonica KCh J3.4 with sequence 1, hydroxylation at the carbon C- 7, oxidation of the hydroxyl group located at this carbon to the carbonyl group and stereoselective hydroxylation at the C-11 carbon atom. The product thus obtained is separated from the aqueous culture of the microorganism in a known manner by extraction with a water-immiscible organic solvent (chloroform).

PL417198A 2016-05-13 2016-05-13 3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione PL232297B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL417198A PL232297B1 (en) 2016-05-13 2016-05-13 3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL417198A PL232297B1 (en) 2016-05-13 2016-05-13 3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione

Publications (2)

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PL417198A1 true PL417198A1 (en) 2017-01-16
PL232297B1 PL232297B1 (en) 2019-06-28

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PL417198A PL232297B1 (en) 2016-05-13 2016-05-13 3β, 11α-dihydroxyandrost-5-en-7,17-dione and method for producing new 3β, 11α-dihydroxyandrost-5-en-7,17-dione

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PL232297B1 (en) 2019-06-28

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