JPS54147998A - Preparation of 9alpha-hydroxysteroid - Google Patents

Info

Publication number

JPS54147998A

JPS54147998A JP5426578A JP5426578A JPS54147998A JP S54147998 A JPS54147998 A JP S54147998A JP 5426578 A JP5426578 A JP 5426578A JP 5426578 A JP5426578 A JP 5426578A JP S54147998 A JPS54147998 A JP S54147998A

Authority

JP

Japan

Prior art keywords

medium containing

bacteria belonging

genus

corynebacterium

androst

Prior art date

1978-05-08

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• BTTWKVFKBPAFDK-UHFFFAOYSA-N (9beta,10alpha)-Androst-4-ene-3,17-dione Natural products OC1CCC2(C)C3CCC(C)(C(CC4)O)C4C3CCC2=C1 BTTWKVFKBPAFDK-UHFFFAOYSA-N 0.000 abstract 4
• AEMFNILZOJDQLW-QAGGRKNESA-N androst-4-ene-3,17-dione Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 AEMFNILZOJDQLW-QAGGRKNESA-N 0.000 abstract 4
• AEMFNILZOJDQLW-UHFFFAOYSA-N androstenedione Natural products O=C1CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 AEMFNILZOJDQLW-UHFFFAOYSA-N 0.000 abstract 4
• 241000894006 Bacteria Species 0.000 abstract 3
• 241000186216 Corynebacterium Species 0.000 abstract 2
• HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 abstract 2
• 238000012258 culturing Methods 0.000 abstract 2
• 150000003431 steroids Chemical class 0.000 abstract 2
• OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 abstract 1
• OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 abstract 1
• 241000186359 Mycobacterium Species 0.000 abstract 1
• 241001532512 Mycobacterium parafortuitum Species 0.000 abstract 1
• 241000158504 Rhodococcus hoagii Species 0.000 abstract 1
• 229930182558 Sterol Natural products 0.000 abstract 1
• HZYXFRGVBOPPNZ-UHFFFAOYSA-N UNPD88870 Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)=CCC(CC)C(C)C)C1(C)CC2 HZYXFRGVBOPPNZ-UHFFFAOYSA-N 0.000 abstract 1
• LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 abstract 1
• 235000012000 cholesterol Nutrition 0.000 abstract 1
• 229940088597 hormone Drugs 0.000 abstract 1
• 239000005556 hormone Substances 0.000 abstract 1
• 235000015097 nutrients Nutrition 0.000 abstract 1
• 230000003647 oxidation Effects 0.000 abstract 1
• 238000007254 oxidation reaction Methods 0.000 abstract 1
• 239000002994 raw material Substances 0.000 abstract 1
• 150000003432 sterols Chemical class 0.000 abstract 1
• 235000003702 sterols Nutrition 0.000 abstract 1
• HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 abstract 1
• 235000016831 stigmasterol Nutrition 0.000 abstract 1
• 229940032091 stigmasterol Drugs 0.000 abstract 1
• BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 abstract 1
• 239000000758 substrate Substances 0.000 abstract 1

Cited By (1)