Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols
4,4-Dimethyl-5α-cholesta-8,14,24-trien-3β-ol (I) from human follicular fluid and 4,4-dimethyl-5α-cholesta-8,24-dien-3β-ol (II) from bull testes have been reported to activate meiosis in mouse oocytes (Byskov et al., 1995. Nature. 374: 559–562). Described herein are new chemical syntheses of I, II, a...
| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
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Elsevier
1998-10-01
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| Series: | Journal of Lipid Research |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520324998 |
| _version_ | 1818972054980919296 |
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| author | Benfang Ruan Shinya Watanabe John J. Eppig Christopher Kwoh Natasha Dzidic Jihai Pang William K. Wilson George J. Schroepfer, Jr. |
| author_facet | Benfang Ruan Shinya Watanabe John J. Eppig Christopher Kwoh Natasha Dzidic Jihai Pang William K. Wilson George J. Schroepfer, Jr. |
| author_sort | Benfang Ruan |
| collection | DOAJ |
| description | 4,4-Dimethyl-5α-cholesta-8,14,24-trien-3β-ol (I) from human follicular fluid and 4,4-dimethyl-5α-cholesta-8,24-dien-3β-ol (II) from bull testes have been reported to activate meiosis in mouse oocytes (Byskov et al., 1995. Nature. 374: 559–562). Described herein are new chemical syntheses of I, II, and the Δ8(14),24 analog XXII. A critical step in these syntheses was a remarkably high yield side chain oxidation of 3β-acetoxy-4,4-dimethyl-5α-cholest-8(14)-en-15-one to the corresponding C24 24-hydroxy compound VI. Oxidation of VI to the aldehyde, followed by Wittig olefination gave 3β-acetoxy-4,4-dimethyl-5α-cholesta-8(14),24-dien-15-one. Reduction with sodium borohydride to the 15β-hydroxysteryl ester, dehydration with sulfuric acid in CHCl3, and saponification furnished I in high purity. Reduction of VI with sodium borohydride to the 15-hydroxysteroid followed by dehydration gave 3β-acetoxy-4,4-dimethyl-5α-chola-8,14-dien-24-ol. Hydrogenation over Raney nickel gave the monounsaturated Δ8(14) and Δ8 compounds. Oxidation to the corresponding aldehydes followed by Wittig olefination and saponification gave II and XXII. Chromatographic, mass spectral, and 1H and 13C nuclear magnetic resonance spectral data have been presented for the synthetic sterols and their derivatives. I, II, XXII, and their Δ8,14 and Δ7,14 analogs, at 3 μg per ml, caused a resumption of meiosis in mouse oocytes in the presence of hypoxanthine (3.5 mm). Under the same conditions, Δ5 and Δ5,7 sterols were inactive.—Ruan, B., S. Watanabe, J. J. Eppig, C. Kwoh, N. Dzidic, J. Pang, W. K. Wilson, and G. J. Schroepfer, Jr. Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols. J. Lipid. Res. 1998. 39: 2005–2020. |
| first_indexed | 2024-12-20T15:02:11Z |
| format | Article |
| id | doaj.art-6e1289a21e394d7890b29866ce405844 |
| institution | Directory Open Access Journal |
| issn | 0022-2275 |
| language | English |
| last_indexed | 2024-12-20T15:02:11Z |
| publishDate | 1998-10-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Journal of Lipid Research |
| spelling | doaj.art-6e1289a21e394d7890b29866ce4058442022-12-21T19:36:36ZengElsevierJournal of Lipid Research0022-22751998-10-01391020052020Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterolsBenfang Ruan0Shinya Watanabe1John J. Eppig2Christopher Kwoh3Natasha Dzidic4Jihai Pang5William K. Wilson6George J. Schroepfer, Jr.7Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892Jackson Laboratory, Bar Harbor, ME 04609-1500Jackson Laboratory, Bar Harbor, ME 04609-1500Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892To whom correspondence should be addressed.; Departments of Chemistry and of Biochemistry and Cell Biology, Rice University, 6100 Main Street, Houston, TX 77251-1892; To whom correspondence should be addressed.4,4-Dimethyl-5α-cholesta-8,14,24-trien-3β-ol (I) from human follicular fluid and 4,4-dimethyl-5α-cholesta-8,24-dien-3β-ol (II) from bull testes have been reported to activate meiosis in mouse oocytes (Byskov et al., 1995. Nature. 374: 559–562). Described herein are new chemical syntheses of I, II, and the Δ8(14),24 analog XXII. A critical step in these syntheses was a remarkably high yield side chain oxidation of 3β-acetoxy-4,4-dimethyl-5α-cholest-8(14)-en-15-one to the corresponding C24 24-hydroxy compound VI. Oxidation of VI to the aldehyde, followed by Wittig olefination gave 3β-acetoxy-4,4-dimethyl-5α-cholesta-8(14),24-dien-15-one. Reduction with sodium borohydride to the 15β-hydroxysteryl ester, dehydration with sulfuric acid in CHCl3, and saponification furnished I in high purity. Reduction of VI with sodium borohydride to the 15-hydroxysteroid followed by dehydration gave 3β-acetoxy-4,4-dimethyl-5α-chola-8,14-dien-24-ol. Hydrogenation over Raney nickel gave the monounsaturated Δ8(14) and Δ8 compounds. Oxidation to the corresponding aldehydes followed by Wittig olefination and saponification gave II and XXII. Chromatographic, mass spectral, and 1H and 13C nuclear magnetic resonance spectral data have been presented for the synthetic sterols and their derivatives. I, II, XXII, and their Δ8,14 and Δ7,14 analogs, at 3 μg per ml, caused a resumption of meiosis in mouse oocytes in the presence of hypoxanthine (3.5 mm). Under the same conditions, Δ5 and Δ5,7 sterols were inactive.—Ruan, B., S. Watanabe, J. J. Eppig, C. Kwoh, N. Dzidic, J. Pang, W. K. Wilson, and G. J. Schroepfer, Jr. Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols. J. Lipid. Res. 1998. 39: 2005–2020.http://www.sciencedirect.com/science/article/pii/S0022227520324998mass spectrometrynuclear magnetic resonance |
| spellingShingle | Benfang Ruan Shinya Watanabe John J. Eppig Christopher Kwoh Natasha Dzidic Jihai Pang William K. Wilson George J. Schroepfer, Jr. Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols Journal of Lipid Research mass spectrometry nuclear magnetic resonance |
| title | Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| title_full | Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| title_fullStr | Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| title_full_unstemmed | Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| title_short | Sterols affecting meiosis: novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| title_sort | sterols affecting meiosis novel chemical syntheses and the biological activity and spectral properties of the synthetic sterols |
| topic | mass spectrometry nuclear magnetic resonance |
| url | http://www.sciencedirect.com/science/article/pii/S0022227520324998 |
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