CAS: 178064-13-6; (2S,3R,4S,5S,6R)-2-(((2S,3R,4S,5S)-3-(((2S,3R,4R,5S)-3,4-Dihydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-yl)Oxy)-5-Hydroxy-2-(((1S,2R,4Ar,6As,6Br,8Ar,10S,12Ar,12Br,14Ar,14Bs)-1-Hydroxy-1,6B,9,9,12A-Pentamethyl-2-(2-Methylprop-1-En-1-yl)Hexadecahydro-1H,6H-4A,6A-Methanonaphtho[1,2-H]Pyrano[2,3-C]Isochromen-10-yl)Oxy)Tetrahydro-2H-Pyran-4-yl)Oxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol
- 英文名称(2S,3R,4S,5S,6R)-2-(((2S,3R,4S,5S)-3-(((2S,3R,4R,5S)-3,4-Dihydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-yl)Oxy)-5-Hydroxy-2-(((1S,2R,4Ar,6As,6Br,8Ar,10S,12Ar,12Br,14Ar,14Bs)-1-Hydroxy-1,6B,9,9,12A-Pentamethyl-2-(2-Methylprop-1-En-1-yl)Hexadecahydro-1H,6H-4A,6A-Methanonaphtho[1,2-H]Pyrano[2,3-C]Isochromen-10-yl)Oxy)Tetrahydro-2H-Pyran-4-yl)Oxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol
- 中文名称(-)-假马齿苋皂苷 C
- IUPAC名称(2S,3R,4S,5S,6R)-2-(((2S,3R,4S,5S)-3-(((2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-5-hydroxy-2-(((1S,2R,4aR,6aS,6bR,8aR,10S,12aR,12bR,14aR,14bS)-1-hydroxy-1,6b,9,9,12a-pentamethyl-2-(2-methylprop-1-en-1-yl)hexadecahydro-1H,6H-4a,6a-methanonaphtho[1,2-h]pyrano[2,3-c]isochromen-10-yl)oxy)tetrahydro-2H-pyran-4-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- 其它别名Bascopasaponin C; Bascopasaponin C, (-)-; (2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S)-3,4-Dihydroxy-5-(Hydroxymethyl)Oxolan-2-Yl]Oxy-5-Hydroxy-2-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,17R,20R)-16-Hydroxy-2,6,6,10,16-Pentamethyl-17-(2-Met
- CAS编号178064-13-6
- MFCD编号:MFCD09265218
- FDA UNII编号:26FG38011G
- 分子式:C46H74O17分子量:899.08
- 产品CID: 908600
- 产品分类生物化工 → 提取物 → 植物提取物
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主要参考文献
1: Vinod A, Sathianarayanan S, Babu AE, Sadanandan P, Venu AK, Venkidasamy B. Bacopa monnieri for Disorders Affecting Brain: Current Perspectives. Curr Top Med Chem. 2022;22(23):1909-1929. doi: 10.2174/1568026622666220119111538. 9(1):55-62. doi: 10.1080/107175402753413181. 17(5):438-446. doi: 10.2174/1570159X16666180419123022.
5: Deepak M, Amit A. 'Bacoside B'--the need remains for establishing identity. Fitoterapia. 2013 Jun;87:7-10. doi: 10.1016/j.fitote.2013.03.011. Epub 2013 Mar 16. 45(5):829-841. doi: 10.1007/s00449-022-02700-4. Epub 2022 Feb 4. 22(3):407-413. doi: 10.1007/s12298-016-0366-y. Epub 2016 Jul 26.
8: Murthy PB, Raju VR, Ramakrisana T, Chakravarthy MS, Kumar KV, Kannababu S, Subbaraju GV. Estimation of twelve bacopa saponins in Bacopa monnieri extracts and formulations by high-performance liquid chromatography. Chem Pharm Bull (Tokyo). 2006 Jun;54(6):907-11. doi: 10.1248/cpb.54.907. 52(4):1791-1805. doi: 10.1007/s42770-021-00586-0. Epub 2021 Aug 2.
合成参考文献
参考文献:10.1016/0031-9422(96)00250-6
摘要:Garai S, Mahato SB, Ohtani K, Yamasaki K. Bacopasaponin D--a pseudojujubogenin glycoside from Bacopa monniera. Phytochemistry. 1996 Sep;43(2):447–9. doi: 10.1016/0031-9422(96)00250-6.
参考文献:10.1248/cpb.54.907
摘要:Murthy PB, Raju VR, Ramakrisana T, Chakravarthy MS, Kumar KV, Kannababu S, Subbaraju GV. Estimation of twelve bacopa saponins in Bacopa monnieri extracts and formulations by high-performance liquid chromatography. Chem Pharm Bull (Tokyo). 2006 Jun;54(6):907–11. doi: 10.1248/cpb.54.907.
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