CAS: 62025-49-4; (2R,3R,4S,5S,6R)-2-(((3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-Hydroxy-4,4,8,10,14-Pentamethyl-17-((S)-6-Methyl-2-(((2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-yl)Oxy)Hept-5-En-2-yl)Hexadecahydro-1H-Cyclopenta[a]Phenanthren-3-yl)Oxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol

该化合物是源自Panax gunseng的原丙烷二型沙邦素,以其潜在的药理活动著称;作为二级代谢物,它表现出显著的生物活性,包括抗炎,抗氧化剂和...

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CAS号6892-79-1 Folienetriol | CAS号51116-90-6 12β,20-Dihydrox... | CAS号108194-57-6 3,20-di-O-(2',3...

合成工艺路线路线简述

  • 41753-43-9 = 62025-49-4 + 110261-98-8 + 39262-14-1 + 52705-93-8 + 80321-69-3
    反应条件:1.1 Catalysts: Ginsenoside Glycosidase Solvents: Water; 100 Min,Ph 5.0,45 °C1.2 Reagents: 1-Butanol Solvents: Water
    标题:Biotransformation Pathway And Kinetics Of The Hydrolysis Of The 3-O- And 20-O-Multi-Glucosides Of Ppd-Type Ginsenosides By Ginsenosidase Type I
    作者:Liu,Chunying; Et Al
    参考文献:Process Biochemistry (Oxford 日期:2014 卷标:49(5) 页码:813-820]

    41753-43-9 = 62025-49-4 + 39262-14-1 + 52705-93-8 + 80321-69-3 + 30636-90-9
    反应条件:1.1 Reagents: (+)-Lactose Catalysts: Glucosidase,β- Solvents: Water; 72 H,37 °C
    标题:Enzymatic Transformation Of Ginsenoside Rb1 By Lactobacillus Pentosus Strain 6105 From Kimchi
    作者:Kim,Se-Hwa; Et Al
    参考文献:Journal Of Ginseng Research 日期:2012 卷标:36(3) 页码:291-297]

    11021-13-9 = 62025-49-4 + 83480-64-2
    反应条件:1.1 Solvents: Water; 30 H,Ph 6.0,37 °C1.2 Reagents: 1-Butanol
    标题:Fungal Sensitivity To And Enzymatic Deglycosylation Of Ginsenosides
    作者:Zhao,Xuesong; Et Al
    参考文献:Phytochemistry (Elsevier) 日期:2012 卷标:78 页码:65-71]

    68406-26-8 = 62025-49-4 + 39262-14-1 + 80321-63-7 + 52705-93-8 + 80325-22-0
    反应条件:1.1 Catalysts: Ginsenoside Glycosidase Solvents: Water; 120 Min,Ph 5.0,45 °C1.2 Reagents: 1-Butanol Solvents: Water
    标题:Biotransformation Pathway And Kinetics Of The Hydrolysis Of The 3-O- And 20-O-Multi-Glucosides Of Ppd-Type Ginsenosides By Ginsenosidase Type I
    作者:Liu,Chunying; Et Al
    参考文献:Process Biochemistry (Oxford 日期:2014 卷标:49(5) 页码:813-820]

    41753-43-9 = 62025-49-4 + 80321-69-3
    反应条件:1.1 Solvents: Water; 30 H,Ph 6.0,37 °C1.2 Reagents: 1-Butanol
    标题:Fungal Sensitivity To And Enzymatic Deglycosylation Of Ginsenosides
    作者:Zhao,Xuesong; Et Al
    参考文献:Phytochemistry (Elsevier) 日期:2012 卷标:78 页码:65-71]

    41753-43-9 = 62025-49-4 + 39262-14-1 + 80321-69-3 + 30636-90-9
    反应条件:1.1 Reagents: Glucose Catalysts: Glucosidase,β- Solvents: Water; 72 H,37 °C
    标题:Enzymatic Transformation Of Ginsenoside Rb1 By Lactobacillus Pentosus Strain 6105 From Kimchi
    作者:Kim,Se-Hwa; Et Al
    参考文献:Journal Of Ginseng Research 日期:2012 卷标:36(3) 页码:291-297
人参皂甙置于β-Galactosidase From Aspergillus Saponins,水体系中,用 甲醇 作为反应溶剂,化学反应 96.0H,反应生成 人参皂苷f2
参考文献:Highly Efficient Biotransformation Of Ginsenoside Rb1 And Rg3 Using β-Galactosidase From Aspergillus Sp.
标题:Highly Efficient Biotransformation Of Ginsenoside Rb1 And Rg3 Using β-Galactosidase From Aspergillus Sp.
摘要:从曲霉中的β-半乳糖苷酶可以将主要的人参皂苷rb1转化为罕见的人参皂苷f2,通过人参皂苷rd.人参皂苷rg3可以通过这种β-半乳糖苷酶进行选择性水解,同时也只得到了人参皂苷rh2.
DOI:10.1039/c5Ra11519A

海关参考信息

专利信息


专利号:CN-114507676-B
优先权日:2022-02-11
标题 :A kind of PgJAR1 gene regulated by ginsenoside synthesis and its encoded protein and application

专利号:CN-114507676-A
优先权日:2022-02-11
标 题:A kind of ginsenoside synthesis-regulated PgJAR1 gene and its encoded protein and application
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主要参考文献


1: Shin HS, Park SY, Hwang ES, Lee DG, Mavlonov GT, Yi TH. Ginsenoside F2 reduces hair loss by controlling apoptosis through the sterol regulatory element-binding protein cleavage activating protein and transforming growth factor-β pathways in a dihydrotestosterone-induced mouse model. Biol Pharm Bull. 2014;37(5):755-63. doi: 10.3109/14756366.2013.871006. Epub 2014 Mar 25. doi: 10.1016/j.ejphar.2014.02.024. Epub 2014 Mar 12. doi: 10.1007/s10529-014-1472-y. Epub 2014 Feb 23. doi: 10.4014/jmb.1605.05052. doi: 10.1016/j.canlet.2012.01.045. Epub 2012 Feb 7. Epub 2016 Oct 18.
8: Park SH, Seo W, Eun HS, Kim SY, Jo E, Kim MH, Choi WM, Lee JH, Shim YR, Cui CH, Kim SC, Hwang CY, Jeong WI. Protective effects of ginsenoside F2 on 12-O-tetradecanoylphorbol-13-acetate-induced skin inflammation in mice. Biochem Biophys Res Commun. 2016 Sep 30;478(4):1713-9. doi: 10.1016/j.bbrc.2016.09.009. Epub 2016 Sep 3. doi: 10.5142/jgr.2012.36.4.418.
10: Li L, Shin SY, Lee SJ, Moon JS, Im WT, Han NS. Production of Ginsenoside F2 by Using Lactococcus lactis with Enhanced Expression of β-Glucosidase Gene from Paenibacillus mucilaginosus. J Agric Food Chem. 2016 Mar 30;64(12):2506-12. doi: 10.1021/acs.jafc.5b04098. Epub 2015 Nov 5. doi: 10.1371/journal.pone.0085727. eCollection 2014.

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参考文献:10.1038/s41592-019-0358-2]
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