CAS: 58543-17-2; (4R,4As,6Ar,9S,11Ar,11Bs)-9-(((2S,3R,4S,5R,6R)-5-Hydroxy-6-(Hydroxymethyl)-3,4-Bis(((2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-yl)Oxy)Tetrahydro-2H-Pyran-2-yl)Oxy)-4,11B-Dimethyl-8-Methylenetetradecahydro-6A,9-Methanocyclohep

该化合物是来自Stevia rebaudiana叶叶叶的螺旋藻,以其高纯度糖性而著称. 作为非卡罗里加糖的甜食者,它表现出的糖糖的甜度大约是其甜度的150至200倍,使它在食品和饮料应用中成为替代糖的可行替代物. 与其他标准糖质相比, Rebaudioside B有清洁,温和的口味,其苦味或余味都很低,提高了其适合需要中性口味的配方. 高温和酸性条件下的稳定性进一步支持了其在加工食品和饮料中的使用. 其低糖性影响也适用于对糖尿病有利的产品.

结构式图片

上下游产品

CAS号57817-89-7 甜菊苷 | CAS号58543-16-1 甜菊双糖苷A

合成工艺路线路线简述

    📜瑞鲍迪甙 A置于sodium Hydroxide体系中,用 甲醇 作为反应溶剂,化学反应生成 瑞鲍迪甙 B
    参考文献:甜叶菊叶中含甜菊糖苷的鼠李糖或木糖的鉴定,化学合成及甜度评价
    标题:甜叶菊叶中含甜菊糖苷的鼠李糖或木糖的鉴定,化学合成及甜度评价
    摘要:从甜叶菊叶中获得的甜菊糖苷越来越多地作为天然低热量甜味剂用于食品工业.其中,由葡萄糖残基组成的主要苷类(如甜菊苷和莱鲍迪苷a)的甜味已被广泛研究.然而,含有鼠李糖或木糖残基的次要天然产物的性质研究很少.在这项研究中,从我们正在发育的甜菊叶中提取了五种未报道的含有鼠李糖或木糖的甜菊糖苷,并评估了它们的甜度.鉴定了高度糖基化的甜菊糖苷,并使用质谱法通过碎片分析检查了它们的结构.这些糖苷的化学合成证实了它们的结构,并允许对少量甜菊醇糖苷进行感官评价.我们的研究表明,一种含木糖的糖苷莱鲍迪甙 Fx1 具有均衡的甜味,因此,它是食品工业中使用的天然甜味剂的有前途的候选者.
    DOI:10.1021/acs.Jafc.3C01753

    专利信息


    专利号:US-10533205-B1
    优先权日:2013-10-09
    标 题:Kaurenoic acid glycoside precursors and methods of synthesis
    发明人:ZIPP BRANDON
    权利人:VITALITY BIOPHARMA INC
    摘要:Ent-kaurenoic acid glycoside precursor compositions and synthesis methods are provided. The KA-19-monoside, KA-19-bioside and KA-19-trioside precursors can be used as starting materials for a variety of kaurenoic acid based reactions. The precursors provide alternative synthesis pathways for steviol glycosides to the natural pathway based on Steviol biosynthesis. The alternative synthesis pathways using the precursors also circumvent the rate limiting step of the natural Steviol biosynthesis pathway. The precursors can be used individually or in combination to produce a mixture or individual steviol glycosides such as Rebaudioside A, Rebaudioside D or Rebaudioside M. Control over the precursor quantities and composition allows control over the composition of the resulting steviol glycosides that are finally produced.

    专利号:US-2024287479-A1
    优先权日:2021-08-23
    标 题 :Glycosyltransferase mutant, and method for catalytic synthesis of rebaudioside m using glycosyltransferase mutant

    专利号:BR-112017006139-B1
    优先权日:2014-10-03
    标题 :Method for the synthesis of rebaudioside m or rebaudioside m and rebaudioside m

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    Wu X, Qiao T, Huang J, Li J, Wei S, Yang J, Zhang Y, Li Y. Rebaudioside B Attenuates Lung Ischemia-reperfusion Injury-associated Apoptosis and Inflammation. Recent Adv Inflamm Allergy Drug Discov. 2024 Apr 5. doi: 10.2174/0127722708295154240327035857. Epub ahead of print. 25(22):5399. doi: 10.3390/molecules25225399.
    2: Dong J, Yang Z. Characterization of a new hemihydrate rebaudioside B crystal having lower aqueous solubility. Food Chem. 2020 Jan 30;304:125444. doi: 10.1016/j.foodchem.2019.125444. Epub 2019 Aug 29.
    162:141-147. doi: 10.1016/j.phytochem.2019.03.008. Epub 2019 Mar 18. 19(9):844-52. doi: 10.1089/jmf.2016.0014. Epub 2016 Aug 11. 29(5):733-8. doi: 10.1002/bmc.3349. Epub 2014 Oct 9. 68(2):259-68. doi: 10.1016/j.yrtph.2013.12.004. Epub 2013 Dec 18. 14(8):15669-80. doi: 10.3390/ijms140815669.
    8: Jaworska K, Krynitsky AJ, Rader JI. Simultaneous analysis of steviol and steviol glycosides by liquid chromatography with ultraviolet detection on a mixed-mode column: application to Stevia plant material and Stevia-containing dietary supplements. J AOAC Int. 2012 Nov-Dec;95(6):1588-96. doi: 10.5740/jaoacint.11-435. 13(11):15126-36. doi: 10.3390/ijms131115126.

    合成参考文献


    摘要:https://pubs.acs.org/doi/abs/10.1021/acs.analchem.7b00741
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