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  • 大豆皂苷 III

    Soyasaponin III

    大豆皂苷 III
    产品编号 CFN91596
    CAS编号 55304-02-4
    分子式 = 分子量 C42H68O14 = 796.99
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The seeds of Glycine max
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    大豆皂苷 III CFN91596 55304-02-4 1mg QQ客服:1457312923
    大豆皂苷 III CFN91596 55304-02-4 5mg QQ客服:1457312923
    大豆皂苷 III CFN91596 55304-02-4 10mg QQ客服:1457312923
    大豆皂苷 III CFN91596 55304-02-4 20mg QQ客服:1457312923
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
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  • Universidad de Antioquia (Colombia)
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  • Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
  • Institute of Tropical Disease Universitas Airlangga (Indonesia)
  • University of Fribourg (Switzerland)
  • University of Malaya (Malaysia)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Molecules.2020, 25(20):4851.
  • Korean Herb. Med. Inf.2021, 9(2):231-239.
  • J of Dentistry & Oral Health2019, 2641-1962
  • Environ Toxicol.2020, doi: 10.1002
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  • Mol Med Rep.2023 Oct;28(4):193.
  • Plants (Basel).2021, 10(5):951.
  • Molecules.2018, 23(10):E2638
  • Molecules.2021, 26(18):5665.
  • Horticulture Research2023, uhad164.
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  • Journal of Apicultural Research2021, 60(1)
  • Curr Issues Mol Biol.2022, 44(5):2300-2308.
  • Int J Biol Macromol.2020, 161:1230-1239.
  • Sci Rep.2018, 8:9267
  • Asian Pac J Tropical Bio.2020, 10(6):239-247
  • Sains Malaysiana2022, 51(4):1143-1154
  • Molecules. 2013, 18(11):14105-21
  • Cell Physiol Biochem.2017, 44(4):1381-1395
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  • Cell Death Differ.2021, 1-8.
  • Biomed Pharmacother.2024, 174:116598.
  • ...
  • 生物活性
    Description: Soyasaponin III, a monodesmodic oleanane triterpenoid, is one of the main potentially bioactive saponins found in soy (Glycine max) and related products. Soyasaponin III can induce apoptosis in Hep-G2 cells. Effects on immunohemolysis: Soyasaponin III plays an active role in anticomplementary activity in vitro
    In vitro:
    Planta Med . 2000 Aug;66(6):506-510.
    Effects of triterpenoids from Pueraria lobata on immunohemolysis: beta-D-glucuronic acid plays an active role in anticomplementary activity in vitro[Pubmed: 10985074]
    The anticomplementary properties of kaikasaponin III (4) and soyasaponin I (8) from Pueraria lobata and their hydrolytic analogs were investigated in vitro. Diglycosidic saponins [kaikasaponin I (3), soyasaponin III (7)] showed most potent anticomplementary activities, followed by monoglycosidic saponins [soyasapogenol B monoglucuronide (6), sophoradiol monoglucuronide (2)] and triglycosidic saponins [soyasaponin I (8), kaikasaponin III (4)], whereas sophoradiol (1) and soyasapogenol B (5) showed enhancement of hemolysis under the presence of serum on the classical pathway of complement system. But all of them showed very weak or no anticomplementary activities on the alternative pathway of complement system. The anticomplementary activity of the saponins was influenced by the nature of glucuronic acid, where the free acid forms (-COOH) showed much more potent activity than the sodium salt forms (-COO-Na+) or methyl ester forms (-COOCH3), and the reduced forms (-CH2OH) decreased the activity significantly.
    Planta Med . 1998 Apr;64(3):233-236.
    Structure-hepatoprotective relationships study of soyasaponins I-IV having soyasapogenol B as aglycone[Pubmed: 9581521]
    As a part of our study on the leguminous plants, we investigated the constituents of the aerial parts of Glycine soya. We isolated and identified four known saponins, soyasaponins I, II, III, and IV which have the same aglycone, soyasapogenol B. As a part of our studies concerning hepatoprotective drugs, we also examined the hepatoprotective actions of these saponins towards immunologically induced liver injury on primary cultured rat hepatocytes. The action of soyasaponin II was almost comparable with that of soyasaponin I, whereas those of soyasaponin III and IV were more effective than soyasaponins I and II. This means that the disaccharide group shows greater action than the trisaccharide group. Furthermore, the saponin having a hexosyl unit shows a slightly greater action than that of the pentosyl unit in each disaccharide group or trisaccharide group. Structure-activity relationships suggest that the sugar moiety linked at C-3 may play an important role in hepatoprotective actions of soybean saponins.
    In vivo:
    Vaccine . 2003 May 16;21(17-18):2145-2151.
    Relationship between adjuvant activity and amphipathic structure of soyasaponins[Pubmed: 12706705]
    A correlation between adjuvant activity and amphipathic structure of saponin was first demonstrated on an experimental basis using structurally consecutive analogues. To clarify the physicochemical factors regulating the adjuvanticity of saponin, we compared the profile of the antibody response against chicken ovalbumin (OVA) in mice and hydrophile-lipophile balance (HLB) of eight purified soyasaponins. Soyasaponins bearing sugar chain(s) showed adjuvanticity stimulating anti-OVA total-IgG and IgG1 antibody responses, while their corresponding aglycones soyasapogenols A and B, did not. Among bisdesmosidic soyasaponins, soyasaponin A(1) (HLB: 26.9) with a long sugar side chain induced stronger total-IgG and IgG1 antibody responses than soyasaponin A(2) (HLB: 21.4). For monodesmosidic soyasaponins, the ranking in terms of antibody response was soyasaponin I (which has the highest HLB value (13.6) among the monodesmosidic soyasaponins) > soyasaponin II (HLB: 12.2) > soyasaponin III (HLB: 10.0). The adjuvant activity increased with the HLB value. The length, the number, and the composition of sugar side chains affecting the HLB value would give the overall conformation of each saponin molecule, and the amphipathic structure may define the fundamental adjuvanticity of saponins.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.2547 mL 6.2736 mL 12.5472 mL 25.0944 mL 31.368 mL
    5 mM 0.2509 mL 1.2547 mL 2.5094 mL 5.0189 mL 6.2736 mL
    10 mM 0.1255 mL 0.6274 mL 1.2547 mL 2.5094 mL 3.1368 mL
    50 mM 0.0251 mL 0.1255 mL 0.2509 mL 0.5019 mL 0.6274 mL
    100 mM 0.0125 mL 0.0627 mL 0.1255 mL 0.2509 mL 0.3137 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    大豆皂苷Be甲酯; Soyasaponin Be methyl Ester CFN90777 N/A C49H78O18 = 955.2 5mg QQ客服:1457312923
    大豆皂苷Bd; Soyasaponin Bd CFN90775 135272-91-2 C48H76O19 = 957.1 5mg QQ客服:3257982914
    大豆皂苷IV; Soyasaponin IV CFN93251 108906-97-4 C41H66O13 = 767.0 5mg QQ客服:2056216494
    大豆皂苷 III; Soyasaponin III CFN91596 55304-02-4 C42H68O14 = 796.99 5mg QQ客服:3257982914
    大豆皂苷II; Soyasaponin II CFN93159 55319-36-3 C47H76O17 = 913.1 5mg QQ客服:2056216494
    大豆皂苷Bb; Soyasaponin Bb CFN90456 51330-27-9 C48H78O18 = 943.12 20mg QQ客服:1457312923
    大豆皂苷 Ba; Soyasaponin Ba CFN90722 114590-20-4 C48H78O19 = 959.1 20mg QQ客服:1413575084
    大豆皂苷Aa; Soyasaponin Aa CFN90455 117230-33-8 C64H100O31 = 1365.46 5mg QQ客服:1413575084
    大豆皂苷Ab; Soyasaponin Ab CFN90773 118194-13-1 C67H104O33 = 1437.6 5mg QQ客服:2159513211
    大豆皂苷Ac; Soyasaponin Ac CFN90774 133882-74-3 C67H104O32 = 1421.6 5mg QQ客服:3257982914

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