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  • 土荆皮甲酸-O-β-D-葡萄糖苷

    Pseudolaric acid A-O-beta-D-glucopyranoside

    土荆皮甲酸-O-β-D-葡萄糖苷
    产品编号 CFN90725
    CAS编号 98891-44-2
    分子式 = 分子量 C28H38O11 = 550.6
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The root bark of Pseudolarix amabilis
    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
    土荆皮甲酸-O-β-D-葡萄糖苷 CFN90725 98891-44-2 1mg QQ客服:215959384
    土荆皮甲酸-O-β-D-葡萄糖苷 CFN90725 98891-44-2 5mg QQ客服:215959384
    土荆皮甲酸-O-β-D-葡萄糖苷 CFN90725 98891-44-2 10mg QQ客服:215959384
    土荆皮甲酸-O-β-D-葡萄糖苷 CFN90725 98891-44-2 20mg QQ客服:215959384
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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
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Instytut Nawozów Sztucznych w Pu?awach (Poland)
  • Kamphaengphet Rajabhat University (Thailand)
  • Center for protein Engineering (CIP) (Belgium)
  • Universidade do Porto (Portugal)
  • The Vancouver Prostate Centre (VPC) (Canada)
  • University of Eastern Finland (Finland)
  • University of Ioannina (Greece)
  • Instituto Politécnico de Bragan?a (Portugal)
  • Semmelweis Unicersity (Hungary)
  • Institute of Pathophysiology Medical University of Vienna (Austria)
  • University of East Anglia (United Kingdom)
  • Gyeongsang National University (Korea)
  • MTT Agrifood Research Finland (Finland)
  • National Cancer Institute (USA)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Industrial Crops and Products2021, 163:113313.
  • Biosci. Rep.2020, 10.1024
  • J Chem Inf Model.2021, 61(11):5708-5718.
  • Phytomedicine.2019, 58:152893
  • Pharmacol Res.2020, 161:105205.
  • Korean Herb. Med. Inf. 2016, 4(1):35-42
  • Molecules.2019, 24(6):E1177
  • Sci Rep.2021, 11(1):21038.
  • Asian J of Pharmaceutical&Clinical 2018, 11(2)
  • Phytother Res.2022, 10.1002:ptr.7602.
  • J Ethnopharmacol.2020, 254:112733.
  • Acta Physiologiae Plantarum2016, 38:7
  • Molecules.2023, 28(9):3685.
  • Comput Biol Chem.2019, 83:107096
  • Am J Chin Med.2016, 44(8):1719-1735
  • Pharmaceuticals (Basel).2021, 14(3):260.
  • Molecules2022, 27(12):3824.
  • J Ethnopharmacol.2017, 197:157-164
  • Front Microbiol.2019, 10:2806
  • Nat Prod Sci.2019, 25(3):238
  • J Cell Biochem.2018, 119(2):2231-2239
  • Cell Prolif.2021, 54(8):e13083.
  • Food Sci Biotechnol.2021, 30(2):217-226.
  • ...
  • 生物活性
    In vitro:
    J Pharm Biomed Anal. 2007 Jul 27;44(3):730-6.
    Simultaneous determination of seven major diterpenoids in Pseudolarix kaempferi by high-performance liquid chromatography DAD method.[Pubmed: 17446030 ]

    METHODS AND RESULTS:
    A reversed phase high-performance liquid chromatography method was established for the first time to simultaneously qualify the seven major diterpenoids in Pseudolarix kaempferi, namely pseudolaric acid B O-beta-D-glucopyranoside (1), pseudolaric acid C2 (2), pseudolaric acid C1 (3), deacetylpseudolaric acid A (4), Pseudolaric acid A-O-beta-D-glucopyranoside (5), pseudolaric acid B (6) and pseudolaric acid A (7). The optimal conditions of separation and detection were achieved on an Inertsil ODS-3 column with gradient elution of methanol and 0.5% aqueous acetic acid (v/v) at the flow rate of 0.6 ml min(-1) within 40 min and detection wavelength set at 262 nm. All calibration curves showed good linear regression (r2>0.9999) within test ranges. This method provided good accuracy with recoveries in the range of 94.3-106.1% and good precision with R.S.D.s of repeatability and intermediate precision less than 0.57% and 4.67%, respectively. The method was successfully applied to qualitative and quantitative determination of 20 P. kaempferi among the 54 samples collected from different areas.
    CONCLUSIONS:
    The results revealed that the commercial crude drugs were seriously confused and the developed HPLC assay could be used as a suitable qualitative and quantitative determination method for P. kaempferi.
    In vivo:
    Yao Xue Xue Bao. 2014 Aug;49(8):1169-74.
    Metabolic pathway and metabolites of total diterpene acid isolated from Pseudolarix kaempferi.[Pubmed: 25322560]
    The preliminary metabolic profile of total diterpene acid (TDA) isolated from Pseudolarix kaempferi was investigated by using in vivo and in vitro tests.
    METHODS AND RESULTS:
    Pseudolaric acid C2 (PC2) was identified as the predominant metabolite in plasma, urine, bile and feces after both oral and intravenous administrations to rats using HPLC-UV and HPLC-ESI/MS(n), and demethoxydeacetoxypseudolaric acid B (DDPB), a metabolite proposed to be the glucoside of PC2 (PC2G), as well as pseudolaric acid C (PC), pseudolaric acid A (PA), Pseudolaric acid A-O-beta-D-glucopyranoside (PAG), pseudolaric acid B O-beta-D glucopyranoside (PBG) and deacetylpseudolaric acid A (DPA) originated from TDA could also be detected. It was demonstrated by tests that the metabolism of TDA is independent of intestinal microflora, and neither of pepsin and trypsin is in charge of metabolism of TDA, TDA is also stable in both pH environments of gastric tract and intestinal tract. The metabolites of TDA in whole blood in vitro incubation were found to be PC2, DDPB and PC2G, which demonstrated that the metabolic reaction of TDA in vivo is mainly occurred in blood and contributed to be the hydrolysis of plasma esterase to ester bond, as well as the glucosylation reaction.
    CONCLUSIONS:
    These results clarified the metabolic pathway of TDA for the first time, which is of great significance to the in vivo active form and acting mechanism research of P. kaempferi.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.8162 mL 9.081 mL 18.162 mL 36.324 mL 45.405 mL
    5 mM 0.3632 mL 1.8162 mL 3.6324 mL 7.2648 mL 9.081 mL
    10 mM 0.1816 mL 0.9081 mL 1.8162 mL 3.6324 mL 4.5405 mL
    50 mM 0.0363 mL 0.1816 mL 0.3632 mL 0.7265 mL 0.9081 mL
    100 mM 0.0182 mL 0.0908 mL 0.1816 mL 0.3632 mL 0.4541 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
    去乙酰基土槿甲酸; Deacetylpseudolaric acid A CFN97313 82508-37-0 C20H26O5 = 346.4 5mg QQ客服:215959384
    土槿皮甲酸; Pseudolaric acid A CFN92814 82508-32-5 C22H28O6 = 388.5 20mg QQ客服:3257982914
    土荆皮甲酸-O-β-D-葡萄糖苷 ; Pseudolaric acid A-O-beta-D-glucopyranoside CFN90725 98891-44-2 C28H38O11 = 550.6 10mg QQ客服:2056216494
    土槿甲酸甲酯A; Methyl pseudolarate A CFN97310 82508-33-6 C23H30O6 = 402.5 5mg QQ客服:1413575084
    去甲氧基去乙酰氧基土槿甲酸B; Demethoxydeacetoxypseudolaric acid B CFN97312 82508-36-9 C20H24O7 = 376.4 5mg QQ客服:3257982914
    土荆皮丙酸; Pseudolaric Acid C CFN90724 82601-41-0 C21H26O7 = 390.4 10mg QQ客服:2056216494
    土槿皮乙酸; 土荆皮乙酸; Pseudolaric Acid B CFN99527 82508-31-4 C23H28O8 = 432.46 20mg QQ客服:3257982914
    土荆皮乙酸葡萄糖苷; Pseudolaric acid B-O-beta-D-glucopyranoside CFN90726 98891-41-9 C29H38O13 = 594.6 20mg QQ客服:2159513211
    土槿甲酸甲酯B; Methyl pseudolarate B CFN97311 82508-34-7 C24H30O8 = 446.5 5mg QQ客服:2159513211
    叶含荚宁C; Vibsanin C CFN97692 74690-89-4 C25H36O5 = 416.56 5mg QQ客服:3257982914

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