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  • 芹菜苷

    Apiin

    芹菜苷
    产品编号 CFN90165
    CAS编号 26544-34-3
    分子式 = 分子量 C26H28O14 = 564.49
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Flavonoids
    植物来源 The herbs of Petroselinum crispum.
    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
    芹菜苷 CFN90165 26544-34-3 10mg QQ客服:1457312923
    芹菜苷 CFN90165 26544-34-3 20mg QQ客服:1457312923
    芹菜苷 CFN90165 26544-34-3 50mg QQ客服:1457312923
    芹菜苷 CFN90165 26544-34-3 100mg 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
    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
  • National Cancer Center Research Institute (Japan)
  • Kamphaengphet Rajabhat University (Thailand)
  • Universite Libre de Bruxelles (Belgium)
  • University of Parma (Italy)
  • St. Jude Children Research Hospital (USA)
  • Molecular Biology Institute of Barcelona (IBMB)-CSIC (Spain)
  • Macau University of Science and Technology (China)
  • Shanghai Institute of Organic Chemistry (China)
  • Biotech R&D Institute (USA)
  • CSIRO - Agriculture Flagship (Australia)
  • Warszawski Uniwersytet Medyczny (Poland)
  • Pennsylvania State University (USA)
  • Srinakharinwirot University (Thailand)
  • Instituto Politécnico de Bragan?a (Portugal)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Asian J Beauty Cosmetol2019, 17(3):287-294
  • Phytomedicine.2019, 55:229-237
  • Analytical sci. & Tech2016, 186-193
  • Molecules.2019, 24(4):E709
  • Sci Rep.2021, 11(1):11936.
  • Plant Cell Tiss Org2017, 479-486
  • Sci Rep.2015, 5:13194
  • Agronomy2023, 13(6), 1435.
  • Antioxidants (Basel).2020, 9(6):544.
  • J of Health Science and Alternative Medicine2019, 1(1)
  • Chem Biol Interact.2016, 260:168-175
  • Nutrients.2018, 10(10)
  • JAOCS2021, 98(7):779-794.
  • Food Analytical Methods2020, 1-10
  • Chin J Appl. Physiol.2019, 35(3):283-288
  • Appl Microbiol Biotechnol.2016, 100(9):3965-77
  • Environ Toxicol.2020, doi: 10.1002
  • Antioxidants (Basel).2021, 10(11): 1802.
  • Cell.2022, 185(23):4298-4316.e21.
  • Eur J Pharmacol.2021, 899:174010.
  • Korean Journal of Medicinal Crop Science2018, 26(5):382-390
  • Phytomedicine.2019, 65:153089
  • J Biochem Mol Toxicol.2021, 35(5):e22731.
  • ...
  • 生物活性
    Description: Apiin as a reducing agent, used in biological synthesis of silver and gold nanoparticles. Apiin has anti-inflammatory properties, it has inhibitory activity in-vitro on iNOS expression and nitrite production when added before LPS stimulation in the medium of J774.A1 cells.
    Targets: NOS
    In vitro:
    J Pharm Pharmacol. 2007 Jun;59(6):891-7.
    An extract of Apium graveolens var. dulce leaves: structure of the major constituent, apiin, and its anti-inflammatory properties.[Pubmed: 17637182]
    Flavonoids, natural compounds widely distributed in the plant kingdom, are reported to affect the inflammatory process and to possess anti-inflammatory as well as immunomodulatory activity in-vitro and in-vivo.
    METHODS AND RESULTS:
    Since nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) is one of the inflammatory mediators, the effects of the ethanol/water (1:1) extract of the leaves of Apium graveolens var. dulce (celery) on iNOS expression and NO production in the J774.A1 macrophage cell line stimulated for 24 h with Escherichia coli lipopolysaccharide (LPS) were evaluated. The extract of A. graveolens var. dulce contained apiin as the major constituent (1.12%, w/w, of the extract). The extract and apiin showed significant inhibitory activity on nitrite (NO) production in-vitro (IC50 0.073 and 0.08 mg mL(-1) for the extract and apiin, respectively) and iNOS expression (IC50 0.095 and 0.049 mg mL(-1) for the extract and apiin, respectively) in LPS-activated J774.A1 cells. The croton-oil ear test on mice showed that the extract exerted anti-inflammatory activity in-vivo (ID50 730 microg cm(-2)), with a potency seven-times lower than that of indometacin (ID50 93 microg cm(-2)), the non-steroidal anti-inflammatory drug used as reference.
    CONCLUSIONS:
    Our results clearly indicated the inhibitory activity of the extract and apiin in-vitro on iNOS expression and nitrite production when added before LPS stimulation in the medium of J774.A1 cells. The anti-inflammatory properties of the extract demonstrated in-vivo might have been due to reduction of iNOS enzyme expression.
    Pharm Biol. 2016;54(1):174-9.
    Compounds from Sedum caeruleum with antioxidant, anticholinesterase, and antibacterial activities.[Pubmed: 25845643]
    This is the first study on the phytochemistry, antioxidant, anticholinesterase, and antibacterial activities of Sedum caeruleum L. (Crassulaceae). The objective of this study is to isolate the secondary metabolites and determine the antioxidant, anticholinesterase, and antibacterial activities of S. caeruleum.
    METHODS AND RESULTS:
    Six compounds (1-6) were isolated from the extracts of S. caeruleum and elucidated using UV, 1D-, 2D-NMR, and MS techniques. Antioxidant activity was investigated using DPPH(•), CUPRAC, and ferrous-ions chelating assays. Anticholinesterase activity was determined against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes using the Ellman method. Antibacterial activity was performed according to disc diffusion and minimum inhibitory concentration (MIC) methods. Isolated compounds were elucidated as ursolic acid (1), daucosterol (2), β-sitosterol-3-O-β-D-galactopyranoside (3), apigenin (4), apigetrin (5), and apiin (6). The butanol extract exhibited highest antioxidant activity in all tests (IC50 value: 28.35 ± 1.22 µg/mL in DPPH assay, IC50 value: 40.83 ± 2.24 µg/L in metal chelating activity, and IC50 value: 23.52 ± 0.44 µg/L in CUPRAC), and the highest BChE inhibitory activity (IC50 value: 36.89 ± 0.15 µg/L). Moreover, the chloroform extract mildly inhibited (MIC value: 80 µg/mL) the growth of all the tested bacterial strains.
    CONCLUSIONS:
    Ursolic acid (1), daucosterol (2), β-sitosterol-3-O-β-D-galactopyranoside (3), apigenin (4), apigetrin (5), and apiin (6) were isolated from Sedum caeruleum for the first time. In addition, a correlation was observed between antioxidant and anticholinesterase activities of bioactive ingredients of this plant.
    In vivo:
    Ann Nutr Metab. 2006;50(3):167-72.
    Bioavailability of apigenin from apiin-rich parsley in humans.[Pubmed: 16407641]
    Absorption and excretion of apigenin after the ingestion of apiin-rich food, i.e. parsley, was tested.
    METHODS AND RESULTS:
    Eleven healthy subjects (5 women, 6 men) in the age range of 23-41 years and with an average body mass index of 23.9 +/- 4.1 kg/m2 took part in this study. After an apigenin- and luteolin-free diet, a single oral bolus of 2 g blanched parsley (corresponding to 65.8 +/- 15.5 micromol apigenin) per kilogram body weight was consumed. Blood samples were taken at 0, 4, 6, 7, 8, 9, 10, 11 and 28 h after parsley consumption and 24-hour urine samples were collected. Apigenin was analyzed in plasma, urine and red blood cells by means of HPLC-ECD. On average, a maximum apigenin plasma concentration of 127 +/- 81 nmol/l was reached after 7.2 +/- 1.3 h with a high range of variation between subjects. For all participants, plasma apigenin concentration rose after bolus ingestion and fell within 28 h under the detection limit (2.3 nmol/l). The average apigenin content in 24-hour urine was 144 +/- 110 nmol/24 h corresponding to 0.22 +/- 0.16% of the ingested dose. The flavone could be detected in red blood cells without showing dose-response characteristics.
    CONCLUSIONS:
    A small portion of apigenin provided by food reaches the human circulation and, therefore, may reveal biological effects.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.7715 mL 8.8576 mL 17.7151 mL 35.4302 mL 44.2878 mL
    5 mM 0.3543 mL 1.7715 mL 3.543 mL 7.086 mL 8.8576 mL
    10 mM 0.1772 mL 0.8858 mL 1.7715 mL 3.543 mL 4.4288 mL
    50 mM 0.0354 mL 0.1772 mL 0.3543 mL 0.7086 mL 0.8858 mL
    100 mM 0.0177 mL 0.0886 mL 0.1772 mL 0.3543 mL 0.4429 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
    密蒙花新甙; Neobudofficide CFN95640 194602-91-0 C34H42O18 = 738.7 10mg QQ客服:3257982914
    金柑苷-6''-beta-D-葡萄糖苷; Fortunellin-6''-beta-D-glucopyranoside (Acacetin-7-O-[2''-O-rhamnosyl-6''-O-glucosyl]-glucoside) CFN95315 1218774-64-1 C34H42O19 = 754.7 5mg QQ客服:2159513211
    5-(beta-D-吡喃葡萄糖氧基)-7-甲氧基-2-(4-甲氧基苯基)-4H-1-苯并吡喃-4-酮; 7,4-Di-O-methylapigenin 5-O-glucoside CFN99900 197018-71-6 C23H24O10 = 460.4 5mg QQ客服:215959384
    7,4'-Di-O-methylapigenin 5-O-xylosylglucoside; 7,4'-Di-O-methylapigenin 5-O-xylosylglucoside CFN98099 221257-06-3 C28H32O14 = 592.6 5mg QQ客服:3257982914
    芹菜素-5-O-新橙皮苷; Apigenin 5-O-neohesperidoside CFN96527 850630-40-9 C27H30O14 = 578.52 5mg QQ客服:3257982914
    山茶黄酮苷 A; Camellianin A CFN90992 109232-77-1 C29H32O15 = 620.56 5mg QQ客服:3257982914
    Angeflorin; Angeflorin CFN96365 57498-69-8 C23H24O11 = 476.4 5mg QQ客服:2159513211
    Gelomuloside B; Gelomuloside B CFN96348 149998-39-0 C28H32O15 = 608.6 5mg QQ客服:3257982914
    Gelomuloside A; Gelomuloside A CFN96347 149998-38-9 C29H34O15 = 622.6 5mg QQ客服:1413575084
    大蓟苷; Pectolinarin CFN99727 28978-02-1 C29H34O15 = 622.57 20mg QQ客服:215959384

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