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  • 盐酸帕洛诺司琼

    Palonosetron hydrochloride

    盐酸帕洛诺司琼
    产品编号 CFN90009
    CAS编号 135729-62-3
    分子式 = 分子量 C19H25ClN2O = 332.87
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 From Streptomycetaceae
    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
    盐酸帕洛诺司琼 CFN90009 135729-62-3 10mg QQ客服:1457312923
    盐酸帕洛诺司琼 CFN90009 135729-62-3 20mg QQ客服:1457312923
    盐酸帕洛诺司琼 CFN90009 135729-62-3 50mg QQ客服:1457312923
    盐酸帕洛诺司琼 CFN90009 135729-62-3 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
  • Leibniz-Institut für Pflanzenbiochemie (IPB) (Germany)
  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
  • University of Wuerzburg (Germany)
  • Sri Ramachandra University (India)
  • Shanghai Institute of Organic Chemistry (China)
  • The University of Newcastle (Australia)
  • Uniwersytet Jagielloński w Krakowie (Poland)
  • Mahidol University (Thailand)
  • Melbourne University (Australia)
  • China Medical University (Taiwan)
  • Instytut Nawozów Sztucznych w Pu?awach (Poland)
  • Universidad de Buenos Aires (Argentina)
  • Seoul National University of Science and Technology (Korea)
  • Helmholtz Zentrum München (Germany)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Applied Biological Chemistry2020, 63:37.
  • HortTechnology2016, 26(6):816-819
  • JPC-Journal of Planar Chromatography 2017, 30(2)
  • LWT2020, 130:109535
  • Molecules.2022, 27(19):6681.
  • J Med Food.2020, 23(6):633-640.
  • Pol J Microbiol.2021, 70(1):117-130.
  • Molecules.2019, 24(9):E1719
  • Antioxidants (Basel).2020, 9(2): E119
  • Int J Mol Sci.2020, 21(9):3239.
  • BMB Rep.2018, 51(5):249-254
  • Biosci Biotechnol Biochem.2021, 85(10):2153-2160.
  • ScientificWorldJournal.2022, 2022:4806889.
  • Proc Natl Acad Sci USA.2016, 113(30):E4407-1
  • J of Advanced Scientific R.2020, 11(3), p109-120.
  • J Mass Spectrom.2022, 57(2):e4810.
  • Int. J. Mol. Sci.2022, 23(8), 4130.
  • Naunyn Schmiedebergs Arch Pharmacol.2021, 394(1):107-115.
  • Front Immunol.2023, 14:1240800.
  • Pharmacol Res.2022, 182:106346.
  • Research on Crops.2017, 18(2)
  • Industrial Crops and Products2019, 140:111612
  • International J of Green Pharmacy2019, 13(3)
  • ...
  • 生物活性
    Description: Palonosetron hydrochloride is the only serotonin receptor antagonist approved for prevention of delayed chemotherapy-induced nausea and vomiting (CINV) caused by moderate emetogenic chemotherapy (MEC).
    Targets: 5-HT Receptor
    In vitro:
    Expert Opin Pharmacother. 2013 Apr;14(5):629-41.
    An update on palonosetron hydrochloride for the treatment of radio/chemotherapy-induced nausea and vomiting.[Pubmed: 23414148]
    Nausea and vomiting are well recognized in different clinical situations, suggesting that no single mechanism is likely to be responsible for their production.
    METHODS AND RESULTS:
    Chemotherapy-induced nausea and vomiting (CINV) can have a negative impact on quality of life and this may lead to a refusal of curative therapy or to a decline in palliative benefits offered by cytotoxic treatment. Palonosetron hydrochloride is a new agent in the class of 5-HT3 receptor antagonists (5-HT3RAs), and differs from the other agents by its higher receptor-binding affinity and longer half-life. These pharmacological properties have resulted in improved antiemetic activity in clinical trials, particularly in the treatment of delayed CINV following moderate emetogenic chemotherapy (MEC). A systematic review of the medical literature was completed to inform this update. MEDLINE, the Cochrane Collaboration Library and meeting materials from ASCO and MASCC were all searched.
    CONCLUSIONS:
    Palonosetron hydrochloride was the only serotonin receptor antagonist approved for prevention of delayed CINV caused by MEC and its use was incorporated in guideline recommendations. To date, several treatment settings such as multiple day chemotherapy require further studies to improve emesis related to therapy.
    In vivo:
    Exp Ther Med. 2013 May;5(5):1418-1426.
    The effect of palonosetron hydrochloride in the prevention of chemotherapy-induced moderate and severe nausea and vomiting.[Pubmed: 23737892]
    The current study aimed to evaluate the efficacy and safety of Palonosetron hydrochloride injection for preventing chemotherapy-induced moderate and severe nausea and vomiting.
    METHODS AND RESULTS:
    A multi-centered, randomly stratified, double-blind, double-dummy, parallel-group and positive-controlled trial was performed. A total of 240 patients who underwent chemotherapy treatment which induced moderate or severe vomiting were divided into the experimental and control groups. Half an hour before chemotherapy, the experimental group received a 0.25-mg Palonosetron hydrochloride injection, whereas the control group received a 3-mg granisetron injection. The acute vomiting complete remission rate (CRR) of the experimental group was not significantly different compared with that of the control group (P=0.35). The delayed vomiting CRR of the experimental group was significantly higher compared with that of the control group (P=0.002). No difference in full course vomiting CRR, vomiting control time, treatment failure time or acute nausea CRR was identified between the two groups. No significant differences in adverse events were observed between the experimental group and the control group. No significant differences in adverse reactions occurred between the experimental group and the control group (12.50%).
    CONCLUSIONS:
    Palonosetron hydrochloride injection had a better effect on delayed vomiting CRR than granisetron hydrochloride injection. The two injections exhibited similar effects on acute vomiting CRR, full course vomiting CRR, vomiting control time, treatment failure time (days), acute nausea CRR and adverse events.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.0042 mL 15.0209 mL 30.0418 mL 60.0835 mL 75.1044 mL
    5 mM 0.6008 mL 3.0042 mL 6.0084 mL 12.0167 mL 15.0209 mL
    10 mM 0.3004 mL 1.5021 mL 3.0042 mL 6.0084 mL 7.5104 mL
    50 mM 0.0601 mL 0.3004 mL 0.6008 mL 1.2017 mL 1.5021 mL
    100 mM 0.03 mL 0.1502 mL 0.3004 mL 0.6008 mL 0.751 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
    2-环己基乙胺; 2-Cyclohexylethylamine CFN00069 4442-85-7 C8H17N = 127.23 5mg QQ客服:2159513211
    N-甲基环己烷乙胺; N-Methylcyclohexaneethaneamine CFN00070 62141-38-2 C9H19N = 141.29 5mg QQ客服:3257982914
    3,3'-[Iminobis(methylene)]bis-2(3H)furanone; 3,3'-[Iminobis(methylene)]bis-2(3H)furanone CFN00082 96562-86-6 C10H15NO4 = 213.23 5mg QQ客服:1457312923
    Cassipourine; Cassipourine CFN00442 14051-10-6 C14H22N2S4 = 346.60 5mg QQ客服:2159513211
    酒石酸伐仑克林; Varenicline tartrate CFN90008 375815-87-5 C13H13N3.C4H6O6 = 361.35 5mg QQ客服:2056216494
    盐酸帕洛诺司琼; Palonosetron hydrochloride CFN90009 135729-62-3 C19H25ClN2O = 332.87 20mg QQ客服:2056216494
    盐酸普拉克索; Pramipexole dihydrochloride CFN90019 104632-25-9 C10H19Cl2N3S = 284.25 5mg QQ客服:2056216494
    雷美替胺; Ramelteon CFN90021 166597-26-9 C13H21NO2 = 259.34 5mg QQ客服:3257982914
    凝血酸,氨甲环酸; Tranexamic acid CFN90569 1197-18-8 C8H15NO2 = 157.21 20mg QQ客服:1413575084

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