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  • 氯化乙酰胆碱; 乙酰氯化胆碱

    Acetylcholine chloride

    氯化乙酰胆碱; 乙酰氯化胆碱
    产品编号 CFN90038
    CAS编号 60-31-1
    分子式 = 分子量 C7H16ClNO2 = 181.66
    产品纯度 >=98%
    物理属性 White powder
    化合物类型 Alkaloids
    植物来源
    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
    氯化乙酰胆碱; 乙酰氯化胆碱 CFN90038 60-31-1 10mg QQ客服:3257982914
    氯化乙酰胆碱; 乙酰氯化胆碱 CFN90038 60-31-1 20mg QQ客服:3257982914
    氯化乙酰胆碱; 乙酰氯化胆碱 CFN90038 60-31-1 50mg QQ客服:3257982914
    氯化乙酰胆碱; 乙酰氯化胆碱 CFN90038 60-31-1 100mg QQ客服:3257982914
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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
  • MTT Agrifood Research Finland (Finland)
  • Universidade da Beira Interior (Germany)
  • University of Hawaii Cancer Center (USA)
  • University of Ioannina (Greece)
  • The University of Newcastle (Australia)
  • University of Lodz (Poland)
  • Universidade Católica Portuguesa (Portugal)
  • Mendel University in Brno (Czech Republic)
  • Srinakharinwirot University (Thailand)
  • University of Madras (India)
  • Stanford University (USA)
  • Mahatma Gandhi University (India)
  • Semmelweis Unicersity (Hungary)
  • University of Illinois at Chicago (USA)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Research Square2023, 2883170.
  • Toxicol Appl Pharmacol.2021, 427:115668.
  • Res Rep Urol.2022, 14:313-326.
  • Sci Rep.2023, 13(1):13610.
  • Pharmaceuticals (Basel).2020, 13(10):302.
  • J Asian Nat Prod Res.2019, 5:1-17
  • J Cell Mol Med.2021, 25(5):2645-2654.
  • Journal of Ginseng Research2021, 3 June.
  • Eur J Pharmacol.2021, 906:174220.
  • Appl. Sci.2020, 10(16),5482.
  • Integr Cancer Ther.2018, 17(3):832-843
  • Front Aging Neurosci.2018, 10:269
  • Applied Biological Chemistry2020, 63:37.
  • Food Chem.2021, 337:128023.
  • Food and Fermentation Industries2018, 44(371)
  • J Bone Miner Res.2017, 32(12):2415-2430
  • J Cell Biochem.2018, 119(2):2231-2239
  • Viruses.2017, 9(10)
  • Nutrients2023, 15(18), 4016.
  • Food Sci Biotechnol.2016, 25(5):1437-1442
  • Anticancer Res.2021, 41(3):1357-1364.
  • RSC Adv.2018, 32621-32636
  • Molecules.2022, 27(2):451.
  • ...
  • 生物活性
    Description: Acetylcholine Chloride is a neurotransmitter in both the peripheral nervous system (PNS) and central nervous system (CNS) in many organisms including humans. Acetylcholine chloride in micromolar concentrations significantly inhibit p53 mutant peptide aggregation in vitro, and could be promising candidate for p53 mutant/ misfolded protein aggregation inhibition, and mutations of tumor suppressor protein p53 are present in almost about 50% of all cancers.
    Targets: p53 | AChR
    In vitro:
    Protein Pept Lett. 2017;24(4):353-357.
    Inhibition of p53 Mutant Peptide Aggregation In Vitro by Cationic Osmolyte Acetylcholine Chloride.[Pubmed: 28117010]
    Mutations of tumor suppressor protein p53 are present in almost about 50% of all cancers. It has been reported that the p53 mutations cause aggregation and subsequent loss of p53 function, leading to cancer progression.
    METHODS AND RESULTS:
    Here in this study we focus on the inhibitory effects of cationic osmolyte molecules acetylcholine chloride, and choline on an aggregation prone 10 amino acid p53 mutant peptide WRPILTIITL, and the corresponding wildtype peptide RRPILTIITL in vitro. The characterization tools used for this study include Thioflavin- T (ThT) induced fluorescence, transmission electron microscopy (TEM), congo red binding, turbidity, dynamic light scattering (DLS), and cell viability assays.
    CONCLUSIONS:
    The results show that acetylcholine chloride in micromolar concentrations significantly inhibit p53 mutant peptide aggregation in vitro, and could be promising candidate for p53 mutant/ misfolded protein aggregation inhibition.
    In vivo:
    Microvasc Res. 2011 Sep;82(2):190-7.
    Acetylcholine chloride as a potential source of variability in the study of cutaneous vascular function in man.[Pubmed: 21601579]
    Laser-Doppler flowmetry (LDF) coupled with Acetylcholine chloride (ACh) iontophoresis is increasingly recognized as a reliable non-invasive method to study the endothelial function. However, Acetylcholine chloride-vasodilation measurement appears highly variable possibly due to the Acetylcholine chloride pharmacological properties itself. These problems may be partially overcome by using methacholine chloride (MCh), a more stable synthetic agonist of muscarinic receptors, instead of Acetylcholine chloride. Therefore, we first studied the correlation between the two drugs and then the effects of (1) spatial variability (inter-site measurements), (2) temporal variability (inter-day measurements), (3) intra-day variability (morning versus evening), and (4) age on the variability of both Acetylcholine chloride-vasodilation and MCh-vasodilation.
    METHODS AND RESULTS:
    The endothelium-dependent vasodilation response to simultaneous iontophoretic applications (4 doses of 10s at 0.1mA with 2min of current-free interval) of Acetylcholine chloride(11mM) or MCh (10mM) was studied on the forearm of 40 healthy subjects (36 males, median 28yr, range 21-59yr). The percent change in perfusion (CVCpeak) from baseline and the area under the curve (CVC(AUC)) during iontophoresis were assessed. Inter-site, inter-day and intra-day coefficients of variation (CV) were studied for each drug as well as correlations between drugs and age. A linear relationship was found between ACh- and MCh-CVCpeak (r²=0.75, p=0.01) and between ACh- and MCh-CVC(AUC) (r²=0.55, p=0.02). MCh inter-site CV for both CVCpeak (12.2%) and CVC(AUC) (13.8%) was significantly lower than ACh inter-site CV for CVCpeak (15.5%) and CVC(AUC) (15.3%), respectively. MCh inter-day CV for CVCpeak (17.2%) and CVC(AUC) (14.6%) was significantly lower than ACh inter-day CV for CVCpeak (19.7%) and ACh CVC(AUC) (21.2%). For ACh and MCh, the CVCpeak and CVC(AUC) were higher at 16:00pm than at 11:00am (p<0.05 for all). Finally, both ACh- and MCh-CVCpeak exhibited a logarithmic decrease with age (r²=0.61, p<0.01 and r²=0.58, p<0.01).
    CONCLUSIONS:
    Although both drugs exhibited circadian and age variability, MCh exhibited less inter-site and interday variabilities than did Acetylcholine chloride for the evaluation of cutaneous endothelium-dependent vasodilation. These findings should be taken into account in studies of cutaneous vascular function by iontophoresis coupled with laser Doppler flowmetry.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 5.5048 mL 27.5239 mL 55.0479 mL 110.0958 mL 137.6197 mL
    5 mM 1.101 mL 5.5048 mL 11.0096 mL 22.0192 mL 27.5239 mL
    10 mM 0.5505 mL 2.7524 mL 5.5048 mL 11.0096 mL 13.762 mL
    50 mM 0.1101 mL 0.5505 mL 1.101 mL 2.2019 mL 2.7524 mL
    100 mM 0.055 mL 0.2752 mL 0.5505 mL 1.101 mL 1.3762 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
    四甲基铵; Tetramethylammonium CFN00093 51-92-3 C4H12N+ = 74.14 5mg QQ客服:2056216494
    三甲胺氧化物; Trimethylamine oxide CFN00096 1184-78-7 C3H9NO = 75.11 5mg QQ客服:1413575084
    N,N,N-Trimethyl-2-aminoethylphosphonate; N,N,N-Trimethyl-2-aminoethylphosphonate CFN00097 14596-57-7 C5H14NO3P = 167.14 5mg QQ客服:215959384
    Trimethyl[3-(methylthio)propyl]ammonium(1+); Trimethyl[3-(methylthio)propyl]ammonium(1+) CFN00098 61672-50-2 C7H18NS+ = 148.29 5mg QQ客服:2056216494
    3-(Dimethylsulfonio)-N,N,N-trimethylpropanaminium(2+); 3-(Dimethylsulfonio)-N,N,N-trimethylpropanaminium(2+) CFN00099 61672-51-3 C8H21NS2+ = 163.33 5mg QQ客服:215959384
    4-羟基苯甲酰胆碱; 4-Hydroxybenzoyl choline CFN95158 5094-31-5 C12H18NO3 = 224.3 20mg QQ客服:215959384
    Trimethylvinylammonium(1+); Trimethylvinylammonium(1+) CFN00100 13448-18-5 C5H12N+ = 86.16 5mg QQ客服:2056216494
    氯化乙酰胆碱; 乙酰氯化胆碱; Acetylcholine chloride CFN90038 60-31-1 C7H16ClNO2 = 181.66 20mg QQ客服:1413575084
    甜菜碱; Betaine CFN99546 107-43-7 C5H11NO2 = 117.15 20mg QQ客服:2159513211
    盐酸甜菜碱; Betaine hydrochloride CFN99547 590-46-5 C5H12ClNO2 = 153.60 20mg QQ客服:2159513211

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