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  • 士的宁

    Strychnine

    士的宁
    产品编号 CFN98130
    CAS编号 57-24-9
    分子式 = 分子量 C21H22N2O2 = 334.41
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The seeds of Strychnos nu r-vomica L.
    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
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    士的宁 CFN98130 57-24-9 10mg QQ客服:1413575084
    士的宁 CFN98130 57-24-9 20mg QQ客服:1413575084
    士的宁 CFN98130 57-24-9 50mg QQ客服:1413575084
    士的宁 CFN98130 57-24-9 100mg QQ客服:1413575084
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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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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Plants (Basel).2021, 10(2):278.
  • Appl. Sci.2022, 12(4), 2032.
  • ACS Chem Biol.2019, 14(5):873-881
  • Revista Brasileira de Farmacognosia2021, 31:794-804.
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  • Molecules.2019, 24(16):E3003
  • Foods.2021, 10(11):2754.
  • ACS Omega.2021, 6(36):23460-23474.
  • Int Immunopharmacol.2021, 101(Pt A):108181.
  • Nat Prod Sci.2014, 20(3):182-190
  • Nutr Res Pract.2020, 14(5):478-489.
  • Food Res Int.2022, 157:111207.
  • Planta Med.2018, 84(6-07):465-474
  • Free Radic Biol Med.2016, 97:307-319
  • Molecules.2020, 25(9):2111.
  • Evid Based Complement Alternat Med.2021, 2021:5319584.
  • bioRxiv - Molecular Biology2023, 535548.
  • Food Chem.2018, 262:78-85
  • Front Microbiol.2019, 10:2806
  • American Association for Anatomy2020, doi: 10.1002.
  • Planta Med.2018, 84(15):1101-1109
  • Asian J of Pharmaceutical&Clinical 2018, 11(2)
  • Plants (Basel).2021, 10(4):702.
  • ...
  • 生物活性
    Description: Strychnine-insensitive glycine site NMDA antagonist ( R )-HA-966 have neuroprotective effects in an experimental model of Parkinson's disease. Strychnine insensitive glycine receptor has anticonvulsant properties.Strychnine can block binaural inhibition in lateral superior olivary neurons, decrease the voltage-dependent Ca2+ current of both Aplysia and frog ganglion neurons. Strychnine also has inhibitory effects on GABA- and glycine-induced responses.
    Targets: Calcium Channel | Sodium Channel | ATPase | Potassium Channel | GABA Receptor
    In vitro:
    Brain Res. 1991 Oct 4;561(1):77-83.
    Differential blockade of bicuculline and strychnine on GABA- and glycine-induced responses in dissociated rat hippocampal pyramidal cells.[Pubmed: 1797352]

    METHODS AND RESULTS:
    The inhibitory effects of bicuculline (BIC) and strychnine (STR) on GABA- and glycine-induced responses were studied in the rat dissociated hippocampal CA1 pyramidal neurons in whole-cell mode by using the conventional patch-clamp technique. Both GABA and glycine elicited inward Cl- currents in a dose-dependent manner and had almost the same maximal responses. The half-maximum dose (Ka) and Hill coefficient were 6.4 microM and 1.1 for the GABA response, and 74 microM and 1.5 for the glycine response. BIC and STR antagonized both GABA and glycine responses in a competitive manner. The blocking potency of BIC and STR on the GABA response was comparable. The half inhibition dose (IC50) was 2.7 microM for BIC and 6.7 microM for STR. STR blocked the glycine response about 3,000 x more effectively than BIC. The IC50 was 28 nM for STR and 100 microM for BIC. The BIC and STR did not have voltage-dependent blocking effects on either GABA or glycine responses.
    CONCLUSIONS:
    Neither GABA nor glycine showed outward rectification in their current-voltage relationships. The functional role of glycine in the rat hippocampal CA1 region is discussed.
    In vivo:
    Eur J Pharmacol. 1989 Dec 19;174(2-3):197-204.
    A potent antagonist of the strychnine insensitive glycine receptor has anticonvulsant properties.[Pubmed: 2560979]

    METHODS AND RESULTS:
    5.7-Dinitro-quinoxaline-2.3-dione (MNQX) displaced [3H]glycine binding to cortical membranes but had no effect n [3H]3-((+/-)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid ([3H]CPP) binding. MNQX potently antagonized N-methyl-D-aspartate (NMDA)-evoked release of [3H]GABA from cultured cortical neurones, NMDA evoked spreading depression and NMDA depolarizations in the rat neo-cortex. All of these responses were reversed by addition of glycine to the perfusion media.
    CONCLUSIONS:
    These results suggested that MNQX is an antagonist at the strychnine-insensitive glycine receptor associated with the NMDA receptor/ionophore complex. Furthermore the compound was found to antagonise audiogenic seizures in DBA-2 mice indicating the potential of glycine antagonists of this type in anticonvulsant therapy.
    Physiol. Behav., 1970, 5(12):1437-42.
    Strychnine effects on discrimination learning in mice: Effects of dose and time of administration.[Reference: WebLink]

    METHODS AND RESULTS:
    Experiment 1 examined the dose response effects of posttrial injections of strychnine sulphate (0.012–1.25 mg/kg) on learning in mice. Injections were given each day immediately after 3 massed training trials on a food reward visual discrimination task. Facilitation was found with low (0.25, 0.05, 0.10 mg/kg) and high (1.0 and 1.25 mg/kg) doses, but not with intermediate doses (0.20, 0.40, 0.80 mg/kg). Experiment 2 examined the effects of time of pre- or posttrial drug injection of two doses: 0.10 and 1.00 mg/kg. With both doses significant facilitation of learning was obtained with posttrial injection intervals of one hour or less. With 1.0 mg/kg facilitation was obtained with all pretrial injection times examined (longest interval was 1 hr). With 0.10 mg/kg significant facilitation was obtained with injections given 30 min but not 60 min pretrial.
    CONCLUSIONS:
    These findings are interpreted as providing further evidence that strychnine facilitates learning by affecting posttrial neurobiological processes underlying memory storage.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.9903 mL 14.9517 mL 29.9034 mL 59.8068 mL 74.7585 mL
    5 mM 0.5981 mL 2.9903 mL 5.9807 mL 11.9614 mL 14.9517 mL
    10 mM 0.299 mL 1.4952 mL 2.9903 mL 5.9807 mL 7.4759 mL
    50 mM 0.0598 mL 0.299 mL 0.5981 mL 1.1961 mL 1.4952 mL
    100 mM 0.0299 mL 0.1495 mL 0.299 mL 0.5981 mL 0.7476 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
    马钱子碱; Brucine CFN90244 357-57-3 C23H26N2O4 = 394.46 20mg QQ客服:3257982914
    硫酸马钱子碱; Brucine sulfate CFN90316 4845-99-2 C46H54N4O12S = 887.01 20mg QQ客服:2056216494
    士的宁; Strychnine CFN98130 57-24-9 C21H22N2O2 = 334.41 20mg QQ客服:2056216494
    番木鳖次碱; Vomicine CFN96442 125-15-5 C22H24N2O4 = 380.4 5mg QQ客服:1457312923
    葫芦箭毒素,葫芦素; Calebassine CFN90130 7257-29-6 C42H52N4O2 = 644.9 5mg QQ客服:1413575084
    长春花碱; Conophylline CFN99473 142741-24-0 C44H50N4O10 = 794.9 5mg QQ客服:215959384

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