品牌咨询
联系方式
公司地址
苏州工业园区生物纳米园A4#216
联系电话
4000-520-616 / 18915418616
传真号码
0512-67156496
电子邮箱
info@ebiomall.com
公司网址
https://www.ebiomall.com

Discovery Antibodies/Biperiden hydrochloride/25 mg/B-115-25 mg

价格
¥1920.00
货号:B-115-25mg
浏览量:85
品牌:Discovery
服务
全国联保
正品保证
正规发票
签订合同
商品描述
Cat #: B-115
Alternative Name Akineton®, Akinophyl®
  • Lyophilized Powder
  • Bioassay Tested
  • Source Synthetic
    MW: 347.92
    Purity: >99%
    Effective concentration 0.5 nM - 100 μM.
      • Biperiden hydrochloride
    Chemical name α-Bicyclo[2.2.1]hept-5-en-2-yl-α-phenyl-1-piperidinepropanol hydrochloride.
    Molecular formula C21H29NO*HCl.
    CAS No.: 1235-82-1.
    Activity Biperiden hydrochloride is a muscarinic acetylcholine receptor (mAChR) antagonist that displays selectivity for the M1 subtype (Ki values are 0.48, 2.4, 3.9, 6.3 and 6.3 nM for M1, M4, M3, M2 and M5 receptors respectively)1. It alleviates extrapyramidal symptoms associated with antipsychotic drugs2 and displays antiparkinsonian activity3.
      • Bolden, C. et al. (1992) J. Pharmacol. Exp. Ther.  260, 576.
      • Sudo, Y. et al. (1999) Life Sci. 64, PL99.
      • Brocks, D.R. (1999) J. Pharm. Pharmaceut. Sci. 2, 39.
    Shipping and storage Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C. Store with a desiccant in a cool place.
    Solubility DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
    Storage of solutions Up to four weeks at 4°C or three months at -20°C.
      • Biperiden hydrochloride
        Alomone Labs Biperiden hydrochloride inhibits carbachol’s effect on M1 mAChR expressed in C6 cells.
        Cells were loaded with Fluo-3 AM and changes in intracellular Ca2+ were detected via changes in Fluo-3 emission following application. A. Normalized fluorescence following application (arrow) of 10 μM Carbachol without (control) and with 10 or 100 μM Biperiden hydrochloride (#B-115), as indicated. B. Inhibition of 10 μM Carbachol effect, plotted against Biperiden hydrochloride concentrations.
    References - Scientific background
    • 1. Bonner, T.I. (1989) Trends. Neurosci. 12, 148.
    • 2. Felder, C.C. (1995) FASEB. J. 9, 619.
    • 3. Bolden, C. et al. (1992) J. Pharmacol. Exp. Ther. 260, 576.
    • 4. Eltze, M. and Figala, V. (1988) Eur. J. Pharmacol. 158, 11.
    • 5. Brocks, D.R. (1999) J. Pharm. Pharmaceut. Sci. 2, 39.
    • 6. Sudo, Y. et al. (1999) Life Sci. 64, PL99.
      • Muscarinic acetylcholine receptors (mAChR) regulate a number of important basic physiologic functions including heart rate, motor and sensory control and more complex behaviors including arousal, memory, and learning. Loss of muscarinic receptor number or function has been implicated in the etiology of several neurological disorders including Alzheimer"s dementia, Down"s syndrome, and Parkinson"s disease. Five subtypes of muscarinic receptors (m1-m5) have been identified by molecular cloning1 and much has been learned about their distribution, pharmacology, and structure2.

        Biperiden hydrochloride is a non-selective muscarinic receptor antagonist that displays selectivity for the M1 subtype (Ki values are 0.48, 2.4, 3.9, 6.3 and 6.3 nM for M1, M4, M3, M2 and M5 receptors respectively)3-4. It is antiparkinsonian5 and therefore used for the adjunctive treatment of all forms of Parkinson"s disease (postencephalitic, idiopathic, and arteriosclerotic), also commonly used to improve parkinsonian signs and symptoms related to antipsychotic drug therapy6.

    Target M1-M5 muscarinic receptors
    receive a 5 mg free trial sample!
    Last update: 25/09/2019

    Biperiden hydrochloride (#B-115) is a highly pure, synthetic, and biologically active compound.

    For research purposes only, not for human use
    Discovery Antibodies的Cyclin dependant kinase 2 (CDK2) is a serine/threonine protein kinase which controls both G1/S and G2/M transitions. CDKs along with cyclins and CDK inhibitors regulate cell cycle progression. Specific cyclins activate different CDKs; in early G1, CDK2 pairs with cyclin E to promote entry into the S phase before switching to partner with cyclin A to drive the cell through S phase. Once activated CDKs phosphorylate downstream proteins to initiate signalling cascades. CDK2 phosphorylates and inactivates the RB1 (pRb) tumour suppressor family of proteins.CDK的活动受到严格控制。CDK2活性可以被包括P21在内的一系列抑制剂抑制。细胞周期失调和增殖控制的丧失与细胞转化和癌症密切相关。CDK2在DNA损伤反应(DDR)中的细胞周期停滞中也似乎起着积极作用,它的抑制作用会阻碍DDR,并使细胞对电离辐射敏感,从而诱导细胞死亡。该抗体与AlexaFluor®488偶联。AlexaFluor®488是一种流行的鲜绿色荧光染料,具有高pH稳定性。
    • 资质认证

      获得国家资质,权威认证!

    • 全国联保

      全国联保,官方无忧售后

    • 正规发票

      正规发票,放心购买

    • 签订合同

      签订合同,保障您的权益

    /**/