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当前位置: 首页 > 产品中心 > acid_base_buffer_solution > 你好Bio/VU 0357017盐酸盐/HB1498/10mg
商品详细你好Bio/VU 0357017盐酸盐/HB1498/10mg
你好Bio/VU 0357017盐酸盐/HB1498/10mg
你好Bio/VU 0357017盐酸盐/HB1498/10mg
商品编号: HB1498-10mg
品牌: hellobio
市场价: ¥1345.50
美元价: 1035.00
产地: 美国(厂家直采)
公司:
产品分类: 酸碱缓冲液
公司分类: acid_base_buffer_solution
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Product overview

  • Name
    VU 0357017 hydrochloride
  • Short description
    Potent, selective M1 receptor allosteric agonist
  • Biological description
    Potent and selective M1 muscarinic receptor allosteric agonist (EC50 = 198 nM). Binds to the orthosteric ACh site at high concentrations to act as an antagonist. Reverses contextual fear conditioning deficits. Shows cognitive enhancing actions. Blood-brain barrier permeable.
  • Biological action
    Agonist
  • Purity
    >98%
  • Our products in action
    Submit Your Citation Now

Properties

  • Chemical name
    4-[[2-[(2-Methylbenzoyl)amino]ethyl ]amino]-1-piperidinecarboxylic acid ethyl ester hydrochloride
  • Molecular Weight
    369.89
  • Chemical structure
    VU 0357017 hydrochloride  [1135242-13-5]
  • Molecular Formula
    C18H27N3O3.HCl
  • CAS Number
    1135242-13-5

Storing and Using Your Product

  • Storage instructions
    +4°C
  • Solubility overview
    soluble in water (25mM) or DMSO (5mM)
  • Important
    This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

References for VU 0357017 hydrochloride

  • Discovery and characterization of novel subtype-selective allosteric agonists for the investigation of M(1) receptor function in the central nervous system.

    Lebois EP et al (2010) ACS Chem Neurosci 1(2) : 104-121.
    PubMedID: 21961051
  • Novel allosteric agonists of M1 muscarinic acetylcholine receptors induce brain region-specific responses that correspond with behavioral effects in animal models.

    Digby GJ et al (2012) J Neurosci 32(25) : 8532-44.
    PubMedID: 22723693
  • Further exploration of M₁ allosteric agonists: subtle structural changes abolish M₁ allosteric agonism and result in pan-mAChR orthosteric antagonism.

    Sheffler DJ et al (2013) Bioorg Med Chem Lett 23(1) : 223-7.
    PubMedID: 23200253
品牌介绍
Hello Bio是由一群经验丰富的科学家和化学家们创立的充满活力的生物企业,总部位于英国布里斯托尔,在美国普林斯顿设有分公司,主旨在于提供质优价廉的生命科学研究工具,主要产品线为小分子化合物,如激动剂、拮抗剂、抑制剂等,部分产品价格甚至低至其他供应商的50%。热销产品线:酶抑制剂和激动剂ROCK inhibitor Y-27632, PKA inhibitor KT 5720 , adenylyl cyclase activator Forskolin, and novel GRK2/3 inhibitor Cmpd101等。 离子通道调节剂NMDA antagonist D-AP5, sodium channel blocker tetrodotoxin citrate, TRP antagonist capsazepine, and GABAA antagonist SR 95531 等。信号通路工具各种信号通路抑制剂、激动剂表观遗传学研究工具potent HDAC inhibitor Trichostatin A, DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine,BET bromodomain inhibitor (+)-JQ1 and potent,selective GLP / G9a HMTase inhibitor BIX 01294 等受体配体novel selective GRK2/3 inhibitor,  NMDA antagonist D-AP5, Group I mGlu agonist (S)-3,5-DHPG, and GABAA antagonist SR 95531.等干细胞调节剂ROCK inhibitor Y-27632,  SB 431542 DAPT.