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当前位置: 首页 > 产品中心 > acid_base_buffer_solution > Hello Bio/PEAQX (NVP-AAM 077)/HB2841/
商品详细Hello Bio/PEAQX (NVP-AAM 077)/HB2841/
Hello Bio/PEAQX (NVP-AAM 077)/HB2841/
Hello Bio/PEAQX (NVP-AAM 077)/HB2841/
商品编号: HB2841
品牌: hellobio
市场价: ¥838.50
美元价: 645.00
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
    PEAQX (NVP-AAM 077)
  • Short description
    Potent, competitive NMDA receptor antagonist
  • Biological description

    Potent and competitive NMDA receptor antagonist. Binds at the glutamate site.

    Shows some selectivity (~7-10-fold) for GluN1/2A (NR1/2A) over GluN1/2B (NR1/2B) subunit containing receptors (IC50 values are 31 and 215 nM at GluN1/2A and GluN1/2B respectively).

    Shows anticonvulsant activity. Active in vivo.

  • Alternative names
    NVP-AAM 007
  • Biological action
    Antagonist
  • Purity
    >98%
  • Our products in action
    1 citation Submit Your Citation Now

Images

Properties

  • Chemical name
    [[[(1S)-1-(4-Bromophenyl)ethyl]amino](1,2,3,4-tetrahydro-2,3-dioxo-5-quinoxalinyl)methyl] phosphonic acid tetrasodium salt
  • Molecular Weight
    542.14
  • Chemical structure
    PEAQX [459836-30-7]
  • Molecular Formula
    C17H13BrN3Na4O5P
  • CAS Number
    459836-30-7
  • PubChem identifier
    101043065
  • SMILES
    CC(C1=CC=C(C=C1)Br)NC(C2=C3C(=CC=C2)N=C(C(=N3)[O-])[O-])P(=O)([O-])[O-].[Na+].[Na+].[Na+].[Na+]
  • InChi
    InChI=1S/C17H17BrN3O5P.4Na/c1-9(10-5-7-11(18)8-6-10)19-17(27(24,25)26)12-3-2-4-13-14(12)21-16(23)15(22)20-13;;;;/h4-9,17,19H,1H3,(H,20,22)(H,21,23)(H2,24,25,26);;;;/q;4*+1/p-4
  • InChiKey
    QBVOZIDKUFSQIL-UHFFFAOYSA-J

Storing and Using Your Product

  • Storage instructions
    -20°C
  • Solubility overview
    Soluble in water (10mM)
  • 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 PEAQX (NVP-AAM 077)

  • 5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition.

    Auberson et al (2002) Bioorg Med Chem Lett 12(7) : 1099-102.
    PubMedID: 11909726
  • Equilibrium constants for (R)-[(S)-1-(4-bromo-phenyl)-ethylamino]-(2,3-dioxo-1,2,3,4-tetrahydroquinoxalin-5-yl)-methyl]-phosphonic acid (NVP-AAM077) acting at recombinant NR1/NR2A and NR1/NR2B NMDA receptors: Implications for studies of sy

    Frizelle et al (2006) Mol Pharmacol. 70(3) : 1022-32
    PubMedID: 16778008
  • The effects of an acute challenge with the NMDA receptor antagonists, MK-801, PEAQX, and ifenprodil, on social inhibition in adolescent and adult male rats.

    Morales and Spear (2014) Psychopharmacology (Berl). 231(8) : 1797-807
    PubMedID: 24043344
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.