
Hello Bio/MDCPG/HB1602/50mg
商品编号:
HB1602-50mg
品牌:
hellobio
市场价:
¥10588.50
美元价:
8145.00
产品分类:
酸碱缓冲液
联系Q Q:
3392242852
电话号码:
4000-520-616
电子邮箱:
info@ebiomall.com
商品介绍
Productoverview
- NameMDCPG
- ShortdescriptionSelectivemGlu8receptorantagoNIST
- BIOLOGicaldescriptionSelectivemGlu8receptorantagonist(Ki=2.3μMinmousehippocampalslices).CanbeusedtodistinguishactionsofDCPGonmGlu8receptorsversusoff-targeteffectsonmGlu2receptors.AlsoshowntoreverseDCPGinducedlongtermdepression.
- Alternativenames(RS)-MDCPG
- OurproductsinactionSubmitYourCitationNow
Properties
- Chemicalname(RS)-4-(1-Amino-1-carboxyethyl)phthalicacid
- MolecularWeight253.06
- Chemicalstructure
- MolecularFormulaC11H11NO6
- PubChemidentifier91996985
- SMILESCC(C1=CC(=C(C=C1)C(=O)O)C(=O)O)(C(=O)O)N
- InChiInChI=1S/C11H11NO6/c1-11(12,10(17)18)5-2-3-6(8(13)14)7(4-5)9(15)16/h4-4H,12H2,1H3,(H,13,14)(H,15,16)(H,17,18)
- InChiKeyIGLGZJSKFBLMKQ-UHFFFAOYSA-N
StoringandUsingYourProduct
- Storageinstructions+4°C(desiccate)
- SolubilityoverviewSolublein0.1MNaOH(100mM)andinDMSO
- ImportantThisproductisforRESEARCHUSEONLYandisnotintendedfortherapeuticordiagnosticuse.Notforhumanorveterinaryuse.
ReferencesforMDCPG
CharacterisationofanmGlu8receptor-selectiveagonistandantagonistinthelateralandmedialperforantpathinputstothedentategyrus.
MercierMSetal(2013)Neuropharmacology67:294-303PubMedID:23220400AntagonistsreversIBLyreversechemicalLTDinducedbygroupI,groupIIandgroupIIImetabotropicglutamatereceptors.
LodgeDetal(2013)Neuropharmacology74:135-46PubMedID:23542080
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.
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