Hello Bio/VU 0361737/HB0638/10mg
商品编号:
HB0638-10mg
品牌:
hellobio
市场价:
¥1033.50
美元价:
795.00
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
- NameVU0361737
- ShortdescriptionmGlu4positiveallostericmodulator
- BIOLOGicaldescriptionmGlu4receptorpositiveallostericmodulator(EC50=0.24µM).DisplayslittleactivityatmGlu5andmGlu8receptorsandnoactivityatmGlu1,2,3,6and7receptors.Blood-brainbarrierpermeable.
- BiologicalactionPAM
- Purity>99%
- OurproductsinactionSubmitYourCitationNow
Properties
- ChemicalnameN-(4-Chloro-3-methoxyphenyl)-2-pyridinecarboxamide
- MolecularWeight262.69
- Chemicalstructure
- MolecularFormulaC13H11ClN2O2
- CASNumber1161205-04-4
StoringandUsingYourProduct
- Storageinstructionsroomtemperature
- SolubilityoverviewsolubleinDMSO(100mM)
- ImportantThisproductisforRESEARCHUSEONLYandisnotintendedfortherapeuticordiagnosticuse.Notforhumanorveterinaryuse.
ReferencesforVU0361737
RADIosynthesisofN-(4-chloro-3-[(11)C]methoxyphenyl)-2-picolinamide([(11)C]ML128)asaPETradiotracerformetabotropicglutamatereceptorsubtype4(mGlu4).
KilKEetal(2013)BioorgMedChem21(19):5955-62.PubMedID:23978356Discovery,synthesis,andstructure-activityrelationshipdevelopmentofaseriesofN-(4-acetamido)phenylpicolinamidesaspositiveallostericmodulatorsofmetabotropicglutamatereceptor4(mGlu(4))withCNSexposureinrats.
EngersDWetal(2011)JMedChem54(4):1106-10.PubMedID:21247167Synthesisandevaluationofaseriesofheterobiarylamidesthatarecentrallypenetrantmetabotropicglutamatereceptor4(mGluR4)positiveallostericmodulators(PAMs).
EngersDWetal(2009)JMedChem52(14):4115-8.PubMedID:19469556
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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