Hello Bio/Fluoxetine hydrochloride/HB1600/
市场价：
¥1989.00
美元价：
1530.00
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
- NameFluoxetinehydrochloride
- ShortdescriptionSelective5-HTuptakeinhibitor
- BIOLOGicaldescriptionPotent,selective5-HTreuptakeinhibitor(Ki=2nMatrSERT).Alsoactsatotherreceptorsandchannels.Shows~150-900foldselectivityover5-HT1a,-2A,muscarinic,α1,α2-adrenoceptorsandH1receptors.Showsantidepressanteffects.Activeinvivo.
- BiologicalactionInhibitor
- Purity>99%
- OurproductsinactionSubmitYourCitationNow
Properties
- ChemicalnameN-Methyl-3-[(4-trifluoromethyl)phenoxy]-3-phenylpropylaminehydrochloride
- MolecularWeight345.78
- Chemicalstructure
![Fluoxetine hydrochloride [56296-78-7]](images/hellobio/201710/hb1600.png "Fluoxetine hydrochloride [56296-78-7]")
- MolecularFormulaC17H18F3NO.HCl
- CASNumber56296-78-7
- PubChemidentifier62857
- SMILESCNCCC(C1=CC=CC=C1)OC2=CC=C(C=C2)C(F)(F)F.Cl
- InChiInChI=1S/C17H18F3NO.ClH/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20;/h4-10,16,21H,11-12H2,1H3;1H
- InChiKeyGIYXAJPCNFJEHY-UHFFFAOYSA-N
- MDLnumberMFCD00214288
StoringandUsingYourProduct
- StorageinstructionsRoomtemperature
- SolubilityoverviewSolubleinwater(10mM)andinDMSO(100mM)
- ImportantThisproductisforRESEARCHUSEONLYandisnotintendedfortherapeuticordiagnosticuse.Notforhumanorveterinaryuse.
ReferencesforFluoxetinehydrochloride
Fluoxetine,aselectiveinhibitorofSEROtoninuptake.
FullerRWetal(1991)MedResRev11(1):17-34.PubMedID:1994152Fluoxetineanditstwoenantiomersasselectiveserotoninuptakeinhibitors.
WongDTetal(1990)ActaPharmNord2(3):171-80.PubMedID:2200429Fluoxetine.Areviewofitspharmacodynamicandpharmacokineticproperties,andtherapeuticefficacyindepressiveillness.
BenfieldPetal(1986)Drugs32(6):481-508.PubMedID:2878798
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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