Ro 67-7476

Ro 67-7476 Suppliers list
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:Ro 67-7476
CAS:298690-60-5
Purity:98% Package:5mg Remarks:V3342
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:Ro 67-7476
CAS:298690-60-5
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:Ro 67-7476
CAS:298690-60-5
Purity:>=99%(HPLC) Package:$173.9/10mg;$652.9/50mg;Bulk package Remarks:99%(HPLC)
Company Name: Nanjing Norris-Pharm Technology Co., Ltd  
Tel: 13901585132
Email: 799750417@qq.com
Products Intro: Product Name:Ro 67-7476
CAS:298690-60-5
Purity:0.95 Package:5KG;1KG;100G
Company Name: MedChemexpress LLC  
Tel: 021-58955995
Email: sales@medchemexpress.cn
Products Intro: Product Name:Ro 67-7476
CAS:298690-60-5
Ro 67-7476 Basic information
Product Name:Ro 67-7476
Synonyms:Ro 67-7476;Pyrrolidine, 2-(4-fluorophenyl)-1-[(4-methylphenyl) sulfonyl]-, (2S)-;(2S)-2-(4-Fluorophenyl)-1-[(4-methylphenyl)sulfonyl]-pyrrolidine;RO67-7476;RO-67-7476;excitatory postsynaptic potentials,Ro 67-7476,cAMP accumulation,mGluR,neuronal culture,Metabotropic glutamate receptors,Ro 67 7476,inhibit,Ro 677476,traumatic injury,mGluR1,Inhibitor
CAS:298690-60-5
MF:C17H18FNO2S
MW:319.39
EINECS:
Product Categories:
Mol File:298690-60-5.mol
Ro 67-7476 Structure
Ro 67-7476 Chemical Properties
Boiling point 452.9±55.0 °C(Predicted)
density 1.268±0.06 g/cm3(Predicted)
storage temp. Store at RT
solubility DMSO:30.0(Max Conc. mg/mL);93.9(Max Conc. mM)
pka-5.53±0.40(Predicted)
form Powder
Safety Information
MSDS Information
Ro 67-7476 Usage And Synthesis
DescriptionRo 67-7476 is a positive allosteric modulator of metabotropic glutamate receptor 1 (mGluR1) that enhances glutamate-induced calcium release in HEK293 cells expressing rat mGluR1a (EC50 = 1.74 μM). It is selective for rat mGluR1 over rat mGluR2, mGluR4, and mGluR8 at a concentration of 10 μM. Ro 67-7476 increases the amplitude of mGluR1 excitatory postsynaptic potentials (EPSCs) evoked by 2,3-dihydroxy-6-nitro-7-sulfamoylbenzoquionxaline, picrotoxin, or AP5 in the Purkinje cells of rat cerebellar slices. It activates ERK1/2 phosphorylation in the absence of exogenously added glutamate (EC50 = 163.3 nM).
UsesRo 67-7476 is a positive allosteric metabotropic mGlu1 receptor modulator.
storageStore at RT
Ro 67-7476 Preparation Products And Raw materials
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