XPC-6444

XPC-6444 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:XPC-6444
CAS:2230144-21-3
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185
Email: sales-cpd@caerulumpharma.com
Products Intro: Product Name:XPC-6444; XPC 6444; XPC6444;
CAS:2230144-21-3
Purity:98% Package:1g;10g;100g
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com
Products Intro: Product Name:XPC-6444
CAS:2230144-21-3
Purity:97.0% Package:5mg
Company Name: DC Chemicals  
Tel: 021-58447131 13564518121
Email: sales@dcchemicals.com
Products Intro: Product Name:XPC6444
CAS:2230144-21-3
Purity:98% HPLC Package:100mg,250mg,1g
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Email: marketing@tsbiochem.com
Products Intro: Product Name:XPC-6444;XPC 6444,XPC6444
CAS:2230144-21-3
Purity:98% Package:10 mg
XPC-6444 Basic information
Product Name:XPC-6444
Synonyms:XPC-6444;https://pubmed.ncbi.nlm.nih.gov/34355886/;XPC 6444,XPC6444;Benzenesulfonamide, 4-[[[2-[[(1,1-dimethylethyl)methylamino]methyl]-6-fluorophenyl]methyl]amino]-2,6-difluoro-N-4-thiazolyl-
CAS:2230144-21-3
MF:C22H25F3N4O2S2
MW:498.58
EINECS:
Product Categories:
Mol File:2230144-21-3.mol
XPC-6444 Structure
XPC-6444 Chemical Properties
Boiling point 574.8±60.0 °C(Predicted)
density 1.384±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 125 mg/mL (250.71 mM; Need ultrasonic)
pka5.73±0.10(Predicted)
form Solid
color Off-white to yellow
Safety Information
MSDS Information
XPC-6444 Usage And Synthesis
Biological ActivityXPC-6444 is a highly potent, isoform-selective, and CNS-penetrant NaV1.6 inhibitor (IC50=41 nM for hNaV1.6). XPC-6444 also displays potent block of NaV1.2 (IC50=125 nM). XPC-6444 shows anticonvulsant activity[1]. XPC-6444 shows high selectivity over NaV1.1 and NaV1.5[1]. XPC-6444 exhibits good metabolic stability in human liver microsomes and hepatocytes, and low potential for MDR1 mediated efflux[1].
References[1]. Focken T, et al. Identification of CNS-Penetrant Aryl Sulfonamides as Isoform-Selective NaV1.6 Inhibitors with Efficacy in Mouse Models of Epilepsy. J Med Chem. 2019 Oct 3.
XPC-6444 Preparation Products And Raw materials
Tag:XPC-6444(2230144-21-3) Related Product Information