VX661

  Cat. No.:  DC7531   Featured
Chemical Structure
1152311-62-0
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More than 5000 active chemicals with high quality for research!
Field of application
VX-661 is a second F508del CFTR corrector and is believed to help CFTR protein reach the cell surface.
Cas No.: 1152311-62-0
Chemical Name: Cyclopropanecarboxamide, 1-(2,2-difluoro-1,3-benzodioxol-5-yl)-N-[1-[(2R)-2,3-dihydroxypropyl]-6-fluoro-2-(2-hydroxy-1,1-dimethylethyl)-1H-indol-5-yl]-
Synonyms: VX 661; VX661,VX-661
SMILES: C(C1=CC=C2OC(F)(F)OC2=C1)(C(NC1C(F)=CC2=C(C=1)C=C(C(C)(C)CO)N2C[C@H](O)CO)=O)1CC1
Formula: C26H27F3N2O6
M.Wt: 520.5
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: VX-661 is a second F508del CFTR corrector and help CFTR protein reach the cell surface.
In Vitro: In vitro, a combination of VX-661 and ivacaftor results in greater CFTR activity compared with VX-661 alone[2].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC1059 Lumacaftor(vx-809,vx809) VX-809 is a CFTR modulator with EC50 of 0.1 μM.
DC7531 VX661 VX-661 is a second F508del CFTR corrector and is believed to help CFTR protein reach the cell surface.
DC7100 CFTRinh 172 Voltage-independent, selective CFTR chloride channel blocker (Ki = 300 nM) that alters channel gating.
DC7483 PPQ-102 PPQ-102 is a potent CFTR inhibitor which can completely inhibited CFTR chloride current with IC 50approximately 90 nM.
DC9276 KM 11060 KM 11060 corrects F508del-CFTR trafficking, increasing the amount of functional CFTR at the plasma membrane (~75%) and Inhibits PDE5 activity.
DC4128 Ivacaftor (VX-770) Ivacaftor (VX-770, Kalydeco) is a potentiator of CFTR targeting G551D-CFTR and F508del-CFTR with EC50 of 100 nM and 25 nM, respectively.
DC10753 GLPG-1837(ABBV-974) GLPG-1837(ABBV-974) is a novel cystic fibrosis transmembrane conductance regulator CFTR potentiator.
DC7039 CFTR Inhibitor II CFTR Inhibitor II is a cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (< 1 min; 95% inhibition at 50 µM; Ki = 4.3 µM in CFTR-expressing FRT cells.
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