VRT-325
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


VRT-325
Description:
VRT-325 is a novel small molecule discovered by screening a compound library designed to address the genetic defect in cystic fibrosis (CF) caused by the ΔF508 mutation in CFTR. VRT-325 belongs to a class of compounds that promote ΔF508-CFTR efflux from the endoplasmic reticulum and restores chloride transport levels in epithelial cells of CF-derived bronchi[1].Product Name Alternative:
4-Hydroxy-TEMPO-d17,15NUNSPSC:
12352005Hazard Statement:
H302, H315, H319, H335Target:
CFTRType:
Reference compoundRelated Pathways:
Membrane Transporter/Ion ChannelField of Research:
OthersAssay Protocol:
https://www.medchemexpress.com/vrt-325.htmlPurity:
99.15Smiles:
CC(N1CCN(CC1)S(=O)(C2=CC=C(C=C2)OC)=O)C3=NC(OC4CCCCC4)=C5C=CC=CC5=N3Molecular Formula:
C27H34N4O4SMolecular Weight:
510.65Precautions:
H302, H315, H319, H335References & Citations:
[1]Van Goor F, et al. Rescue of ホ508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules[J]. American Journal of Physiology-Lung Cellular and Molecular Physiology, 2006, 290 (6) : L1117-L1130.Shipping Conditions:
Room TemperatureStorage Conditions:
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category:
Reference compound1Clinical Information:
No Development ReportedCAS Number:
[815592-21-3]
