An IKs and ICTFR blocker
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Chromanol 293B

Item No. 19993

Technical Information
Formal Name
rel-N-[(3R,4S)-6-cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-yl]-N-methyl-ethanesulfonamide
CAS Number
163163-23-3
Synonyms
  • Chromanol 239B
Molecular Formula
C15H20N2O4S
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 2 mg/ml
λmax
252 nm
SMILES
CC1(C)[C@H](O)[C@@H](N(S(CC)(=O)=O)C)C2=C(C=CC(C#N)=C2)O1
InChi Code
InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3/t13-,14+/m0/s1
InChi Key
HVSJHHXUORMCGK-UONOGXRCSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Chromanol 293B is a blocker of slowly activating delayed-rectifier K+ current (IKs) with an IC50 value of 6.89 μM in Xenopus oocytes expressing rat IKs channels.1 It is selective, having no activity at rat Kv1.1 or Kir2.1 channels at a concentration of 30 μM. Chromanol 293B increases the rate and extent of IKs in guinea pig ventricular cells in a dose-dependent manner.2 It also inhibits cystic fibrosis transmembrane conductance regulator (CTFR) Cl- currents (ICTFR) with an IC50 value of 19 μM in Xenopus oocytes expressing human CTFR.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Suessbrich, H., Bleich, M., Ecke, D., et alSpecific blockade of slowly activating IsK channels by chromanols -- Impact on the role of IsK channels in epithelia. FEBS Lett. 396(2-3), 271-275 (1996).

    2. Fujisawa, S., K., O., and Iijima, T. Time-dependent block of the slowly activating delayed rectifier K+ current by chromanol 293B in guinea-pig ventricular cells. Br. J. Pharmacol. 129(5), 1007-1013 (2000).

    3. Bachmann, A., Quast, U., and Russ, U. Chromanol 293B, a blocker of the slow delayed rectifier K+ current (IKs), inhibits the CFTR Cl- current. Naunyn Schmiedebergs Arch. Pharmacol. 363(6), 590-596 (2001).