| Identification | Back Directory | [Name]
6,12,19,20,25,26-HEXAHYDRO-5,27:13,18:21,24-TRIETHENO-11,7-METHENO-7H-DIBENZO [B,N] [1,5,12,16]TETRAAZACYCLOTRICOSINE-5,13-DIIUM DITRIFLUOROACETATE | [CAS]
199934-16-2 | [Synonyms]
UCL 1684
UCL-1684 Br
UCL 1684 dibromide
6,12,19,20,25,26-Hexahydro-5,27:13,18:21,24-trietheno-11,7-metheno-7H-dibenzo[b,n][1,5,12,16]tetraazacyclotricosine-5,
6,12,19,20,25,26-Hexahydro-5,27:13,18:21,24-trietheno-11,7-metheno-7H-dibenzo[b,n][1,5,12,16]tetraazacyclotricosine-5,13-diiumdibromide
6,12,19,20,25,26-HEXAHYDRO-5,27:13,18:21,24-TRIETHENO-11,7-METHENO-7H-DIBENZO [B,N] [1,5,12,16]TETRAAZACYCLOTRICOSINE-5,13-DIIUM DITRIFLUOROACETATE | [Molecular Formula]
C38H30F6N4O4 | [MDL Number]
MFCD06798362 | [MOL File]
199934-16-2.mol | [Molecular Weight]
720.66 |
| Hazard Information | Back Directory | [Uses]
UCL 1684 is a highly potent and selective, nonpeptidic blocker of the Apamin-sensitive Ca2+-activated K+ channel of which inhibition potentially terminates and protects against atrial fibrillation. | [Biological Activity]
Highly potent, non-peptidic blocker of the apamin-sensitive Ca 2+ -activated K + channel (SK Ca ) (IC 50 = 3 nM in rat sympathetic neurons). Blocks hSK1 and rSK2 channels expressed in HEK 293 cells with IC 50 values of 762 and 364 pM respectively. | [in vivo]
UCL 1684 (dibromide) (3 mg/kg; i.v.) increases wenckebach cycle length to 115.0±5.1 % of baseline value[3]. | [storage]
Desiccate at RT |
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