Arrhythmia
Products Related to Arrhythmia(82)
- GC520483-hydroxy-4-Methoxyphenethylamine (hydrochloride)CAS: 645-33-0Purity: >98.00%
3-hydroxy-4-Methoxyphenethylamine (hydrochloride) is a catecholamine compound that has an inhibitory effect on dihydropteridine reductase.
- GC52058AcebutololCAS: 37517-30-9Purity: >99.50%
Acebutolol is an orally active β1 adrenergic receptor (β1AR) antagonist.
- GC52221EleclazineCAS: 1443211-72-0Purity: >98.00%
Eleclazine is a novel, highly selective inhibitor of the cardiac late sodium current, with an IC 50 value of <1μM.
- GC52390Spexin 1 (human, mouse, rat, bovine) (acetate)Purity: >98.00%
An endogenous peptide and agonist of GAL 2 and GAL 3
- GC91424S1PL-IN-31CAS: 1538574-95-6Purity: >98.00%
S1PL-IN-31 is an inhibitor of sphingosine-1-phosphate (S1P) lyase (IC50 = 210 nM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC52048 | 3-hydroxy-4-Methoxyphenethylamine (hydrochloride) | 645-33-0 | >98.00% | |
3-hydroxy-4-Methoxyphenethylamine (hydrochloride) is a catecholamine compound that has an inhibitory effect on dihydropteridine reductase. | ||||
| GC52052 | Dofetilide N-oxide | 144449-71-8 | >98.00% | |
| GC52058 | Acebutolol | 37517-30-9 | >99.50% | |
Acebutolol is an orally active β1 adrenergic receptor (β1AR) antagonist. | ||||
| GC52221 | Eleclazine | 1443211-72-0 | >98.00% | |
Eleclazine is a novel, highly selective inhibitor of the cardiac late sodium current, with an IC 50 value of <1μM. | ||||
| GC52390 | Spexin 1 (human, mouse, rat, bovine) (acetate) | - | >98.00% | |
An endogenous peptide and agonist of GAL 2 and GAL 3 | ||||
| GC52438 | CGRP (8-37) (mouse, rat) (trifluoroacetate salt) | - | >95.00% | |
A CGRP receptor antagonist | ||||
| GC72527 | S-(-)-Warfarin | 5543-57-7 | - | |
| GC90516 | VK-II-86 | 955371-84-3 | >90.00% | |
An inhibitor of SOICR | ||||
| GC91410 | RA-2 | 1867107-62-7 | >95.00% | |
RA-2 is an inhibitor of small-conductance calcium-activated potassium channel 2.3 (KCa2.3/SK3) and intermediate-conductance calcium-activated potassium channel 3.1 (KCa3.1/IK1) (IC50s = 2 and 17 nM, respectively). | ||||
| GC91424 | S1PL-IN-31 | 1538574-95-6 | >98.00% | |
S1PL-IN-31 is an inhibitor of sphingosine-1-phosphate (S1P) lyase (IC50 = 210 nM). | ||||