ICA
CAS No. 3374-88-7
ICA( N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine )
Catalog No. M26713 CAS No. 3374-88-7
ICA is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 μM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 402 | Get Quote |
|
| 10MG | 593 | Get Quote |
|
| 25MG | 888 | Get Quote |
|
| 50MG | 1251 | Get Quote |
|
| 100MG | 1692 | Get Quote |
|
| 500MG | 3402 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameICA
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NoteResearch use only, not for human use.
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Brief DescriptionICA is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 μM).
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DescriptionICA is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 μM).(In Vitro):ICA exhibited antiarrhythmic effects. ICA prevented electrically induced runs of atrial fibrillation in the isolated right atrium and induced atrial postrepolarization refractoriness and depolarized RMP. ICA (1-10 μM) was found to slow CV; however, because of a marked prolongation of effective refractory period, the calculated wavelength was increased. Furthermore, at increased pacing frequencies, SK channel inhibition by ICA (10-30 μM) demonstrated prominent depression of other sodium channel-dependent parameters. ICA did not inhibit IK,ACh, but at concentrations above 10 μM, ICA use dependently inhibited INa.
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In VitroThe SK channel inhibitor ICA exhibits antiarrhythmic effects. ICA prevents electrically induced runs of atrial fibrillation in the isolated right atrium and induces atrial postrepolarization refractoriness and depolarizes resting membrane potential. ICA at 1 to 10 μM slows conduction velocity. At increased pacing frequencies, SK channel inhibition by ICA (10-30 μM) demonstrates prominent depression of other sodium channel-dependent parameters.
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In Vivo——
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SynonymsN-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine
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PathwayCell Cycle/DNA Damage
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TargetPotassium Channel
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RecptorAlkyl/ether
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Research Area——
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Indication——
Chemical Information
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CAS Number3374-88-7
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Formula Weight254.31
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Molecular FormulaC13H10N4S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 49.5 mg/mL (194.64 m)
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SMILESN(c1nc(cs1)-c1ccccn1)c1ccccn1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Zhang F, et al. Discovery of a new class of PROTAC BRD4 degraders based on a dihydroquinazolinone derivative and lenalidomide/pomalidomide.Bioorg Med Chem. 2020 Jan 1;28(1):115228.
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