Cart
sales@molnova.com
Acecainide hydrochloride
CAS No. 34118-92-8
Acecainide hydrochloride( —— )
Catalog No. M17487 CAS No. 34118-92-8
Acecainide hydrochloride is a major metabolite of procainamide. Its anti-arrhythmic action may cause cardiac toxicity in kidney failure.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 32 | In Stock |
|
| 5MG | 51 | In Stock |
|
| 10MG | 82 | In Stock |
|
| 25MG | 147 | In Stock |
|
| 50MG | 246 | In Stock |
|
| 100MG | 357 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameAcecainide hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionAcecainide hydrochloride is a major metabolite of procainamide. Its anti-arrhythmic action may cause cardiac toxicity in kidney failure.
-
DescriptionAcecainide hydrochloride is a major metabolite of procainamide. Its anti-arrhythmic action may cause cardiac toxicity in kidney failure.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number34118-92-8
-
Formula Weight313.83
-
Molecular FormulaC15H24ClN3O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC(=O)Nc1ccc(C(=O)NCCN(CC)CC)cc1.Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Ikramuddin S,et al. JAMA. 2013 Jun 5;309(21):2240-9.
molnova catalog
related products
-
Dehydromiltirone
Dehydromiltirone has antioxidant activity, it shows significant anti-neuroinflammatory effects through inhibiting PI3K/Akt phosphorylation and then inhibiting NF-κB signaling pathway.
-
dITP trisodium salt
dITP trisodium salt (2'-Deoxyinosine-5'-triphosphate trisodium salt) is present in the hyperthermophilic bacterium Thermotoga maritima and can be used as a mutation reagent in mutagenesis PCR.
-
L-Selenocystine
L-Selenocystine can be used as a building block in biologically active selenol compounds.
