Cart
sales@molnova.com
Sulcardine sulfate
CAS No. 343935-61-5
Sulcardine sulfate( —— )
Catalog No. M34432 CAS No. 343935-61-5
Sulcardine sulfate (B-87823) is a multi-ion channel blocker with antiarrhythmic activity, inhibits Na+, K+ and Ca2+ channels, and inhibits hNav1.5 channels in a concentration-dependent and reversible manner.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 686 | In Stock |
|
| 10MG | 938 | In Stock |
|
| 25MG | 1444 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSulcardine sulfate
-
NoteResearch use only, not for human use.
-
Brief DescriptionSulcardine sulfate (B-87823) is a multi-ion channel blocker with antiarrhythmic activity, inhibits Na+, K+ and Ca2+ channels, and inhibits hNav1.5 channels in a concentration-dependent and reversible manner.
-
DescriptionSulcardine sulfate (B-87823) is a multi-ion channel blocker with antiarrhythmic activity, inhibits Na+, K+ and Ca2+ channels, and inhibits hNav1.5 channels in a concentration-dependent and reversible manner.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
RecptorPotassium Channel | Calcium Channel | Sodium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number343935-61-5
-
Formula Weight557.68
-
Molecular FormulaC24H35N3O8S2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=S(=O)(O)O.O=S(=O)(NCC=1C=C(C(O)=C(C1)CN2CCCC2)CN3CCCC3)C4=CC=C(OC)C=C4
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
GAL-021
A novel respiratory stimulant that acts as a potent calcium-activated potassium (BKCa) channel blocker blocker.
-
NS6180
NS6180 is a novel potent and selective KCa3.1 channel inhibitor(IC50= 9 nM) prevents T-cell activation and inflammation.
-
PF-04895162
PF-04895162 (ICA-105665, PF 4895162) is an orally available agonist of neuronal Kv7 potassium channel, opens Kv7.2/7.3 and Kv7.3/7.5 potassium channels.
