Benzamil (hydrochloride)
CAS No. 2898-76-2
Benzamil (hydrochloride)( —— )
Catalog No. M20570 CAS No. 2898-76-2
Benzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 45 | In Stock |
|
10MG | 54 | In Stock |
|
25MG | 113 | In Stock |
|
50MG | 215 | In Stock |
|
100MG | 389 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBenzamil (hydrochloride)
-
NoteResearch use only, not for human use.
-
Brief DescriptionBenzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
-
DescriptionBenzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
-
In VitroBenzamil (Benzylamiloride) inhibits neuronal and heterologously expressed small conductance Ca2+-activated K2+ channels.
-
In VivoBenzamil (Benzylamiloride) (0.7 mg/kg/day; s.c.) treated stroke-prone spontaneously hypertensive rats (SHRSP) survived, on average, until 16.1 weeks of age in SHRSP rats.
-
Synonyms——
-
PathwayMembrane Transporter/Ion Channel
-
TargetSodium Channel
-
RecptorENaC
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2898-76-2
-
Formula Weight356.21
-
Molecular FormulaC13H15Cl2N7O
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESNc1nc(N)c(nc1Cl)C(=O)NC(=N)NCc1ccccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Jeong S Lee S H Kim Y O et al. Antinociceptive Effects of Amiloride and Benzamil in Neuropathic Pain Model Rats[J]. Journal of Korean Medical Science 2013 28(8).
molnova catalog
related products
-
Ambroxol hydrochlori...
Ambroxol HCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block.
-
NHE3-IN-1
NHE3-IN-1 is a inhibitor of Na+/H+-exchanger 3 (NHE-3).
-
GS967
GS967 is a novel, potent, and selective inhibitor of cardiac late sodium current(late INa).