Cart
sales@molnova.com
Tolbutamide
CAS No. 64-77-7
Tolbutamide ( D 860; NSC 23813; NSC 87833; U-2043 )
Catalog No. M15457 CAS No. 64-77-7
Tolbutamide is an inhibitor of potassium channel, used for type II diabetes.
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 500MG | 37 | In Stock |
|
| 1G | 53 | In Stock |
|
Biological Information
-
Product NameTolbutamide
-
NoteResearch use only, not for human use.
-
Brief DescriptionTolbutamide is an inhibitor of potassium channel, used for type II diabetes.
-
DescriptionTolbutamide is an inhibitor of potassium channel, used for type II diabetes.
-
SynonymsD 860; NSC 23813; NSC 87833; U-2043
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
RecptorPotassium Channel
-
Research AreaMetabolic Disease
-
Indication——
Chemical Information
-
CAS Number64-77-7
-
Formula Weight270.35
-
Molecular FormulaC12H18N2O3S
-
Purity>98%(HPLC)
-
SolubilityEthanol: 54 mg/mL warmed (199.74 mM); DMSO: 54 mg/mL (199.74 mM)
-
SMILESO=C(NS(=O)(C1=CC=C(C)C=C1)=O)NCCCC
-
Chemical Name1-butyl-3-(4-methylphenyl)sulfonylurea
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Wray HL, et al, Biochem Biophys Res Commun. 1973, 53(1), 291-294.
molnova catalog
related products
-
Hexachlorophene
Hexachlorophene(Hexachlorofen) is a potent KCNQ1/KCNE1 potassium channel activator with EC50 of 4.61 ± 1.29 μM; also is an inhibitor of Wnt/beta-catenin signaling.
-
Margatoxin
Potent KV1.3 channel blocker (IC50 = 36 pM). Displays no effect at calcium-activated channels. Reduces VEGF-induced transmembrane calcium influxes and nitric oxide production in human endothelial cells.
-
P-1075
P-1075 is a potent sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6) activator (EC50 = 45 nM).
