MAO-B-IN-2
CAS No. 1253978-24-3
MAO-B-IN-2( —— )
Catalog No. M37635 CAS No. 1253978-24-3
MAO-B-IN-2 is a selective and competitive inhibitor of MAO-B and BChE with IC50 values of 0.51 μM and 7.00 μM, respectively. It attenuates H2O2-induced cellular damage due to its strong ROS scavenging properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 93 | Get Quote |
|
| 5MG | 140 | Get Quote |
|
| 10MG | 225 | Get Quote |
|
| 25MG | 394 | Get Quote |
|
| 50MG | 592 | Get Quote |
|
| 100MG | 869 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMAO-B-IN-2
-
NoteResearch use only, not for human use.
-
Brief DescriptionMAO-B-IN-2 is a selective and competitive inhibitor of MAO-B and BChE with IC50 values of 0.51 μM and 7.00 μM, respectively. It attenuates H2O2-induced cellular damage due to its strong ROS scavenging properties.
-
DescriptionMAO-B-IN-2 is a selective and competitive inhibitor of MAO-B and BChE with IC50 values of 0.51 and 7.00 μM, respectively.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1253978-24-3
-
Formula Weight310.73
-
Molecular FormulaC18H11ClO3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 10 mg/mL (32.18 mM; Ultrasonic (<80°C)
-
SMILESClc1ccccc1\C=C\C(=O)c1cc2ccccc2oc1=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Rehuman NA, et al. Halogenated Coumarin-Chalcones as Multifunctional Monoamine Oxidase-B and Butyrylcholinesterase Inhibitors. ACS Omega. 2021 Oct 12;6(42):28182-28193. ?
molnova catalog
related products
-
Parishin C
Parishin C is a phenolic glycoside and a major component of G. elata have antioxidant property.
-
Labetalone hydrochlo...
Labetalone hydrochloride is an impurity of Labetalol. Labetalol is an orally active adrenoceptor blocking drug, Labetalol is a competitive antagonist at both alpha- and beta-adrenoceptor sites.
-
TRAM-34
TRAM-34(Kd=20 nM), an effective and specific inhibitor of the intermediate-conductance Ca2+-activated K+ channel (IKCa1, KCa3.1), does not block cytochrome P450.
Cart
sales@molnova.com