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ML192

ML192 is a selective ligand antagonist of GPR55. ML192 inhibits the β-arrestin trafficking, ERK1/2 phosphorylation and PKCβII translocation[1].

Product Specifications

CAS Number

460331-61-7

UNSPSC

12352005

Hazard Statement

H302, H315, H319

Target

Arrestin; ERK; GPR55; PKC

Type

Reference compound

Related Pathways

Epigenetics; GPCR/G Protein; MAPK/ERK Pathway; Neuronal Signaling; Stem Cell/Wnt; TGF-beta/Smad

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Metabolic Disease

Assay Protocol

https://www.medchemexpress.com/ml192.html

Concentration

10mM

Purity

99.70

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

O=C(N1CCN(CC1)C2=C3C(CCCC4)=C4SC3=NC(C)=N2)C5=CC=CO5

Molecular Formula

C20H22N4O2S

Molecular Weight

382.48

Precautions

H302, H315, H319

References & Citations

[1]Kotsikorou E, et al. Identification of the GPR55 antagonist binding site using a novel set of high-potency GPR55 selective ligands. Biochemistry. 2013 Dec 31;52 (52) :9456-69.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

ERK1; ERK2; PKCβ

Available Sizes

Frequently Asked Questions

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