ML-SA1 TRP Channel activator

Cat.No.S9926

ML-SA1 (Mucolipin synthetic agonist 1) is an activator of TRPML channels. This compound also inhibits Dengue virus 2 (DENV2) and Zika virus (ZIKV) by promoting lysosomal acidification and protease activity. The IC50 values of this chemical against DENV2 RNA and ZIKV RNA are 8.93 μM and 52.99 μM, respectively. It induces autophagy. It can be used for the research of broad-spectrum antiviral.

ML-SA1 TRP Channel activator Chemical Structure

Chemical Structure

Molecular Weight: 362.42

Quality Control

Batch: S992601 DMSO]18 mg/mL]false]Ethanol]2 mg/mL]false]Water]Insoluble]false Purity: 99.84%
99.84

Chemical Information, Storage & Stability

Molecular Weight 362.42 Formula

C22H22N2O3

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 332382-54-4 -- Storage of Stock Solutions

Synonyms Mucolipin synthetic agonist 1 Smiles CC1CC(C)(C)N(C(=O)CN2C(=O)C3=C(C=CC=C3)C2=O)C4=C1C=CC=C4

Solubility

In vitro
Batch:

DMSO : 18 mg/mL (49.66 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 2 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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Mechanism of Action

Targets/IC50/Ki
DENV2 [2]
(A549 cells cells)
8.93 µM
TRPML channel [1]
ZIKV [2]
(A549 cells cells)
52.99 µM
In vitro

ML-SA1, as a potent inhibitors of DENV2 and ZIKV, can inhibit these viruses by promoting lysosome acidification and protease activity to cause viral degradation.[2]

In vivo

Administration of ML-SA1 before transient global ischemia ameliorated neurological dysfunction possibly through the promotion of autophagy and the inhibition of apoptosis.[3]

References

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