research use only
Cat.No.S7296
| Related Targets | HDAC JAK BET Histone Methyltransferase PKC PARP HIF PRMT EZH2 AMPK |
|---|---|
| Other Histone Demethylase Inhibitors | GSK-J4 Hydrochloride SP2509 CPI-455 HCl GSK-LSD1 2HCl Ladademstat (ORY-1001) Dihydrochloride JIB-04 OG-L002 IOX1 GSK J1 CPI-455 |
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In vitro |
DMSO
: 28 mg/mL
(80.13 mM)
Ethanol : 6 mg/mL Water : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
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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| Molecular Weight | 349.43 | Formula | C21H23N3O2 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 1222800-79-4 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CN(C)CCCNC(=O)C1=CC=C(C=C1)C2=CC(=C3C(=C2)C=CC=N3)O | ||
| Targets/IC50/Ki |
JMJD2
(Cell-free assay) 920 nM
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| In vitro |
ML324 exhibits good Caco-2 cell permeability, and possesses excellent microsomal stability in the presence of both mouse and rat liver microsomes. This compound demonstrates potent anti-viral activity against both herpes simplex virus (HSV) and human cytomegalovirus (hCMV) infection by inhibiting viral IE gene expression.
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| In vivo |
In a mouse ganglia explant model of latently infected mice, ML324 suppresses the formation of HSV plaques, and blocks HSV-1 reactivation.
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References |
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