[CAS NO. 1357302-64-7]  OG-L002

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PRODUCTS SPECIFICATIONS [1357302-64-7]

Catalog
HY-19333
Brand
MCE
CAS
1357302-64-7

DESCRIPTION [1357302-64-7]

Overview

MDLMFCD27997969
Molecular Weight225.29
Molecular FormulaC15H15NO
SMILESOC1=CC(C2=CC=C([C@@H]3[C@@H](N)C3)C=C2)=CC=C1

For research use only. We do not sell to patients.

1 Publications Citing Use of MCE


Summary

OG-L002 is a potent and highly selective LSD1 inhibitor with an IC 50 of 0.02 μM. OG-L002 is a potent monoamine oxidases (MAO) inhibitor with IC 50 s of 1.38 μM and 0.72 μM for MAO-A and MAO-B , respectively. OG-L002 potently inhibits the expression of HSV IE genes [1] .


IC50 & Target

IC50: 0.02 μM (LSD1), 1.38 μM (MAO-A), 0.72 μM (MAO-B), HSV IE [1]


In Vitro

OG-L002 inhibits viral IE gene expression in both cells with a significantly reduced IC 50 (IC 50 : ~10 µM in HeLa cells; IC 50 : ~3 µM in HFF cells) relative to the control MAOI TCP (IC 50 : ~1 mM) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

OG-L002 (i.p.; 6-40 mg/kg; daily; for 7 days) reduces the levels of detectable viral genomes in the ganglia in a dose-dependent manner at both 3 and 5 days postinfection [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 4-week-old BALB/c female mice [1]
Dosage: 6, 20, 40 mg/kg
Administration: Intraperitoneal; daily; for 7 days
Result: Reduced the levels of detectable viral genomes in the ganglia in a dose-dependent manner at both 3 and 5 days postinfection.

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 250 mg/mL ( 1109.68 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.4387 mL 22.1936 mL 44.3872 mL
5 mM 0.8877 mL 4.4387 mL 8.8774 mL
10 mM 0.4439 mL 2.2194 mL 4.4387 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 1.67 mg/mL (7.41 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 1.67 mg/mL (7.41 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 1.67 mg/mL (7.41 mM); Clear solution

* All of the co-solvents are available by MCE.