| OG-L002 |
| [1,1’-Biphenyl]-3-ol, 4’-[(1R,2S)-2-aminocyclopropyl]-4’-((1R,2S)-2-Aminocyclopropyl)biphenyl-3-o |
| (CAS 1357302-64-7) |
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| Description： |
OG-L002 is a potent and specific LSD1 inhibitor with IC50 of 20 nM, exhibiting 36- and 69-fold selectivity over MAO-B and MAO-A, respectively.
OG-L002 potently inhibits HSV IE gene expression in both HeLa and HFF cells with IC50 of ~10 μM and ~3 μM , respectively. OG-L002 treatment (50 μM ) results in the reduced production of progeny virus with no significant toxicity in HeLa or HFF cells. OG-L002 (50 μM ) increases the levels of repressive chromatin on viral IE gene promoters. In addition, OG-L002 also represses the expression of hCMV IE genes and adenovirus E1A gene.
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| Product No. |
KT00620 |
| Product Name |
OG-L002 |
| Synonyms |
OGL002;OG L002 |
| Formal Name |
[1,1’-Biphenyl]-3-ol, 4’-[(1R,2S)-2-aminocyclopropyl]-4’-((1R,2S)-2-Aminocyclopropyl)biphenyl-3-o |
| CAS Number |
1357302-64-7 |
| Molecular Formula |
C15H15NO |
| Formula Weight |
225.29 |
| Formulation |
A crystalline solid |
| Purity |
98%min |
| Stability |
2 years |
| Storage |
-20°C |
| Shipping |
USD45 for Europe and USA. No shipping charge once amount reach USD500 |
| Quality Control |
HNMR,CNMR,LCMS,HPLC,IR,etc. |
| Price & Availability |
In Stock. Price Negotiated. |
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