LSD1/HDAC-IN-2
Based on 1 publication(s) in Google Scholar
LSD1/HDAC-IN-2 (Compound 20c) is the inhibitor for LSD and HDAC, that inhibits LSD1, HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8, with IC50s of 39.0, 1.4, 1.0, 1.3, 2.9 and 16.0 nM, respectively. LSD1/HDAC-IN-2 inhibits the proliferation of cancer cells, especially the colorectal cancer cells. LSD1/HDAC-IN-2 arrests the cell cycle at G2/M phase, inhibits cell migration, and induces apoptosis in HCT-116 and HT-29 cells. LSD1/HDAC-IN-2 exhibits antitumor efficacy in mouse model without significant toxicity.
For research use only. We do not sell to patients.
- CAS No.: 2966782-82-9
- Formula: C23H26N4O2
- Molecular Weight:390.48
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) LSD1/HDAC-IN-2
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Biological Activity
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HDAC2 1.0 nM (IC50) |
HDAC3 1.3 nM (IC50) |
HDAC1 1.4 nM (IC50) |
HDAC6 2.9 nM (IC50) |
HDAC8 16.0 nM (IC50) |
KDM1/LSD1 39.0 nM (IC50) |
Chemical Information
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CAS No. 2966782-82-9
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Molecular Weight 390.48
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Formula C23H26N4O2
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SMILES
NC1=C(C)C(C2=CN(CCCCCCC(NO)=O)C3=C2C=C(C#N)C=C3)=CC=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
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Journal Impact Factor
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Most Recent
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)