1. Epigenetics Neuronal Signaling
  2. Histone Demethylase Monoamine Oxidase
  3. LSD1-IN-10

LSD1-IN-10 is a LSD1/MAO inhibitor with LSD1 IC50 of 5 nM, MAO-A IC50 of 16 μM, and MAO-B IC50 of 7.4 μM. LSD1-IN-10 suppresses enzymatic activity of LSD1, MAO-A, and MAO-B. LSD1-IN-10 can be used for the research of cancer, alzheimer's disease, parkinson's disease, huntington's disease.

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

LSD1-IN-10

LSD1-IN-10 Chemical Structure

CAS No. : 1235864-15-9

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Description

LSD1-IN-10 is a LSD1/MAO inhibitor with LSD1 IC50 of 5 nM, MAO-A IC50 of 16 μM, and MAO-B IC50 of 7.4 μM. LSD1-IN-10 suppresses enzymatic activity of LSD1, MAO-A, and MAO-B. LSD1-IN-10 can be used for the research of cancer, alzheimer's disease, parkinson's disease, huntington's disease[1].

IC50 & Target[1]

LSD1

5 nM (IC50)

MAO-A

16 μM (IC50)

MAO-B

7.4 μM (IC50)

In Vitro

LSD1-IN-10 (Compound 76) potently inhibits LSD1 with an IC50 of 0.005 μM, and is far less potent against MAO-A (IC50 16 μM) and MAO-B (IC50 7.4 μM) in cell-free enzymatic assays[1].

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

Molecular Weight

295.38

Formula

C19H21NO2

CAS No.
SMILES

N(C(C)C=1C=C2C(=CC1)OCCO2)[C@H]3[C@@H](C3)C4=CC=CC=C4

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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LSD1-IN-10
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HY-136878
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