2170347-90-5

2170347-90-5 structure
2170347-90-5 structure
  • Name: LSD1-IN-13 hydrochloride
  • Chemical Name: LSD1-IN-13 hydrochloride
  • CAS Number: 2170347-90-5
  • Molecular Formula: C23H30ClN3O2S
  • Molecular Weight: 448.02
  • Catalog: Signaling Pathways Epigenetics Histone Demethylase
  • Create Date: 2022-08-30 15:51:40
  • Modify Date: 2024-01-17 18:03:02
  • LSD1-IN-13 hydrochloride (compound 7e) is an orally active and potent LSD1 inhibitor, with an IC50 of 24.43 nM. LSD1-IN-13 hydrochloride can activate CD86 expression, with an EC50 of 470 nM. LSD1-IN-13 hydrochloride induces differentiation of AML (acute myeloid leukemia) cell lines[1].

Name LSD1-IN-13 hydrochloride
Description LSD1-IN-13 hydrochloride (compound 7e) is an orally active and potent LSD1 inhibitor, with an IC50 of 24.43 nM. LSD1-IN-13 hydrochloride can activate CD86 expression, with an EC50 of 470 nM. LSD1-IN-13 hydrochloride induces differentiation of AML (acute myeloid leukemia) cell lines[1].
Related Catalog
Target

IC50: 24.43 ± 1.08 nM (LSD1), 5.00 ± 0.28 μM (LSD2), >100 μM (MAO-A), >100 μM (MAO-B)[1]

In Vitro LSD1-IN-13 hydrochloride (compound 7e) shows good selectivity over LSD2 (205-fold) and MAOs (>4000-fold)[1]. LSD1-IN-13 hydrochloride shows potent and selective antiproliferative activity in MV-4-11, with an IC50 of 1.36 μM[1].
In Vivo LSD1-IN-13 hydrochloride (compound 7e) (MV-4-11 xenograft mice, 0-20 mg/kg, Orally, daily for 15 days) suppresses tumor growth significantly in a dose-dependent manner[1].
References

[1]. Li C, et al. Structure-Activity Relationship Study of Indolin-5-yl-cyclopropanamine Derivatives as Selective Lysine Specific Demethylase 1 (LSD1) Inhibitors. J Med Chem. 2022 Mar 10;65(5):4335-4349.

Molecular Formula C23H30ClN3O2S
Molecular Weight 448.02
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