CBB1007 (trihydrochloride)
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CBB1007 (trihydrochloride)
Description :
CBB1007 trihydrochloride is a reversible and selective LSD1 inhibitor with an IC50 of 5.27 µM for human LSD1. CBB1007 trihydrochloride significantly blocks the demethylase activity of LSD1 on H3K4Me2 and H3K4Me. CBB1007 trihydrochloride shows selectivity for LSD1 over LSD2 or JARID1A, and induces differentiation-related genes in pluripotent cells. CBB1007 trihydrochloride is studied in non-pluripotent cancer research, targeting teratocarcinoma, embryonic carcinoma, and seminoma[1][2].CAS Number :
[2070015-03-9]UNSPSC :
12352005Target :
Histone DemethylaseType :
Reference compoundRelated Pathways :
EpigeneticsApplications :
Cancer-programmed cell deathField of Research :
Cancer; Metabolic DiseaseAssay Protocol :
https://www.medchemexpress.com/CBB1007-trihydrochloride.htmlPurity :
97.08Solubility :
DMSO : 25 mg/mL (ultrasonic; warming; heat to 80°C)Smiles :
NC(N1CCN(CC1)CC2=CC(C(OC)=O)=CC(C(N3CCN(CC3)C(C4=CC=C(C=C4)C(N)=N)=O)=O)=C2)=N.[H]Cl.[H]Cl.[H]ClMolecular Formula :
C27H37Cl3N8O4Molecular Weight :
643.99References & Citations :
[1]Wang J, et al. Novel histone demethylase LSD1 inhibitors selectively target cancer cells with pluripotent stem cell properties. Cancer Res. 2011 Dec 1;71 (23) :7238-49.|[2]Xiong Y, et al. Inhibition of Lysine-Specific Demethylase-1 (LSD1/KDM1A) Promotes the Adipogenic Differentiation of hESCs Through H3K4 Methylation. Stem Cell Rev Rep. 2016;12 (3) :298-304.Shipping Conditions :
Room TemperatureStorage Conditions :
4°C (Powder, sealed storage, away from moisture)Scientific Category :
Reference compound1Clinical Information :
No Development ReportedIsoform :
KDM1/LSD1Citation 01 :
Clin Exp Med. 2025 Nov 25;26 (1) :33.|BMC Neurosci. 2022 Nov 10;23 (1) :63.

