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CBB1007

CAT: 0804-HY-15313Size: 1 EachDry Ice: NoHazardous: No
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CAT#:0804-HY-15313Size:1 Each
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Description
CBB1007 is a reversible and selective LSD1 inhibitor with an IC50 of 5.27 µM for human LSD1. CBB1007 significantly blocks the demethylase activity of LSD1 on H3K4Me2 and H3K4Me. CBB1007 shows selectivity for LSD1 over LSD2 or JARID1A, and induces differentiation-related genes in pluripotent cells. CBB1007 is studied in non-pluripotent cancer research, targeting teratocarcinoma, embryonic carcinoma, and seminoma[1][2].
CAS Number
1379573-92-8
UNSPSC
12352005
Target
Histone Demethylase
Type
Reference compound
Related Pathways
Epigenetics
Applications
Cancer-programmed cell death
Field of Research
Cancer; Metabolic Disease
Assay Protocol
https://www.medchemexpress.com/cbb1007.html
Solubility
10 mM in DMSO
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
Molecular Formula
C27H34N8O4
Molecular Weight
534.61
References & 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 temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
KDM1/LSD1
Citation 01
BMC Neurosci. 2022 Nov 10;23 (1) :63.|Clin Exp Med. 2025 Nov 25;26 (1) :33.

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A16374-10CBB1007 10mg
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A16374-100CBB1007 100mg
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T10699L2-01CBB1007 trihydrochloride (1379573-92-8 free base)
T10699-01CBB1007 hydrochloride (1379573-92-8 free base)

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