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KDOAM-25 (citrate)

KDOAM-25 citrate is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 citrate increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells[1].

Product Specifications

CAS Number

[2448475-08-7]

UNSPSC

12352005

Target

Histone Demethylase

Type

Reference compound

Related Pathways

Epigenetics

Applications

Cancer-programmed cell death

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/kdoam-25-citrate.html

Purity

98.56

Solubility

DMSO : 200 mg/mL (ultrasonic) |H2O : 100 mg/mL (ultrasonic)

Smiles

NC(C1=CC=NC(CNCC(N(CC)CCN(C)C)=O)=C1)=O.OC(CC(C(O)=O)(O)CC(O)=O)=O

Molecular Formula

C21H33N5O9

Molecular Weight

499.51

References & Citations

[1]Tumber A, et al. Potent and Selective KDM5 Inhibitor Stops Cellular Demethylation of H3K4me3 at Transcription Start Sites and Proliferation of MM1S Myeloma Cells. Cell Chem Biol. 2017 Mar 16;24 (3) :371-380.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, stored under nitrogen)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

KDM5

Citation 01

BioRxiv. 2024 October 03.|Cancer Sci. 2018 Nov;109 (11) :3602-3610.|Clin Exp Med. 2025 Nov 25;26 (1) :33.|Nat Cell Biol. 2024 Feb;26 (2) :263-277.|Research Square Preprint. 2023 Dec 2.|Sci Adv. 2025 Jun 6;11 (23) :eadu2695.|Clin Transl Med. 2024 Jun;14 (6) :e1692.|University of Gothenburg. 2023 Jun 27.

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