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TP-064

TP-064, a chemical probe, is a potent and selective proteinarginine methyltransferase 4 (PRMT4; CARM1) inhibitor (IC50 IC50 of 340 nM) and MED12 (IC50 of 43 nM) . TP-064 is inactive against the other family members except for PRMT6 (IC50 of 1.3 μM) . TP-064 has anticancer activities[1].

Product Specifications

CAS Number

2080306-20-1

Product Name Alternative

1-hydroxycholecalciferol-d7; 1.alpha.-Hydroxyvitamin D3-d7

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Histone Methyltransferase

Type

Reference compound

Related Pathways

Epigenetics

Applications

COVID-19-immunoregulation

Field of Research

Cancer; Inflammation/Immunology

Assay Protocol

https://www.medchemexpress.com/tp-064.html

Purity

99.61

Solubility

DMSO : 125 mg/mL (ultrasonic; warming; heat to 60°C) |H2O : ≥ 50 mg/mL

Smiles

O=C(C1=CC=CC(OC2=CC=CC=C2)=C1)N(CC3=CC(C4CCN(CC4)CCNC)=NC=C3)C

Molecular Formula

C28H34N4O2

Molecular Weight

458.60

Precautions

H302, H315, H319, H335

References & Citations

[1]Kazuhide Nakayama, et al. TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myeloma. Oncotarget. 2018 Apr 6;9 (26) :18480-18493.|[2]Yiheng Zhang, et al. PRMT4 inhibitor TP-064 inhibits the pro-inflammatory macrophage lipopolysaccharide response in vitro and ex vivo and induces peritonitis-associated neutrophilia in vivo. Biochim Biophys Acta Mol Basis Dis. 2021 Jul 24;1867 (11) :166212.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

PRMT4; PRMT6

Available Sizes

Frequently Asked Questions

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