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TJ-M2010-2

Chemical Structure : TJ-M2010-2

CAS No.: 1333465-88-5

TJ-M2010-2

Catalog No.: PC-20347Not For Human Use, Lab Use Only.

TJ-M2010-2 is a small molecule inhibitor of MyD88 homodimerization, interacts with MyD88 TIR domain.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

TJ-M2010-2 is a small molecule inhibitor of MyD88 homodimerization, interacts with MyD88 TIR domain.
TJ-M2010-2 partially inhibited MyD88 homodimerization at 10 μM and completely inhibited MyD88 homodimerization at 40 μM.
TJ-M2010-2 alone or with CD154 antagonist mAb MR1 improves survival rate, prevents renal dysfunction and attenuates pathologic damage after IRI.
TJ-M2010-2 alone or with MR1 decreases IRI-induced apoptosis, inhibits DC maturation in vitro and decreases DC-mediated T-cell proliferation.
TJ-M2010-2 attenuates renal fibrosis after IRI and prevents EMT in vitro.
TJ-M2010-2 down-regulates the TLR/MyD88 signaling pathway.

Physicochemical Properties

M.Wt 392.52
Formula C22H24N4OS
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-(4-phenylthiazol-2-yl)-2-(4-p-tolylpiperazin-1-yl) acetamide

References

1. Zhang LM, et al. Sci Rep. 2016 Jun 1;6:26954. doi: 10.1038/srep26954.

2. Liu JH, et al. Exp Cell Res. 2020 Sep 15;394(2):112157.

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