Free shipping on all orders over $ 500

K-7174 dihydrochloride

Cat. No. M4814

All AbMole products are for research use only, cannot be used for human consumption.

K-7174 dihydrochloride Structure
Synonym:

K7174 2HCl

Size Price Availability Quantity
10mM*1mL in Water USD 100 In stock
1mg USD 32 In stock
5mg USD 75 In stock
10mg USD 115 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

K-7174, a GATA-specific inhibitor, is a putative anti-inflammatory agent that attenuates effects of inflammatory cytokines in certain cell types. K-7174 inhibited the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either tumor necrosis factor alpha or interleukin-1beta, without affecting the induction of intercellular adhesion molecule-1 or E-selectin. K-7174 had no effect on the stability of VCAM-1 mRNA. Electrophoretic mobility shift assay revealed that its inhibitory effect on VCAM-1 induction was mediated by an effect on the binding to the GATA motifs in the VCAM-1 gene promoter region. K-7174 did not influence the binding to any of the following binding motifs: octamer binding protein, AP-1, SP-1, ets, NFkappaB, or interferon regulatory factor. K-7174 had the potential to induce endoplasmic reticulum (ER) stress evidenced by induction of GRP78 and CHOP. K7174 inhibits hepcidin expression partly by inducing GDF15.

Chemical Information
Molecular Weight 641.67
Formula C33H50Cl2N2O6
CAS Number 191089-60-8
Solubility (25°C) Water 15 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Fujiwara T, et al. PLoS One. A low-molecular-weight compound K7174 represses hepcidin: possible therapeutic strategy against anemia of chronic disease.

[2] Kikuchi J, et al. J Biol Chem. The novel orally active proteasome inhibitor K-7174 exerts anti-myeloma activity in vitro and in vivo by down-regulating the expression of class I histone deacetylases.

[3] Shimada T, et al. Biochem Biophys Res Commun. Unexpected blockade of adipocyte differentiation by K-7174: implication for endoplasmic reticulum stress.

[4] Takano Y, et al. Biochem Biophys Res Commun. Suppression of cytokine response by GATA inhibitor K-7174 via unfolded protein response.

[5] Imagawa S, et al. FASEB J. A GATA-specific inhibitor (K-7174) rescues anemia induced by IL-1beta, TNF-alpha, or L-NMMA.

[6] Umetani M, et al. Biochem Biophys Res Commun. A novel cell adhesion inhibitor, K-7174, reduces the endothelial VCAM-1 induction by inflammatory cytokines, acting through the regulation of GATA.

Related Proteasome Products
Bortezomib (PS-341)

Bortezomib (PS-341) is a highly selective proteasome inhibitor with a ki value of 6nM.

CTP-518

CTP-518 is a novel HIV protease inhibitor. CTP-518 has the potential to be the first HIV protease inhibitor toeliminate the need to co-dose with a boosting agent.

ITMN-191

ITMN-191 (Danoprevir, RG7227) is a potent and orally active inhibitor of hepatitis C virus (HCV) NS3/4A serine protease with an IC50 of 1.6 nM.

MG132

MG132 is a specific and potent cell-permeable proteasome inhibitor (IC50 = 100 nM, Ki = 4 nM). MG-132 effectively blocks the proteolytic activity of the 26S proteasome complex. MG-132 is also a calpain inhibitor with IC50 of 1.2 μM.

IU1

IU1 is a reversible, small molecule inhibitor of deubiquitination by USP14 that demonstrates an IC50 value of 4-5 μM.

  Catalog
Abmole Inhibitor Catalog




Keywords: K-7174 dihydrochloride, K7174 2HCl supplier, Proteasome, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.