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Elesclomol

Cat. No. M2083

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Elesclomol Structure
Synonym:

STA-4783

Size Price Availability Quantity
10mM*1mL in DMSO USD 40  USD40 In stock
2mg USD 29  USD29 In stock
5mg USD 39  USD39 In stock
10mg USD 60  USD60 In stock
50mg USD 127  USD127 In stock
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Quality Control & Documentation
Biological Activity

Elesclomol (STA-4783) is a novel oxidative stress inducer that acts on tumor cells and promotes their apoptosis, and is a strong copper ion-carrier that can be used for cuproptosis studies. By Affymetrix microarray analysis, Elesclomol significantly induced the expression of heat shock stress response genes and metallothionein genes in Hs294T cells treated at 100 nM for 6 h. Ramos Burkitt's lymphoma B cells were treated with Elesclomol (100 nM) for 1 h and 6 h, respectively, and the Hsp70 RNA level was rapidly increased by 4.8 times and 160 times, which was consistent with the intracellular ROS content. After 0.5 h and 6 h Elesclomol treatment, ROS content increased by 20% and 385%, respectively. Antioxidant N-acetylcysteine (NAC) and Tiron pretreatment could inhibit the induction of Hsp70. HSB2 cells treated with 200 nM Elesclomol for 18 h could induce oxidative stress and increase the apoptotic cells in early stage and late stage by 3.7 times and 11 times, respectively. The above effects could be completely inhibited by NAC, but had no effect on normal cells.

Chemical Information
Molecular Weight 400.52
Formula C19H20N4O2S2
CAS Number 488832-69-5
Solubility (25°C) DMSO 50 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Blackman RK, et al. PLoS One. Mitochondrial electron transport is the cellular target of the oncology drug elesclomol.

[2] Qu Y, et al. Breast Cancer Res Treat. Elesclomol, counteracted by Akt survival signaling, enhances the apoptotic effect of chemotherapy drugs in breast cancer cells.

[3] Kirshner JR, et al. Mol Cancer Ther. Elesclomol induces cancer cell apoptosis through oxidative stress.

Related Cuproptosis Products
Cu(II)-Elesclomol

Cu(II)-Elesclomol is a Cu2+ complex of Elesclomol. Cu(II)-Elesclomol induces cuproptosis. Cu(II)-Elesclomol also inducesapoptosis, causes a G1 cell cycle block and induces DNA double strand breaks in K562 cells.

DL-Penicillamine

DL-Penicillamine is a copper chelating agent. DL-Penicillamine can cause pyridoxine deficiency and then induce optic axial neuritis. DL-Penicillamine can also depress primary immune response.

UM4118

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Ammonium tetrathiomolybdate

Ammonium tetrathiomolybdate is a copper chelator and also is a class of sulfide donor. Ammonium tetrathiomolybdate has neuroprotection effects. Tetrathiomolybdate, an orally active anti-copper agent, reduces copper levels in the body.

2,2'-Bipyridine

2,2'-Bipyridine has been used in the preparation of copper(II)-bipyridine-naringenin complexes. It can be used for the preparation of 2,2'-bipyridine hydrobromide. 2,2'-Bipyridine has good redox stability and glucose elevating activity.

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Keywords: Elesclomol, STA-4783 supplier, Cuproptosis, inhibitors, activators

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