[CAS NO. 488832-69-5]  Elesclomol (STA-4783)

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PRODUCTS SPECIFICATIONS [488832-69-5]

Distributor
Catalog
SLK-S1052
Brand
Selleck
CAS
488832-69-5

DESCRIPTION [488832-69-5]

Overview

MDLMFCD12911784
Molecular Weight400.5
Molecular FormulaC19H20N4O2S2
SMILESC(N(NC(CC(NN(C(=S)C1=CC=CC=C1)C)=O)=O)C)(=S)C2=CC=CC=C2

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.4969 mL12.4844 mL24.9688 mL
5 mM0.4994 mL2.4969 mL4.9938 mL
10 mM0.2497 mL1.2484 mL2.4969 mL
50 mM0.0499 mL0.2497 mL0.4994 mL

Description

Elesclomol (STA-4783) is a novel potent inducer that elicits pro-apoptosis events among tumor cells. Phase 3.Elesclomol specifically binds ferredoxin 1 (FDX1) α2/α3 helices and β5 strand and inhibits FDX1-mediated Fe-S cluster biosynthesis.

Targets

HSP70 [1]
(Cell-free assay)

In vitro

Elesclomol significantly induces the expression of heat shock stress response genes and metallothionein genes, a signature transcription profile indicative of oxidative stress in Hs294T cells. Elesclomol (100 nM) rapidly induces Hsp70 RNA levels with a 4.8-fold increase at 1 hour and a 160-fold increase at 6 hours in Ramos Burkitt's lymphoma B cells in consistent with the intracellular ROS content which increases by 20% as early as 0.5 hour and 385% at 6 hours, and the induction of Hsp70 can be blocked by antioxidants N-acetylcysteine (NAC) and Tiron pretreatment. Elesclomol increases the number of early and late apoptotic cells with 3.7- and 11-fold through the induction of oxidative stress, which can be completely blocked by NAC, while having little effect on normal cells. Elesclomol significantly inhibits the cell viability of SK-MEL-5, MCF-7, and HL-60 with IC50 of 110 nM, 24 nM and 9 nM, respectively. Elesclomol induces copper-dependent ROS generation and cytoxicity in yeast. Instead of working through a specific cellular protein target, Elesclomol interacts with the electron transport chain (ETC), a biologically coherent set of processes occurring in the mitochondrion, to generate high levels of ROS within the organelle and consequently cell death.

In vivo

Although Elesclomol (25-100 mg/kg) as a single agent shows no antitumor activity in nude mouse xenograft models of human breast cancers (MDA435, MCF7 and ZR-75-1), lung cancer (RER) or lymphoma (U937), Elesclomol substantially enhances the efficacy of chemotherapeutic agents such as paclitaxel in these models, both in terms of tumor regression and extended survival of mice.


Synonyms

Propanedioic acid, 1,3-bis[2-methyl-2-(phenylthioxomethyl)hydrazide]
Propanedioic acid, bis[2-methyl-2-(phenylthioxomethyl)hydrazide]
NSC 174939
Elesclomol
STA 4783
GSK 842879A
1-N′,3-N′-Bis(benzenecarbonothioyl)-1-N′,3-N′-dimethylpropanedihydrazide