GLPBio

Cu(II)-Elesclomol

Catalog No.: GC73634Purity:>99.00%
Cu(II)-Elesclomol ist ein Cu2+-Komplex von Elesclomol.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Cu(II)-Elesclomol
Cas No.: 1224195-72-5
1 mgIn Stock
$140.00
1
5 mgIn Stock
$216.00
1
10 mgIn Stock
$302.00
1
25 mgIn Stock
$447.00
1

Zitate (Citations)

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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Cu (II) -Elesclomol is a 1:1 chelate formed by Elesclomol and Cu (II) ions, which can induce copper death and has anti-cancer activity[1]. Elesclomol is a highly novel anti-cancer drug that has completed Phase 3 clinical trials for patients with advanced melanoma[2]. Both Elesclomol and Cu (II) -elesclomol are highly effective in vitro and usually inhibit the growth of cancer cells at low concentrations[3]. Cu (II) -Elesclomol inhibits the growth of cancer cells by inducing Cu2+ -mediated apoptosis and oxidative stress[1,2].

In vitro, K562 cells were treated with Cu (II) -Elesclomol (0.04, 0.2, 1, 5μM) for 72 hours to induce intracellular H2O2 production, increase intracellular reactive oxygen species levels, and cause oxidative stress in the cells. The IC50 of Cu (II) -Elesclomol on K562 cells was 6.2nM[1,4]. CHO cells were treated with Cu (II) -Elesclomol (50nM) for 30 minutes to induce G1 phase arrest of CHO cells, resulting in rapid cessation of cell growth and induction of cell apoptosis[5].

References:
[1]Hasinoff BB, Yadav AA, Patel D, Wu X. The cytotoxicity of the anticancer drug elesclomol is due to oxidative stress indirectly mediated through its complex with Cu(II). J Inorg Biochem. 2014 Aug;137:22-30.
[2] Nagai M, Vo NH, Shin Ogawa L, Chimmanamada D, Inoue T, Chu J, Beaudette-Zlatanova BC, Lu R, Blackman RK, Barsoum J, Koya K, Wada Y. The oncology drug elesclomol selectively transports copper to the mitochondria to induce oxidative stress in cancer cells. Free Radic Biol Med. 2012 May 15;52(10):2142-50.
[3]Hasinoff BB, Yadav AA, Patel D, Wu X. The cytotoxicity of the anticancer drug elesclomol is due to oxidative stress indirectly mediated through its complex with Cu(II). J Inorg Biochem. 2014 Aug;137:22-30.Nov;71(11):1788-1800.
[4]Wu L, Zhou L, Liu DQ, Vogt FG, Kord AS. LC-MS/MS and density functional theory study of copper(II) and nickel(II) chelating complexes of elesclomol (a novel anticancer agent). J Pharm Biomed Anal. 2011 Jan 25;54(2):331-6.
[5]Fleischmann R, Pangan AL, Song IH, Mysler E, Bessette L, Peterfy C, Durez P, Ostor AJ, Li Y, Zhou Y, Othman AA, Genovese MC. Upadacitinib Versus Placebo or Adalimumab in Patients With Rheumatoid Arthritis and an Inadequate Response to Methotrexate: Results of a Phase III, Double-Blind, Randomized Controlled Trial. Arthritis Rheumatol. 2019 Nov;71(11):1788-1800.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

K562 cells

Preparation Method

The K562 cells were seeded into 96-well plates at a density of 5x104 cells/mL.The K562 cells were treated with TM just prior to the addition of either Cu(II)-Elesclomoll. Cell growth inhibition was evaluated by an MTS assay after 72h. The curved lines were calculated from non-linear least squares fits to 4-parameter logistic equations to yield IC50 values.

Reaction Conditions

0, 0.001, 0.01, 0.1, 1, 10, 100, 1000μM;72 hours

Applications

The results that showed that the copper chelators TM and TRIEN greatly reduced the growth inhibitory effects of elesclomol and Cu(II)-Elesclomol strongly suggests that copper present in the medium has a role in the K562 cell growth inhibitory effects of elesclomol and Cu(II)-Elesclomol.

Cell experiment [2]:

Cell lines

CHO cells

Preparation Method

CHO cells were seeded into 96-well plates at a density of 2x104 cells/mL.CHO cells that had been synchronized in G0/G1 through serum starvation were repleted with serum and were treated with 50nM Cu(II)-Elesclomol , elesclomol, or the DMSO vehicle control directly after repletion and allowed to grow for the times indicated, after which they were subjected to cell cycle analysis of their propidium iodide-stained DNA.

Reaction Conditions

50nM;30min

Applications

Cu(II)-Elesclomol causes G1 phase arrest in CHO cells, resulting in rapid cessation of cell growth, induction of apoptosis, and may also partially inhibit cell growth through its ability to destroy DNA.

References:
[1]Hasinoff BB, Yadav AA, Patel D, Wu X. The cytotoxicity of the anticancer drug elesclomol is due to oxidative stress indirectly mediated through its complex with Cu(II). J Inorg Biochem. 2014 Aug;137:22-30.
[2]Fleischmann R, Pangan AL, Song IH, Mysler E, Bessette L, Peterfy C, Durez P, Ostor AJ, Li Y, Zhou Y, Othman AA, Genovese MC. Upadacitinib Versus Placebo or Adalimumab in Patients With Rheumatoid Arthritis and an Inadequate Response to Methotrexate: Results of a Phase III, Double-Blind, Randomized Controlled Trial. Arthritis Rheumatol. 2019 Nov;71(11):1788-1800.

Produktdokumente (Product Documents)

Purity:>99.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
1224195-72-5
Summenformel
C19H18CuN4O2S2
Molekulargewicht
462.05
Löslichkeit
DMSO : 6.67 mg/mL (14.44 mM; ultrasonic and warming and heat to 80°C)
Lagerung
-20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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