GLPBio

Misonidazole

Catalog No.: GC16331Purity:>95.00%Synonyms: NSC 261037,Ro 7-0582,SR 1354
Misonidazol (Ro 7-0582; SR 1354) ist ein hypoxischer Radiosensibilisator fÜr Tumorzellen.

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Misonidazole
Cas No.: 13551-87-6
1mgIn Stock
$96.00
1
5mgIn Stock
$165.00
1
10mgIn Stock
$232.00
1
25mgIn Stock
$270.00
1

Zitate (Citations)

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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    35, 97–116 (2025)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Misonidazole (MISO), a hypoxic cell radiosensitizer, is selectively metabolized by hypoxic cells to reactive products that bind covalently to cellular constituents. The drug also possesses a substantial cytotoxic effect, independent of radiation, which is selectively expressed in hypoxic cells. Misonidazole may be cytotoxic to the normal hypoxic tissues in the human body, making this became a major concern in the clinical application of the drug. Misonidazole leads to strand breaks in cellular DNA and those cells which fail to survive also fail to repair these strand breaks. Misonidazole depletes intracellular glutathione and is more toxic in glutathione depleted cells. The depletion is time, temperature, drug concentration and cell line dependent.

In vitro: In cultured CHO cells, pretreatment with 5 mM MISO for 2 hr exihibited the marginal toxicity [2].

In vivo: Pretreatment with misonidazole (MISO) enhanced the number of cross-links formed in a fibrosarcoma and in the spleen and gut of mice for periods up to 48 h following a single injection of melphalan (MEL). MISO pretreatment could result in a greater amount of binding of MEL to DNA at early times after injection. MISO may exert its affect by inhibiting the repair of cross-links or monoadducts at early times post-injection [3].

Clinical trials: Various dose schedules of misonidazole have proven to be tolerable, with a moderate incidence of nausea and vomiting and mild peripheral neuropathy, and a low incidence of more severe peripheral neuropathy or central neuropathy [4].

References:
[1] Josephy P D, Palcic B, Skarsgard L D.  Ascorbate-enhanced cytotoxicity of misonidazole[J]. Nature, 1978, 271(5643): 370-372.
[2]Taylor Y C, Bump E A, Brown J M.  Studies on the mechanism of chemosensitization by misonidazole in vitro[J]. International Journal of Radiation Oncology Biology Physics, 1982, 8(3-4): 705-708.
[3] Murray D, Meyn R E.  Enhancement of the DNA cross-linking activity of melphalan by misonidazole in vivo[J]. British journal of cancer, 1983, 47(2): 195.
[4] Wasserman T H, Stetz J A, Phillips T L.  Clinical trials of misonidazole in the United States[J]. Cancer clinical trials, 1980, 4(1): 7-16.

Produktdokumente (Product Documents)

Purity:>95.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
13551-87-6
Synonyme
NSC 261037,Ro 7-0582,SR 1354
Chemischer Name
α-(methoxymethyl)-2-nitro-1H-imidazole-1-ethanol
SMILES
OC(COC)CN1C=CN=C1[N+]([O-])=O
Summenformel
C7H11N3O4
Molekulargewicht
201.2
Löslichkeit
≤5mg/ml in ethanol;15mg/ml in DMSO;15mg/ml in dimethyl formamide
Lagerung
Store at -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

Reviews

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