GLPBio

Midostaurin (PKC412)

Catalog No.: GC10496Purity:>98.00%Synonyms: CGP 41251
Midostaurin (PKC412) (PKC412; CGP 41251) ist ein oral aktiver, reversibler, mehrfach zielgerichteter Proteinkinase-Inhibitor. Midostaurin (PKC412) hemmt PKCα/β/γ, Syk, Flk-1, Akt, PKA, c-Kit, c-Fgr, c-Src, FLT3, PDFR&7#946; und VEGFR1/2 mit IC50s im Bereich von 22-500 nM. Midostaurin (PKC412) reguliert auch die Genexpression der endothelialen Stickoxidsynthase (eNOS) hoch. Midostaurin (PKC412) zeigt starke Antikrebswirkungen.

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


Midostaurin (PKC412)
Cas No.: 120685-11-2
1mgIn Stock
$34.00
1
5mgIn Stock
$100.00
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10mgIn Stock
$157.00
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25mgIn Stock
$323.00
1

Zitate (Citations)

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    610, 366–372 (2022)
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    187(9):2288-2304 (2024)
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Beschreibung (Description)

Midostaurin (PKC412) is an oral, multi-targeted tyrosine kinase inhibitor that inhibits multiple kinases, including FLT3, KIT, PDGFR, and VEGFR (IC50 = 22-500nM) [1-2]. Midostaurin competitively inhibits the binding of ATP to kinases, thereby blocking tumor cell proliferation and promoting apoptosis [3]. Midostaurin is commonly used to treat acute myeloid leukemia (AML) harboring FLT3 mutations [4].

In peripheral blood mononuclear cells (PBMCs), Midostaurin (1µM; 72h) significantly reduced the CD4+CD25+FOXP3+ T cell population and FOXP3 mRNA expression in PBMCs [5]. In MDA -MB-468 cells, Midostaurin (1µM; 72h) directly inhibits Aurora kinases A and B and subsequently reduces cell viability in TNBC cells [6]. In HMC-1 cells, ponatinib cooperates with Midostaurin (0-0.1µM; 48h) to induce growth inhibition and apoptosis [7].

In CT26 cells xenograft tumor mouse model, Midostaurin (100mg/kg; po; 7d) treatment significantly inhibited tumor growth [8]. In HL-60 cells xenograft tumor mouse model, All-trans retinoic acid combined with Midostaurin (50mg/kg; po; 10d) treatment significantly inhibited tumor growth [9].

References:
[1]. Fabbro D, Buchdunger E, Wood J, et al. Inhibitors of protein kinases: CGP 41251, a protein kinase inhibitor with potential as an anticancer agent[J]. Pharmacology & therapeutics, 1999, 82(2-3): 293-301.
[2]. Fabbro D, Ruetz S, Bodis S, et al. PKC412-a protein kinase inhibitor with a broad therapeutic potential[J]. Anti-cancer drug design, 2000, 15(1): 17-28.
[3]. Gallogly M M, Lazarus H M, Cooper B W. Midostaurin: a novel therapeutic agent for patients with FLT3-mutated acute myeloid leukemia and systemic mastocytosis[J]. Therapeutic advances in hematology, 2017, 8(9): 245-261.
[4]. Levis M. Midostaurin approved for FLT3-mutated AML[J]. Blood, The Journal of the American Society of Hematology, 2017, 129(26): 3403-3406.
[5]. Gutierrez L, Jang M, Zhang T, et al. Midostaurin reduces regulatory T cells markers in acute myeloid leukemia[J]. Scientific reports, 2018, 8(1): 17544.
[6]. Kawai M, Nakashima A, Kamada S, et al. Midostaurin preferentially attenuates proliferation of triple-negative breast cancer cell lines through inhibition of Aurora kinase family[J]. Journal of biomedical science, 2015, 22(1): 48.
[7]. Gleixner K V, Peter B, Blatt K, et al. Synergistic growth-inhibitory effects of ponatinib and midostaurin (PKC412) on neoplastic mast cells carrying KIT D816V[J]. Haematologica, 2013, 98(9): 1450.
[8]. Lai C T, Chi C W, Wu S H, et al. Midostaurin modulates tumor microenvironment and enhances efficacy of anti-PD-1 against colon cancer[J]. Cancers, 2022, 14(19): 4847.
[9]. Lu H, Weng X, Sheng Y, et al. Combination of midostaurin and ATRA exerts dose-dependent dual effects on acute myeloid leukemia cells with wild type FLT3[J]. BMC cancer, 2022, 22(1): 749.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

Peripheral blood mononuclear cells (PBMCs)

Preparation Method

PBMCs were cultured in Roswell Park Memorial Institute 1640 1x (RPMI) medium supplemented with 20% fetal bovine serum (FBS). In addition, PBMCs were treated with IL-2 (5ng/mL) and IL-7 (10ng/mL), as well as 1µM of Midostaurin. PBMCs were seeded at 2 million cells per well in a 6 well plate, and allowed to incubate at 5% CO2, 37 ℃ for 72 hours before analysis via flow cytometry or quantitative polymerase chain reaction.

Reaction Conditions

1µM; 72h

Applications

Midostaurin reduces CD4 + CD25 + FOXP3 + T cell population in healthy PBMC.
Animal experiment [2]:

Animal models

CT26 cells xenograft tumor mouse model

Preparation Method

Male BALB/c mice at five weeks old were purchased from the National Laboratory Animal Center of Taiwan and housed under 12-h light/dark cycle under a specific pathogen-free facility. The 4 × 106 CT26 cells in 100μL PBS were subcutaneously inoculated on the right hindlimb of the mice. After the tumors grew for 7 days to achieve a mean diameter of approximate 5mm, mice were randomly allocated into 4 groups as follows: (1) control, (2) Midostaurin (100mg/kg), (3) intraperitoneal anti-PD-1 injection (200μg), and (4) Midostaurin in combination with anti-PD-1.

Dosage form

100mg/kg; po; 7d

Applications

Midostaurin treatment significantly inhibited tumor growth.

References:
[1]. Gutierrez L, Jang M, Zhang T, et al. Midostaurin reduces regulatory T cells markers in acute myeloid leukemia[J]. Scientific reports, 2018, 8(1): 17544.
[2]. Lai C T, Chi C W, Wu S H, et al. Midostaurin modulates tumor microenvironment and enhances efficacy of anti-PD-1 against colon cancer[J]. Cancers, 2022, 14(19): 4847.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
120685-11-2
Synonyme
CGP 41251
SMILES
CC12C(C(CC(O1)N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N2C7=C53)CNC6=O)N(C)C(=O)C9=CC=CC=C9)OC
Summenformel
C35H30N4O4
Molekulargewicht
570.64
Löslichkeit
≥ 57.1mg/mL in DMSO with ultrasonic
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

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