GLPBio

Midostaurin (PKC412)

Catalog No.: GC10496Purity:>98.00%Synonyms: CGP 41251
Midostaurin (PKC412) (PKC412 ؛ CGP 41251) هو مثبط بروتين كينيز نشط عن طريق الفم وقابل للعكس ومتعدد الأهداف. Midostaurin (PKC412) يثبط PKCα؛ / β؛ / γ ؛، Syk، Flk-1، Akt، PKA، c-Kit، c-Fgr، c-Src، FLT3، PDFRβ؛ و VEGFR1 / 2 مع IC50s تتراوح من 22-500 نانومتر. كما ينظم Midostaurin (PKC412) التعبير الجيني لأكسيد النيتريك البطاني (eNOS). يُظهر Midostaurin (PKC412) تأثيرات قوية مضادة للسرطان.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


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

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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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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    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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الوصف (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.

البروتوكول (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.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
120685-11-2
المرادفات
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
الصيغة الجزيئية
C35H30N4O4
الوزن الجزيئي
570.64
الذوبانية
≥ 57.1mg/mL in DMSO with ultrasonic
التخزين
Store at -20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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