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Midostaurin (PKC412) (Synonyms: CGP 41251)

Katalog-Nr.GC10496

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.

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Midostaurin (PKC412) Chemische Struktur

Cas No.: 120685-11-2

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1mg
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Sample solution is provided at 25 µL, 10mM.

Product Documents

Quality Control & SDS

View current batch:

Protocol

Cell experiment [1-3]:

Cell lines

Ba/F3-FLT3-ITD cells, Ba/F3 cells, M0-91 and IMS-M2 cells

Preparation method

The solubility of this compound in DMSO is > 10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

0.01–1 μM, 24–72 hr

Applications

PKC412 showed a broad antiproliferative activity against various tumor and normal cell lines in vitro, and was able to reverse the Pgp-mediated multidrug resistance of tumor cells. PKC412 resulted in a dose-dependent increase in the G2/M phase of the cell cycle concomitant with increased polyploidy, apoptosis and enhanced sensitivity to ionizing radiation. PKC412 inhibited the proliferation of Ba/F3-FLT3-ITD cells with an IC50 of less than 10 nM within 24–72 hr, and was nontoxic toward parental Ba/F3 cells at concentrations up to 100 nM. PKC412 inhibited proliferation and viability of Ba/F3-FLT3-D835Y cells. PKC412 (0.01–1 μM, 15 min) potently inhibited FLT3 tyrosine phosphorylation in Ba/F3-FLT3-ITD and Ba/F3-FLT3-D835Y cells. In Ba/F3-FLT3-ITD cells, treatment with PKC412 (up to 0.04 μM) over a span of two months generated a polyclonal subline of Ba/F3-FLT3-ITD cells less sensitive to PKC412. PKC412 inhibited EN fusion tyrosine kinase in hematopoietic Ba/F3 cells. PKC412 significantly inhibited EN phosphorylation in M0-91 and IMS-M2 cells in a dose-dependent manner.

Animal experiment [1,2,4]:

Animal models

Balb/c mice with FLT3/ITD-induced myeloproliferative disorder (MPD)

Dosage form

Oral administration, 100 mg/kg

Application

Combination of PKC412 with loco-regional ionizing irradiation showed significant antitumor activity against tumors which are resistant to both ionizing radiation and chemotherapeutic agents (dysfunctional p53). Orally administered PKC412 strongly inhibited retinal neovascularization as well as laser-induced choroidal neovascularization in murine models. In Balb/c mice with FLT3/ITD-induced myeloproliferative disorder (MPD), PKC412 prolonged survival. PKC412 inhibited FLT3-ITD-mediated transformation. PKC412-treated mice displayed only a slight increase in mean spleen weight (80 mg). PKC412 (25 mg/kg, i.p.) protected cultured A549 cells that expressed mutant or wild-type K18 and mouse livers of the K18 Arg90Cys-overexpressing transgenic mice from Fas-induced apoptosis.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. 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.

[2]. Weisberg E, Boulton C, Kelly L M, et al. Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412[J]. Cancer cell, 2002, 1(5): 433-443.

[3]. Chi HT, et al. ETV6-NTRK3 as a therapeutic target of small molecule inhibitor PKC412. Biochem Biophys Res Commun. 2012 Dec 7;429(1-2):87-92.

[4]. Juarez JC, et al. Copper binding by tetrathiomolybdate attenuates angiogenesis and tumor cell proliferation through the inhibition of superoxide dismutase 1. Clin Cancer Res. 2006 Aug 15;12(16):4974-82.

Background

Midostaurin is an inhibitor of PKC with IC50 values of 22nM, 30nM, 31nM, 24nM, 330nM, 160nM and 1.25μM for PKC-α, PKC-β1, PKC-β2, PKC-γ, PKC-δ, PKC-η and PKC-ε, respectively [1].

Midostaurin is a PKC inhibitor with potent activity against most PKC subtypes. It also has inhibitory activity against KDR and its mouse homologue Flk-1. Other protein kinases involved in angiogenesis, cell cycle and cell growth are not sensitive to midostaurin. Midostaurin shows reversible inhibition of intracellular PKC activity with IC50 value of 0.5μM. Besides PKC, midostaurin inhibits the autophosphorylation of the receptors for PDGF, VEGF and stem cell factor with IC50 values of 80nM, 1μM and 30nM, respectively. Midostaurin also inhibits the FGF-induced c-fos transcription and MAPK activation. Moreover, midostaurin suppresses cell growth of different cell lines through inducing cell cycle arrest in G2/M and inducing apoptosis [1].

Furthermore, midostaurin exerts antitumor activity via inhibiting tumor angiogenesis and proliferation due to its effects on VEGFR and PKC, respectively. Administration of midostaurin prolongs the life span of mice bearing B16 melanoma at dose of 75mg/kg 3 times daily for 9 days [1].

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. Pharmacology & therapeutics, 1999, 82(2): 293-301.

Chemical Properties

Cas No. 120685-11-2 SDF
Überlieferungen CGP 41251
Canonical 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
Formula C35H30N4O4 M.Wt 570.64
Löslichkeit ≥ 57.1mg/mL in DMSO with ultrasonic Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.7524 mL 8.7621 mL 17.5242 mL
5 mM 0.3505 mL 1.7524 mL 3.5048 mL
10 mM 0.1752 mL 0.8762 mL 1.7524 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 9 reference(s) in Google Scholar.)

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