- Midostaurin
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- $0.00 / 25kg
-
2024-04-12
- CAS:120685-11-2
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 2000ton
- Midostaurin
-
- $0.00 / 1KG
-
2024-03-16
- CAS:120685-11-2
- Min. Order: 100g
- Purity: 98%+
- Supply Ability: 100kg
- Midostaurin
-
- $0.00 / 1g
-
2024-03-12
- CAS:120685-11-2
- Min. Order: 1g
- Purity: 98% HPLC
- Supply Ability: 1kg
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| | Midostaurin Basic information |
| Product Name: | Midostaurin | | Synonyms: | CGP 41251MIDOSTAURIN(PKC412);N-((5S,6R,7R,9R)-6-Methoxy-14-oxo-5,6,7,8,9,14,15,16-octahydro-17-oxa-4b,9a,15-triaza-5,9-Methanodibenzo[b,h]cyclonona[jkl]cyclopenta[e]-as-indacen-7-yl)-N-MethylbenzaMide;PKC-412, CGP-41251;Midostaurin (PKC412);PKC412 (Midostaurin);CGP 41231;N-Benzoylstaurosporine;(Midostaurin) Benzoylstaurosporine | | CAS: | 120685-11-2 | | MF: | C35H30N4O4 | | MW: | 570.64 | | EINECS: | 999-999-2 | | Product Categories: | antibiotic;Pharmaceutical | | Mol File: | 120685-11-2.mol |  |
| | Midostaurin Chemical Properties |
| Melting point | 235-260℃ | | density | 1.47±0.1 g/cm3(Predicted) | | storage temp. | Sealed in dry,Store in freezer, under -20°C | | solubility | Soluble in DMSO (15 mg/ml), MDC (10 mg/ml), methanol (5 mg/ml), 100% ethanol (2.5 mg/ml), and DMF (20 mg/ml). | | pka | 14.19±0.70(Predicted) | | form | Tan solid | | color | White | | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 2 months. |
| Hazard Codes | T | | Risk Statements | 36/37/38 | | HS Code | 29329990 |
| | Midostaurin Usage And Synthesis |
| Description | PKC-412 (120685-11-2) is a broad spectrum kinase inhibitor. Inhibited kinases include, but are not limited to; PKA, PKC, S6 Kinase, KDR, PKC, Akt, EGFR, VEGFR, PDGFR, c-kit, and FLT-3. Acute myeloid leukemia related mutant forms of FLT-3 are also inhibited both in vitro and in vivo. PKC-412 has been demonstrated to induce apoptosis and shows broad antiproliferative activity in various tumor cell lines. Cell Permeable | | Uses | Midostaurin is used as a broad spectrum protein kinase inhibitor. Inhibits conventional PKC isoforms (α, β, γ), PDFRβ, VEGFR2, Syk, PKCη, Flk-1, Flt3, Cdk1/B, PKA, c-Kit, c-Fgr, c-Src, VEGFR1 and EGFR. Displays potent antitumor activity. Due to this act which may result in disruption of the cell cycle, inhibition of proliferation, apoptosis, and inhibition of angiogenesis in susceptible tumors. Midostaurin was shown to possess antiproliferative characteristics via inhibition of protein kinase C, kinase insert domain receptor, and c-kit. | | Definition | ChEBI: An organic heterooctacyclic compound that is the N-benzoyl derivative of staurosporine. | | Biological Activity | Broad spectrum protein kinase inhibitor. Inhibits conventional PKC isoforms ( α , β , γ ), PDFR β , VEGFR2, Syk, PKCη, Flk-1, Flt3, Cdk1/B, PKA, c-Kit, c-Fgr, c-Src, VEGFR1 and EGFR. Displays potent antitumor activity. | | storage | Store at -20°C | | References | 1) Odgerel et al. (2008) The FLT3 inhibitor PKC412 exerts differential cell cycle effects on leukemic cells depending on the presence of FLT3 mutations; Oncogene, 27 3102
2) El Fitori et al. (2007) PKC 412 small-molecule tyrosine kinase inhibitor: single-compound therapy for pancreatic cancer; Cancer, 110 1457
3) Miyatake, et al. ( 2007) PKC412 (CGP41251) modulates the proliferation and lipopolysaccharide-induced inflammatory responses of RAW 264.macrophages; Biochem. Biophys. Res. Commun., 360 115
4) Bahlis et.al. (2005) N-Benzoylstaurosporine (PKC412) inhibits Akt kinase inducing apoptosis in multiple myeloma cells; Leuk. Lymphoma, 46 899
5) Fabbro et al., (2000) PKC-412 – a protein kinase inhibitor with a broad therapeutic potential; Anticancer Drug Des., 15 17 |
| | Midostaurin Preparation Products And Raw materials |
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