- Search results for SYN-1075-M100
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18 products were found matching "SYN-1075-M100"!
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Item number: SYN-1057-M100
Soluble in DMSO or ethanol. Nilotinib is an orally bio-available aminopyrimidine-derivative Bcr-Abl tyrosine kinase inhibitor (IC(50) <30nM) with anti-neoplastic activity. Target: Abl - PDGFR - BCR , Kinase Group: RTK, PTK , Substrate: Tyrosine
Keywords: | AMN107, Tasigna |
Application: | Bcr-Abl / PDGFR inhibitor |
CAS | 641571-10-0 |
MW: | 529,5 D |
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Item number: SYN-1175-M001
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. IPI-145 is a potent, oral inhibitor of Class I phosphoinositide-3-kinase (PI3K)-delta and PI3K-gamma (IC(50) of 243 pM and 50nM), and is clinically active in patients with advanced hematological malignancies. Target: PI3K , Kinase Group: Atypical (PIKK) ,...
Keywords: | IPI 145 |
Application: | PI3K gamma / delta inhibitor |
CAS | 1201438-56-3 |
MW: | 416,9 D |
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Item number: SYN-1035-M100
Soluble in DMSO. CYT387 is selective inhibitor of JAK1 and JAK2 kinases including the JAK2V617F mutant . Using ATP kinase assays IC(50) values for JAK1 (11nm), JAK2, (18nM), JAK2, JAK2V617F (23nM) JAK3 (155nM), and TYK2 (17nM). In testing kinase arrays, CYT387 also had activity (defined as an IC(50) < 100nM)...
Keywords: | CYT387, Momelotinib |
Application: | JAK1 / JAK2 inhibitor |
CAS | 1056634-68-4 |
MW: | 414,5 D |
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Item number: SYN-1045-M100
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. IC87114 is a potent, ATP-competitive, and selective inhibitor of PI3Kdelta. IC(50) values (130-500nM) for IC87114 are sub-micromolar over a wide range of ATP concentrations from 10µM to 200µM. IC87114 can selectively inhibit cellular migration but not...
Keywords: | IC-87114 |
Application: | PI3K delta inhibitor |
CAS | 371242-69-2 |
MW: | 397,4 D |
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Item number: SYN-1055-M100
Soluble in DMSO or ethanol. Motesanib (AMG 706) is a multi-targeted anti-cancer agent with an inhibitory action on human vascular endothelial growth factor receptors 1, 2 and 3 (VEGFR1-3) with IC(50) values of 2nM, 3nM and 6nM. It also inhibits platelet-derived growth factor receptor (PDGFR) and cellular stem-cell...
Keywords: | AMG706 |
Application: | VEGFR / PDGFR inhibitor |
CAS | 453562-69-1 |
MW: | 373,5 D |
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Item number: SYN-1077-M100
Soluble in DMSO or ethanol. SB-590885 is a novel, potent and selective small molecule inhibitor of B-Raf kinase, with a Ki of 0.16nM. It shows an 11-fold greater selectivity for B-Raf over c-Raf. It was used to address the dependence of MAPK signalling and tumor cell growth on B-Raf kinase activity. Target: ARaf -...
Keywords: | SB-590885 |
Application: | BRAF inhibitor |
CAS | 405554-55-4 |
MW: | 453,5 D |
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Item number: SYN-1078-M100
Soluble in DMSO. SD-06 is a p38 MAP kinase inhibitor. It inhibits p38alpha with an IC(50) value of 170nM and inhibits LPS-stimulated TNF-release in rats. Target: p38 , Kinase Group: CMGC , Substrate: Serine-Threonine
Keywords: | SD06 |
Application: | p38 inhibitor |
CAS | 271576-80-8 |
MW: | 397,9 D |
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Item number: SYN-1095-M100
Soluble in DMSO or ethanol. Aurora kinases are key regulators of protein phosphorylation during mitosis, and these serine/threonine kinases interact with other cellular proteins to help control chromosome assembly and segregation during mitosis. Aurora kinases are often highly expressed in malignancies and solid...
Keywords: | PHA-739358 |
Application: | Aurora inhibitor |
CAS | 827318-97-8 |
MW: | 474,6 D |
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Item number: SYN-1070-M100
Soluble in DMSO or ethanol. Purvalanol B is a cyclin-dependent kinase inhibitor with IC(50) values of 6, 6, 9, > 10,000, and 6nM for cdc2/cyclin B, cdk2/cyclin A, cdk2/cyclin E, cdk4/cyclin D1 and cdk5-p35, respectively. Purvalanol B has also been shown to have anti-proliferative properties, mediated by p42/p44...
Keywords: | NG95 |
Application: | Cyclin-dependent kinase inhibitor inhibitor |
CAS | 212844-54-7 |
MW: | 432,9 D |
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Item number: SYN-1072-M100
Soluble in DMSO or ethanol. The cytokine Tumor necrosis factor-alpha (TNF-alpha) is secreted by activated monocytes/macrophages and T lymphocytes and has been implicated in several disease states, including rheumatoid arthritis, inflammatory bowel disease, septic shock, and osteoporosis. Monocyte/macrophage...
Keywords: | RWJ67657 |
Application: | p38 inhibitor |
CAS | 215303-72-3 |
MW: | 425,5 D |
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Item number: SYN-1079-M100
Soluble in DMSO or ethanol. SD169 is an orally available, ATP-competitive, isoenzyme-selective Mitogen-Activated Protein Kinase (MAPK) inhibitor. It is 38 times more potent against p38alpha MAP kinase (IC(50) of 3.2nM) over p38beta MAP kinase (IC(50) of 122nM). Target: MAPK - p38 , Kinase Group: CMGC , Substrate:...
Keywords: | SD169 |
Application: | p38 alpha inhibitor |
CAS | 1670-87-7 |
MW: | 160,2 D |
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Item number: SYN-1005-M100
Soluble in DMSO. The compound (Akt-I-1) inhibits only Akt1 (IC(50) 4.6 µM) and does not inhibit AKT2, or AKT3. The compound is a reversible inhibitor, and exhibits a linear mixed-type inhibition against ATP and peptide substrate. In addition to inhibiting kinase activity of AKT1 isoform, AKT-I-1 blocked the...
Keywords: | AktI1 |
Application: | Akt1 inhibitor |
CAS | 473382-39-7 |
MW: | 378,5 D |
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