- Search results for SYN-1043-M100
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18 products were found matching "SYN-1043-M100"!
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Item number: SYN-1034-M100
Soluble in DMSO or ethanol. CYC116 is an orally active small molecule multi-kinase inhibitor with anti-neoplastic activity. CYC116 inhibits Aurora kinases A/B and vascular endothelial growth factor receptor 2 (VEGFR2), resulting in disruption of the cell cycle, rapid cell death, and the inhibition of angiogenesis....
Keywords: | CYC-116 |
Application: | Aurora A / B inhibitor |
CAS | 693228-63-6 |
MW: | 368,5 D |
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Item number: SYN-1143-M001
Soluble in DMSO. AMG-1 is a potent inhibitor of human c-Met and RON with IC(50) values of 4 and 9nM respectively. Target: c-Met - RON , Kinase Group: RTK , Substrate: Tyrosine
Keywords: | AMG1 |
Application: | c-Met / RON inhibitor |
CAS | 913376-84-8 |
MW: | 556,6 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-1093-M100
Soluble in DMSO or ethanol. The kinases called p38 MAP kinases (MAPKs) are intracellular, soluble serine-threonine kinases which belong to a large family of proteins that include the extracellular regulated kinases (ERKs) and c-Jun N-terminal kinases (JNKs). So far four p38 isoforms have been identified, namely...
Keywords: | VX702 |
Application: | P38 inhibitor |
CAS | 745833-23-2 |
MW: | 404,3 D |
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Item number: SYN-1041-M100
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. GDC-0941 is a potent class I PI3 kinase (PI3K) inhibitor. It selectively binds to PI3K isoforms in an ATP-competitive manner. It has an IC(50) of 3nM, and shows slight selectivity toward p110beta (11-fold) and p110gamma (25-fold). Target: PI3K , Kinase Group:...
Keywords: | GDC0941 |
Application: | PI3K inhibitor |
CAS | 957054-30-7 |
MW: | 513,6 D |
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Item number: SYN-1042-M100
Soluble in DMSO or ethanol. Gefitinib is a selective, orally available epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. In NR6wtEGFR and NR6W cells, it inhibits Tyr1173, Tyr992, Tyr1173 and Tyr992 with IC(50) values of 37nM, 37nM, 26nM and 57nM, respectively. Target: EGFR , Kinase Group: RTK ,...
Keywords: | ZD1839, Iressa |
Application: | EGFR inhibitor |
CAS | 184475-35-2 |
MW: | 446,9 D |
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Item number: SYN-1003-M100
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. Quizartinib (AC220) is a second-generation FLT3 inhibitor that has shown promising activity in AML in Phase II clinical trials. It inhibits mutant and wild-type FLT3 in vivo at 0.1 and 0.5µM, respectively, and has shown favorable activity and tolerability in...
Keywords: | AC220 |
Application: | FLT3 inhibitor |
CAS | 950769-58-1 |
MW: | 560,7 D |
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Item number: SYN-1013-M100
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. Tivozanib is a potent inhibitor of VEGFR-1, 2 & 3 (IC(50) 0.21, 0.16 and 0.24nM respectively). Target: VEGFR , Kinase Group: RTK , Substrate: Tyrosine
Keywords: | AV-951 |
Application: | VEGFR inhibitor |
CAS | 475108-18-0 |
MW: | 454,9 D |
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Item number: SYN-1033-M100
Soluble in DMSO or ethanol. CP-724714 is an oral, selective and potent ErbB-2 (HER2) kinase inhibitor with an IC(50) of 10 nM. It has >640-fold selectivity for ErbB-2 (HER2) over EGFR, InsR, IRG-1R, PDGFR, VEGFR2, Abl, Src, c-Met. Target: HER2 , Kinase Group: RTK , Substrate: Tyrosine
Keywords: | CP724714 |
Application: | HER2 inhibitor |
CAS | 383432-38-0 |
MW: | 469,5 D |
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Item number: SYN-1047-M100
Soluble in DMSO. Slightly soluble (<1mg/ml) in ethanol. JNJ38877605 is an orally bio-available, small-molecule, c-MET tyrosine kinase inhibitor with potential anti-neoplastic activity. It is potent (c-MET enzyme and Phospho-MET IC(50) values of 4nM and 50nM, respectively) and highly specific (selective over 229...
Keywords: | JNJ38877605 |
Application: | c-MET inhibitor |
CAS | 943540-75-8 |
MW: | 377,4 D |
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Item number: SYN-1048-M100
Soluble in DMSO or ethanol. JNJ-7706621 is a dual inhibitor of cyclin-dependent kinases (CDK) and aurora kinases. It demonstrates highest potency on CDK1/2 with IC(50) values of 9nM and 4nM respectively. It shows more than 6-fold selectivity for CDK1/2 over CDK3/4/6. Target: Aurora - CDK , Kinase Group: Other ,...
Keywords: | JNJ7706621 |
Application: | Aurora / CDK1 / CDK2 inhibitor |
CAS | 443797-96-4 |
MW: | 394,4 D |
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Item number: SYN-1083-M100
Soluble in DMSO. SR-3677 had an IC(50) of approximately 3nM in enzyme and cell based assays and had an off-target hit rate of 1.4% against 353 kinases, and inhibited only 3 out of 70 non-kinase enzymes and receptors. Pharmacology studies showed that 5 was efficacious in both, increasing ex vivo aqueous humor outflow...
Keywords: | SR-3677 |
Application: | ROCK2 inhibitor |
CAS | 1072959-67-1 |
MW: | 408,5 D |
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