For research use only, not for therapeutic use.
PHA-680632（Cat No.:I003454）is a potent and selective inhibitor of Aurora kinases, particularly targeting Aurora A, B, and C, which are critical regulators of cell division. By inhibiting these kinases, PHA-680632 disrupts mitosis, leading to cell cycle arrest and apoptosis in rapidly dividing cells, making it a valuable tool for cancer research. Its high specificity for Aurora kinases offers insights into novel therapeutic strategies for cancer treatment, particularly in studies exploring mitotic dysregulation. This compound is widely used in preclinical models for investigating the role of Aurora kinases in tumorigenesis.
| Catalog Number | I003454 |
| CAS Number | 398493-79-3 |
| Synonyms | N-(2,6-diethylphenyl)-3-[[4-(4-methylpiperazin-1-yl)benzoyl]amino]-4,6-dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxamide |
| Molecular Formula | C₂₈H₃₅N₇O₂ |
| Purity | ≥95% |
| Target | Aurora Kinase |
| Solubility | DMSO ≥95mg/mL Water <1.2mg/mL Ethanol ≥95mg/mL |
| Storage | 3 years -20C powder |
| IC50 | 27 nM (Aurora A); 135 nM (Aurora B); 120 nM(Aurora C) |
| IUPAC Name | N-(2,6-diethylphenyl)-3-[[4-(4-methylpiperazin-1-yl)benzoyl]amino]-4,6-dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxamide |
| InChI | InChI=1S/C28H35N7O2/c1-4-19-7-6-8-20(5-2)25(19)29-28(37)35-17-23-24(18-35)31-32-26(23)30-27(36)21-9-11-22(12-10-21)34-15-13-33(3)14-16-34/h6-12H,4-5,13-18H2,1-3H3,(H,29,37)(H2,30,31,32,36) |
| InChIKey | OBWNXGOQPLDDPS-UHFFFAOYSA-N |
| SMILES | CCC1=C(C(=CC=C1)CC)NC(=O)N2CC3=C(C2)NN=C3NC(=O)C4=CC=C(C=C4)N5CCN(CC5)C |
| Reference | 1:Clin Cancer Res. 2006 Jul 1;12(13):4080-9. PHA-680632, a novel Aurora kinase inhibitor with potent antitumoral activity.Soncini C,Carpinelli P,Gianellini L,Fancelli D,Vianello P,Rusconi L,Storici P,Zugnoni P,Pesenti E,Croci V,Ceruti R,Giorgini ML,Cappella P,Ballinari D,Sola F,Varasi M,Bravo R,Moll J, PMID: 16818708 DOI: 10.1158/1078-0432.CCR-05-1964 </br><span>Abstract:</span> PURPOSE: Aurora kinases play critical roles during mitosis in chromosome segregation and cell division. The aim of this study was to determine the preclinical profile of a novel, highly selective Aurora kinase inhibitor, PHA-680632, as a candidate for anticancer therapy.EXPERIMENTAL DESIGN: The activity of PHA-680632 was assayed in a biochemical ATP competitive kinase assay. A wide panel of cell lines was evaluated for antiproliferative activity. Cell cycle analysis. Immunohistochemistry, Western blotting, and Array Scan were used to follow mechanism of action and biomarker modulation. Specific knockdown of the targets by small interfering RNA was followed to validate the observed phenotypes. Efficacy was determined in different xenograft models and in a transgenic animal model of breast cancer.RESULTS: PHA-680632 is active on a wide range of cancer cell lines and shows significant tumor growth inhibition in different animal tumor models at well-tolerated doses. The mechanism of action of PHA-680632 is in agreement with inhibition of Aurora kinases. Histone H3 phosphorylation in Ser10 is mediated by Aurora B kinase, and our kinetic studies on its inhibition by PHA-680632 in vitro and in vivo show that phosphorylation of histone H3 is a good biomarker to follow activity of PHA-680632.CONCLUSIONS: PHA-680632 is the first representative of a new class of Aurora inhibitors with a high potential for further development as an anticancer therapeutic. On treatment, different cell lines respond differentially, suggesting the absence of critical cell cycle checkpoints that could be the basis for a favorable therapeutic window. |
