Chemical Structure
Phenylmethylene hydantoin [PMH] [80171-33-1]
AG-CN2-0041
Overview
- SupplierAdipoGen Life Sciences
- Product NamePhenylmethylene hydantoin [PMH]
- Delivery Days Customer10
- CAS Number80171-33-1
- CertificationResearch Use Only
- Estimated Purity>97%
- Molecular FormulaC10H8N2O3
- Molecular Weight204.2
- Scientific DescriptionAnticancer compound [2, 3, 5, 6]. Chemopreventive [2, 3, 5, 6, 7]. Shows anti-metastatic activity in prostate cancer cells through enhancement of cell-cell adhesion [2, 3]. Anti-invasive compound [5, 6, 7]. Glycogen synthase kinase-3beta (GSK-3 beta) inhibitor [4]. - Chemical. CAS: 80171-33-1. Formula: C10H8N2O3. MW: 204.2. Isolated from an unidentifed marine sponge. Anticancer compound. Chemopreventive. Shows anti-metastatic activity in prostate cancer cells through enhancement of cell-cell adhesion. Anti-invasive compound. Glycogen synthase kinase-3beta (GSK-3 beta) inhibitor.
- SMILESOC1=CC=C(\C=C2/NC(=O)NC2=O)C=C1
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC12352200
References
- The synthesis of amino-acids: Piperidine and diethylamine as catalysts in the condensation of aromatic aldehydes with hydantoins: W.J. Boyd & W. Robson; Biochem. J. 29, 542 (1935)
- Identification of a small molecule class to enhance cell-cell adhesion and attenuate prostate tumor growth and metastasis: G.V. Shah, et al.; Mol. Cancer Ther. 8, 509 (2009)
- Discovery, design, and synthesis of anti-metastatic lead phenylmethylene hydantoins inspired by marine natural products: M. Mudit, et al.; Bioorg. Med. Chem. 17, 1731 (2009)
- The marine natural-derived inhibitors of glycogen synthase kinase-3beta phenylmethylene hydantoins: In vitro and in vivo activities and pharmacophore modeling: M.A. Khanfar, et al.; Bioorg. Med. Chem. 17, 6032 (2009)
- Phenylmethylene hydantoins as prostate cancer invasion and migration inhibitors. CoMFA approach and QSAR analysis: M.A. Khanfar & K.A. El Sayed; Eur. J. Med. Chem. 45, 5397 (2010)
- Phenyl-methylene hydantoins alter CD44-specific ligand binding of benign and malignant prostate cells and suppress CD44 isoform expression: K. Yang, et al.; Am. J. Transl. Res. 2, 88 (2010)
- Methods for evaluation of structural and biological properties of antiinvasive natural products: M. Mudit, et al.; Meth. Mol. Biol. 716, 55 (2011)