RG7112

RG7112

Catalog Number:
L002368839APE
Mfr. No.:
APE-A3762
Price:
$394
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      • Overview
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          Background

          RG7112 is a selective inhibitor of p53-MDM2 binding that frees p53 from negative control, activating the p53 pathway in cancer cells leading to cell cycle arrest and apoptosis. [1]P53 is a potent tumor suppressor that activates the transcription of a subset of genes controlling cell-cycle progression and apoptosis. MDM2 is a negative regulator of p53 that binds the transactivation domain of p53 and inhibits its ability to activate transcription. MDM2 is also an E3 ubiquitin ligase that targets p53 for proteosomal degradation. MDM2 overexpression is one of the mechanisms by which the wild type p53 function is impaired. [2]RG7112 has been profiled extensively in many cell lines. In 15 cancer cell lines expressing wild-type p53, it shows IC50 in the range of 0.18 - 2.2 μM. However, the inhibition is much less in seven cancer cell lines with p53 mutation, IC50 5.7 - 20.3 μM. The overall selectivity is 14-fold.In the animal models, RG7112-induced thrombocytopenia occurred rather late during the treatment period and persisted after drug discontinuation, suggesting that the drug acts on early hematopoietic progenitor cells. This is supported by the RG7112 ability to inhibit CFU-MK colonies formation by the CD34t cells in vitro. Administration of RG7112 in rats and monkeys reduces WBC counts and, to a lesser extent, hemoglobin levels. In patients treated with RG7112, neutropenia is among the serious adverse events while anemia occurred only in 2 of 20 patients. Interestingly, when tested in vitro, the same concentration of RG7112 that reduced CFU-MK colony formation do not significantly affect the formation of BFU-E and CFU-GM derived colonies.

          [1] Hernan Carol, C. Patrick Reynolds, Min H. Kang et al. Initial Testing of the MDM2 Inhibitor RG7112 by the Pediatric Preclinical Testing Program. Pediatr Blood Cancer 2013;60:633–641
          [2] Binh Vu, Peter Wovkulich, Giacomo Pizzolato et al. Discovery of RG7112: A Small-Molecule MDM2 Inhibitor in Clinical Development. ACS Med. Chem. Lett. 2013, 4, 466−469
          [3] Camelia Iancu-Rubina, Goar Mosoyana, Kelli Glenn et al. Activation of p53 by the MDM2 inhibitor RG7112 impairs thrombopoiesis. Experimental Hematology 2014;42:137–145

      • Properties
        • Alternative Name
          RG-7112;RG 7112; [(4S,5R)-2-(4-tert-butyl-2-ethoxyphenyl)-4,5-bis(4-chlorophenyl)-4,5-dimethylimidazol-1-yl]-[4-(3-methylsulfonylpropyl)piperazin-1-yl]methanone
          CAS Number
          939981-39-2
          Molecular Formula
          C38H48Cl2N4O4S
          Molecular Weight
          727.78
          Appearance
          A solid
          Purity
          98.58%
          Solubility
          ≥36.4 mg/mL in DMSO; insoluble in H2O; ≥31.87 mg/mL in EtOH
          Storage
          Store at -20°C

          * For Research Use Only

      • Reference
        • 1. Makii C, Ikeda Y, et al. ”Anti-tumor activity of dual inhibition of phosphatidylinositol 3-kinase and MDM2 against clear cell ovarian carcinoma." Gynecol Oncol. 2019 Nov;155(2):331-339. PMID:31493899
          2. Her NG, Oh JW, et al. "Potent effect of the MDM2 inhibitor AMG232 on suppression of glioblastoma stem cells." Cell Death Dis. 2018 Jul 18;9(8):792. PMID:30022047
          3. Miyazaki M, Otomo R, et al. "The p53 activator overcomes resistance to ALK inhibitors by regulating p53-target selectivity in ALK-driven neuroblastomas." Cell Death Discov. 2018 May 10;4:56. PMID:29760954
          4. Chen R, Zhou J, et al. "A Fusion Protein of the p53 Transaction Domain and the p53-Binding Domain of the Oncoprotein MdmX as an Efficient System for High-Throughput Screening of MdmX Inhibitors." Biochemistry. 2017 Jun 27;56(25):3273-3282. PMID:28581721
          5. Makii C, Oda K, et al. "MDM2 is a potential therapeutic target and prognostic factor for ovarian clear cell carcinomas with wild type TP53." Oncotarget. 2016 Nov 15;7(46):75328-75338. PMID:27659536
          6. Kwon DH, Eom GH, et al. "MDM2 E3 ligase-mediated ubiquitination and degradation of HDAC1 in vascular calcification." Nat Commun.2016 Feb 1;7:10492. PMID:26832969

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