Serdemetan (JNJ-26854165)

製品コードS1172 バッチS117203

印刷

化学情報

Chemical Structure Synonyms N/A Storage
(From the date of receipt)		 3 years -20°C powder
1 years -80°C in solvent
化学式

C21H20N4
分子量 328.41 CAS No. 881202-45-5
Solubility (25°C)* 体外 DMSO 66 mg/mL (200.96 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明 Serdemetan (JNJ-26854165) acts as a HDM2 ubiquitin ligase antagonist and also induces early apoptosis in p53 wild-type cells, inhibits cellular proliferation followed by delayed apoptosis in the absence of functional p53. Phase 1.
in vitro JNJ 26854165 is a novel tryptamine derivative which activates p53 and acts as a HDM2 ubiquitin ligase antagonist. JNJ 26854165 inhibits cell growth and induces apoptosis in leukemia cell lines with IC50 values of 0.24, 0.33, 0.32 and 0.44 μM at 72 hours for OCI-AML-3, MOLM-13, NALM-6 and REH cells, respectively. In addition, JNJ 26854165 accelerates proteasome-mediated degradation of p21 and antagonizes the transcriptional induction of p21 by p53. It also induces S-phase delay and upregulates E2F1 expression in p53 mutant cells, resulting in preferential apoptosis of S-phase cells. [1] JNJ 26854165 is an oral Mdm2 inhibitor which can inhibit the interaction of Mdm2-p53 complex with the proteasome and increase p53 levels by binding to RING domain of Mdm2. [2] A recent study shows that JNJ 26854165 inhibits clonogenic survival in four human cancer cell lines: H460, A549, p53-WT-HCT116, and p53-null-HCT116. [3]
in vivo JNJ 26854165 leads to significant differences in EFS distribution in 17 of the 36 (47%) evaluable solid tumor xenografts and in 5 of 7 (71%) of the evaluable ALL xenografts using a dose of 20 mg/kg administered via oral gavage daily for 5 days, repeated for 6 weeks. [4]

プロトコル(参考用のみ)

細胞アッセイ 細胞株 OCI-AML-3, MOLM-13, NB4 and U937 cells
濃度 0-10 μM
反応時間 72 hours
実験の流れ Cell lines are maintained in RPMI 1640 medium containing 10% heat-inactivated fetal calf serum (FCS). OCI-AML-3, MOLM-13, NB4 and U937 cells are derived from acute myelogenous leukemia (AML) patients, K562 from a chronic myelogenous leukemia (CML) patient in blast crisis, and NALM-6, REH, P12-ICHIK
動物実験 動物モデル CB17SC scid-/- female mice.
投薬量 ≤20 mg/kg
投与方法 Administered via p.o.

カスタマーフィードバック

Data from [Mol Pharmacol, 2014, 85(3), 408-19]

Data from [Sci Rep, 2014, 4, 4663]

Data from [Sci Rep, 2014, 4, 4663]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

Nuclear Aurora kinase A switches m6A reader YTHDC1 to enhance an oncogenic RNA splicing of tumor suppressor RBM4 [ Signal Transduct Target Ther, 2022, 7(1):97] PubMed: 35361747
Prediction and identification of synergistic compound combinations against pancreatic cancer cells [ iScience, 2021, 24(9):103080] PubMed: 34585118
MDM2-Mediated Ubiquitination of ACE2 Contributes to the Development of Pulmonary Arterial Hypertension [ Circulation, 2020, 10.1161/CIRCULATIONAHA.120.048191] PubMed: 32755395
Subcellular distribution of p53 by the p53-responsive lncRNA NBAT1 determines chemotherapeutic response in neuroblastoma [ Cancer Res, 2020, canres.3499.2019] PubMed: 33372039
Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras. [ Cell, 2019, 36(2):179-193] PubMed: 28162770
A Pharmacogenomic Landscape in Human Liver Cancers. [ Cancer Cell, 2019, 36(2):179-193] PubMed: 31378681
The novel anticancer agent JNJ-26854165 is active in chronic myeloid leukemic cells with unmutated BCR/ABL and T315I mutant BCR/ABL through promoting proteosomal degradation of BCR/ABL proteins [ Oncotarget, 2017, 8(5):7777-7790] PubMed: 27999193
Inhibitors of ubiquitin E3 ligase as potential new antimalarial drug leads. [Jain J, et al. BMC Pharmacol Toxicol, 2017, 18(1):40] PubMed: 28577368
Quantitative phosphoproteomic analysis identifies the critical role of JNK1 in neuroinflammation induced by Japanese encephalitis virus. [ Sci Signal, 2016, 9(448):ra98] PubMed: 27703031
Host-based Prophylaxis Successfully Targets Liver Stage Malaria Parasites [Douglass AN, et al. Mol Ther, 2015, 23(5):857-65] PubMed: 25648263

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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