DNMT-IN-5
DNMT-IN-5 is a stable and efficient DNA methyltransferase (DNMT) inhibitor with high stability and high activity with an IC50 of 0.78 nM. DNMT-IN-5 exhibits sub-micromolar DNMT3A inhibitory activity, upregulates the expression of DNMT-targeted genes, impairs cell proliferation, and triggers a critical cell cycle arrest. DNMT-IN-5 can be used for the study of p53-depleted colorectal cancer.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 3126555-64-1
- 分子式: C16H12BrClO3
- 分子量:367.62
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
生物活性
-
化学情報
- 純度とドキュメンテーション
- 参考文献
-
Help & FAQs
DNA Methyltransferase アイソフォーム固有の製品をすべて表示
More
生物活性
|
DNMT3A 9.15 μM (IC50) |
DNMT-IN-5 (compound 34b) (0.1-30 μM; 3 days) still exhibits the activity of a DNMT 3A inhibitor at the nanomolar level, with an IC50 value of 9.15 μM in HCT-116 cells[1].
DNMT-IN-5 (5 μM; 0-5 days) significantly induces the upregulation of p15 and p16 expression by 1.76 (88%)-fold and 1.34 (67%)-fold, respectively in HCT-116 cells[1].
DNMT-IN-5 (5 μM; 5 days) on DNMT-regulated genes varies by cell type and is most pronounced in HCT-116 cells[1].
DNMT-IN-5 (5 μM; 5 days) triggers a critical cell cycle arrest in the G1/S transition, notably in p53-depleted HCT-116 colorectal cancer cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:HCT-116
-
Concentration:0.1 μM; 1 μM; 10 μM; 100 μM
-
Incubation Time:3 days
-
Result:Showed very similar cytotoxicity (IC50 = 9.15 μM) among themselves and reference compound MLo1506 (IC50 = 8.18 μM).
-
Cell Line:HCT-116
-
Concentration:5 μM
-
Incubation Time:0 d; 2 d; 5d
-
Result:Significantly induced the upregulation of p15 expression by 1.76 (88%)-fold, compared to nontreated cells.
Increased p16 expression by 1.34 (67%)-fold.
-
Cell Line:HCT-116, DU-145, U2OS
-
Concentration:5 μM
-
Incubation Time:5 days
-
Result:Did not alter p15 expression in p53-KO cells but successfully induced p16 re-expression.
Strongly impaired the G1/S transition in the absence of p53 and led to a substantial population of defective replicating cells.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
-
CAS 番号 3126555-64-1
-
分子量 367.62
-
分子式 C16H12BrClO3
-
SMILES
CO[C@]1(C2=CC=CC=C2)OC3=CC=CC=C3C([C@@]1(Cl)Br)=O
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
DNMT-IN-5 関連分類
HY-176230 関連分類
Powered by Bioz