NSD2-IN-6
NSD2-IN-6 is a selective and orally active NSD2 inhibitor with IC50s of 3.8 and 274 nM for NSD2 and NSD1 respectively. NSD2-IN-6 reduces H3K36me2 levels, reverses cell plasticity by restoring the androgen receptor (AR) signaling pathway. NSD2-IN-6 reduces a shift from cluster 2 and 3 states towards the cluster 1 state in organoids. NSD2-IN-6 exerts antitumor activity by reversing tumor cell plasticity, suppressing growth, and promoting apoptosis in vivo. NSD2-IN-6 can be used for prostate cancer research.
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。
- 分子式: C25H26F4N8O2
- 分子量:546.52
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Histone Methyltransferase アイソフォーム固有の製品をすべて表示
More
生物活性
|
EZH1 3.8 nM (IC50) |
EZH1 274 nM (IC50) |
NSD2-IN-6 (compound NSD2i) shows a substantial reduction in H3K36me2 domains in NPPO-1NE organoids[1].
NSD2-IN-6 results a substantial shift from cluster 2 and 3 states towards the cluster 1 state and enrichment of canonical AR target expression in NPPO-1NE organoids[1].
NSD2-IN-6 has little or no effect on AR expression in non-neuroendocrine organoids with combined Enzalutamide [1].
NSD2-IN-6 (1 µM, 17 days) increases sensitivity to enzalutamide in NPPO-1NE, NPPO-2, NPPO-4 and NPPO-6 organoids with EC50 values of 0.34, 2.7, 1.6 and 20 µM respectively[1].
NSD2-IN-6 (0.3-10 µM, 26 days ) not affect on NSD2 knockout NPPO-1 and NPPO-2 organoids, has a slight effect on NSD2 knockout MSKPCa10[1].
NSD2-IN-6 (10 µM, 21 days) reduces H3K36me2 expression and modest upregulates H3K27me3 in MSKPCa10, MSKPCa14, WCM154, WCM1262 and MSKPCa2 human CRPC organoid lines, loss the lineage marker CD56 and upregulates AR in WCM1262 human CRPC organoid lines, results a reduction in organoid size and immunostaining for cleaved caspase 3 in MSKPCa2 organoids[1].
NSD2-IN-6 (0.3-10 µM, 21 days) lead a decreasing cell viability after enzalutamide treatment, a high Bliss synergy score and a concentration-dependent induction of apoptosis in MSKPCa10, MSKPCa14, WCM154, WCM1262 and MSKPCa2 human CRPC organoid lines when combinate with Enzalutamide [1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:H3K27me3 in MSKPCa10, MSKPCa14, WCM154, WCM1262 and MSKPCa2 human CRPC organoid lines
-
Concentration:0.3, 1, 3 and 10 μM
-
Incubation Time:21 days
-
Result:Progressively decreased cell viability after enzalutamide treatment.
-
Cell Line:H3K27me3 in MSKPCa10, MSKPCa14, WCM154, WCM1262 and MSKPCa2 human CRPC organoid lines
-
Concentration:0.3, 1, 3 and 10 μM
-
Incubation Time:21 days
-
Result:Significantly increased caspase 3 and caspase 7 activity in a concentration-dependent manner.
NSD2-IN-6 (150 mg/kg, p.o., daily for 42 days) exerts antitumor activity by by reversing plasticity, suppressing growth and promoting tumour cell apoptosis in mice xenografts of human prostate organoids[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:Subcutaneous grafts of human CRPC organoids in NOD/SCID mice[1]
-
Dosage:75, 150 and 300 mg/kg
-
Administration:p.o., daily for 5 days
-
Result:Reduced H3K36me2 levels at each con centration without any adverse effects on mouse body weights.
-
Animal Model:Subcutaneous grafts of human CRPC organoids in NOD/SCID mice[1]
-
Dosage:150 mg/kg
-
Administration:p.o., daily for 42 days
-
Result:Had modest effects on tumour growth for MSKPCa10, MSKPCa14 and WCM1262 xenografts.
Resulted strong growth suppression when combined with Enzalutamide.
Displayed a strong responses when combined with or with not Enzalutamide.
Showed loss of neuroendocrine phenotypes accompanied by overt necrosis and fibrosis, and increased adenocarcinoma features in MSKPCa10, MSKPCa14 and WCM1262 xenografts when combine with Enzalutamide.
Showed Loss of H3K36me2 , neuroendocrine markers CHGA and SYP in MSKPCa10 and MSKPCa14, and loss of CD56 in WCM1262 when combined with Enzalutamide.
Displayed strong downregulation of Ki67 and upregulation of CC3 when combine with Enzalutamide.
化学情報
-
分子量 546.52
-
分子式 C25H26F4N8O2
-
SMILES
NC1=NC=NC2=C1N=CN2CC3=CC(C4=C(F)C=C(OC)C(F)=C4)=NC=C3N5C[C@]([C@@H](O)C(F)F)(N)CCC5
-
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)