QN523
Based on 1 Customer Validation
QN523 is a novel scaffold with agent-like properties, showing potent in vitro cytotoxicity in a panel of 12 cancer cell lines. QN523 induces apoptosis and autophagy. QN523 can be used in research of 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。
- 純度: 99.19%
- CAS 番号: 878581-60-3
- 分子式: C14H10N4O
- 分子量:250.26
-
保管条件:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
生物活性
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| BXPC-3 | IC50 |
1.8 μM
Compound: QN523
|
Antiproliferative activity against human BXPC-3 cells measured after 72 hrs by MTT assay
Antiproliferative activity against human BXPC-3 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| BXPC-3 | IC50 |
3.3 μM
Compound: QN523; 2
|
Cytotoxicity against human BXPC-3 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Cytotoxicity against human BXPC-3 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HCT-116 | IC50 |
0.1 μM
Compound: QN523; 2
|
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HEK293 | IC50 |
0.15 μM
Compound: QN523; 2
|
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HEK293 | IC50 |
0.2 μM
Compound: QN523
|
Cytotoxicity against HEK293 cells measured after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| Hep 3B2 | IC50 |
0.21 μM
Compound: QN523; 2
|
Antiproliferative activity against human Hep3B cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human Hep3B cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HepG2 | IC50 |
0.5 μM
Compound: QN523; 2
|
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HFF-1 | IC50 |
>30 μM
Compound: QN523; 2
|
Cytotoxicity against human HFF-1 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Cytotoxicity against human HFF-1 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| HFF-1 | IC50 |
>30 μM
Compound: QN523
|
Cytotoxicity against HFF-1 cells measured after 72 hrs by MTT assay
Cytotoxicity against HFF-1 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| Jurkat | IC50 |
0.1 μM
Compound: QN523; 2
|
Antiproliferative activity against human Jurkat cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human Jurkat cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| MIA PaCa-2 | IC50 |
0.11 μM
Compound: QN523; 2
|
Cytotoxicity against human MIA PaCa-2 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Cytotoxicity against human MIA PaCa-2 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| MIA PaCa-2 | IC50 |
0.3 μM
Compound: QN523
|
Antiproliferative activity against human MIA PaCa-2 cells measured after 72 hrs by MTT assay
Antiproliferative activity against human MIA PaCa-2 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| OVCAR-8 | IC50 |
0.3 μM
Compound: QN523; 2
|
Antiproliferative activity against human OVCAR-8 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human OVCAR-8 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| Panc02 | IC50 |
0.3 μM
Compound: QN523
|
Antiproliferative activity against mouse Panc02 cells measured after 72 hrs by MTT assay
Antiproliferative activity against mouse Panc02 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| PANC-1 | IC50 |
0.5 μM
Compound: QN523; 2
|
Cytotoxicity against human PANC-1 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Cytotoxicity against human PANC-1 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| PANC-1 | IC50 |
1.7 μM
Compound: QN523
|
Antiproliferative activity against human PANC-1 cells measured after 72 hrs by MTT assay
Antiproliferative activity against human PANC-1 cells measured after 72 hrs by MTT assay
|
[PMID: 36692906] |
| SNU-387 | IC50 |
5.73 μM
Compound: QN523; 2
|
Antiproliferative activity against human SNU-387 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human SNU-387 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| SNU-398 | IC50 |
1.9 μM
Compound: QN523; 2
|
Antiproliferative activity against human SNU-398 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human SNU-398 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| SNU-449 | IC50 |
0.4 μM
Compound: QN523; 2
|
Antiproliferative activity against human SNU-449 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human SNU-449 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
| SNU-475 | IC50 |
2.67 μM
Compound: QN523; 2
|
Antiproliferative activity against human SNU-475 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
Antiproliferative activity against human SNU-475 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
|
[PMID: 35439009] |
QN523 (72 h) has cytotoxicity with IC50 values ranging from 0.1 to 5.7 μM across 12 cell lines[1].
QN523 (0.1 and 0.5 μM; 24 and 48 h; MIA PaCa-2 cells) arrests cell cycle at S phase and delays for pancreatic cancer cells to enter the G2-M phase. QN523 induces apoptosis and autophagy of MIA PaCa-2 Cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:MIA PaCa-2 cells
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Concentration:0.1 and 0.5 μM
-
Incubation Time:24 and 48 hours
-
Result:Delayed for pancreatic cancer cells to enter the G2-M phase because of accumulation of cells in the S phase.
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Cell Line:MIA PaCa-2 cells
-
Concentration:0.1 and 0.5 μM
-
Incubation Time:24 and 48 hours
-
Result:Increased the number of apoptotic cell in time- and dose-dependent manner.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:NOD/SCID mice of pancreatic cancer xenografts (6 weeks of age)
-
Dosage:10 and 20 mg/kg
-
Administration:Intraperitoneal administration; 1-9 days (10 mg/kg), 10-44 days (20 mg/kg)
-
Result:Delayed growth of the tumors, and no systemic toxicity.
化学情報
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CAS 番号 878581-60-3
-
性状 Solid
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分子量 250.26
-
分子式 C14H10N4O
-
Color Light brown to brown
-
SMILES
O=C(C1=NC=CN=C1)NC2=CC=CC3=CC=CN=C32
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輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
溶剤 & 溶解度
DMSO : ≥ 16.67 mg/mL (66.61 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
純度とドキュメンテーション
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データシート (276 KB)
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SDS (393 KB)
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- Deutsch - DE (393 KB)
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- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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取扱説明書 (2659 KB)
参考文献
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.9958 mL | 19.9792 mL | 39.9584 mL | 99.8961 mL |
| 5 mM | 0.7992 mL | 3.9958 mL | 7.9917 mL | 19.9792 mL | |
| 10 mM | 0.3996 mL | 1.9979 mL | 3.9958 mL | 9.9896 mL | |
| 15 mM | 0.2664 mL | 1.3319 mL | 2.6639 mL | 6.6597 mL | |
| 20 mM | 0.1998 mL | 0.9990 mL | 1.9979 mL | 4.9948 mL | |
| 25 mM | 0.1598 mL | 0.7992 mL | 1.5983 mL | 3.9958 mL | |
| 30 mM | 0.1332 mL | 0.6660 mL | 1.3319 mL | 3.3299 mL | |
| 40 mM | 0.0999 mL | 0.4995 mL | 0.9990 mL | 2.4974 mL | |
| 50 mM | 0.0799 mL | 0.3996 mL | 0.7992 mL | 1.9979 mL | |
| 60 mM | 0.0666 mL | 0.3330 mL | 0.6660 mL | 1.6649 mL |