CCT374705
Based on 1 Customer Validation
CCT374705 is an orally active BCL6 inhibitor (IC50 = 4.8 nM) with potent antiproliferative effects in vitro. CCT374705 effectively inhibits tumor growth in a lymphoma xenograft mouse model.
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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: 99.29%
- CAS 番号: 2640647-90-9
- 分子式: C21H18ClF3N4O2
- 分子量:450.84
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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
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HT | GI50 |
545 nM
Compound: 17; CCT374705
|
Antiproliferative activity against human HT cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
Antiproliferative activity against human HT cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
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[PMID: 37026591] |
| KARPAS-422 | GI50 |
14.9 nM
Compound: 17; CCT374705
|
Antiproliferative activity against human KARPAS-422 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
Antiproliferative activity against human KARPAS-422 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
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[PMID: 37026591] |
| OCI-Ly1 | GI50 |
38.5 nM
Compound: 17; CCT374705
|
Antiproliferative activity against human OCI-Ly1 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
Antiproliferative activity against human OCI-Ly1 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
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[PMID: 37026591] |
| OCI-Ly3 | GI50 |
1850 nM
Compound: 17; CCT374705
|
Antiproliferative activity against human OCILY3 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
Antiproliferative activity against human OCILY3 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
|
[PMID: 37026591] |
| SUD4 | GI50 |
1380 nM
Compound: 17; CCT374705
|
Antiproliferative activity against human SU-DHL-4 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
Antiproliferative activity against human SU-DHL-4 cells assessed as cell growth inhibition incubated for 14 days by luminescence based CellTiter Glo assay
|
[PMID: 37026591] |
CCT374705 (50 mg/kg, p.o., 35 d) results in a significant increase in ARID3A mRNA expression in Karpas 422 tumor xenograft mice model, indicating the modulation of BCL6 activity[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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CAS 番号 2640647-90-9
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性状 Solid
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分子量 450.84
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分子式 C21H18ClF3N4O2
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Color White to off-white
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SMILES
O=C1N(C)C2=C(C=C(NC3=C(Cl)C(F)=NC=C3)C=C2)C4=C1OCC(F)(F)[C@H](C5CC5)N4
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輸送条件
Room temperature in continental US; may vary elsewhere.
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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 : 100 mg/mL (221.81 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: 2.5 mg/mL (5.55 mM); Suspended solution; Need ultrasonic
This protocol yields a suspended solution of 2.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
純度とドキュメンテーション
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データシート (277 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 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 | 2.2181 mL | 11.0904 mL | 22.1808 mL | 55.4520 mL |
| 5 mM | 0.4436 mL | 2.2181 mL | 4.4362 mL | 11.0904 mL | |
| 10 mM | 0.2218 mL | 1.1090 mL | 2.2181 mL | 5.5452 mL | |
| 15 mM | 0.1479 mL | 0.7394 mL | 1.4787 mL | 3.6968 mL | |
| 20 mM | 0.1109 mL | 0.5545 mL | 1.1090 mL | 2.7726 mL | |
| 25 mM | 0.0887 mL | 0.4436 mL | 0.8872 mL | 2.2181 mL | |
| 30 mM | 0.0739 mL | 0.3697 mL | 0.7394 mL | 1.8484 mL | |
| 40 mM | 0.0555 mL | 0.2773 mL | 0.5545 mL | 1.3863 mL | |
| 50 mM | 0.0444 mL | 0.2218 mL | 0.4436 mL | 1.1090 mL | |
| 60 mM | 0.0370 mL | 0.1848 mL | 0.3697 mL | 0.9242 mL | |
| 80 mM | 0.0277 mL | 0.1386 mL | 0.2773 mL | 0.6932 mL | |
| 100 mM | 0.0222 mL | 0.1109 mL | 0.2218 mL | 0.5545 mL |