CG428
Based on 1 Customer Validation
CG428 is a potent and selective CRBN-dependent tropomyosin receptor kinase (TRK) PROTAC degrader that has anti-tumor activity. CG428 reduces levels of the tropomyosin 3 TPM3-TRKA fusion protein in KM12 colorectal carcinoma cells (DC50 = 0.36 nM) and inhibits downstream PLCγ1 phosphorylation (IC50 = 0.33 nM). CG428 has a higher binding affinity for TRKA than TRKB and TRKC (Kd = 1 nM, 28 nM and 4.2 nM, respectively). CG428 can be used for the research of colorectal carcinoma.
(Pink: Trk Receptor ligand (HY-118271); Blue: Cereblon ligand (HY-41547); Black: linker (HY-W067489)).
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 : 98.18%
- CAS 番号: 2412055-93-5
- 分子式: C43H43FN10O6
- 分子量:814.86
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
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生物活性
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化学情報
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溶剤 & 溶解度
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
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生物活性
製品説明
IC50 & Target
[1]|
TrkA 1 nM (Kd) |
TrkC 4.2 nM (Kd) |
TrkB 28 nM (Kd) |
Cereblon |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| KM12 | IC50 |
52 nM
Compound: 6; CG428
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Antiproliferative activity against human KM12 cells assessed as reduction in cell viability measured after 3 days by Celltiter-Glo assay
Antiproliferative activity against human KM12 cells assessed as reduction in cell viability measured after 3 days by Celltiter-Glo assay
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[PMID: 33058680] |
体外実験
CG428 binds with high affinity to recombinant TRKA, TRKB, and TRKC kinases, with Kd values of 1.0, 28.0 and 4.2 nM[1].
CG428 degrades endogenous TPM3-TRKA fusion protein (DC50 = 0.36 nM) and inhibits PLCγ1 phosphorylation (IC50 = 0.33 nM) in KM12 cells[1].
CG428 potently degrades endogenous wild-type TRKA in HEL cells with a DC50 of 2.23 nM[1].
CG428 (0.7-500 nM; 6 h) exhibits reduced potency for degradation of ectopically expressed AGBL4-TRKB and ETV6-TRKC fusion protein in KM12 cells, with a hook effect at high concentrations[1].
CG428 potently inhibits the growth of KM12 cells with an IC50 of 2.9 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:KM12 human colorectal carcinoma cells
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Concentration:0.04, 0.12, 0.4, 1.1, 3.3, 10, 30 nM
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Incubation Time:6 h
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Result:Induced potent degradation of TPM3-TRKA with a DC50 of 0.36 ± 0.06 nM.
Inhibited downstream PLCγ1 phosphorylation with an IC50 of 0.33 ± 0.06 nM.
Caused 96 ± 3% TPM3-TRKA degradation at 10 nM.
Caused 82 ± 2% TPM3-TRKA degradation at 1 nM.
Caused 46 ± 6% TPM3-TRKA degradation at 0.1 nM.
Parmacokinetics
| Species | Dose | Route | Cmax | Tmax | T1/2 |
|---|---|---|---|---|---|
| Mice[1] | 10 mg/kg | i.p. | 1640 nM | 1 h | 0.9 h |
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:ICR (male)[1]
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Dosage:10 mg/kg
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Administration:i.p.; single dose
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Result:Reached a maximum plasma concentration of 1640 ± 120 nM at 1 h post dosing.
Plasma concentration was 12.4 ± 13.6 nM at 8 h post dosing.
Exhibited a half-life of 0.9 h.
臨床実験
| NCT Number | Sponsor | Condition | Start Date |
Phase
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|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
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CAS 番号 2412055-93-5
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性状 Solid
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分子量 814.86
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分子式 C43H43FN10O6
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Color Light yellow to yellow
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SMILES
O=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC=C3NCCOCCC(N4CCN(C5=NC(C6=CN=C7C=CC(N8[C@@H](C9=CC=CC(F)=C9)CCC8)=NN76)=CC=C5)CC4)=O)=O
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
溶剤 & 溶解度
体外:
DMSO : 100 mg/mL (122.72 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. 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. 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 (272 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 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. 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 | 1.2272 mL | 6.1360 mL | 12.2720 mL | 30.6801 mL |
| 5 mM | 0.2454 mL | 1.2272 mL | 2.4544 mL | 6.1360 mL | |
| 10 mM | 0.1227 mL | 0.6136 mL | 1.2272 mL | 3.0680 mL | |
| 15 mM | 0.0818 mL | 0.4091 mL | 0.8181 mL | 2.0453 mL | |
| 20 mM | 0.0614 mL | 0.3068 mL | 0.6136 mL | 1.5340 mL | |
| 25 mM | 0.0491 mL | 0.2454 mL | 0.4909 mL | 1.2272 mL | |
| 30 mM | 0.0409 mL | 0.2045 mL | 0.4091 mL | 1.0227 mL | |
| 40 mM | 0.0307 mL | 0.1534 mL | 0.3068 mL | 0.7670 mL | |
| 50 mM | 0.0245 mL | 0.1227 mL | 0.2454 mL | 0.6136 mL | |
| 60 mM | 0.0205 mL | 0.1023 mL | 0.2045 mL | 0.5113 mL | |
| 80 mM | 0.0153 mL | 0.0767 mL | 0.1534 mL | 0.3835 mL | |
| 100 mM | 0.0123 mL | 0.0614 mL | 0.1227 mL | 0.3068 mL |
CG428 関連分類
HY-137465 関連分類
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