PUMAi
PUMAi is a PUMA inhibitor that disrupts the interaction between PUMA and BCL-xL. PUMAi inhibits apoptosis, caspase-3 activation, WNT/NOTCH pathway activation, and DNA damage. PUMAi protects intestinal tissues in mice, promotes the growth of colonoids, and reduces chemotherapy-induced weight loss, gastrointestinal damage, and lethality. PUMAi alleviates acetaminophen-induced liver injury and cytoplasmic translocation of HMGB1 in mice. PUMAi can be used in studies related to gastrointestinal injury, intestinal injury, and liver injury.
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: 470695-03-5
- 分子式: C19H28Cl2N2O3
- 分子量:403.34
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Caspase アイソフォーム固有の製品をすべて表示
More
生物活性
|
Caspase 3 |
Bcl-xL |
PUMAi (25 μM; 15 min) inhibits the protein-protein interaction between PUMA and BCL-xL in HEK293 cell lysates, without affecting the interaction between BIM and MCL-1[1].
PUMAi (50 μM; 24 h) protects mouse colon organoids and human primary colon organoids from CPT-induced growth inhibition, apoptosis, and WNT/Notch pathway activation[1].
PUMAi effectively disrupts the interaction between PUMA and BCL-XL in cell-free biochemical assays[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
PUMAi (10 mg/kg; i.p.; 2 hours before CPT-11) reduces LGR5+ intestinal stem cell apoptosis, niche cell expansion, and DNA damage in mice treated with CPT-11[1].
PUMAi (10 mg/kg; i.p.; 2 hours before and 20 hours after each of 6 CPT-11 doses) prevents LGR5+ intestinal stem cell exhaustion and preserves niche integrity in mice treated with repeated doses of CPT-11[1].
PUMAi (10 mg/kg; i.p.; 2 hours before and 20 hours after each of 6 CPT-11 doses) protects tumor-bearing mice from CPT-11-induced gastrointestinal injury and weight loss without compromising tumor response to chemotherapy[1].
PUMAi (10 mg/kg; i.p.; 30 minutes before irradiation, 30 minutes after irradiation, and daily for 4 subsequent days) improves survival in mice with radiation-induced gastrointestinal injury[1].
PUMAi (10 mg/kg; i.p.; single dose) administered 2 hours after acetaminophen overdose significantly reduces acetaminophen-induced liver necrosis and injury in mice, as evidenced by reduced serum ALT/AST levels, necrotic liver area, TUNEL-positive cells, and HMGB1 cytoplasmic translocation[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
-
CAS 番号 470695-03-5
-
分子量 403.34
-
分子式 C19H28Cl2N2O3
-
SMILES
OCCN1CCN(CC(COC2=CC3=C(C=CC=C3)C=C2)O)CC1.Cl.Cl
-
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)