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.
For research use only. We do not sell to patients.
- CAS No.: 470695-03-5
- Formula: C19H28Cl2N2O3
- Molecular Weight:403.34
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Caspase Isoforms
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Biological Activity
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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.
Chemical Information
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CAS No. 470695-03-5
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Molecular Weight 403.34
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Formula C19H28Cl2N2O3
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SMILES
OCCN1CCN(CC(COC2=CC3=C(C=CC=C3)C=C2)O)CC1.Cl.Cl
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)