ISM-PR44
ISM-PR44 is an orally active PROTAC degrader targeting BTK, with a DC50 of 0.05 nM in BTK-HiBiT Ramos cells. ISM-PR44 recruits CRBN E3 ligase to induce ubiquitination and proteasomal degradation of BTK. ISM-PR44 exhibits antiproliferative and cytotoxic activities in B-cell lymphoma cells. ISM-PR44 can be used for research on B-cell lymphoma.
(Pink: Btk ligand (HY-170324); Blue: Cereblon E3 ligase ligand; Black: linker).
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Formel: C43H52ClN11O6
- Molecular Weight:854.40
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
BTK 0.05 nM (DC50) |
In Vitro
ISM-PR44 (compound 44) (1 mM; 4 h) potently degrades BTK in BTK-HiBiT Ramos cells with a DC50 of 0.05 nM[1].
ISM-PR44 (30 μM; 15-60 min) exhibits potent binding to CRBN with an IC50 of 16 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Parmacokinetics
| Species | Dose | Route | AUC0-t | Cmax | T1/2 |
|---|---|---|---|---|---|
| Mice[1] | 1 mg/kg | i.v. | 7991 ng·h/mL | 1693 ng/mL | 1.2 h |
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:BALB/c nude mice (female, 6-8 weeks)[1]
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Dosage:3 mg/kg
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Administration:p.o.; single dose
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Result:Demonstrated comparable BTK degradation at both 2 h and 24 h postdose.
Chemical Information
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Molecular Weight 854.40
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Formel C43H52ClN11O6
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SMILES
O=C(C1=NC=C(N2C[C@H](N3CCN(C)C3=O)CCC2)N=C1NC4=CC=C(C5CCN(CC6=CC=CC(C(N[C@@]7(C)C(N([C@@H](CC8)C(NC8=O)=O)CC7)=O)=O)=C6Cl)CC5)C=C4)N
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)