PROTAC PD-1/PD-L1 degrader-1
CAS No. 2447066-37-5
PROTAC PD-1/PD-L1 degrader-1( —— )
Catalog No. M35183 CAS No. 2447066-37-5
PROTAC PD-1/PD-L1 degrader-1, a Cereblon E3 ligand-based compound, is a PD-1/PD-L1 PROTAC that effectively inhibits the PD-1/PD-L1 interaction with an IC50 of 39.2 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 385 | Get Quote |
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| 5MG | 588 | Get Quote |
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| 10MG | 938 | Get Quote |
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| 25MG | 1398 | Get Quote |
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| 50MG | 1822 | Get Quote |
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| 100MG | 2493 | Get Quote |
|
| 200MG | 3357 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NamePROTAC PD-1/PD-L1 degrader-1
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NoteResearch use only, not for human use.
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Brief DescriptionPROTAC PD-1/PD-L1 degrader-1, a Cereblon E3 ligand-based compound, is a PD-1/PD-L1 PROTAC that effectively inhibits the PD-1/PD-L1 interaction with an IC50 of 39.2 nM.
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DescriptionPROTAC PD-1/PD-L1 degrader-1, a PD-1/PD-L1 PROTAC based on Cereblon E3 ligand, inhibits PD-1/PD-L1 interaction with an IC50 of 39.2 nM. PROTAC PD-1/PD-L1 degrader-1 significantly restores the immunity repressed in a co-culture model of Hep3B/OS-8/hPD-L1 and CD3 T cells. PROTAC PD-1/PD-L1 degrader-1 moderately reduces the protein levels of PD-L1 in a lysosome-dependent manner.
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In VitroPROTAC PD-1/PD-L1 degrader-1 (compound p22) reduces cell surface PD-L1 expression for more than 14%.PROTAC PD-1/PD-L1 degrader-1 (1-10 μM; 24 hours) reduces PD-L1 expression in a dose-dependent manner by 21% and 35% at 1 μM and 10 μM, respectively.Western Blot Analysis Cell Line:MDA-MB-231 cells Concentration:1-10 μM Incubation Time:24 hours Result:Reduced PD-L1 expression in a dose-dependent manner by 21% and 35% at 1 μM and 10 μM, respectively.
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorPROTACs | PD-1/PD-L1
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Research Area——
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Indication——
Chemical Information
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CAS Number2447066-37-5
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Formula Weight1076.59
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Molecular FormulaC59H58ClN7O11
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 210 mg/mL (195.06 mM; Ultrasonic )
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SMILESN#CC1=CC=CC(=C1)COC2=CC(OCC3=CC=CC(C4=CC=C5OCCOC5=C4)=C3C)=C(Cl)C=C2CN6CCCCC6C(=O)N7CCN(C(=O)CCCC(=O)NC8=CC=CC=9C(=O)N(C(=O)C89)C%10C(=O)NC(=O)CC%10)CC7
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Cheng B, Ren Y, Cao H, Chen J. Discovery of novel resorcinol diphenyl ether-based PROTAC-like molecules as dual inhibitors and degraders of PD-L1. Eur J Med Chem. 2020;199:112377.?
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