4 Results for "

GBM43 cells

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "GBM43 cells" in MCE Product Catalog:

Cat. No.: HY-151886
CAS No.: 2759420-43-2
NU223612 is a cereblon (CRBN)-recruiting IDO1 PROTAC degrader, with a DC50 value of 0.329-0.5438 μM against human IDO1, and it is capable of penetrating the blood-brain barrier. NU223612 directly binds to IDO1, mediates the degradation of both wild-type and catalytically inactive mutant IDO1 proteins, and does not degrade TDO2. NU223612 inhibits IDO1-mediated enzymatic activity. NU223612 directly binds to CRBN and promotes the formation of a cooperative ternary complex with IDO1. NU223612 induces ubiquitin-dependent proteasomal degradation of the IDO1 protein. NU223612 suppresses IDO1-mediated non-enzymatic phosphorylation of NF-κB p65 and the DNA-binding activity of downstream transcription factors. NU223612 can be used in studies of glioblastoma (malignant glioma) .
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Cat. No.: HY-173066
CAS No.: 3048196-52-4
Research Areas:  

Cancer

NU227326 is a blood-brain barrier penetrant IDO1 PROTAC degrader, with a DC50 of 4.5 nM in HiBiT degradation assays. NU227326 degrades IDO1 in U87 and GBM43 cells, with DC50 values of 7.1 nM and 11.8 nM, respectively (WB assays). NU227326 is applicable to research related to glioblastoma, prostate cancer, triple-negative breast cancer, pancreatic cancer, and ovarian cancer .
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Cat. No.: HY-134983
CAS No.: 2222114-22-7
Purity:  96.47%
Thalidomide-piperazine hydrochloride is a synthetic E3 ligase ligand-linker conjugate, containing a cereblon ligand based on Thalidomide (HY-14658) and one linker. Thalidomide-piperazine hydrochloride can be used in studies related to PROTAC synthesis .
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Cat. No.: HY-159093
Target:  

Drug Derivative

Research Areas:  

Cancer

Antitumor agent-178 (compound 4 h) is a potent and selective GSCs inhibitor. Antitumor agent-178 has the potential for the research of cancer .
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