4 Results for "

IDO1-PROTAC

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

4 Results for "IDO1-PROTAC" in MCE Product Catalog:

Cat. No.: HY-151886
CAS No.: 2759420-43-2
NU223612 is a potent PROTAC (PROTACs) that degrades indoleamine 2,3-dioxygenase 1 (IDO1) (Indoleamine 2,3-Dioxygenase (IDO)) with a Kd of 640 nM. NU223612 potently degrades the IDO1 protein through CRBN-mediated proteasomal degradation. NU223612 is bound to CRBN with an affinity of 290 nM. NU223612 can cross the blood-brain barrier (BBB) [1].
loading...
    loading...
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 [1].
loading...
    loading...
Cat. No.: HY-131912
CAS No.: 2488761-07-3
Thalidomide-NH-PEG8-Ts is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 8-unit PEG linker used in PROTAC technology, such as IDO1 PROTAC degrader (HY-131911) [1].
loading...
    loading...
Cat. No.: HY-132288
CAS No.: 2488761-03-9
Purity:  95.09%
Research Areas:  

Cancer

Pom-8PEG, an E3 ligase ligand-linker conjugate, incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase and an 8-unit PEG linker. Pom-8PEG can be used in the synthesis of PROTAC, such as IDO1 PROTAC degrader [1].
loading...
    loading...