| Cat. No. |
Product Name |
Information |
| PC-21634 |
Cbl-b inhibitor 3
Cbl-b inhibitor
|
Cbl-b inhibitor 3 is a potent, selective inhibitor of RING finger E3 ligase Cbl-b with IC50 of 5.5 nM in Cbl-b LCK Ub TR-FRET assays. |
| PC-21633 |
Cbl-b inhibitor 2
Cbl-b inhibitor
|
Cbl-b inhibitor 2 is a potent, selective inhibitor of RING finger E3 ligase Cbl-b. |
| PC-21632 |
Cbl-b inhibitor 1
Cbl-b inhibitor
|
Cbl-b inhibitor 1 is a potent, selective inhibitor of RING finger E3 ligase Cbl-b. |
| PC-21631 |
Cbl-b inhibitor 25
Cbl-b inhibitor
|
Cbl-b inhibitor 25 is a potent, selective inhibitor of RING finger E3 ligase Cbl-b with IC50 of 15 nM in TR-FRET assays. |
| PC-21046 |
KLHDC2 E3 ubiquitin ligase ligand 1
KLHDC2 E3 ligand
|
KLHDC2 E3 ubiquitin ligase ligand 1 is a 7 aa C-terminal fragment of the SelK protein used for PROTAC degradation. |
| PC-38765 |
EN106 derivative 2
E3 Ligase Ligand
|
EN106 derivative 2 is a EN106 derivative used for PROTAC design, EN106 is a covalent ligand and recruiter for FEM1B E3 ligase for targeted protein degradation. |
| PC-38764 |
EN106 derivative 1
E3 Ligase Ligand
|
EN106 derivative 1 is a EN106 derivative used for PROTAC design, EN106 is a covalent ligand and recruiter for FEM1B E3 ligase for targeted protein degradation. |
| PC-73170 |
Lenalidomide-Br
E3 Ligase Ligand
|
Lenalidomide-Br is an analog of cereblon (CRBN) ligand Lenalidomide for E3 ubiquitin ligase and recruitment of CRBN protein, can be used for PROTACs design. |
| PC-73169 |
SY2-062
E3 Ligase Ligand
|
SY2-062 is a thalidomide derivative and useful precursor for synthesis of thalidomide-based PROTAC degrader. |
