8 Results for "

DDR1-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "DDR1-IN-1" in MCE Product Catalog:

6
6 Cited Publications
Cat. No.: HY-13979
CAS No.: 1449685-96-4
Purity:  98.20%
Research Areas:  

Cancer

DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with an IC50 of 105 nM; 4-fold less potent for DDR2 (IC50 = 413 nM) .
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6
6 Cited Publications
Cat. No.: HY-13979A
CAS No.: 1780303-76-5
Research Areas:  

Cancer

DDR1-IN-1 dihydrochloride is a potent and selective DDR1 receptor tyrosine kinase inhibitor with an IC50 of 105 nM; 4-fold less potent for DDR2 (IC50 = 413 nM) .
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Cat. No.: HY-W018931
CAS No.: 1644069-80-6
Research Areas:  

Cancer

DDR Inhibitor is a potent discoidin domain receptor (DDR) inhibitor, with an IC50 of 3.3 nM for DDR2, and shows 53% inhibition on DDR1 at 1.5 nM.
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Cat. No.: HY-176184
CAS No.: 3081612-73-6
Research Areas:  

Cancer

PROTAC DDR1 degrader-1 is a potent and selective DDR1-targeting PROTAC degrader. PROTAC DDR1 degrader-1 selectively induces full-length DDR1 degradation via the ubiquitin proteasome system, blocking downstream signaling pathways. PROTAC DDR1 degrader-1 inhibits tumor cell migration and invasion. PROTAC DDR1 degrader-1 exhibits anti-tumor activity in mice. PROTAC DDR1 degrader-1 can be used for the research of DDR1-driven cancers .
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Cat. No.: HY-176185
DDR1 ligand 1 is a PROTAC target protein ligand (Ligands for Target Protein for PROTACs). DDR1 ligand 1 can be used for the synthesis of PROTAC DDR1 degrader-1 (HY-176184) .
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Cat. No.: HY-176187
CAS No.: 3081612-71-4
Research Areas:  

Cancer

DDR1 ligand 1-piperidine is a target protein ligand and linker conjugate, which can be used for the synthesis of PROTAC DDR1 degrader-1 (HY-176184) .
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Cat. No.: HY-176186
CAS No.: 1056123-56-8
Target:  

PROTAC Linkers

Research Areas:  

Cancer

4-Hydroxy-1-piperidinepropanamide is a PROTAC linker that can be used in the synthesis of PROTAC DDR1 degrader-1 (HY-176184) .
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Cat. No.: HY-176188
CAS No.: 3081612-41-8
Research Areas:  

Cancer

Lenalidomide-5-Br-amide-C2-Br is an E3 ligase ligand-linker conjugate. Lenalidomide-5-Br-amide-C2-Br can be used to synthesize PROTAC DDR1 degrader-1 (HY-176184) .
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