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Aromatic organic compounds that consist of a phenyl functional group (−C6H5) bonded to a hydroxyl functional group (−OH). Includes compounds with more substitutions and derivatives.
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OARV-771 is a VHL-based BET degrader (PROTAC) that induces proteasomal degradation of BET family proteins BRD2, BRD3, and BRD4. It demonstrates low-nanomolar degradation potency in cellular assays and is supplied as a solid with high chemical purity for research use.
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OARV-771 is a VHL-based BET degrader (PROTAC) with improved cell permeability. It demonstrates an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells.
Exhibits DC50 values of 6 nM for Brd4, 1 nM for Brd2, and 4 nM for Brd3.
Improved cell permeability.
Shows antiproliferative effect in MV4;11 cells.
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OARV-771 is a VHL-based BET degrader (PROTAC) with improved cell permeability. It demonstrates an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells. It is for research use only.
Shows DC50s of 6, 1, and 4 nM for Brd4, Brd2 and Brd3, respectively
Demonstrates an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells
Targets BRD4, BRD2, BRD3, and VHL
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
OARV-771 is a VHL-based BET degrader (PROTAC) with improved cell permeability. It shows DC50s of 6 nM for Brd4, 1 nM for Brd2, and 4 nM for Brd3. It also exhibits an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells.
VHL-based BET degrader (PROTAC)
Enhanced cell permeability
Demonstrates DC50s of 6 nM for Brd4, 1 nM for Brd2, and 4 nM for Brd3
Exhibits an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
OARV-771 is a VHL-based BET degrader (PROTAC) with improved cell permeability. It demonstrates DC50 values of 6 nM for Brd4, 1 nM for Brd2, and 4 nM for Brd3, and shows an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells.
VHL-based BET degrader (PROTAC)
Improved cell permeability
DC50 for Brd4: 6 nM
DC50 for Brd2: 1 nM
DC50 for Brd3: 4 nM
Antiproliferative effect with EC50 of 4 nM in MV4;11 cells
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
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LL-37 (CAS 154947-66-7) is a naturally occurring antimicrobial peptide derived from human cathelicidin consisting of 37 amino acids with amphipathic structure Its mechanism involves interaction with bacterial membranes resulting in membrane disruption and broad-spectrum antibacterial activity In addition to its antimicrobial role LL-37 modulates immune response contributes to inflammatory regulation and participates in wound healing through influencing cell migration and proliferation Current biomedical research employs LL-37 for investigating infection control immune modulation pathways and tissue repair processes
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AMA-37 is an arylmorpholine ATP-competitive inhibitor of DNA-dependent protein kinase (DNA-PK) used for biochemical and cellular research. The compound is provided in both solution and solid formats to support assay work and synthesis.
Inhibits DNA-PK with IC50 0.27 μM and shows activity against p110α (32 μM), p110β (3.7 μM), and p110γ (22 μM).
Available as a 10 mM solution in DMSO (1 mL) and in solid vials for scale flexibility.
CAS number 404009-46-7 for unambiguous chemical identification.
High reported purity (~99.5%) suitable for research applications.
Molecular weight 283.32 g/mol for formulation and dosing calculations.
Appropriate for DNA-PK signaling studies, kinase selectivity profiling, and preclinical assay development.
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