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- PROTAC-Linker Conjugates for PAC
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- Tumor
- Anti-infective
- Cardiovascular disease
- Development and reproduction
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- Inflammation and immunity
- Metabolic diseases
- Neurological disorders
- Other Fields
- Alangiaceae
- Aquifoliaceae
- Cephalotaxaceae
- Costaceae
- Daphniphyllaceae
- Dioscoreaceae
- Eucommiaceae
- Ginkgoaceae
- Hippocastanaceae
- Illiciaceae
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- Hematologic Malignancies Target Proteins
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- B Cell CD Proteins
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- Cytokines
- Epidermal Growth Factor Family, EGFs
- Growth Factors
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- Hydrolases,EC 3
- Isomerases,EC 5
- Ligases or Synthetases,EC 6
- Lyases,EC 4
- Oxidoreductases,EC 1
- Transferases,EC 2
- Translocases,EC 7
- Butyrophilins
- Co-inhibitory Immune Checkpoint Proteins
- Co-stimulatory Immune Checkpoint Proteins
- Cell Adhesion Receptors
- Cytokines and Growth Factor Receptors
- Enzyme-Linked Receptors
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- G Protein-Coupled Receptors, GPCRs
- Ion Channel-Linked Receptors
- Nuclear Receptors
- Receptor Serine/Threonine Kinases
- Receptor Tyrosine Kinases
- Others
- Coronavirus (CoV) Proteins
- DENV Proteins
- EBOV Proteins
- HBV Proteins
- HCV Proteins
- HIV Proteins
- Influenza Proteins
- RSV Proteins
- Others
- Molecular Docking
- Virtual Screening
- Biomolecular Interaction
- Custom Synthesis
- AI-driven Ultra High-throughput Virtual Screening
PROTAC-Linker Conjugates for PAC
- PROTAC BRD4 degrader for PAC-1T18603PROTAC BRD4 degrader for PAC-1 (compound 5) is a chimeric BET degrader GNE-987 conjugated with a disulfide-containing linker[1]. This PROTAC-linker conjugate specifically targets and degrades BRD4, enabling selective proteolysis of PAC-1.
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