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Chloramphenicol Palmitate 25mg | Purity Not Available
Selleck Chemicals
CX-3543(Quarfloxin) 5mg | Purity Not Available
Selleck Chemicals
Quarfloxin (CX-3543), a fluoroquinolone derivative inhibits RNA pol I activity. Quarfloxin disrupts the interaction between the nucleolin protein and a G-quadruplex DNA structure in the ribosomal DNA (rDNA) template.
More Information Supplier PageGANT58(NSC75503) 5mg | Purity Not Available
Selleck Chemicals
GANT 58 (NSC 75503) is a potent antagonist of GLI-mediated transcription with IC50 of ≈5 μM. It can be used for research in Ewing Sarcoma and several forms of solid cancer.
More Information Supplier PageGW501516 5mg | Purity Not Available
Selleck Chemicals
GW501516 is a potent and highly selective PPARβ/δ agonist, with EC50 of 1 nM, with 1000-fold selectivity over hPPARα and hPPARγ. Phase 4.
More Information Supplier PageLenalidomide-Br 100mg | Purity Not Available
Selleck Chemicals
Lenalidomide-Br is a brominated analog of lenalidomide, designed for use as a chemical tool in PROTAC research. It serves as a cereblon (CRBN)-recruiting ligand, enabling targeted protein degradation through the CRL4CRBN E3 ubiquitin ligase complex.
More Information Supplier PageLenalidomide-Br 25mg | Purity Not Available
Selleck Chemicals
Lenalidomide-Br is a brominated analog of lenalidomide, designed for use as a chemical tool in PROTAC research. It serves as a cereblon (CRBN)-recruiting ligand, enabling targeted protein degradation through the CRL4CRBN E3 ubiquitin ligase complex.
More Information Supplier PageAZD1152(Barasertib) 5mg | Purity Not Available
Selleck Chemicals
Lenalidomide-Br 1g | Purity Not Available
Selleck Chemicals
Lenalidomide-Br is a brominated analog of lenalidomide, designed for use as a chemical tool in PROTAC research. It serves as a cereblon (CRBN)-recruiting ligand, enabling targeted protein degradation through the CRL4CRBN E3 ubiquitin ligase complex.
More Information Supplier PageEdpetiline 1mg | Purity Not Available
Selleck Chemicals
Edpetiline is a steroidal alkaloid derived from Fritillaria species that exhibits potent anti-inflammatory and antioxidant effects. It suppresses proinflammatory mediators and reactive oxygen species (ROS) production while inhibiting NF-κB nuclear translocation and selectively blocking p38 and ERK MAPK phosphorylation.
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