ARL3 (ADP-Ribosylation Factor-like 3) inhibitors constitute a class of small molecules designed to target and modulate the activity of the ARL3 protein, which belongs to the ADP-ribosylation factor (ARF) family of GTP-binding proteins. These inhibitors play a pivotal role in the realm of cell biology and molecular research by aiding in the investigation of ARL3's cellular functions and its involvement in various intracellular processes. ARL3, known for its essential roles in cellular trafficking, ciliary function, and intracellular signaling, is a key regulator of vesicular transport and is particularly associated with the ciliary transport machinery in eukaryotic cells.
The mechanisms of ARL3 inhibitors generally involve interfering with the GTPase activity of ARL3, thereby modulating its nucleotide-bound state. By binding to ARL3 and affecting its GTPase cycle, these inhibitors can perturb the dynamic equilibrium between the active GTP-bound form and the inactive GDP-bound form of ARL3. This modulation can result in altered intracellular transport processes, disruptions in ciliary function, and downstream effects on cellular signaling pathways. Researchers have employed ARL3 inhibitors as valuable tools to decipher the intricate roles of ARL3 in various cellular contexts, shedding light on its contributions to cell division, intracellular trafficking, and ciliogenesis. These inhibitors offer insights into the fundamental biology of ARL3, enabling a deeper understanding of its physiological and pathological significance in cellular processes. As a result, ARL3 inhibitors are indispensable for advancing our knowledge of cell biology and may hold potential implications for the development of future research and therapies targeting ARL3-related cellular dysfunctions.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Apalutamide | 956104-40-8 | sc-507442 | 5 mg | $290.00 | ||
Apalutamide is a competitive androgen receptor antagonist. It competes with androgens for binding to the androgen receptor, inhibiting the receptor's activity and suppressing androgen-driven prostate cancer growth. | ||||||
MDV3100 | 915087-33-1 | sc-364354 sc-364354A | 5 mg 50 mg | $245.00 $1051.00 | 7 | |
Enzalutamide is another androgen receptor antagonist that inhibits androgen binding to the receptor, preventing nuclear translocation, and coactivator recruitment. It is studied in the research of castration-resistant prostate cancer. | ||||||
Bicalutamide | 90357-06-5 | sc-202976 sc-202976A | 100 mg 500 mg | $42.00 $146.00 | 27 | |
Bicalutamide is a nonsteroidal antiandrogen that blocks androgen receptor activation by binding to the receptor, preventing its interaction with DNA and coactivators, and inhibiting prostate cancer cell growth. | ||||||
Darolutamide | 1297538-32-9 | sc-507537 | 10 mg | $250.00 | ||
Darolutamide is a high-affinity androgen receptor antagonist that prevents androgen binding to the receptor, inhibiting nuclear translocation and coactivator recruitment. | ||||||
Flutamide | 13311-84-7 | sc-204757 sc-204757A sc-204757D sc-204757B sc-204757C | 1 g 5 g 25 g 500 g 1 kg | $47.00 $156.00 $171.00 $525.00 $941.00 | 4 | |
Flutamide is a nonsteroidal antiandrogen that competitively inhibits androgen receptor activation, reducing androgen-dependent prostate cancer cell proliferation. | ||||||
Abiraterone Acetate | 154229-18-2 | sc-207240 | 5 mg | $231.00 | 1 | |
Abiraterone acetate is an inhibitor of CYP17A1, reducing androgen production. | ||||||
Galeterone | 851983-85-2 | sc-364495 sc-364495A | 5 mg 25 mg | $191.00 $572.00 | 1 | |
Galeterone has a unique mechanism as a selective CYP17 lyase inhibitor and androgen receptor antagonist, targeting both androgen synthesis and receptor activation in prostate cancer therapy. | ||||||
MLN8237 | 1028486-01-2 | sc-394162 | 5 mg | $220.00 | ||
EPI-001 is an androgen receptor N-terminal domain inhibitor that disrupts coactivator recruitment, offering a unique approach to androgen receptor inhibition in prostate cancer. | ||||||