LLH1 inhibitors represent a class of chemical compounds that specifically target and modulate the activity of the LLH1 protein, an enzyme involved in certain cellular processes. These inhibitors work by binding to the active or allosteric sites of the LLH1 protein, effectively reducing its activity or blocking its function entirely. LLH1, a member of a specific protein family, is integral to various biochemical pathways, particularly those related to protein regulation, cell signaling, or metabolic functions. Inhibiting LLH1 may cause changes in intracellular signaling cascades, protein degradation, or other regulatory mechanisms that depend on the normal function of the enzyme. LLH1 inhibitors are often characterized by their specificity, meaning they selectively target LLH1 without significantly affecting related proteins or other pathways, which is crucial for studying specific molecular interactions within cells.
Chemically, LLH1 inhibitors are diverse, and their structures can vary significantly depending on their mode of binding and the type of inhibition they employ. Some inhibitors may act competitively, blocking the substrate from accessing the enzyme's active site, while others may non-competitively alter the enzyme's conformation. The design of LLH1 inhibitors often involves detailed structural analysis of the LLH1 protein to identify binding pockets or regulatory domains that can be exploited for inhibition. Such inhibitors are important for researchers who wish to understand the detailed roles that LLH1 plays in biological systems, allowing for the dissection of pathways where LLH1 is a key regulatory element. Additionally, LLH1 inhibitors can serve as valuable tools in biochemical assays to observe cellular responses when the enzyme is inactivated or downregulated.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
L-Ascorbic acid, free acid | 50-81-7 | sc-202686 | 100 g | $46.00 | 5 | |
Essential for PLOD1 activity, its deficiency can reduce PLOD1 function. | ||||||
3-Aminopropionitrile | 151-18-8 | sc-266473 | 1 g | $104.00 | ||
Inhibitor of lysyl oxidase, indirectly affects collagen cross-linking, influencing PLOD1's role. | ||||||
Minodronic acid monohydrate | 155648-60-5 | sc-482735 | 10 mg | $153.00 | ||
Bisphosphonate, affects bone collagen dynamics, potentially impacting PLOD1 activity. | ||||||
Alendronate acid | 66376-36-1 | sc-337520 | 5 g | $135.00 | 2 | |
Bisphosphonate, used in osteoporosis, can influence bone collagen turnover, indirectly affecting PLOD1. | ||||||
Penicillamine | 52-67-5 | sc-205795 sc-205795A | 1 g 5 g | $46.00 $96.00 | ||
Reduces cross-linking in collagen, potentially influencing PLOD1's role in collagen stability. | ||||||
hydroxychloroquine | 118-42-3 | sc-507426 | 5 g | $57.00 | 1 | |
Used in rheumatoid arthritis, can affect collagen metabolism, indirectly influencing PLOD1. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Methotrexate may influence collagen synthesis and PLOD1 indirectly. | ||||||
Colchicine | 64-86-8 | sc-203005 sc-203005A sc-203005B sc-203005C sc-203005D sc-203005E | 1 g 5 g 50 g 100 g 500 g 1 kg | $100.00 $321.00 $2289.00 $4484.00 $18207.00 $34749.00 | 3 | |
Affects microtubule function and may impact collagen secretion and PLOD1 activity. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $138.00 $380.00 | 101 | |
Known to affect collagen and connective tissue, potentially impacting PLOD1. | ||||||