Isthmin inhibitors are a class of small organic molecules that have garnered significant attention in the field of chemical biology and drug discovery due to their potential in modulating cellular processes. These compounds are primarily designed to target and inhibit isthmin, a secreted signaling protein that plays crucial roles in embryonic development, tissue regeneration, and the regulation of various cellular pathways. Isthmin itself is a member of the BMP (Bone Morphogenetic Protein) family and is known to exert its effects through interactions with specific cell surface receptors. Isthmin inhibitors are characterized by their ability to interfere with the isthmin-receptor interactions, thereby influencing downstream signaling cascades.
Isthmin inhibitors is rooted in the desire to gain a deeper understanding of isthmin's biological functions and its impact on various cellular processes. Researchers have designed these molecules to serve as valuable tools in dissecting isthmin-related pathways, offering insights into the intricate mechanisms that govern cell fate, tissue development, and regeneration. By selectively blocking isthmin's activity, these inhibitors enable scientists to explore the consequences of isthmin inhibition in a controlled manner, paving the way for a more comprehensive understanding of its roles in both normal development and pathological conditions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Suramin sodium | 129-46-4 | sc-507209 sc-507209F sc-507209A sc-507209B sc-507209C sc-507209D sc-507209E | 50 mg 100 mg 250 mg 1 g 10 g 25 g 50 g | $152.00 $214.00 $728.00 $2601.00 $10965.00 $21838.00 $41096.00 | 5 | |
Suramin can interfere with growth factor signaling, which may disrupt the angiogenic processes isthmins are involved in. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $153.00 $938.00 | 5 | |
A tyrosine kinase inhibitor that can disrupt signaling pathways involved in angiogenesis, which isthmins may be a part of. | ||||||
Pazopanib | 444731-52-6 | sc-396318 sc-396318A | 25 mg 50 mg | $130.00 $182.00 | 2 | |
An inhibitor of vascular endothelial growth factor receptor (VEGFR) that can disrupt angiogenic signaling. | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $111.00 $357.00 | 8 | |
Modulates the expression of VEGF and fibroblast growth factor (FGF), which are potentially connected to isthmin action. | ||||||
TNP 470 | 129298-91-5 | sc-296547 | 10 mg | $235.00 | ||
An angiogenesis inhibitor that could potentially alter the cellular environment isthmins function within. | ||||||
2-Methoxyestradiol | 362-07-2 | sc-201371 sc-201371A | 10 mg 50 mg | $71.00 $288.00 | 6 | |
A metabolite of estradiol that can inhibit angiogenesis, possibly affecting isthmin-related processes. | ||||||
Combrestatin A4 | 117048-59-6 | sc-204697 sc-204697A | 1 mg 5 mg | $46.00 $81.00 | ||
A tubulin-binding agent that disrupts the cytoskeleton, influencing angiogenesis where isthmins may play a role. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
A RAF kinase inhibitor that also inhibits VEGFR and PDGFR, which may affect isthmin-mediated processes. | ||||||
Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
An inhibitor of VEGFR, EGFR, and RET tyrosine kinases, possibly influencing isthmin-related angiogenesis. | ||||||