PINX1 Inhibitors, as a chemical class, encompass a diverse range of compounds primarily characterized by their ability to interact with the telomere maintenance mechanisms, either directly or indirectly. These inhibitors do not target the PINX1 protein specifically but instead influence the pathways and processes in which PINX1 is involved, such as telomerase activity and telomere length regulation. This group includes molecules varying in structure from small synthetic compounds to larger biomolecules. A significant portion of these inhibitors function by targeting the telomerase enzyme, an essential component in telomere elongation. Chemicals like BIBR1532, MST-312, and GRN163L are designed to impede the action of the telomerase reverse transcriptase (TERT), the catalytic core of the telomerase complex. By inhibiting TERT, these compounds effectively reduce the enzyme's ability to add telomeric repeats to chromosome ends, indirectly affecting the telomere-related functions of PINX1.
In addition to direct telomerase inhibitors, this class also includes compounds that alter telomere structure or stability. Agents such as Telomestatin and RHPS4 bind to telomeric DNA, specifically targeting the G-quadruplex structures, a unique configuration of nucleic acids found in telomeres. This binding disrupts the normal telomere architecture, potentially affecting the interaction of telomere-associated proteins like PINX1. Furthermore, natural compounds such as Costunolide, Berberine, and Curcumin, although not initially developed as telomerase inhibitors, have shown activity in this area. These natural inhibitors offer a different mode of action, possibly through indirect interactions with telomerase or telomere-related pathways. Their diverse chemical structures, ranging from alkaloids to polyphenols, highlight the chemical diversity within this class. These inhibitors, by influencing telomerase activity or telomere integrity, can indirectly modulate the function of PINX1 in telomere maintenance, reflecting the broad and varied mechanisms of action encompassed within this chemical class. The PINX1 Inhibitors, therefore, represent a unique and chemically diverse group of compounds with a shared focus on modulating telomere dynamics and telomerase activity.
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Produkt | CAS # | Katalog # | Menge | Preis | Referenzen | Bewertung |
---|---|---|---|---|---|---|
BIBR 1532 | 321674-73-1 | sc-203843 sc-203843A | 10 mg 50 mg | $189.00 $733.00 | 6 | |
BIBR 1532 ist ein potenter und spezifischer Telomerase-Inhibitor, der die Telomerase-Aktivität hemmt und damit möglicherweise PINX1-bezogene Signalwege beeinflusst, indem er die Aufrechterhaltung der Telomerlänge beeinträchtigt. | ||||||
Telomerase Inhibitor IX | 368449-04-1 | sc-204333 | 10 mg | $200.00 | 2 | |
Der Telomerase-Inhibitor IX (MST-312) ist ein Telomerase-Inhibitor, der durch Destabilisierung des Telomerase-Komplexes wirkt und damit indirekt die PINX1-Funktion im Zusammenhang mit der Telomer-Regulierung beeinflusst. | ||||||
3′-Azido-3′-deoxythymidine | 30516-87-1 | sc-203319 | 10 mg | $60.00 | 2 | |
Ein antiretroviraler Wirkstoff in der Forschung, der auch telomerasehemmende Eigenschaften aufweist. Es könnte die PINX1-Aktivität indirekt über seine Wirkung auf die Telomerase beeinflussen. | ||||||
Costunolide | 553-21-9 | sc-203555 sc-203555A | 1 mg 10 mg | $81.00 $168.00 | 1 | |
Ein Sesquiterpenlacton, von dem bekannt ist, dass es die Telomerase-Aktivität hemmt und möglicherweise die an PINX1 beteiligten Signalwege verändert. | ||||||
Berberine | 2086-83-1 | sc-507337 | 250 mg | $90.00 | 1 | |
Ein Alkaloid, das nachweislich eine telomerasehemmende Wirkung besitzt und sich möglicherweise indirekt auf PINX1 auswirkt. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Disulfiram hat gezeigt, dass es die Telomerase-Aktivität hemmen kann. |