L-Penicillamine is an orally active serine palmitoyltransferase (SPT) inhibitor. L-Penicillamine inactivates the PLP cofactor by forming adducts, thereby inhibiting SPT activity and reducing sphingolipid biosynthesis. L-Penicillamine not only blocks tumor access to vitamin B6, but also stabilizes the human papillomavirus 16 E6 oncoprotein monomer and inhibits its polymerization, exhibiting a unique anticancer mechanism. L-Penicillamine effectively delays the growth of Sarcoma-180, induces tumor necrosis and prolongs survival (though long-term use may lead to Pyridoxine (HY-B1328) deficiency and weight loss)[1][2][3].
Molekulargewicht:
149.22
Reinheit:
97
CAS Nummer:
[1113-41-3]
Formel:
C5H11NO2S
Target-Kategorie:
Acyltransferase
Anwendungsbeschreibung:
MCE Product type: Peptides
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