WebAug 4, 1998 · Cryptophycin-52 (LY355703) is a new synthetic member of the cryptophycin family of antimitotic antitumor agents that is currently undergoing clinical evaluation. At high concentrations (≥10 times the IC50), cryptophycin-52 blocked HeLa cell proliferation at mitosis by depolymerizing spindle microtubules and disrupting chromosome organization. WebCryptophycin C35H43ClN2O8 CID 381235 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, …
Formal syntheses of cryptophycin A and arenastatin A
WebMar 10, 1997 · The cryptophycins, isolated from blue-green algae (Nostoc sp.) by Schwartz et aL and Moore and collaborators, are potent fungicides2 and antitumor agents.3,4 … WebJun 7, 2024 · RGD‐cryptophycin and isoDGR‐cryptophycin conjugates were synthetized by combining peptidomimetic integrin ligands and cryptophycin, a highly potent tubulin‐binding antimitotic agent across lysosomally cleavable Val‐Ala or uncleavable linkers.The conjugates were able to effectively inhibit binding of biotinylated vitronectin to integrin α v … st thomas six sigma
Cryptophycin 1 C35H43ClN2O8 - PubChem
WebCryptophycin-38 is a stereoisomer of cryptophycin-1 (1) and to date is the only naturally occurring analogue that possesses a S,S epoxide group in unit A. Cryptophycin-327 is a geometric isomer that differs from 1 in having a cis Delta(2)-double bond in unit A. Cryptophycin-326 is related to cryptophycin-21, but has two chlorines ortho to the … WebCryptophycin is a potent antitumor agent that depletes microtubules in intact cells, including cells with the multidrug resistance phenotype. To determine the mechanism of action of … WebJul 1, 1994 · Therefore, cryptophycin is a new antimicrotubule compound which appears to be a poorer substrate for P-glycoprotein than are the Vinca alkaloids. This property may confer an advantage to cryptophycin in the chemotherapy of drug-resistant tumors. 1. st thomas shops