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Epirubicin has a different spatial orientation of the hydroxyl group at the 4' carbon of the sugar - it has the opposite chirality - which may account for its faster elimination and reduced toxicity
Formula: C21H21FN6O
Curr Drug Targets
Chemical Name: N'-(5-chloropyridin-2-yl)-N-[(1S
001-100 μM
Niclosamide olamine 11670 Epirubicin has a different spatialNiclosamide olamine (BAY2353 olamine) is an anthelmintic that disrupts mitochondrial metabolism in parasitic worms and animal models. Niclosamide olamine inhibits STAT3 (IC50 = 0. 25 M) and stimulates autophagy by reversibly inhibiting mammalian target of Rapamycin complex 1 (mTORC1) signaling. Product information CAS Number: 1420 04 8 Molecular Weight: 388. 20 Formula: C15H15Cl2N3O5 Synonym: BAY2353 olamine Chemical Name: 2 aminoethan 1 ol; 5 chloro
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