Pirarubicin

Pirarubicin is an anthracycline antibiotic, and also a DNA/RNA synthesis inhibitor by intercalating into Dna and interacts with topoisomerase II, used as an antineoplastic agent. (In Vitro) :Pirarubicin is a topoisomerase II inhibitor. Pirarubicin shows inhibitory activities against M5076 and Ehrlich cells, with IC50s of 0.366 and 0.078 μM, respectively. The cytotoxicity of Pirarubicin toward M5076 cells is lower than toward Ehrlich cells, and this is due to the much lower expression of topoisomerase II in M5076 cells than in Ehrlich cells. Pirarubicin (2.5, 5, 10 μg/mL) significantly induces autophagy in a dose dependent manner in bladder cancer (T24, EJ, 5637, J82 and UM-UC-3) cells. Furthmore, Pirarubicin (5 μg/mL) induces apoptosis through inhibition of mTOR/p70S6K/4E-BP1 in bladder cancer cells, and this effect is enhanced by inhibition of autophagy. (In Vivo) :Pirarubicin (18 mg/kg, i.v.) significantly elevates serum level of BNP, CK-MB, CTnT, LDH, and MDA compared with those in the control group in acute cardiac toxicity rats. Pirarubicin also lowers heart rate, and depresses R-wave voltage, and prolongation of QT intervals in the acute cardiac toxicity model.

72496-41-4

Tepirubicin | Tetrahydropyranyl-Doxorubicin | THP-Adriamycin | THP-Doxorubicin

Pharmacology & Drug Discovery

>98% (HPLC)

DMSO:7 mg/mL (11.15 mM) ; Ethanol:<1 mg/mL (<1 mM) ; Water:<1 mg/mL (<1 mM)

O=C1C2=C (O) C (C[C@] (C (CO) =O) (O) C[C@@H]3O[C@H]4C[C@H] (N) [C@H] (O[C@H]5CCCCO5) [C@H] (C) O4) =C3C (O) =C2C (C6=C1C=CC=C6OC) =O

C32H37NO12

627.64

Storage temperature: -20°C. Stability: ≥ 2 years

For research use only.