Setomimycin


CAS No. : 69431-87-4

69431-87-4
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Cat. No. : HY-124439
M.Wt: 580.58
Formula: C34H28O9
Purity: >98 %
Solubility: 10 mM in DMSO
Introduction of 69431-87-4 :

Setomimycin is a potent antibiotic. Setomimycin inhibits the SARS-CoV-2 Mpro enzyme with an IC50 value of 12.02 µM. Setomimycin shows anti-inflammatory and antioxidant properties. Setomimycin shows antiproliferative and antitumor activity[1][2]. IC50 & Target:IC50: 12.02 µM (SARS-CoV-2 Mpro)[1] In Vitro: Setomimycin (0.01-1 µM) inhibits the release of cytokines IL-1β, IL-6 and TNF-α and nitric oxide release from LPS stimulated RAW 264.7 cells in a dose-dependent manner[1].
Setomimycin (compound 1) shows antimicrobial activity with MICs of 8, 4, 16, 4 μg/mL for Staphylococcus aureus, Bacillus cereus, Bacillus subtilis, Micrococcus luteus, respectively[2].
Setomimycin (0-100 µM; 5 days) shows antiproliferative activity and inhibits colony formation[2].
Setomimycin (4, 5.5, 7 µM) decreases the protein expression of p-MEK, p-ERK, Bcl-2, increases the expression of Par-4[2]. In Vivo: Setomimycin (20 mg/kg; i.p.; alternate days for two weeks) shows antitumor activity in mice[2].
Pharmacokinetic Parameters of Setomimycin in female BALB/c mice[2].
Pharmacokinetic parameters Value
Cmax (ng/ml) 694 ± 62
Tmax (h) 0.3 ± 0.1
T1/2 (h) 2.3 ± 0.5
AUC0-t (ng.h/mL) 2613 ± 111
AUC0-α (ng.h/mL) 2734 ± 108
Vd (L/Kg) 24 ± 4
Cl (L/h/Kg) 7.4 ± 0.3
Female BALB/c mice, 20 mg/kg ip (1 % DMSO +30 % PEG-200 + 2 % Tween 80 + q.s. water (v/v))[2]

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