Antineoplastic agents

A rotenoid compound with chemopreventive and chemosensitizing effects in models of skin, mammary, colon, and lung carcinogenesis inhibits cell growth (IC50 = 8 M), blocks PI3K/Akt signaling, suppresses COX-2 expression, and induces apoptosis of

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) is a potent, selective and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. (-)-DHMEQ inhibits nuclear translocation of NF-κB and shows anti-inflammatory and anticancer activityIn

Synonyms: D-(-)-Tartaric acid diisopropyl ester Diisopropyl (2S,3S)-dihydroxysuccinate CAS No.: 62961-64-2 Molecular Formula: C10H18O6 Molecular Weight: 234.25 MDL No.: MFCD00008876 Storage Temperature: Store at 0-8°C

(-)-Enitociclib ((R)-Enitociclib) is an enanthiomer of BAY-1251152 with rotation (-). BAY-1251152 is a potent and highly selective PTEF/CDK9 inhibitor.Form:SolidIC50&amp: Target:CDK9.

A natural catechin which inhibits the growth of cancer cells and has anti-inflammatory effects has potent antioxidant activity and facilitates the killing of methicillin-resistant strains of S. aureus.

A natural catechin which inhibits the growth of cancer cells and has anti-inflammatory effects has potent antioxidant activity and facilitates the killing of methicillin-resistant strains of S. aureus.

A natural catechin which inhibits the growth of cancer cells and has anti-inflammatory effects has potent antioxidant activity and facilitates the killing of methicillin-resistant strains of S. aureus.

A natural catechin which inhibits the growth of cancer cells and has anti-inflammatory effects has potent antioxidant activity and facilitates the killing of methicillin-resistant strains of S. aureus.

A 2R,3R stereoisomer of catechin a powerful antioxidant inhibits COX-1 (IC50 = 3.2 &muM) at 100 &microM, induces apoptosis in human adenocarcinoma PC-9 cells and stimulates the inhibition of TNF-&alpha release from BALB-c/3T3 cells treated

A 2R,3R stereoisomer of catechin a powerful antioxidant inhibits COX-1 (IC50 = 3.2 &muM) at 100 &microM, induces apoptosis in human adenocarcinoma PC-9 cells and stimulates the inhibition of TNF-&alpha release from BALB-c/3T3 cells treated

A 2R,3R stereoisomer of catechin a powerful antioxidant inhibits COX-1 (IC50 = 3.2 &muM) at 100 &microM, induces apoptosis in human adenocarcinoma PC-9 cells and stimulates the inhibition of TNF-&alpha release from BALB-c/3T3 cells treated

A 2R,3R stereoisomer of catechin a powerful antioxidant inhibits COX-1 (IC50 = 3.2 &muM) at 100 &microM, induces apoptosis in human adenocarcinoma PC-9 cells and stimulates the inhibition of TNF-&alpha release from BALB-c/3T3 cells treated