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  • Inhibitors & Agonists
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Tetramethylcurcumin
TN226952328-97-9In house
Tetramethylcurcumin is a novel curcumin analog, is an effective inhibitors of STAT3 phosphorylation, DNA binding activity, and transactivation in vitro.it also inhibits colony formation in soft agar, cell invasion, and exhibit synergy with the anti-cancer drug doxorubicin against breast cancer cells.
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Erythromycin estolate
Phtalic anhydride, ilosone
T152453521-62-8
Erythromycin estolate is a semi-synthetic derivative of erythromycin with good oral absorption and bioavailability tolerance. As a macrolide antibiotic, Erythromycin exerts its antibacterial action by inhibiting bacterial protein synthesis and is mainly used in studies for the treatment of respiratory, skin and soft tissue infections caused by susceptible bacteria. Erythromycin estolate may cause liver injury, including mild cholestatic hepatitis, jaundice, and paucity of bile ducts.
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7-10 days
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Trabectedin
ET-743, Ecteinascidin 743
T17155114899-77-3
Trabectedin (Ecteinascidin 743) has potent antitumor activity and the potential for soft tissue sarcoma and ovarian cancer research. Trabectedin inhibits cell growth of MX-1, MCF7 and MCF7 DXR cells with IC50 values of 0.1 nM, 1.5 nM and 3.7 nM, respectively.
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Sarcophine
Sarcophin,Sarcophin A
T3452555038-27-2
Sarcophine is a natural cembranoid from the Red Sea soft coral Sarcophyton glaucum.
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Dipalmitin
1,3-Dipalmitin
T704726657-95-4
Dipalmitin (1,3-Dipalmitin) has templating effects on soft palm mid fraction crystals.
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Eleutherobin
T74761174545-76-7
Eleutherobin, a potent β-microtubule inhibitor with an IC50 value of 2 μM, exhibits cytotoxic activity against cancer cells at a potency comparable to Paclitaxel. This compound is derived from marine soft coral and is known for its anticancer activity. [1] [2]
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