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        [Date : November 13 2025 00:07]

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        Inostamycin A (Sodium Salt), Antitumor
        DatasheetThis may not be the latest data sheet.         		14652 IMCInstitute of Microbial Chemistry 1 mg $500

        Description M.W.: 722.933 (Sodium salt) Purity : >90% (qNMR) Molecular Formula : C38H68O11Na (Sodium salt) Solubility : Soluble in DMSO, DMF, and CHCl3, Poorly soluble in H2O Inostamycin A is an inhibitor of phosphatidylinositol turnover, supplied as sodium salt. It was reported that this compound inhibited EGF-induced inositol incorporation into inositol lipids in the A431 cell assay system. It was also reported that inhibition of in vitro CDP-DG: inositol transferase activity of the A431 cell membrane, antimicrobial activities against gram-positive bacteria, cytocidal activity against srk-NIH-3T3, and potentiated colchicine cytotoxicity toward KB-C4 cells. In addition, it caused Ms-1 cell to accumulate in the G1 phase and induced morphological apoptosis at high concentration.
        Storage -20°C CAS 1884611-95-3 (sodium salt), 129905-10-8 (salt free form)
        Link

        Inostamycin A (sodium salt)
        Bioactive Compounds

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              [Date : November 13 2025 00:07]

              Inostamycin A (Sodium Salt), Antitumor

              DatasheetThis may not be the latest data sheet.


              • Product Code: 14652
              • Supplier: IMC
              • Size: 1mg
              • Price: $500

              Description M.W.: 722.933 (Sodium salt) Purity : >90% (qNMR) Molecular Formula : C38H68O11Na (Sodium salt) Solubility : Soluble in DMSO, DMF, and CHCl3, Poorly soluble in H2O Inostamycin A is an inhibitor of phosphatidylinositol turnover, supplied as sodium salt. It was reported that this compound inhibited EGF-induced inositol incorporation into inositol lipids in the A431 cell assay system. It was also reported that inhibition of in vitro CDP-DG: inositol transferase activity of the A431 cell membrane, antimicrobial activities against gram-positive bacteria, cytocidal activity against srk-NIH-3T3, and potentiated colchicine cytotoxicity toward KB-C4 cells. In addition, it caused Ms-1 cell to accumulate in the G1 phase and induced morphological apoptosis at high concentration.
              Storage -20°C CAS 1884611-95-3 (sodium salt), 129905-10-8 (salt free form)
              Link

              Inostamycin A (sodium salt)
              Bioactive Compounds