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≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Cyclic-di-GMP diammonium is a STING agonist and a bacterial second messenger that coordinates different aspects of bacterial growth and behavior, including motility, virulence, biofilm formation, and cell cycle progression. Cyclic-di-GMP diammonium has anti-cancer cell proliferation activity and also induces elevated CD4 receptor expression and cell cycle arrest. Cyclic-di-GMP diammonium can be used in cancer research
In Vitro
Cyclic-di-GMP diammonium (0.5-50 μM; 5 days) inhibits proliferation of human colon cancer cells. ?\nCyclic-di-GMP diammonium (0.5-50 μM; 5 days) specifically elevates CD4 expression in Jurkat cells. ?\nCyclic-di-GMP diammonium (0.5-50 μM; 5 days) induces cell cycle arrest at the S-phase in Jurkat cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Proliferation AssayCell Line: H508 cells Concentration: 0.5-50 µM Incubation Time: 5 days Result: Reduced basal H508 cell proliferation by approx 15%, even inhibited acetylcholine- and EGF-induced cell proliferation. Cell Viability AssayCell Line: Jurkat cells Concentration: 50 µM Incubation Time: 24 h Result: Specifically induced of CD4 (no effect on the expression of CD8), with a 6.3-fold upregulation over control and in a dose-dependent manner. Cell Cycle AnalysisCell Line: Jurkat cells Concentration: 50 µM Incubation Time: 24 h Result: Increased the percentage of cells in S-phase by 79%, with almost complete disappearance of G2/M-phase cells which decreased by 93%.
In Vivo
Cyclic-di-GMP diammonium (100 μg/per; i.v.; two sequential vaccinations 9 days apart) enhances TriVax-induced immune responses to melanoma in mice and further increased the anti-tumor effects of TriVax. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: C57BL/6 (B6) mice (8- to 10-week-old). Dosage: 100 µg/per Administration: Intravenous injection; two sequential vaccinations 9 days apart; combine with TriVax. Result: Significantly higher numbers of antigen-specific CD8 T cells when combined with TriVax. (TriVax consisted of a mixture of 120 μg Pam-hgp100, 100 µg hgp100 or 100 µg Ova, 50 or 25 μg anti-CD40 antibody, and 25 μg Poly-IC). Enhanced the anti-tumor activity of TriVax.
Form:Solid
IC50& Target:STING
| Molecular Weight | 724.47 |
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Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Solubility | H2O : 50 mg/mL (69.02 mM; Need ultrasonic) |
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