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Last Updated: 3 years ago

Possible Interaction: Sphingosine 1-Phosphate and Colforsin

Research Papers that Mention the Interaction

In Baby Hamster Kidney (BHK) cells expressing wild-type human CFTR, S1P (1μmol/L) attenuates forskolin-stimulated , CFTR-dependent iodide efflux.
PloS one  •  2015  |  View Paper
Pre-exposure to S1P markedly inhibited the augmentation of cAMP accumulation induced by forskolin.
Allergology international : official journal of the Japanese Society of Allergology  •  2012  |  View Paper
SPP markedly inhibited forskolin-stimulated cAMP accumulation in a dose-dependent manner and caused a remarkable elevation of intracellular calcium, both effects being sensitive to pertussis toxin treatment.
Archives of biochemistry and biophysics  •  2000  |  View Paper
Binding of SPP to Edg-1 resulted in inhibition of forskolin-stimulated cAMP accumulation, in a pertussis toxin–sensitive manner.
The Journal of cell biology  •  1998  |  View Paper
Furthermore, SPP inhibited forskolin-stimulated cAMP accumulation in HEK cells and increased binding of guanosine 5′-3-O-(thio)triphosphate to HEK cell membranes.
The Journal of Biological Chemistry  •  1996  |  View Paper
In the presence of forskolin , however, S1P significantly inhibited cAMP accumulation at a lower concentration (1–100 nm) of S1P in a manner sensitive to PTX in the Edg-1-transfected cells but not in either the Edg-3 or AGR16-transfected cells.
The Journal of Biological Chemistry  •  1999  |  View Paper
In a CHO clone stably expressing EDG1 receptor (CHO-EDG1 cells), SP induced increases in the production of inositol phosphates and the [Ca2+] i and inhibited forskolin-induced increase in the cellular cAMP content, all in a manner sensitive to pertussis toxin.
The Journal of Biological Chemistry  •  1998  |  View Paper
In Chinese hamster ovary cells heterologously expressing EDG-8, S1P inhibited forskolin-induced cAMP accumulation and activated c-Jun NH2-terminal kinase.
The Journal of Biological Chemistry  •  2001  |  View Paper