Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

AC1Q1SAB (2S,3R,4S,5S,6R)-2-[5,7- dihydroxy-2-(3,4,5...

Synonyms: AR-1G6328, AC1L4V8W, Delphinidin-3-rutinoside

This record was replaced with 5492231.

Matsumoto, H. et al., Matsumoto, H. et al.

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High impact information on Delphinidin-3-rutinoside

Delphinidin-3-rutinoside relaxes the bovine ciliary smooth muscle through activation of ETB receptor and NO/cGMP pathway [1].
Relative to intravenous injection, oral administration of delphinidin-3-rutinoside resulted in complete bioavailability (0.49 +/- 0.06%) [2].
Setting the bile duct cannulation in a Bollman-type cage, however, significantly increased the bioavailability of orally administered delphinidin-3-rutinoside (18.14 +/- 6.24%) [2].

Biological context of Delphinidin-3-rutinoside

In the present study, we calculated the pharmacokinetic bioavailability of anthocyanins in rats by measuring the plasma concentration of delphinidin-3-rutinoside that had been administered orally or intravenously [2].

References

Delphinidin-3-rutinoside relaxes the bovine ciliary smooth muscle through activation of ETB receptor and NO/cGMP pathway. Matsumoto, H., Kamm, K.E., Stull, J.T., Azuma, H. Exp. Eye Res. (2005) [Pubmed]
Ingested delphinidin-3-rutinoside is primarily excreted to urine as the intact form and to bile as the methylated form in rats. Matsumoto, H., Ichiyanagi, T., Iida, H., Ito, K., Tsuda, T., Hirayama, M., Konishi, T. J. Agric. Food Chem. (2006) [Pubmed]

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