Sphondin

Catalog No. BCN5579
CAS RN 483-66-9
Molecular Weight 216.2
Molecular Formula C12H8O4
Database [PubChem]:382161424
[ChEBI]:81486
[PCIDB]:

Definition

Standard InChI

InChI=1S/C12H8O4/c1-14-9-6-7-2-3-10(13)16-11(7)8-4-5-15-12(8)9/h2-6H,1H3

Biological Activity

Sphondin, a furanocoumarin derivative isolated from Heracleum laciniatum, possesses an inhibitory effect on IL-1beta-induced increase in the level of COX-2 protein and PGE(2) release in A549 cells, the inhibitory mechanism, at least in part, through suppression of NF-kappaB activity, suggests that sphondin may have the therapeutic potential as an anti-inflammatory drug on airway inflammation.[1]
Sphondin, 8-methoxypsoralen, and khellin have delayed phototoxic effects inAedes aegypti.[2]
Sphondin has NO production inhibitory activity, due to the effect of iNOS expression, but not by direct inhibition of iNOS enzyme activity, thus, sphondin may act as a potent inhibitor of NO production under tissue-damaging inflammatory conditions.[3]
Sphondin, one of furanocoumarins isolated from the fruits of the plant, may have anticonvulsant activity.[4]
Sphondin shows anti-proliferative activity and causes G2/M arrest at concentrations of 0.05-15.0 uM, it may have anti-tumor effects.[5]

Product information

English website: Sphondin
Japanese website: Sphondin
Chinese website: Sphondin

References

[1] Yang L L, Liang Y C, Chang C W, et al. Life Sci, 2002, 72(2):199-213.
[2] Kagan J, Szczepanski P, Bindokas V, et al. J Chem Ecol, 1986, 12(4):899-914.
[3] Wang C C, Lai J E, Chen L G, et al. Bioorg Med Chem, 2000, 8(12):2701-7.
[4] Tosun F, Çiğdem Akyüz Kızılay, Erol K, et al. Food Chem, 2008, 107(3):990-3.
[5] Sumiyoshi M, Sakanaka M, Taniguchi M, et al. J Nat Med, 2013, 68(1):83-94.
[6] Fatma M. Al-Barwani, Elsadig A. Eltayeb. SQU Journal For Science, 2004,(9): 7-17.