A lignan polyphenol with diverse biological activities
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Obovatol

Item No. 27553

Technical Information
Formal Name
5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]-1,2-benzenediol
CAS Number
83864-78-2
Synonyms
  • NSC 364150
Molecular Formula
C18H18O3
Formula Weight
Purity
≥98%
A neat oil
SMILES
OC1=C(OC2=CC=C(CC=C)C=C2)C=C(CC=C)C=C1O
InChi Code
InChI=1S/C18H18O3/c1-3-5-13-7-9-15(10-8-13)21-17-12-14(6-4-2)11-16(19)18(17)20/h3-4,7-12,19-20H,1-2,5-6H2
InChi Key
OPGPFZQBCIAFLI-UHFFFAOYSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Obovatol is a lignan polyphenol that has been found in M. officinalis and has diverse biological activities.1,2,3 It inhibits epinephrine- or arachidonate-induced aggregation of isolated rat platelets (IC50s = 59 and 54 µM, respectively).1 Obovatol (50 µM) induces cell cycle arrest at the S phase and apoptosis in SW620 colorectal cancer cells.2 It reduces tumor volume and weight in a SW620 mouse xenograft model when administered at a dose of 6 mg/kg per day. Obovatol (1 mg/kg per day for three months) decreases hippocampal and cortical amyloid-β (Aβ) 1-42 (Aβ42) fibril formation and reduces latency and distance to escape in the Morris water maze in a Tg2576 mouse model of Alzheimer's disease.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Pyo, M.K., Lee, Y., and Yun-Choi, H.S. Anti-platelet effect of the constituents isolated from the barks and fruits of Magnolia obovata. Arch. Pharm. Res. 25(3), 325-328 (2002).

    2. Lee, S.-K., Kim, H.-N., Kang, Y.-R., et alObovatol inhibits colorectal cancer growth by inhibiting tumor cell proliferation and inducing apoptosis. Bioorg. Med. Chem. 16(18), 8397-8402 (2008).

    3. Choi, D.-Y., Lee, J.W., Peng, J., et alObovatol improves cognitive functions in animal models for Alzheimer’s disease. J. Neurochem. 120(6), 1048-1059 (2012).