A diacylglycerol
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1,3-Dipalmitoleoyl Glycerol

Item No. 26797

Technical Information
Formal Name
(9Z,9'Z)-9-hexadecenoic acid, 1,1'-(2-hydroxy-1,3-propanediyl) ester
CAS Number
106352-09-4
Synonyms
  • DG(16:1/0:0/16:1)
  • 1,3-Dipalmitolein
Molecular Formula
C35H64O5
Formula Weight
Purity
≥98%
A 10 mg/ml solution in ethanol
DMF: 10 mg/mlEthanol: 10 mg/mlEthanol:PBS (pH 7.2) (1:1): 0.5 mg/ml
SMILES
OC(COC(CCCCCCC/C=C\CCCCCC)=O)COC(CCCCCCC/C=C\CCCCCC)=O
InChi Code
InChI=1S/C35H64O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-31-33(36)32-40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h13-16,33,36H,3-12,17-32H2,1-2H3/b15-13-,16-14-
InChi Key
UUCZIVACHUFMPO-VMNXYWKNSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    1,3-Dipalmitoleoyl glycerol is a diacylglycerol with palmitoleic acid (Item No. 10009871) at the sn-1 and sn-3 positions. It selectively inhibits α-glucosidase from S. cerevisiae over rat enzyme (IC50s = 4.45 and 9,326.5 μM, respectively).1 1,3-Dipalmitoleoyl glycerol has been used in the formation of lipid bilayers to study the effects of membrane composition and the ionophore valinomycin (Item No. 10009152) on membrane potential.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Nguyen, T.H., and Kim, S.M. α-Glucosidase inhibitory activities of fatty acids purified from the internal organ of sea cucumber Stichopus japonicas. J. Food Sci. 80(4), H841-H847 (2015).

    2. Minami, H., Sato, N., Sugawara, M., et alComparative study on the potentiometric responses between a valinomycin-based bilayer lipid membrane and a solvent polymeric membrane. Anal. Sci. 7(6), 853-862 (1991).