A pyrrolizidine alkaloid
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Australine (hydrochloride)

Item No. 30051

Technical Information
Formal Name
(1R,2R,3R,7S,7aR)-hexahydro-3-(hydroxymethyl)-1H-pyrrolizine-1,2,7-triol, monohydrochloride
CAS Number
186766-07-4
Synonyms
  • 7a-epi-Alexine
  • (+)-Australine
Molecular Formula
C8H15NO4 • HCl
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
Water: 20 mg/ml
SMILES
OC[C@@H]1[C@@H](O)[C@H](O)[C@]2([H])N1CC[C@@H]2O.Cl
InChi Code
InChI=1S/C8H15NO4.ClH/c10-3-4-7(12)8(13)6-5(11)1-2-9(4)6;/h4-8,10-13H,1-3H2;1H/t4-,5+,6-,7-,8-;/m1./s1
InChi Key
VGFORKADSOHYJT-XFAJBIDRSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Australine is a pyrrolizidine alkaloid originally isolated from C. australe that has enzyme inhibitory activities.1,2,3 It is an inhibitor of glucoamylase (IC50 = 5.8 µM) that also inhibits glucosidase I, sucrase, maltase, and A. niger α-glucosidase (IC50s = 20, 28, 35, and 28 µM, respectively).2,3 Australine is selective for these enzymes over glucosidase II, α- and β-mannosidase, and α- and β-galactosidase up to 500 µM, β-glucosidase, with only 5% inhibition at 66 µM, as well as isomaltase and trehalase (IC50 = 97 and 160 µM, respectively). Australine (500 µg/ml) inhibits glycoprotein processing of viral glycoproteins in influenza virus-infected MDCK cells and induces the accumulation of glycoproteins.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Molyneux, R.J., Benson, M., Wong, R.Y., et alAustraline, a novel pyrrolizidine alkaloid glucosidase inhibitor from Castanospermum austral. J. Nat. Prod. 51(6), 1198-1206 (1988).

    2. Tropea, J.E., Molyneux, R.J., Kaushal, G.P., et alAustraline, a pyrrolizidine alkaloid that inhibits amyloglucosidase and glycoprotein processing. Biochemistry 28(5), 2027-2034 (1989).

    3. Kato, A., Kano, E., Adachi, I., et alAustraline and related alkaloids: easy structural confirmation by 13C NMR spectral data and biological activities. Tetrahedron Asymmetry 14(3), 325-331 (2003).