An anthraquinone glycoside with diverse biological activities
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Pulmatin

Item No. 36343

Technical Information
Formal Name
8-(β-D-glucopyranosyloxy)-1-hydroxy-3-methyl-9,10-anthracenedione
CAS Number
13241-28-6
Synonyms
  • Chrysophanol 8-O-glucoside
  • Chrysophanol 8-O-β-D-glucopyranoside
Molecular Formula
C21H20O9
Formula Weight
Purity
≥98%
Formulation
A solid
SMILES
O=C(C1=CC(C)=CC(O)=C12)C3=CC=CC(O[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)=C3C2=O
InChi Code
InChI=1S/C21H20O9/c1-8-5-10-14(11(23)6-8)18(26)15-9(16(10)24)3-2-4-12(15)29-21-20(28)19(27)17(25)13(7-22)30-21/h2-6,13,17,19-23,25,27-28H,7H2,1H3/t13-,17-,19+,20-,21-/m1/s1
InChi Key
WMMOMSNMMDMSRB-JNHRPPPUSA-N
Origin
Plant/Rheum emodi
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Pulmatin is an anthraquinone glycoside that has been found in R. emodi and has diverse biological activities.1,2,3 It inhibits protein tyrosine phosphatase 1B (PTP1B; IC50 = 18.34 µM) and yeast and rat intestinal α-glucosidase when used at a concentration of 50 µg/ml.1,2 Pulmatin (25 µM) increases insulin-induced glucose transport by 255% in L6 myotubes.1 It lowers plasma levels of total cholesterol, phospholipids, LDL, VLDL, and triglycerides in a rat model of Triton WR-1339-induced dyslipidemia when administered at a dose of 100 mg/kg.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Lee, M.S., and Sohn, C.B. Anti-diabetic properties of chrysophanol and its glucoside from rhubarb rhizome. Biol. Pharm. Bull. 31(11), 2154-2157 (2008).

    2. Babu, K.S., Tiwari, A.K., Srinivas, P.V., et alYeast and mammalian a-glucosidase inhibitory constituents from Himalayan rhubarb Rheum emodi Wall.ex Meisson. Bioorg. Med. Chem. Lett. 14(14), 3841-3845 (2004).

    3. Mishra, S.K., Tiwari, S., Shrivastava, A., et alAntidyslipidemic effect and antioxidant activity of anthraquinone derivatives from Rheum emodi rhizomes in dyslipidemic rats. J. Nat. Med. 68(2), 363-371 (2014).