A diterpene with diverse biological activities
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Deacetylforskolin

Item No. 11701

Technical Information
Formal Name
(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-3-ethenyldodecahydro-5,6,10,10b-tetrahydroxy-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-1-one
CAS Number
64657-20-1
Synonyms
  • 7-Deactylcoleonol
  • Forskolin D
Molecular Formula
C20H32O6
Formula Weight
Purity
≥98%
Formulation
A solid
Chloroform: slightly solubleChloroform: Slightly SolubleMethanol: Slightly SolubleMethanol: slightly soluble
SMILES
O=C1C[C@](C)(C=C)O[C@]2(C)[C@@H](O)[C@@H](O)[C@@]3([H])C(C)(C)CC[C@H](O)[C@]3(C)[C@]21O
InChi Code
InChI=1S/C20H32O6/c1-7-17(4)10-12(22)20(25)18(5)11(21)8-9-16(2,3)14(18)13(23)15(24)19(20,6)26-17/h7,11,13-15,21,23-25H,1,8-10H2,2-6H3/t11-,13-,14-,15-,17-,18-,19+,20-/m0/s1
InChi Key
WPDITXOBNLYZHH-KAACEJSMSA-N
Origin
Plant/Coleus forskohlii
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Deacetylforskolin is a diterpene and a derivative of forskolin (Item No. 11018) that has been found in C. forskohlii and has diverse biological activities.1,2,3,4 It activates rat adipocyte adenylyl cyclase (IC50 = 20 µM) and inhibits glucose transport in rat adipocyte plasma membranes.2 Deactylforskolin (30-1,000 µg/kg) reduces blood pressure in spontaneously hypertensive rats.3 It also attenuates hypercapnia-induced impairments in the passive avoidance response in mice.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Gabetta, B., Zini, G., and Danieli, B. Minor Diterpenoids of Coleus forskohlii. Phytochemistry 28(3), 859-862 (1989).

    2. Joost, H.G., Habberfield, A.D., Simpson, I.A., et alActivation of adenylate cyclase and inhibition of glucose transport in rat adipocytes by forskolin analogues: structural determinants for distinct sites of action. Mol. Pharmacol. 33(4), 449-453 (1988).

    3. Bhat, S.V., Dohadwalla, A.N., Bajwa, B.S., et alThe antihypertensive and positive inotropic diterpene forskolin: Effects of structural modifications on its activity. J. Med. Chem. 26(4), 486-492 (1983).

    4. McCulloch, A.J., Thomson, T.A., and Deacon, R. Hypoxic amnesia and its reversal with forskolin. Biochem. Soc. Trans. 17(1), 212-213 (1988).