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Forskolin

Forskolin is a cell-permeable diterpene that directly activates adenylyl cyclase, for the maintenance and reprogramming of stem cells.

Grouped product items
SKUSIZEPRICE QTY
SML19B10 mg
$75.00
- +
SML19BC50 mg
$295.00
- +
Details
Resources
Reviews
Description
Specifications
More Information
SKUSML19-CT
Molecular NameForskolin
Size10 mg (cat. no. SML19B) or 50 mg (cat. no. SML19C)
FormPowder
Alternative NamesColeonol; Colforsin, Coleonol; HL 362; L 75-1362B; NSC 357088; NSC 375489
Chemical Name1H-Naphtho[2,1-b]pyran-1-one, 5-(acetyloxy)-3-ethenyldodecahydro-6,10,10b-trihydroxy3,4a,7,7,10a-pentamethyl-, (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-
Chemical FormulaC22H34O7
Molecular Weight410.50
CAS Number66575-29-92
PubChem ID8709105
Purity≥98% by HPLC
Physical AppearanceWhite to off-white (Solid)
TargetAdenylate Cyclase; FXR; Autophagy
Shelf-Life≥ 2 years (powder)
ShippingRoom Temperature
StorageStore at 2-8°C
Quality StatementThis product is for Research Use Only and is not intended for therapeutic or diagnostic use.

Forskolin is a cell permeable activator and has been used to potentiate neuron differentiation as well as maintain human ES cells in a naïve or ground state. Forskolin induces differentiation of various cell types and activates pregnane X receptor (PXR) and FXR. Forskolin exerts an inotropic effect on the heart, has platelet antiaggregatory and antihypertensive actions. and also induces autophagy.

Forskolin has been shown to enable chemical reprogramming of mouse embryonic fibroblasts to iPS cells in combination with CHIR99021 (SML01B), Tranylcypromine, Valproic Acid, 3-Deazaneplanocin A, and RepSox. (SML06B).

Applications
  • Neural stem and progenitor cell, neurons, pluripotent stem cells, neuronal differentiation, reprogramming of fibroblasts, iPSCs
  • Maintenance, Reprogramming
Resources
References and Publications
  • Fang, Jun, et al. 2021. Chemical cocktail activates stem cells, promotes repair after muscle damage. Nat Biomed Eng.
  • Robbins JD, et al. 1996. Forskolin carbamates: binding and activation studies with type I adenylyl cyclase. J Med Chem. 39(14):2745-52.
  • Matsumiya W, et al. 2012. Forskolin modifies retinal vascular development in Mrp4-knockout mice. Invest Ophthalmol Vis Sci. 53(13):8029-35.
  • Mayati A, et al. 2018. Functional polarization of human hepatoma HepaRG cells in response to forskolin. Sci Rep. 8(1):16115.
  • Awad JA, et al. 1983. Interactions of forskolin and adenylate cyclase. Effects on substrate kinetics and protection against inactivation by heat and N-ethylmaleimide. J Biol Chem. 258(5):2960-5.
  • Seamon KB, et al. 1983. Structure-activity relationships for activation of adenylate cyclase by the diterpene forskolin and its derivatives. J Med Chem. (3):436-9.
  • Hou, P., et al. 2013. Pluripotent stem cells induced from mouse somatic cells by small-molecule compounds. Science 341: 651-654.
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