A synthetic corticosteroid
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Fluocinolone acetonide

Item No. 23027

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
6α,9-difluoro-11β,21-dihydroxy-16α,17-[(1-methylethylidene)bis(oxy)]-pregna-1,4-diene-3,20-dione
CAS Number
67-73-2
Synonyms
  • NSC 92339
Molecular Formula
C24H30F2O6
Formula Weight
452.5
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 20 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5 mg/mlEthanol: 5 mg/ml
λmax
239 nm
SMILES
O=C1C=C[C@@]2(C)C([C@@H](F)C[C@]3([H])[C@]2(F)[C@@H](O)C[C@@]4(C)[C@@]3([H])C[C@]5([H])[C@@]4(C(CO)=O)OC(C)(C)O5)=C1
InChi Code
InChI=1S/C24H30F2O6/c1-20(2)31-19-9-13-14-8-16(25)15-7-12(28)5-6-21(15,3)23(14,26)17(29)10-22(13,4)24(19,32-20)18(30)11-27/h5-7,13-14,16-17,19,27,29H,8-11H2,1-4H3/t13-,14-,16-,17-,19+,21-,22-,23-,24+/m0/s1
InChi Key
FEBLZLNTKCEFIT-VSXGLTOVSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    500 mg

    $117

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    1 g

    $218

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    5 g

    $627

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    Product Description

    Fluocinolone acetonide is a synthetic fluorinated corticosteroid that acts as a glucocorticoid receptor agonist (IC50 = 2.0 nM in a radioligand binding assay).1 It increases transcriptional activity of the glucocorticoid receptor in HeLa cells (EC50 = 0.7 nM). It inhibits VEGF secretion in a dose-dependent manner and decreases TNF-α-induced angiogenesis in a chick chorioallantoic membrane assay.2 Formulations containing fluocinolone acetonide have been used for the treatment of various skin, eye, ear, and nose conditions to reduce inflammation.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Nehmé, A., Lobenhofer, E.K., Stamer, W.D., et al. Glucocorticoids with different chemical structures but similar glucocorticoid receptor potency regulate subsets of common and unique genes in human trabecular meshwork cells. BMC Med. Genomics. 2, 58 (2009).

    2. Ayalasomayajula, S.P., Ashton, P., and Kompella, U.B. Fluocinolone inhibits VEGF expression via glucocorticoid receptor in human retinal pigment epithelial (ARPE-19) cells and TNF-α-induced angiogenesis in chick chorioallantoic membrane (CAM. J. Ocul. Pharmacol. Ther. 25(2), 97-103 (2009).