Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C26H35FO5 |
Molecular Weight | 446.5515 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@H](C)[C@H](C(=O)C(=O)OCCCC)[C@@]1(C)C[C@H](O)[C@@]3([H])[C@@]2([H])C[C@H](F)C4=CC(=O)C=C[C@]34C
InChI
InChIKey=XWTIDFOGTCVGQB-FHIVUSPVSA-N
InChI=1S/C26H35FO5/c1-5-6-9-32-24(31)23(30)21-14(2)10-17-16-12-19(27)18-11-15(28)7-8-25(18,3)22(16)20(29)13-26(17,21)4/h7-8,11,14,16-17,19-22,29H,5-6,9-10,12-13H2,1-4H3/t14-,16+,17+,19+,20+,21-,22-,25+,26+/m1/s1
Fluocortin butyl, a corticosteroid, is available in Germany for nasal application to improve symptoms and signs of perennial rhinitis. This drug is also used in Italy under the brand name Vaspit for the treatment of skin diseases such as dermatitis, eczema, erythema, first-degree burns, and insect bites. Once the cellular environment is reached, the fluocortin butyl induces the expression of protein lipocortin 1, an inhibitor of the enzyme phospholipase A2, an initiator of a cascade of molecular events that leads to the formation of inflammatory mediators such as prostaglandins, and prostacyclins.
Approval Year
PubMed
Title | Date | PubMed |
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[The effect of fluocortin butylester on adrenal function in man (author's transl)]. | 1977 |
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Intranasal fluocortin butyl in patients with perennial rhinitis: a 12-month efficacy and safety study including nasal biopsy. | 1991 Aug |
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Double-blind study of prednicarbate versus fluocortin butyl ester in atopic dermatitis. | 1996 Feb |
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6N7OA9MO7O
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41767-29-7
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C011824
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255-543-8
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25127
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m5453
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C166952
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100000090228
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Fluocortin butyl
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3234
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DTXSID60194590
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15942715
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CHEMBL2105087
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SUB13900MIG
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SUBSTANCE RECORD