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Fluocinonide

Catalog No. DB01047 Name DrugBank
CAS Number 356-12-7 Website http://www.ualberta.ca/
M. F. C26H32F2O7 Telephone (780) 492-3111
M. W. 494.5248864 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 919

SYNONYMS

IUPAC name
2-[(1S,2S,4R,8S,9S,11S,12R,13S,19S)-12,19-difluoro-11-hydroxy-6,6,9,13-tetramethyl-16-oxo-5,7-dioxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosa-14,17-dien-8-yl]-2-oxoethyl acetate
IUPAC Traditional name
fluocinonide
Brand Name
Biscosal
Lyderm
Straderm
Cortalar
Bestasone
Fluzon
Lidex
Metosyn
Synalar acetate
Topsymin
Vanos
Fluonex
Lonide
Lidex E
Topsyn
Lidex-E
Synonyms
Fluocinolide acetate
Fluocinolone acetonide acetate
fluocinonide
Fluocinolide
Fluocinonide Emulsified Base
Fluocinonide [USAN:BAN:INN:JAN]
Fluocinonido [INN-Spanish]
Fluocinonidum [INN-Latin]

DATABASE IDS

PubChem CID 9642
PubChem SID 46504523
CAS Number 356-12-7

PROPERTIES

Hydrophobicity(logP) 1.9
Solubility 4.74 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved; investigational
Description A topical glucocorticoid used in the treatment of eczema. [PubChem]
Indication A topical anti-inflammatory product for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.
Pharmacology Fluocinonide is a potent glucocorticoid steroid used topically as anti-inflammatory agent for the treatment of skin disorders such as eczema. It relieves itching, redness, dryness, crusting, scaling, inflammation, and discomfort. [Wikipedia]
Toxicity Side effects may include acne-like eruptions, burning, dryness, excessive hair growth, infection of the skin, irritation, itching, lack of skin color, prickly heat, skin inflammation, skin loss or softening, stretch marks
Affected Organisms
Humans and other mammals
Absorption The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. In general, percutaneous absorption is minimal.
Elimination Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys.
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

REFERENCES