Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H32O6 |
Molecular Weight | 416.5073 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@]3([H])[C@]4([H])CCC5=CC(=O)C=C[C@]5(C)[C@@]4([H])[C@@H](O)C[C@]3(C)[C@@]1(OC(C)(C)O2)C(=O)CO
InChI
InChIKey=WBGKWQHBNHJJPZ-LECWWXJVSA-N
InChI=1S/C24H32O6/c1-21(2)29-19-10-16-15-6-5-13-9-14(26)7-8-22(13,3)20(15)17(27)11-23(16,4)24(19,30-21)18(28)12-25/h7-9,15-17,19-20,25,27H,5-6,10-12H2,1-4H3/t15-,16-,17-,19+,20+,22-,23-,24+/m0/s1
Molecular Formula | C24H32O6 |
Molecular Weight | 416.5073 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 8 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | DESONIDE Approved UseDesonide Ointment, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. It should not be used for longer than two weeks unless directed by a physician. Launch Date1972 |
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Primary | DESONIDE Approved UseDesonide Cream, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. Launch Date1972 |
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Primary | DESONIDE Approved UseDesonide Cream, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. Launch Date1972 |
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Primary | DESONIDE Approved UseDesonide Cream, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. Launch Date1972 |
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Primary | DESONIDE Approved UseDesonide Cream, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. Launch Date1972 |
Doses
Dose | Population | Adverse events |
---|---|---|
0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.3 |
unhealthy n = 425 Health Status: unhealthy Condition: Atopic dermatitis Population Size: 425 Sources: Page: p.3 |
Disc. AE: Telangiectasia... AEs leading to discontinuation/dose reduction: Telangiectasia Sources: Page: p.3 |
0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Disc. AE: Cushing's syndrome, Hypothalamic pituitary adrenal axis suppression... AEs leading to discontinuation/dose reduction: Cushing's syndrome Sources: Page: p.1Hypothalamic pituitary adrenal axis suppression Atrophy Striae Irritation skin Acneiform eruption Skin hypopigmentation Allergic contact dermatitis |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Telangiectasia | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.3 |
unhealthy n = 425 Health Status: unhealthy Condition: Atopic dermatitis Population Size: 425 Sources: Page: p.3 |
Acneiform eruption | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Allergic contact dermatitis | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Atrophy | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Cushing's syndrome | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Hypothalamic pituitary adrenal axis suppression | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Irritation skin | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Skin hypopigmentation | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Striae | Disc. AE | 0.05 % 2 times / day multiple, topical Recommended Dose: 0.05 %, 2 times / day Route: topical Route: multiple Dose: 0.05 %, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Atopic dermatitis Sources: Page: p.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
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Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 4,8 |
yes | yes (co-administration study) Comment: Concomitant oral administration of ketoconazole (a known inhibitor of CYP3A4 activity in the liver and in the intestinal mucosa) caused an eight-fold increase of the systemic exposure to oral budesonide. If treatment with inhibitors of CYP3A4 activity (such as ketoconazole, intraconazole, ritonavir, indinavir, saquinavir, erythromycin, etc.) is indicated, reduction of the budesonide dose should be considered Page: 4,8 |
PubMed
Title | Date | PubMed |
---|---|---|
Clinical comparison of alclometasone dipropionate and desonide ointments (0.05%) in the management of psoriasis. | 1982 |
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Allergic contact dermatitis from topical corticosteroids. | 1989 Aug |
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Efficacy, cutaneous tolerance and cosmetic acceptability of desonide 0.05% lotion (Desowen) versus vehicle in the short-term treatment of facial atopic or seborrhoeic dermatitis. | 2002 Aug |
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Two case reports of cutaneous adverse reactions following hepatitis B vaccine: lichen planus and granuloma annulare. | 2004 Sep |
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Photochemistry of desonide, a non-fluorinated steroidal anti-inflammatory drug. | 2006 Jun |
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Effect of desonide hydrogel 0.05% on the hypothalamic-pituitary-adrenal axis in pediatric subjects with moderate to severe atopic dermatitis. | 2007 May-Jun |
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Corticosteroid therapy in the treatment of pediatric patients with atopic dermatitis. | 2007 Sep 20 |
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Desonide gel. | 2007 Sep-Oct |
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What's your assessment? Severe seborrheic dermatitis. | 2008 Dec |
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Adverse cutaneous drug reaction. | 2008 Jan |
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Desonide foam: a review. | 2008 Jan |
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A simple and rapid ESI-LC-MS/MS method for simultaneous screening of doping agents in urine samples. | 2009 Apr |
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Fixed drug eruption induced by atenolol. | 2009 Apr 24 |
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Rhabdomyomatous mesenchymal hamartoma: clinical overview and report of a case with spontaneous regression. | 2009 Dec |
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Treatment of scalp and facial seborrheic dermatitis with desonide hydrogel 0.05%. | 2009 Feb |
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Vitiligo after diphencyprone for alopecia areata. | 2010 |
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Lenalidomide-induced acute acneiform folliculitis of the head and neck: not only the anti-EGF receptor agents. | 2010 |
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Good adherence and early efficacy using desonide hydrogel for atopic dermatitis: results from a program addressing patient compliance. | 2010 Apr |
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Generic sample preparation combined with high-resolution liquid chromatography-time-of-flight mass spectrometry for unification of urine screening in doping-control laboratories. | 2010 Apr |
|
Update on the management of chronic eczema: new approaches and emerging treatment options. | 2010 Jul 28 |
|
Pediatric atopic dermatitis: a review of the medical management. | 2010 Sep |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:13:42 GMT 2023
by
admin
on
Fri Dec 15 15:13:42 GMT 2023
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Record UNII |
J280872D1O
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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WHO-ATC |
S01BA11
Created by
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NDF-RT |
N0000175450
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WHO-VATC |
QS01BA11
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WHO-ATC |
D07BB02
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WHO-VATC |
QD07BB02
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WHO-ATC |
D07AB08
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WHO-VATC |
QD07AB08
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NDF-RT |
N0000175576
Created by
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NCI_THESAURUS |
C521
Created by
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Code System | Code | Type | Description | ||
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DTXSID7046756
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638-94-8
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PRIMARY | |||
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CHEMBL1201109
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PRIMARY | |||
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7066
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PRIMARY | |||
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204734
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PRIMARY | |||
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DESONIDE
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PRIMARY | |||
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3135
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2889
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DB01260
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211-351-6
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Desonide
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PRIMARY | |||
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5311066
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D003898
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1173304
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SUB07005MIG
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PRIMARY | |||
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100000083192
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PRIMARY | |||
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3254
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PRIMARY | RxNorm | ||
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J280872D1O
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C61702
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m4199
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PRIMARY | Merck Index | ||
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J280872D1O
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759226
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
This impurity is to be reported under total unspecified impurities. Do not report it under total specified impurities.
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
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|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
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|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |