Motretinide

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Structural formula
Structure of motretinide
General
Non-proprietary name Motretinide
other names

all- trans - N -ethyl-9- (4-methoxy-2,3,6-trimethylphenyl) -3,7-dimethyl-2,4,6,8-nonatetraenamide ( IUPAC )

Molecular formula C 23 H 31 NO 2
External identifiers / databases
CAS number 56281-36-8
EC number 260-094-6
ECHA InfoCard 100.054.613
PubChem 6314185
ChemSpider 4880635
Wikidata Q904009
Drug information
ATC code

D10 AD05

Drug class

mono aromatic retinoid

properties
Molar mass 353.51 g · mol -1
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Motretinide [trade name: Tasmaderm ® (CH)] is a retinoid second generation (monoaromatic retinoids).

operation area

Motretinide is used as a pharmaceutical active ingredient and is used topically as an effective component of creams and solutions in the treatment of acne and other hyperkeratotic skin diseases . The drug is only approved in Switzerland .

effect

Motretinide 0.1% was found to be 0.05% more effective against inflammatory lesions than tretinoin , but not against comedolysis . Overall, it is rated as less effective. The formulation used has good skin tolerance.

Side effects

In the first few weeks of therapy, there may be temporary irritation of the skin and, in very rare cases, deterioration of the skin condition.

Interactions

Other external skin preparations should only be used concurrently with motretinide preparations after medical advice. The combined use of several topical acne medicines can cause dryness and irritation of the skin.

pregnancy and breast feeding period

Animal studies have shown undesirable effects on the fetus after systemic application of motretinide . There are no controlled human studies. Systemic uptake with topical application of the active ingredient is estimated at a maximum of 1%. Since the safety of topical application during pregnancy has not been systematically investigated, preparations containing motretinide should not be administered during pregnancy or if the patient wishes to have children. In addition, it is not known whether motretinide is excreted in breast milk. Use during breastfeeding is not recommended.

Individual evidence

  1. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  2. Zouboulis CC .: Modern Acne Therapy In: Akt Dermatol 2003; 29: 49-57. Georg Thieme Publishing House. Full text (PDF; 116 kB).
  3. Orfanos CE, Garbe C: 16.3.1 Effect on follicular hyperkeratosis In: Therapy of Skin Diseases , p. 383; 2nd edition, Springer 2002. ISBN 3-540-41366-9 .