Details
Stereochemistry | ACHIRAL |
Molecular Formula | C24H30O2S |
Molecular Weight | 382.559 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C\C(=C/C1=CC=C(C=C1)S(C)(=O)=O)C2=CC3=C(C=C2)C(C)(C)CCC3(C)C
InChI
InChIKey=AUCWKKVIBKHRED-BMRADRMJSA-N
InChI=1S/C24H30O2S/c1-17(15-18-7-10-20(11-8-18)27(6,25)26)19-9-12-21-22(16-19)24(4,5)14-13-23(21,2)3/h7-12,15-16H,13-14H2,1-6H3/b17-15+
Molecular Formula | C24H30O2S |
Molecular Weight | 382.559 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Sumarotene (also known as Ro 14-9706) is a third-generation retinoid developed by Hoffmann-La Roche, F., und Co. A.-G., as a topical dermatologic agent for the repair of photodamage, antikeratinization, and antiproliferation. Sumarotene shows activity in standard preclinical and pharmacologic models of repair of photodamage, antikeratinization, and antiproliferation. In clinical trials, Sumarotene effectively decreases the number of actinic keratoses. Sumarotene is well-tolerated and most patients have only slight or absent local inflammation.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2061443
twice daily for 16 weeks as a 0.05% cream
Route of Administration:
Topical
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:46:55 GMT 2023
by
admin
on
Fri Dec 15 15:46:55 GMT 2023
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Record UNII |
8896RX4S4J
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Record Status |
Validated (UNII)
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NCI_THESAURUS |
C938
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SUB10769MIG
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8896RX4S4J
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6738
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CHEMBL2105526
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C74431
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CC-38
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6436127
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C069613
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Related Record | Type | Details | ||
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ACTIVE MOIETY |