Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C13H17NO2 |
Molecular Weight | 219.2796 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](C(O)=O)C1=CC=C(NCC(C)=C)C=C1
InChI
InChIKey=FPHLBGOJWPEVME-SNVBAGLBSA-N
InChI=1S/C13H17NO2/c1-9(2)8-14-12-6-4-11(5-7-12)10(3)13(15)16/h4-7,10,14H,1,8H2,2-3H3,(H,15,16)/t10-/m1/s1
Molecular Formula | C13H17NO2 |
Molecular Weight | 219.2796 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/9933032Curator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/2787705
Sources: http://www.ncbi.nlm.nih.gov/pubmed/9933032
Curator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/2787705
Alminoprofen is a nonsteroidal anti-inflammatory drug (NSAID) of the phenylpropionic acid class. It has anti-inflammatory properties different from the classical NSAID. Alminoprofen possesses both antiphospholipase A2 (PLA2) activity and anti-cycloxygenase (COX) activity.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL230 Sources: http://www.ncbi.nlm.nih.gov/pubmed/9933032 |
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Target ID: Secretory phospholipase A2, Homo sapiens Sources: http://www.ncbi.nlm.nih.gov/pubmed/9933032 |
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Target ID: CHEMBL221 Sources: http://www.genome.jp/dbget-bin/www_bget?D01513 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: http://www.ndrugs.com/?s=minalfen |
Palliative | Minalfen Approved UseIndications: inflammation, pain |
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Sources: http://www.ndrugs.com/?s=minalfen |
Primary | Minalfen Approved UseIndications: inflammation, pain |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/1491485
In rheumatoid arthritis and spondylosis deformans - 200 mg (three times a day) repeated dose for 5 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/1783328
Alminoprofen (10(-6)-10(-4) M) inhibited dose-dependently the chemotaxis of leukocytes induced by chemotactic factors from guinea pig neutrophils stimulated with sodium urate crystals.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:51:16 GMT 2023
by
admin
on
Sat Dec 16 10:51:16 GMT 2023
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Record UNII |
4820D59WLM
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |