Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C16H24FNO |
Molecular Weight | 265.3663 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCN(CCC)[C@@H]1CCC2=C(F)C=CC(O)=C2C1
InChI
InChIKey=FNKBVTBXFLSTPB-GFCCVEGCSA-N
InChI=1S/C16H24FNO/c1-3-9-18(10-4-2)12-5-6-13-14(11-12)16(19)8-7-15(13)17/h7-8,12,19H,3-6,9-11H2,1-2H3/t12-/m1/s1
Molecular Formula | C16H24FNO |
Molecular Weight | 265.3663 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/19837141
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19837141
R(+)-UH-301 is a potent and selective 5-HT1A serotonin receptor agonist and works as an antinociceptive agent. In the experiments on rats were shown, that R(+)-UH-301 significantly decrease formalin-induced flinching.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P08908 Gene ID: 3350.0 Gene Symbol: HTR1A Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/19837141 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19837141
in rats: 0.1-3 microg/paw
Route of Administration:
Other
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:55:17 GMT 2023
by
admin
on
Sat Dec 16 10:55:17 GMT 2023
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Record UNII |
44B1597K8X
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Record Status |
Validated (UNII)
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Record Version |
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admin on Sat Dec 16 10:55:18 GMT 2023 , Edited by admin on Sat Dec 16 10:55:18 GMT 2023
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