Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H25N3O2 |
| Molecular Weight | 387.4742 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C(NC1CCN(CC2=CC3=C(C=CC=C3)C=C2)CC1)NC(=O)C4=CC=CC=C4
InChI
InChIKey=AQFFJGJVFJCQQL-UHFFFAOYSA-N
InChI=1S/C24H25N3O2/c28-23(20-7-2-1-3-8-20)26-24(29)25-22-12-14-27(15-13-22)17-18-10-11-19-6-4-5-9-21(19)16-18/h1-11,16,22H,12-15,17H2,(H2,25,26,28,29)
| Molecular Formula | C24H25N3O2 |
| Molecular Weight | 387.4742 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6514142
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6514142
Panuramine, a selective inhibitor of uptake of 5-hydroxytryptamine that was studied as an antidepressant, however, has never been marketed.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P31652 Gene ID: 25553.0 Gene Symbol: Slc6a4 Target Organism: Rattus norvegicus (Rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/6514142 |
22.0 nM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Examination of the relationship between the uptake site for 5-hydroxytryptamine and the high affinity binding site for [3H]imipramine. II. The role of sodium ions. | 1987-08 |
|
| Panuramine, a selective inhibitor of uptake of 5-hydroxytryptamine in the brain of the rat. | 1984-09 |
Patents
| Substance Class |
Chemical
Created
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1UWS3T8EAB
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C265
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100000082769
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5335
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Panuramine
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1UWS3T8EAB
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SUB09609MIG
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C66305
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80349-58-2
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C043858
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CHEMBL2105324
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DTXSID30230257
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ACTIVE MOIETY |