Cyclopentylamine is a cyclic secondary amine with a cyclopentane ring. It is a colorless liquid with a pungent odor. Cyclopentylamine is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a catalyst in various chemical reactions. Cyclopentylamine has been shown to have antidepressant and anti-anxiety effects in animal studies. However, it is not currently used as a medication for these conditions in humans. Cyclopentylamine is a relatively simple compound, but its properties make it an important building block for the synthesis of more complex molecules. It is also a useful model system for studying the properties of amines. Cyclopentylamine is studied for its potential applications in various fields, including organic synthesis, pharmaceutical chemistry, and materials science.'
| ID Source | ID |
|---|---|
| PubMed CID | 2906 |
| CHEMBL ID | 1171859 |
| MeSH ID | M0066266 |
| Synonym |
|---|
| unii-4259vry3gn |
| 4259vry3gn , |
| 4-12-00-00004 (beilstein handbook reference) |
| ec 213-697-3 |
| 1003-03-8 |
| nsc32389 |
| nsc-32389 |
| cyclopentanamine |
| cyclopentylamine |
| brn 0635706 |
| einecs 213-697-3 |
| nsc 32389 |
| aminocyclopentane |
| cb 1689 |
| nisgsntvmoosjq-uhfffaoysa- |
| inchi=1/c5h11n/c6-5-3-1-2-4-5/h5h,1-4,6h2 |
| cyclopentylamine, 99% |
| CHEMBL1171859 |
| AKOS000119393 |
| BP-11379 |
| FT-0624266 |
| 1-cyclopentylamine |
| cyclo-pentyl amine |
| cyclopentyl-amine |
| n-cyclopentylamine |
| cyclopentyl amine |
| 1-amino cyclopentane |
| amino cyclopentane |
| cylcopentylamine |
| DTXSID4061387 |
| W-108970 |
| mfcd00001380 |
| F2190-0380 |
| Q8457765 |
| EN300-20348 |
| STL196759 |
| BBL036999 |
| AMY3757 |
| Assay ID | Title | Year | Journal | Article |
|---|---|---|---|---|
| AID1081643 | Phytotoxicity against Echinochloa crus-galli (barnyard grass) assessed as mortality measured after 3 days at 5 mg/ml by foliar spraying | 2010 | Journal of agricultural and food chemistry, Sep-22, Volume: 58, Issue:18 | Phytotoxicity of sarmentine isolated from long pepper (Piper longum) fruit. |
| AID489224 | Binding affinity to Influenza A Weybridge(H7N7) virus Matrix protein 2 by spectrophotometry | 2010 | Bioorganic & medicinal chemistry letters, Jul-15, Volume: 20, Issue:14 | Interaction of aminoadamantane derivatives with the influenza A virus M2 channel-docking using a pore blocking model. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||||
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|---|---|
| pre-1990 | 1 (12.50) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.
| This Compound (40.79) All Compounds (24.57) |
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 11 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||