Weight | 175.275 g/mol |
---|---|
Formula | C12H17N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
4-Benzylpiperidine (31252-42-3)
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- N-Benzylpiperidine derivatives of 1,2,4-thiadiazolidinone as new acetylcholinesterase inhibitors (European Journal of Medicinal Chemistry, 2000)
- Highly selective, novel analogs of 4-[2-(diphenylmethoxy)ethyl]- 1-benzylpiperidine for the dopamine transporter: effect of different aromatic substitutions on their affinity and selectivity. (Journal of Medicinal Chemistry, 1997)
- Selective Suppression of Cocaine- versus Food-Maintained Responding by Monoamine Releasers in Rhesus Monkeys: Benzylpiperazine, (+)Phenmetrazine, and 4-Benzylpiperidine (Journal of Pharmacology and Experimental Therapeutics, 2009)
- StructureActivity Relationship Studies of 4-[2-(Diphenylmethoxy)ethyl]-1-benzylpiperidine Derivatives and Their N-Analogues: Evaluation of Behavioral Activity of O- and N-Analogues and Their Binding to Monoamine Transporters (Journal of Medicinal Chemistry, 2001)
- Synthesis and structure-activity relationships of 1-aralkyl-4-benzylpiperidine and 1-aralkyl-4-benzylpiperazine derivatives as potent sigma ligands. (Journal of Medicinal Chemistry, 2005)
- Structure-activity relationship studies of highly selective inhibitors of the dopamine transporter: N-benzylpiperidine analogues of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine. (Journal of Medicinal Chemistry, 2003)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNCCC1CC2=CC=CC=C2
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InChIKeyABGXADJDTPFFSZ-UHFFFAOYSA-N
- Pubchem - 4-Benzylpiperidine
- Wikipedia - 4-benzylpiperidine
4-Benzylpiperidine is a drug and research chemical used in scientific studies. It acts as a monoamine releasing agent with 20- to 48-fold selectivity for releasing dopamine versus serotonin. It has a fast onset of action and a short duration.
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