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Apr 2, 2013 · The present study describes the synthesis of three substituted 1- (1-phenylcyclohexyl)piperidines, (3-MeO-, 4-MeO- and 3-Me-PCP) and three substituted 1- (1-phenylcyclohexyl)pyrrolidine analogues (3-MeO-, 4-MeO- and 3-Me-PCPy).
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- Identification
- Pharmacology
- Interactions
- Chemical Identifiers
- Pharmacoeconomics
- Properties
Generic Name
1. 1-Phenylcyclohexylamine
DrugBank Accession Number
1. DB01506
Background
1. Not Available
Indication
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Contraindications & Blackbox Warnings
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Pharmacodynamics
1. Not Available
Drug Interactions information
1. This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist. Not Available
Food Interactions
1. Not Available
UNII
1. HBO2D49I2S
CAS number
1. 2201-24-3
InChI Key
1. RGZGRPPQZUQUCR-UHFFFAOYSA-N
Manufacturers
1. Not Available
Packagers
1. Not Available
Dosage Forms
1. Not Available
People also ask
Why do arylcyclohexamines cause misperception?
How many substituted 1 phenylcyclohexyl pyrrolidine analogues are there?
When was phencyclidine discovered?
What was the first arylcyclohexamine?
Jan 1, 2016 · The underlying mechanism of the emergence phenomena caused by arylcyclohexamines appears to be due to their depressive effects on visual and auditory relay nuclei in the medial geniculate and inferior colliculus, respectively, leading to misperception and/or misinterpretation of visual and auditory stimuli [287, 288].
The reaction of phenylcyclohexene with hydrogen cyanide in strongly acidic media for 2 hr. yielded a fornianiide which on acid hydrolysis produced an amine hydro- chloride whose spectral data and analysis were in agree- ment with structure IIc (Ar = phenyl).
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Phencyclidine. A.C. Puran, ... T.J. Wiegand, in Encyclopedia of Toxicology (Third Edition), 2014. Toxicokinetics. Phencyclidine, or 1-(1-phenylcyclohexyl) piperidine, is synthesized from piperidine and cyclohexanone. It is a highly lipid-soluble solid that is soluble in both water and alcohol.
Phencyclidine (PCP) is a synthetic arylcycloalkylamine discovered in 1926. It was eventually patented in 1952 by the Parke-Davis pharmaceutical company and marketed under the brand name Sernyl (referring to serenity) for use as a nonnarcotic anesthetic.
N-Phenylcyclohexylamine. Formula: C 12 H 17 N. Molecular weight: 175.2701. IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11 (8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2. Copy Sheet of paper on top of another sheet.
