Prolintane
Basic information
- CAS
493-92-5- Standard SMILES
CCCC(Cc1ccccc1)N1CCCC1- InChIKey
OJCPSBCUMRIPFL-UHFFFAOYSA-N- Molecular formula
- C15H23N
- Average molar mass
- 217.35 g/mol
- Monoisotopic mass
- 217.18304974
Overview
Prolintane is a member of amphetamines.
Names & identifiers
- Preferred name
- Prolintane
- IUPAC
- 1-(1-phenylpentan-2-yl)pyrrolidine
- English name
- prolintane
- Molecular formula
- C15H23N
- Molecular weight
- 217.35
Names & synonyms
ProlintaneProlintan493-92-51-(1-phenylpentan-2-yl)pyrrolidine1-Phenyl-2-pyrrolidinylpentaneProlintanoProlintanum1-(alpha-Propylphenethyl)pyrrolidinePyrrolidine, 1-(1-benzylbutyl)-Pyrrolidine, 1-(1-(phenylmethyl)butyl)-EM4YZW677HPyrrolidine, 1-[1-(phenylmethyl)butyl]-
Show more names
Brn 0144260Prolintan-d8Prolintane-d8Einecs 207-784-5Prolintane [inn:ban]Phenylpyrrolidinopentane-d8
phenylpyrrolidinylpentanRefChem:868592N06BX14207-784-5Phenylpyrrolidinopentane1-(1-Benzylbutyl)pyrrolidineCatovit1-(.alpha.-Propylphenethyl)pyrrolidine
Database identifiers
- CAS
493-92-5- PubChem CID
- 14592
- DTXSID
DTXSID70862031- ChEMBL
CHEMBL2111047- ChEBI
CHEBI:134898- UNII
- EM4YZW677H
- EC Number
- 207-784-5
- Nikkaji
- J6.074G
Properties
Computed structural properties
- XLogP
- 4
- Topological polar surface area
- 3.2 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 5
- Heavy atoms
- 16
- Formal charge
- 0
- Complexity
- 178
Experimental & physicochemical properties
DrugsPharmaceuticals
Human DrugsPharmaceuticals
Boiling Point153 °C
Physical DescriptionSolid
Physicochemical properties
- Boiling point
- 0.5 · bp0.5 105°; bp16 153°
- Density
- 0.963 · 0.963±0.06 g/cm3(Predicted)
- solubility
- Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
- pka
- 10.62 · 10.62±0.20(Predicted)
- form
- Oil
- color
- Colourless
- FDA UNII
- 4 YZW677H · EM4YZW677H
- ATC code
- 6 BX14 · N06BX14
Chemistry & industry
Pharmacology
ATC Code
N - Nervous system
QN - Nervous system
MeSH Pharmacological Classification
A loosely defined group of drugs that tend to increase behavioral alertness, agitation, or excitation. They work by a variety of mechanisms, but usually not by direct excitation of neurons. The many drugs that have such actions as side effects to their main therapeutic use are not included here.
Cellular LocationsMembrane
Uses & manufacturing
UsesUse (kg; approx.) in Germany (2009): >100
Use ClassificationPharmaceuticals
Applications
UsesLabelled Prolintane. Prolintane is a CNS stiumlant used as an analeptic drug. Prolintane acts as a norepinephrine-dopamine reuptake inhibitor.
Additional notes
DefinitionChEBI: Prolintane is a member of amphetamines.
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