Structure via PubChem · Public domain (PubChem)
properidine
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Properidine is an opioid, an analgesic, and the isopropyl analog of pethidine. Properidine is under international control and is listed in the United States under the Controlled Substances Act (1970) as a Schedule I substance. It is a narcotic, with an Administrative Controlled Substances Code Number (ACSCN) of 9644 and a 2 gramme annual aggregate manufacturing quota as of 2014. The salt in use is hydrochloride, with a free base conversion ratio of 0.88.
In the Vinony graph
Vinony's link graph records 14 inbound references to properidine, and connects out to (+)-catechin, butorphanol and opium.
It sits within the topics 4-Phenylpiperidines, Carboxylate esters and Chemical pages without DrugBank identifier.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C16H23NO2
- Molecular weight
- 261.36 g/mol
- IUPAC name
- propan-2-yl 1-methyl-4-phenylpiperidine-4-carboxylate
- SMILES
- CC(C)OC(=O)C1(CCN(CC1)C)C2=CC=CC=C2
- InChIKey
- XJKQCILVUHXVIQ-UHFFFAOYSA-N
- XLogP
- 2.9
- Polar surface area
- 29.5 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 261.173
Show 2 more facts
- chemical formula
- C₁₆H₂₃NO₂
- canonical SMILES
- CC(C)OC(=O)C1(CCN(CC1)C)C2=CC=CC=C2
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Properidine is an opioid, an analgesic, and the isopropyl analog of pethidine. Properidine is under international control and is listed in the United States under the Controlled Substances Act (1970) as a Schedule I substance. It is a narcotic, with an Administrative Controlled Substances Code Number (ACSCN) of 9644 and a 2 gramme annual aggregate manufacturing quota as of 2014. The salt in use is hydrochloride, with a free base conversion ratio of 0.88.
==References==
Excerpted from Wikipedia’s “properidine” article, available under the CC BY-SA 4.0 licence.