<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2971</id>
  <title>T3D2929</title>
  <common-name>Anileridine</common-name>
  <description>Anileridine is a synthetic opioid and strong analgesic medication. It is a narcotic pain reliever used to treat moderate to severe pain. Narcotic analgesics act in the central nervous system (CNS) to relieve pain. Some of their side effects are also caused by actions in the CNS.</description>
  <cas>144-14-9</cas>
  <pubchem-id>8944</pubchem-id>
  <chemical-formula>C22H28N2O2</chemical-formula>
  <weight>352.215080</weight>
  <appearance>White powder.</appearance>
  <melting-point>275-277°C</melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility>1.24e-02 g/L</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Anileridine is absorbed by all routes of administration.</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Opiate receptors are coupled with G-protein receptors and function as both positive and negative regulators of synaptic transmission via G-proteins that activate effector proteins. Binding of the opiate stimulates the exchange of GTP for GDP on the G-protein complex. As the effector system is adenylate cyclase and cAMP located at the inner surface of the plasma membrane, opioids decrease intracellular cAMP by inhibiting adenylate cyclase. Subsequently, the release of nociceptive neurotransmitters such as substance P, GABA, dopamine, acetylcholine and noradrenaline is inhibited. Opioids also inhibit the release of vasopressin, somatostatin, insulin and glucagon. Opioids such as anileridine close N-type voltage-operated calcium channels (OP2-receptor agonist) and open calcium-dependent inwardly rectifying potassium channels (OP3 and OP1 receptor agonist). This results in hyperpolarization and reduced neuronal excitability.</mechanism-of-toxicity>
  <metabolism>Hepatic</metabolism>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>For treatment and management of pain (systemic) and for use as an anesthesia adjunct.</use-source>
  <min-risk-level nil="true"/>
  <health-effects>Medical problems can include congested lungs, liver disease, tetanus, infection of the heart valves, skin abscesses, anemia and pneumonia. Death can occur from overdose.</health-effects>
  <symptoms>Symptoms of overexposure include dizziness, perspiration, a feeling of warmth, dry mouth, visual difficulty, itching, euphoria, restlessness, nervousness and excitement have been reported.</symptoms>
  <treatment nil="true"/>
  <created-at type="dateTime">2009-07-21T20:27:57Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:25:53Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Anileridine</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id></kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>61203</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id>Anileridine</stitch-id>
  <drugbank-id>DB00913</drugbank-id>
  <pdb-id></pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CCOC(=O)C1(CCN(CCC2=CC=C(N)C=C2)CC1)C1=CC=CC=C1</moldb-smiles>
  <moldb-formula>C22H28N2O2</moldb-formula>
  <moldb-inchi>InChI=1S/C22H28N2O2/c1-2-26-21(25)22(19-6-4-3-5-7-19)13-16-24(17-14-22)15-12-18-8-10-20(23)11-9-18/h3-11H,2,12-17,23H2,1H3</moldb-inchi>
  <moldb-inchikey>InChIKey=LKYQLAWMNBFNJT-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">352.4699</moldb-average-mass>
  <moldb-mono-mass type="decimal">352.21507815</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp>3.7</logp>
  <hmdb-id>HMDB15049</hmdb-id>
  <chembl-id>CHEMBL1201347</chembl-id>
  <chemspider-id>8600</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference>&lt;p&gt;Weijlard, J.and Pfister, K., Ill; US. Patent 2,966,490; December 27, 1960; assigned to Merck &amp;amp; Co., Inc.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
