CHEBI:247956 - cinchocaine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name cinchocaine ChEBI ID CHEBI:247956 Definition A monocarboxylic acid amide that is the 2-(diethylamino)ethyl amide of 2-butoxyquinoline-4-carboxylic acid. One of the most potent and toxic of the long-acting local anesthetics, its parenteral use was restricted to spinal anesthesia. It is now generally only used (usually as the hydrochloride) in creams and ointments and in suppositories for temporary relief of pain and itching associated with skin and anorectal conditions. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:4500 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C20H29N3O2 Net Charge 0 Average Mass 343.46320 Monoisotopic Mass 343.22598 InChI InChI=1S/C20H29N3O2/c1-4-7-14-25-19-15-17(16-10-8-9-11-18(16)22-19)20(24)21-12-13-23(5-2)6-3/h8-11,15H,4-7,12-14H2,1-3H3,(H,21,24) InChIKey PUFQVTATUTYEAL-UHFFFAOYSA-N SMILES CCCCOc1cc(C(=O)NCCN(CC)CC)c2ccccc2n1 Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Application(s): topical anaesthetic A local anesthetic that is used to numb the surface of a body part. View more via ChEBI Ontology ChEBI Ontology Outgoing cinchocaine (CHEBI:247956) has role topical anaesthetic (CHEBI:48425) cinchocaine (CHEBI:247956) is a aromatic ether (CHEBI:35618) cinchocaine (CHEBI:247956) is a monocarboxylic acid amide (CHEBI:29347) cinchocaine (CHEBI:247956) is a tertiary amino compound (CHEBI:50996) Incoming cinchocaine hydrochloride (CHEBI:59735) has part cinchocaine (CHEBI:247956) IUPAC Name 2-butoxy-N-[2-(diethylamino)ethyl]quinoline-4-carboxamide INNs Sources cinchocaine ChEBI cinchocainum ChemIDplus cincocainio ChemIDplus Synonyms Sources 2-butoxy-N-(2-(diethylamino)ethyl)cinchoninamide ChemIDplus 2-butoxy-N-(α-diethylaminoethyl)cinchoninamide ChemIDplus 2-butoxy-N-(β-diethylaminoethyl)cinchoninamide NIST Chemistry WebBook 2-butoxy-N-[2-(diethylamino)ethyl]-4-quinolinecarboxamide NIST Chemistry WebBook 2-Butoxy-quinoline-4-carboxylic acid (2-diethylamino-ethyl)-amide ChEMBL 2-butoxyquinoline-4-carboxylic acid diethylaminoethylamide ChemIDplus 2-N-butoxy-N-(2-diethylaminoethyl)cinchoninamide ChemIDplus α-butyloxycinchonic acid-γ-diethylethylenediamine ChemIDplus α-butyloxycinchoninic acid diethylethylenediamide NIST Chemistry WebBook α-butyloxycinchoninic acid diethylethylenediamide ChemIDplus CINCHOCAINE ChEMBL Dibucaine KEGG COMPOUND DIBUCAINE ChEMBL dibucaine ChEMBL dibucaine base ChemIDplus N-(2-(diethylamino)ethyl)-2-butoxycinchoninamide ChemIDplus Manual Xrefs Databases 859 DrugCentral C07879 KEGG COMPOUND D00733 KEGG DRUG DB00527 DrugBank Dibucaine Wikipedia HMDB0014668 HMDB LSM-6018 LINCS US1825623 Patent View more database links Registry Numbers Types Sources 275489 Reaxys Registry Number Reaxys 85-79-0 CAS Registry Number KEGG COMPOUND 85-79-0 CAS Registry Number NIST Chemistry WebBook 85-79-0 CAS Registry Number ChemIDplus Citations Types Sources 23953476 PubMed citation Europe PMC 2873227 PubMed citation Europe PMC Last Modified 22 February 2017