HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
Huagongshe Open Program:[email protected]AI access: llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.7.8
  1. Home
  2. /Compound

Bumecaine

HCID 65770
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
30103-44-7
Standard SMILES
CCCCN1CCCC1C(=O)Nc1c(C)cc(C)cc1C
InChIKey
VEPZOLKTNZOTTQ-UHFFFAOYSA-N
Molecular formula
C18H28N2O
Average molar mass
288.4 g/mol
Monoisotopic mass
288.22016352

Overview

RN given refers to parent cpd; structure

Names & identifiers

Preferred name
Bumecaine
IUPAC
1-butyl-N-(2,4,6-trimethylphenyl)pyrrolidine-2-carboxamide
English name
Bumecaine
Molecular formula
C18H28N2O
Molecular weight
288.43

Names & synonyms

BumecaineBumecainBumecainaBumecaine [INN]BumecainumPyromekainBumecainum [INN-Latin]Bumecaina [INN-Spanish]DTXSID4046109UNII-B77K612SPZB77K612SPZ2-Pyrrolidinecarboxanilide, 1-butyl-2',4',6'-trimethyl-
Show more names
2,4,6-Trimethylanylide-1-butylpyrrolidinecarbonoic 2-acid1-butyl-N-(2,4,6-trimethylphenyl)pyrrolidine-2-carboxamide1-Butyl-N-(2,4,6-trimethylphenyl)-2-pyrrolidinecarboxamide
DTXCID20261092-Pyrrolidinecarboxamide, 1-butyl-N-(2,4,6-trimethylphenyl)-pirromecainepyrromecainBumecainum (INN-Latin)Bumecaina (INN-Spanish)pyromecaine-collagenN-butyl-alpha-pyrrolidine carbonic acid mesidine

Database identifiers

CAS
30103-44-7
PubChem CID
65770
DTXSID
DTXSID4046109
ChEMBL
CHEMBL1870919
UNII
B77K612SPZ
Nikkaji
J20.257F

Properties

Computed structural properties

XLogP
3.4
Topological polar surface area
32.3 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
2
Rotatable bonds
5
Heavy atoms
21
Formal charge
0
Complexity
332

Physicochemical properties

Boiling point
416.6 · 416.6±45.0 °C(Predicted)
Density
1.038 · 1.038±0.06 g/cm3(Predicted)
pka
14.29 · 14.29±0.70(Predicted)
FDA UNII
77 K612SPZ · B77K612SPZ

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 2 items

Drugs that block nerve conduction when applied locally to nerve tissue in appropriate concentrations. They act on any part of the nervous system and on every type of nerve fiber. In contact with a nerve trunk, these anesthetics can cause both sensory and motor paralysis in the innervated area. Their action is completely reversible. (From Gilman AG, et. al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed) Nearly all local anesthetics act by reducing the tendency of voltage-dependent sodium channels to activate.

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.

Suppliers3 total

Lanospharma Laboratories Co.,Ltd13440048448 · [email protected]
Shanghai New Union Textra Import & Export Co., Ltd.[email protected]
CHEMICAL LAND21[email protected]

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes