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Bidisomide

HCID 59798
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
116078-65-0
Standard SMILES
CC(=O)N(CCC(CCN1CCCCC1)(C(N)=O)c1ccccc1Cl)C(C)C
InChIKey
GTEPPJFJSNSNIH-UHFFFAOYSA-N
Molecular formula
C22H34ClN3O2
Average molar mass
408 g/mol
Monoisotopic mass
407.233955

Overview

Bidisomide is a member of acetamides.

Names & identifiers

Preferred name
Bidisomide
IUPAC
2-[2-[acetyl(propan-2-yl)amino]ethyl]-2-(2-chlorophenyl)-4-piperidin-1-ylbutanamide
English name
Bidisomide
Molecular formula
C22H34ClN3O2
Molecular weight
407.97726

Names & synonyms

BIDISOMIDE116078-65-0BidisomidaSC-40230BidisomidumSC 402302X3Z153A4ODTXSID60869599alpha-(2-(acetyl(1-methylethyl)amino)ethyl)-alpha-(2-chlorophenyl)-1-piperidinebutanamidealpha-[2-[acetyl(1-methylethyl)amino]ethyl]-alpha-(2-chlorophenyl)-1-piperidinebutanamideRefChem:917175DTXCID70817561
Show more names
Brn 6536016Bidisomide, 10 mM in DMSO(αR)-α-[2-(Acetylisopropylamino)ethyl]-α-(2-chlorophenyl)-1-piperidinebutanamide(αS)-α-[2-(Acetylisopropylamino)ethyl]-α-(2-chlorophenyl)-1-piperidinebutanamide
103810-45-32-[2-[acetyl(propan-2-yl)amino]ethyl]-2-(2-chlorophenyl)-4-piperidin-1-ylbutanamideSC40230Bidisomide (+-)-Bidisomide [USAN:INN]Bidisomidum [INN-Latin]Bidisomida [INN-Spanish]C22H34ClN3O2

Database identifiers

CAS
116078-65-0
PubChem CID
59798

Properties

Computed structural properties

XLogP
3.1
Topological polar surface area
66.6 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
9
Heavy atoms
28
Formal charge
0
Complexity
522

Physicochemical properties

Melting point
140 · 140-141°
storage temp.
-20 °C · Store at -20°C
solubility
Soluble in DMSO
form
Solid
color
Off-white to light yellow
FDA UNII
2 X3Z153A4O · 2X3Z153A4O

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 1 item

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.

Applications

UsesCardiac depressant (anti-arrhythmic).

Suppliers11 total

Aladdin Scientific[email protected]
北京博奥森生物技术有限公司400-901-9800 18611424007 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
上海陶术生物科技股份有限公司

Related reactions

3 records
New reaction record
HRID 1647546 reaction equation
HRID 1647546As reactantuspto-grants-1995_07
HRID 1647548 reaction equation
HRID 1647548As productuspto-grants-1995_07
HRID 1647554 reaction equation
HRID 1647554As productuspto-grants-1995_07

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
DTXSID
DTXSID60869599
ChEMBL
CHEMBL305745
ChEBI
CHEBI:135658
UNII
2X3Z153A4O
Nikkaji
J444.068D
+1-781-999-5354 · [email protected]
北京新研汇医药研发有限公司13969155946 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]

Additional notes

DefinitionChEBI: Bidisomide is a member of acetamides.