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Nisoxetine

HCID 4500
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
53179-07-0
Standard SMILES
CNCCC(Oc1ccccc1OC)c1ccccc1
InChIKey
ITJNARMNRKSWTA-UHFFFAOYSA-N
Molecular formula
C17H21NO2
Average molar mass
271.35 g/mol
Monoisotopic mass
271.15722891

Overview

Nisoxetine is a secondary amino compound that is N-methyl-3-phenylpropan-1-amine substituted at position 3 by a 2-methoxyphenoxy group. It has a role as an antidepressant and an adrenergic uptake inhibitor. It is an aromatic ether and a secondary amino compound.

Names & identifiers

Preferred name
Nisoxetine
IUPAC
3-(2-methoxyphenoxy)-N-methyl-3-phenylpropan-1-amine
English name
nisoxetine
Molecular formula
C17H21NO2
Molecular weight
271.35414

Names & synonyms

Nisoxetine53179-07-03-(2-methoxyphenoxy)-N-methyl-3-phenylpropan-1-amineNisoxetinaCompound 89218Nisoxetinum3-(2-Methoxyphenoxy)-N-methyl-3-phenylpropylamineDTXSID0045175COMPOUND-89218NSC-28348117NV064B2DDL-N-Methyl-3-(o-methoxyphenoxy)-N-methyl-3-phenylpropylamine
Show more names
3-(o-Methoxyphenoxy)-N-methyl-3-phenylpropylamineN-Methyl-gamma-(2-methylphenoxy)phenylpropanolamineDTXCID8025175CHEBI:73410LY 94939RefChem:85420657226-61-6CHEMBL295467

Database identifiers

CAS
53179-07-0、57226-61-6
PubChem CID
4500
DTXSID
DTXSID0045175
ChEMBL
CHEMBL295467
ChEBI
CHEBI:73410
UNII
17NV064B2D

Properties

Computed structural properties

XLogP
3.1
Topological polar surface area
30.5 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
7
Heavy atoms
20
Formal charge
0
Complexity
253

Experimental & physicochemical properties

Chemical ClassesOther Uses -> Biochemical Research

Chemistry & industry

Uses & manufacturing

UsesPotent inhibitor for norepinephrine uptake into rat brain synaptosomes & brain. [ChemIDplus]

Suppliers14 total

沈阳中申泽康生物医学技术研究有限公司024-88590548 18698872706 · [email protected]
成都超九八生物科技有限公司13348960310 13348960310 · [email protected]
BOC Sciences1-631-485-4226; 16314854226 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
武汉壹加壹生物科技有限公司027-027-16602739303 16602739303 · [email protected]
杭州六可生物科技有限公司+86-0571-86912261 +86-15658003402 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
上海芮晖化工科技有限公司021-31433387 15618786686 · [email protected]
上海超岚化工科技中心QQ:65489617 13301690235 · [email protected]
ATK CHEMICAL COMPANY LIMITED+undefined-21-51877795 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]

Related reactions

8 records
New reaction record
HRID 328999 reaction equation
HRID 328999As productuspto-grants-1977_04
HRID 329000 reaction equation
HRID 329000As productuspto-grants-1977_04
HRID 1248850 reaction equation
HRID 1248850As productuspto-grants-1986_12
HRID 1248851 reaction equation
HRID 1248851As productuspto-grants-1986_12
HRID 1446929 reaction equation
HRID 1446929As productuspto-grants-1982_02
HRID 1446930 reaction equation
HRID 1446930As productuspto-grants-1982_02
HRID 1701555 reaction equation
HRID 1701555As productuspto-grants-1980_03
HRID 1701556 reaction equation
HRID 1701556As productuspto-grants-1980_03

Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
上海传芊化工科技中心15869524721 · [email protected]
常州辰鸿生物科技有限公司+86-0519-85788828 +86-13775037613 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Nisoxetine is a secondary amino compound that is N-methyl-3-phenylpropan-1-amine substituted at position 3 by a 2-methoxyphenoxy group. It has a role as an antidepressant and an adrenergic uptake inhibitor. It is an aromatic ether and a secondary amino compound.