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Reboxetine - 98%, high purity , CAS No.71620-89-8, Inhibitor of NET

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Reboxetine - 98%, high purity , CAS No.71620-89-8, Inhibitor of NET

Moligand™

≥98%

CAS#: 71620-89-8
Formula: C₁₉H₂₃NO₃
Molecular Weight: 313.39
PubChem CID: 127151

Item Number

R304469

Grouped product items
SKU	Size	Availability	Price	Qty
R304469-500mg	500mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$2,524.90

View related series

NET Inhibitor

Basic Description

Synonyms	Reboxetine \| 71620-89-8 \| 98769-81-4 \| Reboxetine [INN] \| 105017-38-7 \| (2R)-2-[(R)-(2-ethoxyphenoxy)-phenylmethyl]morpholine \| 947S0YZ36I \| Reboxetine (INN) \| Norebox \| (2r)-2-[(R)-(2-Ethoxyphenoxy)(Phenyl)methyl]morpholine \| Reboxitine \| Morpholine, 2-[(R)-(2-ethoxyphenoxy)p
Specifications & Purity	Moligand™, ≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice
Grade	Moligand™
Action Type	INHIBITOR
Mechanism of action	Inhibitor of NET

Associated Targets(Human)

SLC6A2 Tclin Sodium-dependent noradrenaline transporter (3 Activities)

Discover Target: SLC6A2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter (0 Activities)

Discover Target: SLC6A4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

Discover Target: SLC6A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CACNA2D1 Tclin Voltage-gated calcium channel alpha2/delta subunit 1 (266 Activities)

Discover Target: CACNA2D1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CACNA2D2 Tclin Voltage-gated calcium channel alpha2/delta subunit 2 (37 Activities)

Discover Target: CACNA2D2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	(2R)-2-[(R)-(2-ethoxyphenoxy)-phenylmethyl]morpholine
INCHI	InChI=1S/C19H23NO3/c1-2-21-16-10-6-7-11-17(16)23-19(15-8-4-3-5-9-15)18-14-20-12-13-22-18/h3-11,18-20H,2,12-14H2,1H3/t18-,19-/m1/s1
InChi Key	CBQGYUDMJHNJBX-RTBURBONSA-N
Canonical SMILES	CCOC1=CC=CC=C1OC(C2CNCCO2)C3=CC=CC=C3
Isomeric SMILES	CCOC1=CC=CC=C1O[C@@H]([C@H]2CNCCO2)C3=CC=CC=C3
PubChem CID	127151
Molecular Weight	313.39

Database links

DrugBank Ligand	DB00234
Wikipedia	Reboxetine
CAS Registry No.	71620-89-8
PubChem CID	65856
ChEMBL Ligand	CHEMBL180101
ChEBI	CHEBI:114263
PEP	reboxetine

Certificates

Certificate of Analysis(COA)

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References

1. Kobayashi T, Washiyama K, Ikeda K. (2010) Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine.. Neuropsychopharmacology, 35 (7): (1560-9). [PMID:20393461] [10.1021/op500134e]

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