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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

Associated Targets(non-human)

SARS-CoV-2 (38078 Activities)

Discover Target:

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

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]

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