Home - Products - GPCR/G Protein - Dopamine Receptor - SPD-473 citrate

SPD-473 citrate

CAS No. 161190-26-7

SPD-473 citrate( —— )

Catalog No. M33235 CAS No. 161190-26-7

SPD-473 citrate (BTS 74398 citrate) is a dopamine reuptake inhibitor, a norepinephrine transporter protein (NET) inhibitor.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
2MG	375	Get Quote
5MG	588	Get Quote
10MG	825	Get Quote
25MG	1279	Get Quote
50MG	1720	Get Quote
100MG	2277	Get Quote
500MG	Get Quote	Get Quote
1G	Get Quote	Get Quote

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

SPD-473 citrate
Note

Research use only, not for human use.
Brief Description

SPD-473 citrate (BTS 74398 citrate) is a dopamine reuptake inhibitor, a norepinephrine transporter protein (NET) inhibitor.
Description

SPD-473 citrate is a serotonin/dopamine/norepinephrine reuptake inhibitior.
In Vitro

SPD-473 inhibits the synaptic reuptake of dopamine, serotonin and noradrenaline, making it a triple reuptake inhibitor potentially for the treatment of Parkinson's Disease.
In Vivo

——
Synonyms

——
Pathway

GPCR/G Protein
Target

Dopamine Receptor
Recptor

Dopamine Receptor | 5-HT Receptor | Norepinephrine
Research Area

——
Indication

——

Chemical Information

CAS Number

161190-26-7
Formula Weight

552.47
Molecular Formula

C23H31Cl2NO8S
Purity

>98% (HPLC)
Solubility

——
SMILES

O=C(O)CC(O)(C(=O)O)CC(=O)O.O=C(CSCCCN(C)C)C1(C2=CC=C(Cl)C(Cl)=C2)CCC1
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

Raclopride

Raclopride is a selective antagonist of dopamine D2/D3 receptor.
Octopamine hydrochlo...

Octopamine (OA), a biogenic monoamine structurally related to noradrenaline.
Dehydroevodiamine

Dehydroevodiamine, a constituent of Evodia rutaecarpa, has various biological effects such as hypotensive, negative chronotropic, ion channel depressant, inhibition of nitric oxide production and cerebral blood flow enhancing activities.

Sign In Join Free