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Rotigotine

A non-selective agonist of the dopamine D3 receptor (Ki=0.71 nM) ; has 10-fold selectivity for the D3 receptor over the D2, D4, and D5 receptors and 100-fold selectivity for the D3 receptor over the D1 receptor; behaves as a full agonist of D1, D2, and D3 with similar potencies (EC50) in functional assay; also demonstrates significant affinity at α-adrenergic (α2B, Ki=27 nM) and serotonin receptors (5-HT1A Ki=30 nM) ; significantly attenuates MPTP-induced acute cell degeneration in mouse model.Parkinson's Disease Approved (In Vitro) :Rotigotine (0.01-10 μM) slightly protects dopaminergic neurons against MPP+ toxicity dopamine, protects dopaminergic neurons against rotenone-induced cell death and significantly inhibits ROS production by rotenone. (In Vivo) :Rotigotine (0.1-5 mg/kg; i.h.; for 14 days; male Sprague–Dawley rats) has antidepressant effect.

Product Specifications

CAS Number

99755-59-6

Product Name Alternative

N-0923 | SPM 962

Field of Research

Pharmacology & Drug Discovery

Purity

>98% (HPLC)

Solubility

10 mM in DMSO

Smiles

CCCN (CCC1=CC=CS1) C2CCC3=C (C2) C=CC=C3O

Molecular Formula

C19H25NOS

Molecular Weight

315.4729

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

1-Naphthalenol, 5,6,7,8-tetrahydro-6-[propyl[2- (2-thienyl) ethyl]amino]-, (6S) -

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