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| Product | Description | |
|---|---|---|
| Vanoxerine | Vanoxerine is a is a potent and selective DRI acts to block cardiac ion channels. Uses: Dat1 antagonist. Synonyms: 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine; GBR-12909; I-893. Grades: ≥98%. CAS No. 67469-69-6. Molecular formula: C28H32F2N2O. Mole weight: 450.56. |  |
| Vanoxerine dihydrochloride | Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) is a competitive, potent, and highly selective dopamine reuptake inhibitor ( K i =1 nM). Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) binds to the target site on the dopamine transporter (DAT) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GBR-12909 dihydrochloride; I893 dihydrochloride. CAS No. 67469-78-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-13217. |  |
| Vanoxerine dihydroChloride | Vanoxerine is a is a potent and selective DRI acts to block cardiac ion channels. Uses: Dat1 antagonist. Synonyms: GBR 12909 Dihydrochloride; GBR12909 Dihydrochloride; GBR-12909 Dihydrochloride; 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine; dihydrochloride. Grades: ≥98%. CAS No. 67469-78-7. Molecular formula: C28H34Cl2F2N2O. Mole weight: 523.49. | |
| GBR 12909 Dihydrochloride | A potent inhibitor of dopamine active transporter (DAT, Ki=1nM, IC50=40 and 51nM) with >100 fold selectivity over noradrenalin and 5-HT re-uptake transporter. Shown to produce behavioral profile in mice for bipolar mania disease model and ADHD disease models. Group: Biochemicals. Alternative Names: 1-[2-[Bis (4-fluorophenyl) methoxy]ethyl]-4- (3-phenylpropyl) -piperazine Dihydrochloride (9CI); GBR 12909; I 893; Vanoxerine Dihydrochloride; 1-[2-[Bis (4-fluorophenyl) methoxy]ethyl]-4- (3-phenylpropyl) -piperazine Hydrochloride (1:2). Grades: Highly Purified. CAS No. 67469-78-7. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C??H??F?N?O 2HCl, Molecular Weight: 450.56 (anhydrous). US Biological Life Sciences. |  Worldwide |
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