Cat. No. |
Product Name |
Information |
PC-20034 |
FFN200
Fluorescent false neurotransmitter
|
FFN200 is a vesicular monoamine transporter 2 (VMAT2) substrate, and the first probe to selectively trace monoamine exocytosis in both neuronal cell culture and brain tissue. |
PC-49497 |
SRI-20041
DAT inhibitor
|
SRI-20041 is a small molecule allosteric dopamine transporter ligand. |
PC-49495 |
SRI-32743
DAT inhibitor
|
SRI-32743 is a novel allosteric modulator of dopamine transporter (DAT), attenuates HIV-1 Tat protein-induced inhibition of the dopamine transporter. |
PC-38458 |
Nisoxetine hydrochloride
SNRI
|
Nisoxetine Hcl is a highly selective and potent noradrenaline reuptake inhibitor (SNRI) with high affinity for the NET (0.7 nM), shows potential antidepressant effect. |
PC-73425 |
lafadofensine
Monoamines reuptake inhibitor
|
Lafadofensine is a small molecule monoamines reuptake inhibitor with antidepressant activity. |
PC-36099 |
Serdexmethylphenidate
|
Serdexmethylphenidate is the dextrorotary form of methylphenidate and a norepinephrine-dopamine reuptake inhibitor (NDRI) and thus a psychostimulant.. |
PC-35618 |
SRI-31142
|
SRI-31142 (SRI31142) is a novel potent, putative allosteric dopamine transporter (DAT) inhibitor with Ki of 1.9 nM.. |
PC-35476 |
CTDP-32476
|
CTDP-32476 is a potent and selective dopamine transporter (DAT) inhibitor and a competitive inhibitor of cocaine binding to the DAT with Ki of 12 nM. |
PC-35438 |
Ampreloxetine
|
Ampreloxetine (TD-9855) is a potent monoamine reuptake inhibitor with pIC50 of 8.0, 8.6 and 6.8 for human NET, SERT, and DAT, respectively. |
PC-63567 |
AMR-2
|
AMR-2 is a highly potent, orally active, triple reuptake inhibitor of SERT, NET, and DAT with IC50 of 3.0, 3.1, and 8.3 nM, respectively. |
PC-43400 |
Vanoxerine
|
Vanoxerine (GBR-12909, I-893, Boxeprazine) is a highly potent inhibitor of dopamine uptake in vitro in tissue slices obtained from rat neostriatum with IC50 of 40-50 nM, also inhibits norepinephrine uptake with IC50 of 560-2600 nM. |
PC-43399 |
Vanoxerine dihydrochloride
|
Vanoxerine (GBR-12909, I-893) is a highly potent inhibitor of dopamine uptake in vitro in tissue slices obtained from rat neostriatum with IC50 of 40-50 nM, also inhibits norepinephrine uptake with IC50 of 560-2600 nM. |