| Cat. No. |
Product Name |
Information |
| PC-20248 |
NV-6297
GLUT-1 inhibitor
|
NV-6297 (NV6297) is a potent, selective mTORC1 pathway signaling inhibitor without inhibition on mTORC2, inhibits S6K1 phosphorylation (pS6K1 T389) in MCF7 cells with IC50 of 120 nM, directly and selectively targets GLUT-1. |
| PC-20247 |
NV-5440
GLUT-1 inhibitor
|
NV-5440 (NV5440) is a potent, selective mTORC1 pathway signaling inhibitor without inhibition on mTORC2, inhibits S6K1 phosphorylation (pS6K1 T389) in MCF7 cells with IC50 of 70 nM, directly targets GLUT-1 with Ki of 69.3 nM. |
| PC-49856 |
GTS467
EAAT2 activator
|
GTS476 (GTS-476) is a potent, selective, orally active activator of EAAT2 with EC50 of 35.1 nM in vitro glutamate uptake assays in COS cells overexpressing EAAT2. |
| PC-49855 |
GT949
EAAT2 activator
|
GT949 (GT-949) is a potent, selective activator (positive allosteric modulator) of EAAT2 with EC50 of 0.26 nM in vitro glutamate uptake assays in COS cells overexpressing EAAT2. |
| PC-49854 |
GTS511
EAAT2 activator
|
GTS511 (GTS-511) is a potent, selective, brain-permeable activator of EAAT2 with EC50 of 3.8 nM in vitro glutamate uptake assays in COS cells overexpressing EAAT2. |
| PC-49853 |
GT951
EAAT2 activator
|
GT951 (GT-951) is a potent, selective activator (positive allosteric modulator) of EAAT2 with EC50 of 0.8 nM in vitro glutamate uptake assays in COS cells overexpressing EAAT2. |
| PC-49277 |
(R)-AS-1
EAAT2 PAM
|
(R)-AS-1 is an orally bioavailable, selective positive allosteric modulator (PAM) of the glutamate transporter EAAT2 with EC50 of 11 nM and Emax of 251%, shows potent antiseizure activity in vivo. |
| PC-72279 |
MC-100093
GLT-1 modulator
|
MC-100093 (MC100093) is a potent, orally bioavailable upregulator of GLT-1 and devoid of antimicrobial properties. |
| PC-36103 |
Troriluzole
Glutamate modulator
|
Trigriluzole (BHV-4157) is a novel glutamate modulator for the treatment of mild-to-moderate Alzheimer’s disease (AD). |
| PC-35512 |
WAY-213613
EAAT2 inhibitor
|
WAY-213613 (WAY213613) is a potent, non-substrate inhibitor of EAAT2 (GLT-1) with IC50 of 85 nM, displays > 44-fold selectivity over EAAT1 and EAAT3. |
| PC-35511 |
NBI-59159
EAAT3 inhibitor
|
NBI-59159 (NBI59159) is a potent EAAT3-preferring inhibitor. |
| PC-62149 |
UCPH-102
EAAT1 inhibitor
|
UCPH-102 is a selective, brain penetrant inhibitor of EAAT1 (Excitatory amino acid transporter 1) with IC50 of 420 nM. |
