R11216 |
Exenatide Acetate;A-1155463 |
N/A
|
R11217 |
Furanylfentanyl |
N/A
|
R11219 |
TA 01 |
TA-01 is a potent CK1 and p38 MAPK inhibitor, with IC50s of 6.4 nM, 6.8 nM, 6.7
|
R11220 |
TA 02;TA-02 |
TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. IC50 value: 20 nM Target: p38
|
R11221 |
M2I-1 |
M2I-1 is a Mad2 inhibitor targeting the binding of Mad2 to Cdc20, an essential p
|
R11223 |
Ym-443 |
N/A
|
R11227 |
ZM241385 |
ZM241385 is a potent, high affinity and selective adenosine A2a receptor (A2AR)
|
R11232 |
NA. |
N/A
|
R11233 |
CPI203 |
CPI-203 is a novel potent, selective and cell permeable inhibitor of BET bromodo
|
R11235 |
Imatinib Mesylate; STI571 Mesylate; CGP-57148B Mesylate |
Imatinib Mesylate (STI571 Mesylate) is a tyrosine kinases inhibitor that inhibit
|
R11237 |
Pemetrexed disodium heptahydrate |
N/A
|
R11239 |
AZ505 |
N/A
|
R11241 |
PJ34 hydrochloride |
PJ34 hydrochloride is an inhibitor of PARP1/2 with IC50 of 110 nM and 86 nM, res
|
R11242 |
NS-1619 |
NS-1619 is a selective large conductance Ca2+-activated K+-channel activator.
|
R11244 |
Indiplon |
Indiplon is a potent GABAA receptor positive allosteric modulator that acts at t
|
R11245 |
Alda 1;Alda-1 |
Alda-1 is a potent ALDH2 agonist, which activates wild-type ALDH2 and restores n
|
R11248 |
Dimethoxycurcumin |
N/A
|
R11252 |
Adjudin(AF-2364) |
Adjudin is an extensively studied male contraceptive with a superior mitoch
|
R11253 |
PFK-015 |
PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFK
|
R11254 |
Pirinixic acid (Wy-14643) |
Pirinixic acid (Wy-14643) is a potent agonist of PPARα, with EC50s of 0.63 μM, 3
|
R11255 |
Dacinostat; NVP-LAQ824 |
Dacinostat is a potent HDAC inhibitor, with an IC50 of 32 nM; Dacinostat also in
|
R11257 |
Lorediplon |
Lorediplon is a novel non-benzodiazepine, hypnotic drug acting as a GABAA recept
|
R11259 |
L67;DNA Ligase Inhibitor |
L67 is a novel, competitive human DNA ligase inhibitor, inhibits DNA ligases I a
|
R11260 |
NS-398 |
N/A
|
R11261 |
Ritalin |
N/A
|