| Cat. No. |
Product Name |
Information |
| PC-73160 |
ALC-0315
Vaccine adjuvant
|
ALC-0315 is a synthetic ionizable amino lipid that has been used in combination with other lipids in the formation of lipid nanoparticles, has attracted attention as a component of the SARS-CoV-2 vaccine. |
| PC-73159 |
JHU37160
DREADD agonist
|
JHU37160 a high affinity, highly potent, BBB penetrant activator (agonist) of hM3Dq and hM4Di DREADDs with Ki 1.9 nM and 3.6 nM for hM3Dq and hM4Di in vitro. |
| PC-73158 |
JHU37152
DREADD agonist
|
JHU37152 is a high affinity and highly potent activator (agonist) of hM3Dq and hM4Di DREADDs with Ki 1.8 nM and 8.7 nM for hM3Dq and hM4Di in vitro. |
| PC-73151 |
Eptifibatide
|
Eptifibatide Integrilin is a synthetic homodetic cyclic peptide, inhibits platelet aggregation by selectively blocking the platelet glycoprotein IIb/IIIa receptor. |
| PC-73150 |
Eptifibatide acetate
|
Eptifibatide acetate is a synthetic homodetic cyclic peptide, inhibits platelet aggregation by selectively blocking the platelet glycoprotein IIb/IIIa receptor. |
| PC-73146 |
FR 901463
|
FR 901463 is an anti-tumor agent isolated from the fermentation broth of Pseudomonas sp. No. 2663. |
| PC-73143 |
MCU-i11
MCU inhibitor
|
MCU-i11 is a specific MICU1 targeting compound that negative modulate mitochondrial Ca2+ uptake. |
| PC-73142 |
MCU-i4
MICU1 inhibitor
|
MCU-i4 is a specific MICU1 targeting compound that negative modulate mitochondrial Ca2+ uptake. |
| PC-73135 |
PGAM1 inhibitor KH3
PGAM1 inhibitor
|
PGAM1 inhibitor KH3 is a potent, allosteric small molecule inhibitor of phosphoglycerate mutase 1 (PGAM1) with IC50 of 105 nM. |
| PC-73134 |
Synucleozid
α-synuclein inhibitor
|
Synucleozid (NSC 377363) is a small molecule that targets the IRE structure and inhibits SNCA gene translation in cells, directly targets the α-synuclein mRNA 5'UTR at the designed site. |
| PC-73123 |
CU-76
cGAS inhibitor
|
CU-76 (cGAS inhibitor CU-76) is a small-molecule human cGAS (hcGAS) inhibitor with IC50 of 0.24 uM. |
| PC-73115 |
AZD9898
LTC4S inhibitor
|
AZD9898 (AZD-9898) is a highly potent, selective and oral inhibitor of leukotriene C4 synthase (LTC4S) with IC50 of 0.28 nM. |
