| Cat. No. |
Product Name |
Information |
| PC-60184 |
Shield-1
FKBP ligand
|
Shield-1 is a cell-permeable FKBP ligand that is designed to protect an otherwise unstable protein domain from degradation. |
| PC-60177 |
CP-312
HO-1 inducer
|
CP-312 (Cardioprotectant 312) is a small molecule inducer of heme oxygenase-1 (HO-1) that protect human iPSC-derived cardiomyocytes from oxidative stress. |
| PC-60175 |
GIBH-130
|
GIBH-130 is a small molecule inhibitor of neuroinflammation, suppresses the proinflammatory cytokine production in LPS-stimulated N9 microglial cells (IC50=3.4 nM). |
| PC-60169 |
Divin
Iron chelator
|
Divin is a potent chelator of iron that arrests late stages of cytokinesis by blocking the physical process of constriction in dividing cells. |
| PC-60154 |
ENT1-IN-39
ENT1 inhibitor
|
ENT1-IN-39 (ENT-1 inhibitor 39) is a potent adenosine transport activity of equilibrative nucleoside transporter I protein (ENT1) with IC50 of 26.9 nM. |
| PC-70005 |
Gue-1654
OXE-R inhibitor
|
Gue-1654 (GUE 1654) is a small-molecule that inhibits Gβγ but not Gα signaling triggered upon activation of Gα(i)-βγ by the chemoattractant receptor OXE-R (Oxoeicosanoid receptor) in both recombinant and human primary cells. |
| PC-70001 |
C1632
Lin28 inhibitor
|
C1632 (Lin28-IN-1632) is a small molecule inhibitor of RNA binding protein Lin28 that blocks the Lin28/let-7 interaction, rescues let-7 processing and function in Lin28-expressing cancer cells. |
| PC-60090 |
trans-AUCB
sEH inhibitor
|
trans-AUCB is a potent, specific and orally bioavailable soluble epoxide hydrolase (sEH) inhibitor with IC50 of 1.3 nM. |
| PC-45343 |
Adrafinil
|
Adrafinil is the prodrug of modafinil that is a mild central nervous system stimulant drug used to relieve excessive sleepiness and inattention, acts as an alpha-1 adrenoceptor agonist. |
| PC-42914 |
PFK-158
PFKFB3 inhibitor
|
PFK-158 is the first potent, selective and competitive small molecule inhibitor of PFKFB3 with IC50 of 137 nM, inhibits glycolysis, induces apoptosis and autophagy. |
| PC-47499 |
Tat-NR2B9c
PSD-95 inhibitor
|
Tat-NR2B9c (NA-1) is a neuroprotective agent, exhibits high-affinity binding to the second PDZ domain of PSD-95, inhibits NR2A-NR2C/PSD-95 interactions (IC50=1-10 uM) and nNOS/PSD-95 interaction (IC50=200 nM). |
| PC-47496 |
Sincalide
CCK Octapeptide
|
Sincalide (CCK-8) is a 8-amino acid C-terminal fragment of cholecystokinin; stimulates gallbladder contraction, Sincalide is a major bioactive segment of CCK that retains most of the biological activities of CCK. Sincalide can promote gallbladder contraction by injection and helps diagnose gallbladder and pancreas disorders. |
