| Cat. No. |
Product Name |
Information |
| PC-42915 |
PFK15
PFKFB3 inhibitor
|
PFK15 (PFK 015) is a potent, selective 6-phosphofructo-2-kinase (PFKFB3) inhibitor with IC50 of 207 nM against recombinant human PFKFB3, displays 100-fold more activity than 3PO. |
| PC-42360 |
γ-Glu-Phe
|
γ-Glu-Phe (γ-Glutamylphenylalanine) is a γ-glutamyl dipeptide.. |
| PC-42359 |
Coproporphyrin III
|
Coproporphyrin III is a diffusible small molecule porphyrin excreted by human-associated Propionibacterium spp., induces Staphylococcus aureus aggregation and biofilm formation, also induces S. aureus to form a plasma-independent surface-attached biofilm. |
| PC-42350 |
TPPU
sHE inhibitor
|
TPPU is a potent soluble epoxide hydrolase (sHE) inhibitor with IC50 of 37 nM and 3.7 nM for monkey and human sHE, respectively. |
| PC-42367 |
Thyroxine sulfate
|
Thyroxine sulfate (T4 Sulfate) is a major Thyroid hormone metabolite secreted by follicular cells of the Thyroid gland, T4 is involved in controlling the rate of metabolic processes in the body and influencing physical development, a prohormone and a reservoir for the active thyroid hormone triiodothyronine (T3). |
| PC-63179 |
TRIF agonist AV-C
TRIF agonist
|
TRIF agonist AV-C is a novel TRIF pathway agonist that activates innate and interferon-associated responses, strongly inhibits replication of ZIKV, CHIKV, and DENV (IC90~5 uM). |
| PC-63145 |
Verdiperstat
MPO inhibitor
|
Verdiperstat (AZD3241) is a potent, selective, reversible, orally active myeloperoxidase (MPO) inhibitor with IC50 of 630 nM, >14-fold selectivity over thyroid peroxidase (TPO). |
| PC-63120 |
MIF-IN-3bb
MIF inhibitor
|
MIF-IN-3bb is a potent inhibitor of Migration inhibitory factor (MIF) tautomerase activity with Ki of 57 nM. |
| PC-63119 |
Orita-13
MIF inhibitor
|
Orita-13 is potent inhibitor of Migration inhibitory factor (MIF) tautomerase activity with Ki of 17 uM. |
| PC-63118 |
ISO-66
MIF inhibitor
|
ISO-66 is a novel, highly stable, small-molecule MIF inhibitor that inhibits MIF tautomerase activity with IC50 of 1.4 uM. |
| PC-63112 |
(R)-CE3F4
EPAC1 inhibitor
|
(R)-CE3F4 is a more potent, selective EPAC1 antagonist than the racemic CE3F4 and (S)-CE3F4, displays 10-fold selectivity for EPAC1 over EPAC2. |
| PC-63111 |
CE3F4
EPAC1 inhibitor
|
CE3F4 is a potent, noncompetitive EPAC1 inhibitor that blocks EPAC1-induced Rap1 activation both in cell-free systems and in intact cells and did not influence protein kinase A holoenzyme activity. |
