| Cat. No. |
Product Name |
Information |
| PC-63231 |
TJ191
|
TJ191 is a selective anti-cancer small molecule that targets low TβRIII-expressing malignant T-cell leukemia/lymphoma cells (MOLT-3 IC50=0.26 uM). |
| PC-63220 |
VUT-MK142
|
VUT-MK142 is a cardiomyogenic small molecule promoting the differentiation of pre-cardiac mesoderm into cardiomyocytes, shows superior cardiomyogenic activity over cardiogenol C. |
| PC-43111 |
Thiamet G
|
Thiamet-G is a potent, selective O-GlcNAcase inhibitor with Ki of 21 nM for human O-GlcNAcase, blocks phosphorylation of tau both in vitro and in vivo. |
| PC-43102 |
Sermorelin
|
Sermorelin is a peptide analogue of growth hormone-releasing hormone (GHRH) which is used as a diagnostic agent to assess growth hormone (GH) secretion for the purpose of diagnosing growth hormone deficiency.. |
| PC-42996 |
FH1
|
FH1 (BRDK4477) is a small molecule that increase function and proliferation of primary human hepatocytes, promotes the differentiation of iPS-derived hepatocytes. |
| PC-42932 |
XEN445
|
XEN445 is a potent, selective endothelial lipase (EL) inhibitor with IC50 of 237 nM, displays no significant activity against lipoprotein lipase (LPL) and hepatic lipase (HL) (IC50=20 and 9.5 uM). |
| PC-42360 |
γ-Glu-Phe
|
γ-Glu-Phe (γ-Glutamylphenylalanine) is a γ-glutamyl dipeptide.. |
| PC-42367 |
Thyroxine sulfate
|
Thyroxine sulfate (T4) 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-42809 |
Alendronate sodium hydrate
|
Alendronate sodium hydrate (Alendronate. |
| PC-63179 |
TRIF agonist AV-C
|
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-63112 |
(R)-CE3F4
|
(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-63110 |
HJC-0338
|
HJC-0338 is a potent and specific EPAC2 antagonist with IC50 of 0.4 uM for competing with 8-NBD-cAMP in binding EPAC2. |
