| Cat. No. |
Product Name |
Information |
| PC-21687 |
BCL3ANT
Bcl-3 inhibitor
|
BCL3ANT (NSC-659509) is a small molecule inhibitor of Bcl-3-mediated cyclin D1 expression, reduces cyclin D1 luciferase activity in Bcl-3-overexpressing melanoma cells with IC50 of 40.4 uM. |
| PC-21646 |
Siastatin B
Glycosidase inhibitor
|
Siastatin B is a potent and effective iminosugar inhibitor of diverse glycosidase classes, namely, sialidases, β-d-glucuronidases, and N-acetyl-glucosaminidases. |
| PC-21645 |
Voclosporin
Calcineurin inhibitor
|
Voclosporin (ISATX247, ISA247) is a small molecule calcineurin inhibitor, more potency than cyclosporine in vitro, substantially inhibits lymphocyte proliferation, T-cell activation and cytokine production. |
| PC-21635 |
Equilin
3βHSD1 inhibitor
|
Equilin (7-Dehydroestrone) is a highly potent 3βHSD1 inhibitor with IC50 of 2.8 nM in VCaP cells, also inhibits the activity of purified 3βHSD1 with SPR KD of 2.23 uM. |
| PC-21628 |
RBS-10
NQO1 inhibitor
|
RBS-10 is a small molecule that shows preferential cytotoxicity against cells pan-resistant to degraders, acts as a prodrug bioactivated by the oxidoreductase enzyme NQO1. |
| PC-21627 |
JA310
MST3 (STK24) inhibitor
|
JA310 is a potent, highly selective inhibitor of the mammalian sterile 20-like serine/threonine (MST) family member MST3 (STK24) with ITC KD value of 115 nM. |
| PC-21595 |
7-Fluorotryptamine
GPRC5A agonist
|
7-fluorotryptamine (7FTA) is a potent synthetic agonist of GPRC5A with EC50 of 7.2 uM for inducing GPRC5A-mediated β-arrestin recruitment. |
| PC-21594 |
7-Fluorotryptamine hydrochloride
GPRC5A agonist
|
7-fluorotryptamine (7FTA) is a potent synthetic agonist of GPRC5A with EC50 of 7.2 uM for inducing GPRC5A-mediated β-arrestin recruitment. |
| PC-21588 |
3-mercaptopicolinic acid hydrochloride
PEPCK inhibitor
|
SKF-34288 (3-Mercaptopicolinic acid) hydrochloride is an orally active phosphoenolpyruvate carboxykinase (PEPCK, PCK) inhibitor with Ki of 2-9 uM, an inhibitor of gluconeogenesis. |
| PC-21580 |
CHD1Li 11
CHD1L inhibitor
|
CHD1Li 11 (CHD1L inhibitor 11) is a small molecule inhibitor of chromodomain helicase DNA-binding protein 1 like (CHD1L) with IC50 of 4.57 uM. |
| PC-21551 |
AQIM-I
ILF3/NF110 inhibitor
|
AQIM-I is a highly potent small molecule survivin inhibitor by targeting ILF3/NF110, binds to ILF3/NF110 with KD value of 163 nM in SPR assays, has broad-spectrum antitumor activity. |
| PC-21548 |
AEP inhibitor 18
APE inhibitor
|
AEP inhibitor 18 is a potent, selective, orally bioavailable, and brain penetrant inhibitor of asparagine endopeptidase (AEP) with IC50 of 7.8 nM. |
