Cat. No. |
Product Name |
Information |
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. |
PC-21541 |
PT-91
GPR27 agonist
|
PT91 is a small-molecule GPR27 (SREB1) agonist with pEC50 of 6.15 (human GPR27) in β-arrestin 2 recruitment-based firefly luciferase complementation assay, Emax=100%. |
PC-21492 |
AP736
|
AP736 is a damantyl benzylbenzamide derivative with anti-melanogenic effects in melanocytes in vitro, acts via the downregulation of tyrosinase, TRP-1 and MITF expression. |
PC-21475 |
AGI-43192
MAT2A inhibitor
|
AGI-43192 is a potent and selective methionine adenosyltransferase 2A (MAT2A) inhibitor with cellular IC50 of 14 nM. |
PC-21474 |
AGI-41998
MAT2A inhibitor
|
AGI-41998 is a potent selective and brain-penetrant methionine adenosyltransferase 2A (MAT2A) inhibitor with IC50 of 22 nM. |
PC-21472 |
RTI-118
NPSR antagonist
|
RTI-118 is a potent, selective neuropeptide S receptor (NPSR, GPR154) antagonist. |
PC-21471 |
RTI-263
NPSR agonist
|
RTI-263 (SerPheLysAsn-NH2) is a potent, selective tetrapeptide neuropeptide S receptor (NPSR, GPR154) biased agonist with EC50 of 3.02 nM for hNPSR calcium mobilization. |