| Cat. No. |
Product Name |
Information |
| PC-22682 |
Hymeglusin
HMGCS1 inhibitor
|
Hymeglusin is a fungal β-lactone antibiotic and HMG-CoA synthase 1 (HMGCS1) inhibitor with IC50 of 0.12 uM, suppresses the growth of AML cells and enhances their chemosensitivity. |
| PC-22678 |
DS28120313
Hepcidin inhibitor
|
DS28120313 is a potent orally active hepcidin production inhibitor with IC50 of 93 nM (hepcidin mRNA expression), shows serum hepcidin-lowering effects. |
| PC-22671 |
GFRα2/GFRα23 inhibitor 16
GFRα2/3 inhibitor
|
GFRα2/GFRα23 inhibitor 16 is a selective small moelcule inhibitor of glycosylphosphatidylinositol-anchored co-receptor GFRa2/GFRa3 with IC50 of 0.1/0.2 uM respectively, selective over RET. |
| PC-22666 |
Myeloperoxidase inhibitor RL6
Myeloperoxidase inhibitor
|
Myeloperoxidase inhibitor RL6 is a potent, reversible inhibitor of myeloperoxidase (MPO) and hypochlorous acid (HOCl) scavenger, inhibits neutrophil extracellular trap release (NETosis). |
| PC-22644 |
TAK-683
KISS1R agonist
|
TAK-683 is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay. |
| PC-22643 |
TAK-683 acetate
KISS1R agonist
|
TAK-683 acetate is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay. |
| PC-22642 |
TAK-448 acetate
KISS1R agonist
|
TAK-448 (MVT-602) acetate is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay. |
| PC-22640 |
(S)-PHA533533
Ube3a unsilencer
|
(S)-PHA533533 is a potent, small molecule unsilencer of paternal UBE3A in mouse primary neurons with EC50 of 0.54 uM, Emax=80%, effectively downregulates Ube3a-ATS/UBE3A ATS and epigenetically unsilences paternal Ube3a/UBE3A in both mouse and human neuron. |
| PC-22636 |
Delphinidin chloride
Hyaluronidase inhibitor
|
Delphinidin chloride is a natural plant compound found in fruits and vegetables, a potent hyaluronidase inhibitor, increases high molecular weight hyaluronic acid (HMW-HA) and inhibits cancer metastasis. |
| PC-22628 |
GGTI-2154 hydrochloride
GGTase I inhibitor
|
GGTI-2154 hydrochloride is a potent, selective inhibitor geranylgeranyltransferase I (GGTase I) with IC50 f 21 nM, >250-fold selective over FTase. |
| PC-22627 |
GGTI-2154
GGTase I inhibitor
|
GGTI-2154 is a potent, selective inhibitor geranylgeranyltransferase I (GGTase I) with IC50 f 21 nM, >250-fold selective over FTase. |
| PC-22615 |
2-BDBPQD
α-glucosidase inhibitor
|
2-BDBPQD is a potent anti-diabetic agent and inhibitor of carbohydrate-degrading enzyme α-glucosidase with IC50 of 63.7 uM, moderately reduces cholesterol and LDL levels, exhibits superior efficacy in reducing glucose levels compared to acarbose. |
