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Cat. No. Product Name Information
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-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-22593

UNC10245380

CIB1 inhibitor

UNC10245380 (UNC5380) is a small molecule ligand/inhibitor of Calcium and Integrin Binding protein 1 (CIB1) with IC50 of 8.0 uM in TR-FRET displacement assay, selectively kills CIB1 depletion-sensitive TNBC cells.
PC-22571

TMLB-C16

B3GAT3 inhibitor

TMLB-C16 is a potent beta-1,3-glucuronosyltransferase (B3GAT3) inhibitor with KD of 3.96 uM, suppresses proliferation and migration in HCC cells.
PC-22540

YK-4-279

EWS-FLI1 inhibitor

YK-4-279 is a specific small molecule inhibitor of EWS-FLI1 interaction with RNA helicase A with SPR KD of 9.48 uM for EWS-FLI1, reduces EWS-FLI1 functional activity, also reduces EWS-FLI1 modulated transcription.
PC-22489

UR778Br

IQGAP1 inhibitor

UR778Br is a potent small molecule inhibitor of scaffolding protein IQGAP1, taregting the IQGAP1-GRD domain, selectively inhibits growth of human acute myeloid leukemia.
PC-22470

PW0729

GPR52 agonist

PW0729 is a potent, selective, G protein-biased agonist of orphan GPR52 with EC50 of 47 nM in cAMP assay, Emax=143%.

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