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首页-小分子抑制剂&激动剂-Others-Other Targets

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Cat. No. Product Name Information
PC-23178

SCR-7952

MAT2A inhibitor

SCR-7952 is a potent, highly selective methionine adenosyltransferase 2A (MAT2A) inhibitor with IC50 of 18.7 nM, Ki of 14.49 nM, shows MTAP-null selective antiproliferative activity.
PC-23069

QC-308

Heme oxygenase inhibitor

QC-308 is a potent heme oxygenase (HO) inhibitor witn IC50 of 0.27 uM and 0.46 uM for hHO-1 and hHO-2 respectively.
PC-23067

CDD-3290

PSA inhibitor

CDD-3290 (CDD3290) is a specific small molecule inhibitor of prostate-specific antigen (PSA; KLK3) with Ki of 216 nM.
PC-23021

SRSF10 inhibitor 1C8

SRSF10 inhibitor

SRSF10 inhibitor 1C8 is a specific small molecule inhibitor of SRSF10, alters splicing regulation mediated by SRSF10, shows strong anti-HIV-1 potency against a variety of clinical strains in vitro.
PC-22980

Peptide SBT-20

ROS-lowering peptide

Peptide SBT-20 (SS-20) is a cell-permeable peptide targeting the inner mitochondrial membrane, reduces ROS, normalizes electron transport chain function and ATP generation.
PC-22799

BCATc inhibitor 2

BCAT1 inhibitor

BCATc inhibitor 2 (Bi2) is a specific inhibitor of cytosolic branched-chain aminotransferase (BCATc, BCAT1) with IC50 of 0.2/ 0.8 uM for rat/human BCATc respectively, weakly inhibits rat mitochondrial isoenzyme rBCATm.
PC-22793

BIIB-TTBKi

TTBK1 inhibitor

BIIB-TTBK1i is a potent selective inhibitor of CNS-specific tau kinase Tau Tubulin Kinase 1 (TTBK1) with IC50 of 9.5 nM in recombinant kinase assay, inhibits tau phosphorylation at S422 (pS422) with IC50 of 9.75 nM in cell-based assays.
PC-22792

TTBK1 inhibitor 31

TTBK inhibitor

TTBK1 inhibitor 31 (TTBK1-IN-1) is a potent, selective and CNS-penetrant Tau Tubulin Kinase 1 (TTBK1) inhibitor with IC50 of 2.7 nM, inhibits tau phosphorylation at the disease-relevant Ser 422 epitope.
PC-22685

NSI-189

Neurogenic compound

NSI-189 (Amdiglurax) is an orally active benzylpiperizine-aminiopyridine compound with neurogenic activity, stimulates neurogenesis of human hippocampus-derived neural stem cells in vitro and stimulates neurogenesis in murine hippocampus in vivo.
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-22641

TAK-448

KISS1R agonist

TAK-448 (MVT-602) is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay.

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