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Wnt/Stem Cell

Chemical Structure Cat. No. Product Name CAS No.
LP-922056 Chemical Structure
 BCP28623 LP-922056 1365060-22-5
LP-922056 is a Notum pectinacetylesterase inhibitor which activates wnt signalling. LP-922056 increases cortical bone thickness in a mouse model of bone growth.
Filgotinib maleate Chemical Structure
 BCP49095 Filgotinib maleate 1802998-75-9
Filgotinib maleate is a potent and selective JAK1 inhibitor under investigation for the treatment of rheumatoid arthritis (RA) and Crohn's disease.
Solcitinib Chemical Structure
 BCP23893 Solcitinib 1206163-45-2
Solcitinib is a Janus kinase 1 (JAK1) inhibitor. Solcitinib may be potential useful for treatment of psoriasis，systemic lupus erythematosus, ulcerative colitis.
Oct3/4-inducer-1 Chemical Structure
 BCP24154 Oct3/4-inducer-1 1016535-83-3
MDK35833, also known as Oct3/4-inducer-1, is a potent Oct3/4 inducer. Oct3/4-inducer-1 promotes expression and stabilization of Oct3/4, and enhances its transcriptional activity in diverse human somatic cells.
Nirogacestat Chemical Structure
 BCP24479 Nirogacestat 1290543-63-3
Nirogacestat is a potent and selective gamma secretase (GS) inhibitor with potential antitumor activity. PF-03084014 binds to GS, blocking proteolytic activation of Notch receptors. Nirogacestat enhances the Antitumor Effect of Docetaxel in Prostate Cancer. Nirogacestat enhances docetaxel-mediated tumor response and provides a rationale to explore GSIs as adjunct therapy in conjunction with docetaxel for men with CRPC (castration-resistant prostate cancer).
Pacritinib citrate Chemical Structure
 BCP48998 Pacritinib citrate 1228923-42-9
Pacritinib Citrate is the citrate salt form of pacritinib, an orally bioavailable inhibitor of Janus kinase 2 (JAK2), the JAK2 mutant JAK2V617F and FMS-like tyrosine kinase 3 (FLT3; CD135; STK1; FLK2), with potential antineoplastic activity.
HA-100 dihydrochloride Chemical Structure
 BCP48930 HA-100 dihydrochloride 210297-47-5
HA-100 dihydrochloride is a protein kinase inhibitor, inhibiting superoxide release from human neutrophils (PMN).
(E/Z)-GSK-3β inhibitor 1 Chemical Structure
 BCP48909 (E/Z)-GSK-3β inhibitor 1 3367-88-2
(E/Z)-GSK-3β inhibitor 1 is a racemic compound of (E)-GSK-3β inhibitor 1 and (Z)-GSK-3β inhibitor 1 isomers.
GSK180736A Chemical Structure
 BCP25022 GSK180736A 817194-38-0
GSK180736A is potent Rho-associated coiled-coil kinase 1 (ROCK1) inhibitor with an IC50 of 100 nM. GSK180736A is also a selective and ATP-competitive G protein-coupled receptor kinase 2 (GRK2) inhibitor with an IC50 of 0.77 μM.
Super-TDU Chemical Structure
 BCP25144 Super-TDU 1599441-71-0
Super-TDU is an inhibitory peptide targeting YAP-TEADs interaction.
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