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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T33514 | MSC 2032964A | MSC-2032964A,MSC2032964A | ASK |
MSC 2032964A is a potent selective ASK1 inhibitor (IC50 = 93 nM) that is oral bioavailable and brain permeable. It inhibited neuroinflammation in mouse EAE models and blocked LPS-induced phosphorylation of ASK1 and p38 i... | |||
T60148 | MSC-4106 | YAP | |
MSC-4106, an orally active and potent YAP/TAZ-TEAD inhibitor, disrupts TEAD1 and TEAD3 auto-palmitoylation and demonstrates significant efficacy in the NCI-H226 tumor xenograft model [1]. | |||
T7727 | Se-Methylselenocysteine | Se MSC,SeMCys,MSeC,Se-MSC,SeMSC | BCL , IAP , Caspase |
Se-Methylselenocysteine (Se-MSC) is a potent chemopreventive agent in many test systems and has been shown to inhibit tumor promotion and induce apoptosis. | |||
T73378 | MSC-1186 | ||
MSC-1186 is a potent and highly selective inhibitor targeting the pan-SRPK family, including SRPK1, SRPK2, and SRPK3, with IC 50 values of 2.7 nM, 81 nM, and 0.6 nM, respectively. Its specificity and effectiveness make i... | |||
T12115 | MSC2360844 | PI3K | |
MSC2360844 is a potent, orally active and selective inhibitor of PI3Kδ(IC50 of 145 nM). | |||
TQ0266 | MSC2530818 | CDK | |
MSC2530818 is an effective, selective and orally available CDK8 inhibitor (IC50: 2.6 nM). | |||
T6121 | Tepotinib | EMD-1214063,MSC2156119 | Trk receptor , c-Met/HGFR , TAM Receptor |
Tepotinib (EMD-1214063) is an inhibitor of MET tyrosine kinase with potential antineoplastic activity. | |||
T60098 | MSC2504877 | 3-(4-(2-Hydroxypropan-2-yl)phenyl)-6-methylpyrrolo[1,2-a]pyrazin-1(2H)-one | Others |
MSC2504877 is an inhibitor of tankyrase and enhances the effects of clinical CDK4/6 inhibitors. MSC2504877 suppresses the upregulation of Cyclin D2 and Cyclin E2 caused by palbociclib and enhances the suppression of phos... | |||
T2771 | Orcinol glucoside | Sakakin | Antioxidant |
Orcinol glucoside (Sakakin) (OG), an active constituent isolated from the rhizomes of Curculigo orchioides Gaertn, shows potent antioxidative and anxiolytic activities without sedative effects. | |||
T12114 | MSC1094308 | p97 | |
MSC1094308 is a reversible and allosteric inhibitor of the type II AAA ATPase. | |||
T71161 | Thiorphan disulfide | ||
Thiorphan disulfide is an impurity of Racecadotril -- an antidiarrheal and enkephalinase inhibitor that reduces the amount of water and electrolytes absorbed into the intestine. | |||
T39094 | MSC2360844 hemifumarate | ||
MSC2360844 hemifumarate is a highly potent and orally active compound that acts as a selective inhibitor of PI3Kδ, with an IC50 value of 145 nM. This compound exhibits exceptional selectivity against a comprehensive pane... | |||
T9238 | KI-7 | Adenosine Receptor | |
KI-7 is an adenosine A2B receptor positive allosteric modulator. | |||
T71383 | NB-533 | ||
NB-533 is a macrocyclic peptidic BACE-1 inhibitor. | |||
T29899 | Alpha-MSCS | alpha-Methylserotonin creatinine sulfate,alpha Methylserotonin creatinine sulfate,alphaMSCS | |
α-MSCs (α-methylserotonin creatinine sulfate) are neurotransmitters. | |||
T4387 | Evobrutinib | MSC2364447C,M2951 | BTK |
Evobrutinib(M2951) , also known as M-2951 and MSC-2364447C, is a highly selective inhibitor of the Bruton's tyrosine kinase (BTK), which is important in the development and functioning of various immune cells including B... | |||
TL0008 | Gigantol | Wnt/beta-catenin , Glucosidase | |
Gigantol is a novel inhibitor of the Wnt/β-catenin pathway. It inhibits Wnt/β-catenin signaling through downregulation of phosphorylated LRP6 and cytosolic β-catenin in breast cancer cells. Gigantol may be developed as a... | |||
TP1300 | GsMTx4 TFA (1209500-46-8 free base) | GsMTx4 TFA | Piezo Channel |
GsMTx4 TFA (1209500-46-8 free base) (GsMTx4 TFA) is a spider venom peptide that selectively inhibits cationic permeable mechanically-sensitive channels (MSCs) belonging to the Piezo and TRP channel families. | |||
T16947 | SU16f | 3-substituted indolin-2-one 16f,SU-16F,SU 16F | PDGFR |
SU16f (3-substituted indolin-2-one 16f) is a potent and selective PDGFRβ inhibitor (IC50s: 10 nM, 140 nM, 2.29 μM for PDGFRβ, PDGFR1, PDGFR2, respectively). Neutralization of PDGFRβ receptor by SU16f blocks the promoting... | |||
TP1152 | Fibronectin Adhesion-promoting Peptide TFA | Heparin Binding Peptide TFA | |
Fibronectin Adhesion-promoting Peptide (Heparin Binding Peptide) is one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. It promotes assembly of mesenchymal... |