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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T61605 | SK3 Channel-IN-1 | ||
SK3 Channel-IN-1 (compound 7a) is a powerful and selective modulator of the SK3 channel. It demonstrates significant efficacy in inhibiting breast cancer MDA-MB-435 cell migration while maintaining low cytotoxicity in ot... | |||
T12256 | NS8593 hydrochloride | NS8593 HCl | Potassium Channel |
NS8593 hydrochloride (NS8593 HCl) is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels) . | |||
T24111 | GSK3i XIII | GSK3 inhibitor XIII,GSK3iXIII,GSK3i-XIII | GSK-3 |
GSK3i XIII (GSK3 inhibitor XIII) is a GSK-3 ATP-binding site inhibitor. | |||
T15440 | GSK376501A | PPAR | |
GSK376501A is a selective and effective modulator of peroxisome proliferator-activated receptor γ (PPARγ) for the study of type 2 diabetes. | |||
T7195 | GSK369796 Dihydrochloride | N-tert-butylisoquine | Potassium Channel , Parasite |
GSK369796 Dihydrochloride (N-tert-butylisoquine),is an anti-malaria drug candidate. is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization(IC50 of 7.5 μM) | |||
T5491 | GSK3179106 | c-RET | |
GSK3179106 is RET kinase inhibitor with an IC50 of 0.4 nM | |||
T21956 | GSK3β inhibitor II | GSK-3 | |
GSK3β inhibitor II is a GSK3β inhibitor. GSK3β inhibitor II exhibits the research potential of Alzheimer's disease (AD). | |||
T64366 | GSK3-IN-4 | GSK-3 | |
GSK3-IN-4 is a GSK-3 inhibitor with IC50 of 0.101-1 μM of GSK-3α and GSK-3β in Calipe Assay. | |||
T6059 | GSK343 | Histone Methyltransferase , Autophagy | |
GSK343, a specific and effective EZH2 inhibitor (IC50=4 nM), exhibits 60 fold specificity activity against EZH1, and >1000 fold specificity activity against other histone methyltransferases. | |||
T15558 | GSK319347A | IκB/IKK | |
GSK319347A is a selective and potent dual inhibitor of TBK1 and IKKε with potential anti-tumor activity and inhibition of IKK2 activity, which can be used in the study of bladder cancer and lung adenocarcinoma. | |||
T73270 | GSK3-IN-2 | GSK-3 | |
GSK3-IN-2 is a potent GSK3 inhibitor for the treatment of diabetes and neurodegenerative diseases. | |||
T5745 | GSK3326595 | EPZ015938 | Histone Methyltransferase |
GSK3326595 (EPZ015938) is an inhibitor of protein arginine methyltransferase 5 (PRMT5)(IC50:6.2 nM.). | |||
T15437 | GSK3145095 | RIP kinase | |
GSK3145095 is an orally active inhibitor of RIPK1 with IC50 of 5 nM, with potential immunomodulatory activities and antineoplastic. | |||
T9573 | GSK3685032 | DNA Methyltransferase | |
GSK3685032 is a non-covalent and selective DNMT1 inhibitor(IC50 = 36 nM). The inhibitory effect is time-independent and reversible. GSK3685032 induces loss of DNA methylation and transcriptional activation and inhibits c... | |||
T11500L | GSK3368715 dihydrochloride | EPZ019997 dihydrochloride,GSK3368715 2HCl,EPZ019997 2HCl | Histone Methyltransferase |
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active and potent inhibitor of type I protein arginine methyltransferases (PRMTs) with anticancer and antitumor activity, inhibiting PRMT1, PRMT3, PRMT4... | |||
T73331 | GSK3-IN-3 | Mitophagy , GSK-3 | |
GSK3-IN-3 is a mitochondrial autophagy (mitophagy) inducer and GSK-3 inhibitor (IC50: 3.01 μM) that induces parkin-dependent mitochondrial autophagy. GSK3-IN-3 is non-ATP and non-substrate competitive and neuroprotective... | |||
T27475 | GSK356278 | GSK-356278,GSK 356278 | PDE |
GSK356278 is an effective and selective inhibitor of phosphodiesterase 4 (PDE4), with pIC50s of 8.6, 8.8, and 8.7 for human PDE4A, PDE4B, and PDE4D, respectively. GSK356278 has anti-inflammatory, anxiolytic, and cognitio... | |||
T24109 | GSK329 | GSK 329,GSK-329 | Others |
GSK329 is an effective and selective inhibitor of TNNI3 Interacting Kinase (TNNI3K). GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury. | |||
T77671 | GSK3a-IN-38 | GSK-3 | |
GSK3a-IN-38 is a novel small molecule compound that has inhibitory effects on GSK-3a. | |||
T27478 | GSK3987 | Liver X Receptor | |
GSK3987 is an LXR ligand. GSK3987 recruits the steroid receptor coactivator-1 to human LXRalpha and LXRbeta with EC50s of 40 nM. |