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Cat. No. Product Name Field of Application Chemical Structure
DC20244 ES9-17 Featured
ES9-17 is a novel CME inhibitor.
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DC26000 EPZ019997 Featured
EPZ019997 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50=3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)).
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DC11287 EHT 5372 Featured
EHT 5372 is a novel DYRK1A (dual specificity tyrosine phosphorylation-regulated kinase 1A) inhibitor for the treatment of Alzheimer's disease: effect on Tau and amyloid pathologies in vitro.
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DC2100 Dasatinib (BMS-354825) Featured
Dasatinib (BMS-354825, Sprycel) is a novel, potent and multi-targeted inhibitor that targets Abl, Src and c-Kit, with IC50 of <1 nM, 0.5 nM and 79 nM, respectively.
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DC10576 Cyantraniliprole Featured
Cyantraniliprole(HGW-86) is an insecticide of the ryanoid class; has activity against pests such as Diaphorina citri that have developed resistance to other classes insecticides.
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DC2062 Ciproxifan (FUB-359) Featured
Ciproxifan is an antagonists of H3-type histamine receptors.
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DC7102 CH5132799 Featured
CH5132799 selectively inhibits class I PI3Ks, such as PI3Kα, PI3Kβ, PI3Kδ, and PI3Kγ with IC50 values of 0.014, 0.12, 0.50, and 0.36 uM, respectively; shows less inhibition of class II PI3Ks, class III PI3ks, and mTOR.
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DC10649 AX15836 Featured
AX15836 is a highly potent and selective ERK5 inhibitor.
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DC7356 Ametantrone Featured
Ametantrone is a new anthracenedione antineoplastic agents, produced a concentration-dependent inhibition of hepatic microsomal lipid peroxidation.
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DC9909 AM2099 Featured
AM-2099 is a potent and selective NaV1.7 Inhibitor.
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DC10117 AC264613 Featured
AC264613 is a potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 7.5). Displays no activity at other PAR subtypes and exhibits no significant activity at over 30 other receptors implicated in nociception and inflammation.
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DC8197 Tyrosine kinase inhibitor Featured
A Tyrosine kinase inhibitor.
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DC26079 GW 803430 Featured
A potent, specific, orally active melanin concentrating hormone receptor 1 (MCHR1) inhibitor with kI of 3.8 nM, >100-fold selectivity over a battery of GPCRs, ion channels and enzymes.
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DC11587 SirReal1 Featured
A novel potent, selective Sirt2 inhibitor with IC50 of 3.745 uM.
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DC11648 2-D08 Featured
A cell permeable, mechanistically unique inhibitor of protein sumoylation.
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DC7604 FAI (5S rRNA modificator) Featured
5S rRNA modificator is a suitable electrophile for 2’-hydroxyl acylation on structured RNA molecules, yielding accurate structural information comparable to that obtained with existing probes; 5S rRNA RNA modification.
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DC23033 Isochlorogenic acid B Featured
3,4-Dicaffeoylquinic acid (3,4-DCQA) is a polyphenol with diverse biological activities.
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