Alternate TextTo enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
Home > Products > Novel inhibitors

Novel inhibitors

You can also try the following methods, and our professionals will serve you Customized Consultation
Cat. No. Product Name Field of Application Chemical Structure
DCC1707 Ddc4002
First-generation allosteric EGFR inhibitor, binding to the allosteric site of EGFR along with ATP that leads to inhibition of cell proliferation and arrest of EGFR L858R/T790M/C797S signalling
More description
DCC1705 Dd-04-015
Novel selective BTK degrader, demonstrating prolonged pharmacodynamic effects
More description
DCC1704 Dcz3112
Novel Hsp90 inhibitor, exerts potent antitumor activity against HER2-positive breast cancer through disruption of Hsp90-Cdc37 interaction
More description
DCC1703 Dc-teadin02
Novel potent and selective TEAD autopalmitoylation inhibitor, inhibiting TEADs transcription activity and downstream gene expression
More description
DCC1702 Dc-s239
Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor
More description
DCC1701 Dc-s238
Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor
More description
DCC1700 Dc-s100
Novel, Selective Histone Methyltransferase SET7 Inhibitor
More description
DCC1699 Dc-prc2in-01
Novel PRC2 Inhibitor, Targeting EZH2-EED Interaction
More description
DCC1698 Dcn1-ubc12 Inhibitor Dn-2
Novel potent and selective DCN1-UBC12 inhibitor for anticardiac fibrotic effects, specifically targetinbg DCN1 at molecular and cellular levels, effectively reversing angiotensin (Ang) II-induced cardiac fibroblast activation
More description
DCC1697 Dc-k2in212
Novel potent CDK2 inhibitor with selectivities above 10-fold over CDK1/4/6/7/9/12 above 10-fold, displaying anti-proliferative activity against A2058 melanoma and MV4-11 leukemia cell lines and low toxicity on human normal cell lines, inhibiting CDK2-medi
More description
DCC1696 dcg-iv
Highly potent agonist for group II mGlu receptors
More description
DCC1695 Dcg066
Novel inhibitor of lysine methyltransferase G9a
More description
DCC1694 Dc-ebio
Activator of IK and SK channels
More description
DCC1693 Dce_42
Novel potent EZH2 inhibitor
More description
DCC1692 Dce_254
Novel potent EZH2 inhibitor
More description
DCC1691 Dc-cpin734
Novel potent CBP bromodomain inhibitor with a TR-FRET IC50 value of 19.5 ± 1.1 nM and over 400-fold of selectivity against BRD4 bromodomains
More description
DCC1690 Dc-bpi-7
Novel potent BPTF-BRD inhibitor, showing selectivities 100-fold higher than those of other BRD targets
More description
DCC1689 Dc-bpi-11
Novel potent BPTF-BRD inhibitor, showing selectivities 100-fold higher than those of other BRD targets, significantly inhibiting leukemia cell proliferation
More description
DCC1688 Dcat Maleate [57915-90-9]
Inhibitor of N-methyl transferases (NMT), preventing the formation of Parkinson's syndrome neurotoxins via methylation of non-methylated pre-neurotoxins.
More description
DCC1687 Dc_ym26
Novel inhibitor of menin-MLL interaction
More description
DCC1686 Dc_ym25
Novel inhibitor of menin-MLL interaction
More description
DCC1685 Dc_ym21 Maleate
Novel inhibitor of menin-MLL interaction
More description
DCC1684 Dc_m5_2
Novel inhibitor of WDR5-MLL1 interaction
More description
DCC1683 Dc_501
Novel selective non-nucleoside inhibitor of DNA methyltransferase 1 (DNMT1)
More description
DCC1682 Dbpr110
Potent HCV NS5A inhibitor
More description
DCC1681 Dbm-1285 Dihydrochloride
p38 MAPK inhibitor, supressing p38 phosphorylation and LPS-induced TNF-α production in macrophages
More description
DCC1680 Dbco-stco
Novel protein cross-linking agent
More description
DCC1679 Db1960
Novel antileishmanial agent, against both intracellular Leishmania donovani and intracellular Leishmania amazonensis and displaying dose-dependent reduction of liver parasitemia
More description
DCC1678 Db1255
Novel ERG/DNA binding inhibitor, targeting the DNA-binding activity of the human ERG transcription factor
More description
DCC1677 Db07107
Novel tyrosine kinase inhibitor for drug resistant T315I mutant BCR-ABL
More description

Customized Consultation X

Your information is safe with us. * Required Fields.

Your name
Company
Email
Procuct Name
Cat. No.
Remark
Verification code
Please fill out the characters in the picture
X