Cat. No. | Product name | CAS No. |
DCC1676 |
Daw-22
Biological Active Reagents |
|
DCC1677 |
Db07107
Novel tyrosine kinase inhibitor for drug resistant T315I mutant BCR-ABL |
552332-71-5 |
DCC1678 |
Db1255
Novel ERG/DNA binding inhibitor, targeting the DNA-binding activity of the human ERG transcription factor |
|
DCC1679 |
Db1960
Novel antileishmanial agent, against both intracellular Leishmania donovani and intracellular Leishmania amazonensis and displaying dose-dependent reduction of liver parasitemia |
|
DCC1680 |
Dbco-stco
Novel protein cross-linking agent |
|
DCC1681 |
Dbm-1285 Dihydrochloride
p38 MAPK inhibitor, supressing p38 phosphorylation and LPS-induced TNF-α production in macrophages |
917811-28-0 |
DCC1682 |
Dbpr110
Potent HCV NS5A inhibitor |
1310694-75-7 |
DCC1683 |
Dc_501
Novel selective non-nucleoside inhibitor of DNA methyltransferase 1 (DNMT1) |
889797-65-3 |
DCC1684 |
Dc_m5_2
Novel inhibitor of WDR5-MLL1 interaction |
713099-37-7 |
DCC1685 |
Dc_ym21 Maleate
Novel inhibitor of menin-MLL interaction |
2001072-35-9 |
DCC1686 |
Dc_ym25
Novel inhibitor of menin-MLL interaction |
|
DCC1687 |
Dc_ym26
Novel inhibitor of menin-MLL interaction |
|
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. |
57915-90-9 |
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 |
|
DCC1690 |
Dc-bpi-7
Novel potent BPTF-BRD inhibitor, showing selectivities 100-fold higher than those of other BRD targets |
|
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 |
|
DCC1692 |
Dce_254
Novel potent EZH2 inhibitor |
673443-80-6 |
DCC1693 |
Dce_42
Novel potent EZH2 inhibitor |
669749-45-5 |
DCC1694 |
Dc-ebio
Activator of IK and SK channels |
60563-36-2 |
DCC1695 |
Dcg066
Novel inhibitor of lysine methyltransferase G9a |
494786-13-9 |
DCC1696 |
dcg-iv
Highly potent agonist for group II mGlu receptors |
147782-19-2 |
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 |