|
T60002 |
DC-S239
|
|
Histone Methyltransferase
|
|
DC-S239 (DC-S239) is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity. |
|
T10682L |
CARM1-IN-1
|
CARM1-IN-7G |
Histone Methyltransferase
|
|
CARM1-IN-1 (CARM1-IN-7G) is a selective inhibitor of CARM1 with IC50 of 8.6 μM. CARM1-IN-1 shows weak activity against PRMT1 and SET7 with IC50 > 600 μM. |
|
T16886 |
Sinefungin
|
Adenosyl-Ornithine,A-9145,Antibiotic 32232RP |
Others
,
Histone Methyltransferase
,
Antibiotic
,
Antifungal
|
|
Sinefungin (Adenosyl-Ornithine) is an effective inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication. Sinefungin is a SET7/9 inhibitor and ameliorates r... |
|
T68613 |
DC-S238
|
|
|
|
DC-S238 is a potent and selective histone methyltransferase SET7 inhibitor. |
|
T71918 |
DC-S100
|
|
|
|
DC-S100 is a selective histone methyltransferase SET7 inhibitor. |
|
T72013 |
Epigenetic Multiple Ligand
|
|
|
|
Epigenetic Multiple Ligand is a cell-permeable inhibitor of substrate processing by several chromatin-associated enzymes, including SIRT1/2, H3/SET7, H3/p300/CBP, H4/RmtA, PABP1/CARM1, and H4/PRMT1. It acts by inducing e... |
|
T26188 |
Setin-1
|
|
|
|
Setin-1 is the most potent Set7 inhibitor that acts by inhibiting the KMTase G9a. |
|
T64186 |
CARM1-IN-1 hydrochloride
|
|
|
|
CARM1-IN-1 hydrochloride is a potent and selective inhibitor of CARM1 (IC50: 8.6 μM) with low inhibition of PRMT1 and SET7. |
