T77787 |
MS023 trihydrochloride
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2108631-19-0
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99.81%
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MS023 trihydrochloride (MS023 3HCl) is a selective and potent human type I protein arginine methyltransferase (PRMT) inhibitor with potential anticancer activity...
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T4334 |
EPZ020411 2HCl (1700663-41-7(free base))
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T4334
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99.2%
|
|
EPZ020411 is an effective and specific small molecule PRMT6 inhibitor (IC50=10 nM).
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T4314 |
EPZ020411
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1700663-41-7
|
|
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EPZ020411 is a specific and effective inhibitor of PRMT6 (IC50=10 nM).
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T1987 |
PFI-2
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1627676-59-8
|
|
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PFI-2 is an effective, specific and cell-active lysine methyltransferase SETD7 inhibitor (Ki/IC50: 0.33/2 nM), 1000-fold selectivity over other methyltransferase...
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T3081L |
EPZ004777 hydrochloride
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1380316-03-9
|
|
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EPZ004777 hydrochloride (EPZ004777 HCl) is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.
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T78152 |
PRMT5-IN-25
|
2691869-82-4
|
98%
|
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PRMT5-IN-25 (compound 503) is a potent inhibitor of PRMT5, exhibiting an inhibition constant (K i) of 0.06 nM and demonstrating antiproliferative properties [1]....
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T78172 |
PRMT5-IN-29
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2242788-69-6
|
98%
|
|
PRMT5-IN-29 is a potent, orally active inhibitor of PRMT5, exhibiting an IC50 value of 1.5 μM, showing promise for use in advanced cancer research [1].
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T78929 |
Anticancer agent 126
|
|
98%
|
|
Anticancer agent 126 (compound 12), a WDR5 inhibitor, exhibits anticancer properties by disrupting the WDR5-MYC interaction in cells, subsequently reducing MYC t...
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T79007 |
CARM1-IN-3
|
912970-67-3
|
98%
|
|
CARM1-IN-3 (compound 17b) is a potent, selective inhibitor of co-activator associated arginine methyltransferase (CARM1), exhibiting IC50 values of 0.07 µM for C...
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T79035 |
PRMT5-IN-28
|
2242753-66-6
|
98%
|
|
PRMT5-IN-28 (compound 36) serves as an inhibitor of the protein arginine methyltransferase 5 (PRMT5) enzyme, which is implicated in various cellular processes in...
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T79120 |
WM-586
|
2894832-05-2
|
98%
|
|
WM-586 is a covalent inhibitor of WDR5 that impedes the WDR5-MYC binding. It selectively reduces the interaction between WDR5 and MYC with an IC50 value of 101 n...
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T79200 |
BBDDL2059
|
2691174-27-1
|
98%
|
|
BBDDL2059 is a selective covalent inhibitor targeting EZH2, exhibiting an IC50 of 1.5 nM against the EZH2-Y641F mutant. It demonstrates potency in inhibiting lym...
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T79249 |
Antitumor agent-101
|
2848632-52-8
|
98%
|
|
Antitumor agent-101 is a selective, covalent inhibitor targeting lysine methyltransferases G9a/GLP, demonstrating IC50 values of 8.5 nM for G9a and 5.5 nM for GL...
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T79274 |
PRMT5-IN-31
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|
98%
|
|
PRMT5-IN-31 (Compound 3m), a selective PRMT5 inhibitor (IC50: 0.31 μM), increases hnRNP E1 protein levels by occupying the substrate site of PRMT5 and establishi...
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T79275 |
Antiproliferative agent-25
|
|
98%
|
|
Antiproliferative Agent-25 (Compound 3s4) is a selective PRMT5 inhibitor displaying an IC50 of 0.11 μM. It elevates hnRNP E1 protein levels and forms hydrogen bo...
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T79355 |
PRMT4-IN-3
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|
98%
|
|
PRMT4-IN-3 (compound 56) serves as a potent class I protein arginine methyltransferase (PRMT) inhibitor, specifically targeting PRMT4 with an IC50 value of 37 nM...
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T79614 |
EML734
|
|
98%
|
|
EML734 is a potent, selective inhibitor of PRMT7 and PRMT9, demonstrating inhibitory concentration 50 (IC50) values of 315 nM for PRMT7 and 0.89 μM for PRMT9.
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T79615 |
MS9715
|
|
98%
|
|
MS9715 is a potent and selective NSD3-targeting PROTAC, designed by leveraging BI-9321, which targets the PWWP1 domain of NSD3, in conjunction with an E3 ligase ...
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T79616 |
UNC7096
|
|
98%
|
|
UNC7096 is a potent, selective degrader of NSD2-PWWP1, exhibiting a dissociation constant (Kd) of 46 nM, and shows promise for treating NSD2-related diseases [1]...
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T79617 |
NSD2-IN-4
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|
98%
|
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NSD2-IN-4 is a potent, selective inhibitor of the NSD2-SET domain, showing promise for the treatment of diseases related to NSD2 [1].
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