Cancer Research
Cancer is a term used to define a group of diseases in which abnormal cells divide without control, are able to invade neighboring tissues/organs and metastasize. Cancer has been characterized by six hallmarks; self sufficiency in proliferative growth signals, insensitivity to growth inhibitors, evasion of apoptosis, limitless replicative potential, ability to develop blood vessels (angiogenesis), and tissue invasion and metastasis.
Cancer Research Products Areas
Products for Cancer Research - Page 54
- Cat.No. Product Name Information/Activity
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BCC2218
EPZ004777
EPZ004777 is a potent, selective DOT1L inhibitor with an IC50 of 0.4 nM.
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BCC2430
UNC 0224
UNC0224 is a potent and selective histone methyltransferase G9a inhibitor with a Ki of 2.6 nM, an IC50 of 15 nM and a Kd of 23 nM. UNC0224 also potently inhibits b>GLP
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BCC8014
UNC 0642
Potent and selective G9a and GLP inhibitor,UNC0642 is a potent and selective <b>G9a/GLP</b> inhibitor, inhibits G9a/GLP with an <b>IC<sub>50</sub></b> of less than 2.5 nM.
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BCC2431
UNC 0646
UNC0646 is a potent and selective histone methyltransferase G9a inhibitor with an IC50 of 6 nM. UNC0646 is also a potent GLP inhibitor (IC50 <15 nM) and highly selective for G9a/GLP over SETD7, SUV39H2, SETD8 and PRMT3. UNC0646 reduces H3K9me2 levels in MDA-MB-231 cells with an IC50 of 26 nM.
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BCC4552
UNC1999
UNC1999 is a SAM-competitive, potent and selective inhibitor of EZH2/1 with IC50s of <10 nM and 45 nM, repectively.
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BCC5625
UNC 2400
1433200-49-7
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BCC5626
WDR5 0103
WDR5-0103 is a potent and selective WD repeat-containing protein 5 (WDR5) antagonist with Kd of 450 nM.
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BCC2445
UNC 926 hydrochloride
UNC-926 is a methyl-lysine (Kme) reader domain inhibitor; inhibits L3MBTL1 with an IC50 of 3.9 μM.
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BCC8013
C 21
Selective PRMT1 inhibitor
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BCC8008
TC-E 5003
Selective PRMT1 inhibitor


