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T11500GSK3368715GSK3368715,EPZ019997,
GSK3368715 produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity. GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (P
价 格：￥电议型 号：T11500产 地：美洲
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T11500LGSK3368715 dihydrochlorideGSK3368715 dihydrochloride,EPZ019997 dihydrochloride,
GSK3368715 dihydrochloride ?produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity.GSK3368715 dihydrochloride ?is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein
价 格：￥电议型 号：T11500L产 地：美洲
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T22342GSK3368715 3HCl；化合物GSK3368715 (EPZ019997) 3HClEPZ019997 3HCl|||GSK3368715(EPZ019997)；EPZ019997 3HCl|
GSK3368715, a potent inhibitor of type I protein arginine methyltransferases (PRMT), could inhibit PRMT1, 3, 4, 6 and 8 with Kiapp vaules ranging from 1.5 to 81 nM.
价 格：￥电议型 号：T22342产 地：中国大陆
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T11500LGSK3368715 dihydrochlorideGSK3368715盐酸盐EPZ019997 dihydrochloride|||GSK3368715 2HCl|||EPZ019997 2HCl
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active and potent inhibitor of type I protein arginine methyltransferases (PRMTs) with anticancer and antitumor activity, inhibiting PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, and can be used to study advanced solid tumors.
价 格：￥电议型 号：T11500L产 地：中国大陆
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T11500GSK3368715；化合物 T11500EPZ019997；EPZ019997
GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50s: 3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). It has strong anti-cancer activity.
价 格：￥电议型 号：T11500产 地：中国大陆
