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Histone Methyltransferase(组蛋白甲基转移酶)

Histone methyltransferases are a group of enzymes that catalyze the methylation of histone lysine and arginine by adding methyl groups to specific histone arginine or lysine residues. Histone methyltransferaes can be classified into 3 classes, including SET domain lysine methyltransferases, non-SET domain lysine methyltransferases and arginine methyltransferases (PRMTs), all of which use S-adenosylmethionine as a cosubstrate for the transfer of the methyl group. Aberrant histone methylation has been associated with a wide range of human cancers (such as hematological malignancies), which leads to the development of novel cancer chemotherapies targeting cancer-associated histone methyltransferases (more than 20 lysine methyltransferases and 9 arginine methyltransferases in humans).

Products for  Histone Methyltransferase

  1. Cat.No. 产品名称 Information
  2. GC33301 BIX-01338 hydrate (BIX01338 hydrate) BIX-01338 hydrate (BIX01338 hydrate) 是一种组蛋白赖氨酸甲基转移酶抑制剂。
  3. GC33278 MM-589 MM-589是WD重复结构域5(WDR5)和混合谱系白血病(MLL)相互作用的有效抑制剂。MM-589结合WDR5的IC50为0.90nM。抑制MLLH3K4甲基转移酶活性的IC50为12.7nM。
  4. GC33220 EBI-2511 EBI-2511是具有口服活性的、EZH2的有效抑制剂,其在Pfeffiera细胞中的IC50值为6nM。
  5. GC33208 Dot1L-IN-1 Dot1L-IN-1是高效,选择性,结构新颖的Dot1L抑制剂,Ki为2pM。
  6. GC33187 A-395 (A395) A-395 (A395) 是一种多梳抑制复合物 2 (PRC2) 蛋白质-蛋白质相互作用的拮抗剂,有效抑制三聚体 PRC2 复合物 (EZH2-EED-SUZ12),IC50 为 18 nM。
  7. GC33184 LLY-283 A PRMT5 inhibitor
  8. GC32988 BRD9539 An inhibitor of EHMT2/G9a and PRC2 in enzyme assays
  9. GC32977 PF-06726304 PF-06726304是有效,选择性的EZH2抑制剂,Ki值为0.7nM。
  10. GC32861 A-196 A selective inhibitor of SUV420H1 and SUV420H2
  11. GC32693 GSK3326595 (EPZ015938)

    EPZ015938

    GSK3326595 (EPZ015938) 是一种具有口服活性的、有效的、选择性protein arginine methyltransferase 5(PRMT5)抑制剂。
  12. GC30530 Dot1L-IN-2 Dot1L-IN-2是一种有效的,选择性的,可口服的Dot1L(一种histonemethyltransferase),IC50值和Ki值分别为0.4nM和0.08nM。
  13. GC30503 A-893 A-893是一个有细胞活性的,SMYD2的抑制剂,其IC50值为2.8nM。
  14. GC19465 JNJ-64619178

    Onametostat

    A PRMT5 inhibitor
  15. GC19388 XY1

    N-2-萘基-N'-[2-氧代-2-(1-吡咯烷基)乙基]脲

    A negative control for SGC707
  16. GC19329 SGC2085 A PRMT4/CARM1 inhibitor
  17. GC19211 JQEZ5 An EZH2 inhibitor
  18. GC19181 GSK2807 Trifluoroacetate GSK2807 Trifluoroacetate 是一种有效的、选择性的、SAM 竞争性的 SMYD3 抑制剂,Ki 为 14 nM,IC50 为 130 nM。
  19. GC19149 EZM 2302

    GSK3359088

    EZM 2302是一种对CARM1有效的且具有选择性的抑制剂,其IC50值为6nM。

  20. GC19141 EPZ011989 An orally bioavailable EZH2 inhibitor
  21. GC19130 EED226 EED226是一种强效的多梳抑制复合物2(PRC2)抑制剂,IC50值为22.3nM。
  22. GC18949 CAY10677

    Icmt Inhibitor 15

    An inhibitor of protein prenylation
  23. GC18650 S-(5'-Adenosyl)-L-methionine (tosylate)

    AdoMet, SAM, SAMe

    S-Adenosyl-L-methioninetosylate(S-Adenosylmethioninetosylate)是通过蛋氨酸腺苷转移酶的作用由蛋氨酸和ATP内源性生产的,是一种重要的具有口服活性的甲基供体。

  24. GC18642 SW155246 A DNA methyltransferase 1 inhibitor
  25. GC18577 CID-2818500

    Α-硝基茋

    An inhibitor of PRMT1
  26. GC18428 SGC2085 (hydrochloride) A PRMT4/CARM1 inhibitor
  27. GC18161 BCI-121 An inhibitor of SMYD3
  28. GC18159 BAY-598 BAY-598是一种氨基吡唑啉基的选择性小分子抑制剂,靶点为含有SET和MYND结构域的蛋白2(SMYD2),半抑制浓度(IC50)为27nM。
  29. GC12530 PFI-2 (hydrochloride)

    (R)-PFI-2 hydrochloride

  30. GC12367 CM-272 An inhibitor of G9a, GLP, and DNA methyltransferases
  31. GC13634 (S)-PFI-2 (hydrochloride)

    (+)-PFI-2

    Negative control of (R)-PFI 2
  32. GC14240 MS049 (hydrochloride) A selective, dual PRMT4/PRMT6 inhibitor
  33. GC16432 MS023 (hydrochloride) An inhibitor of type I PRMTs
  34. GC16298 CPI-1205 EZH2抑制剂
  35. GC17023 HLCL-61 A PRMT5 inhibitor
  36. GC10099 MS023

    N1-甲基-N1-[[4-[4-(异丙氧基)苯基]-1H-吡咯-3-基]甲基]-1,2-乙二胺

    MS023 是 I 型蛋白精氨酸甲基转移酶 (PRMT) 的有效、选择性和细胞活性抑制剂。
  37. GC14585 GSK591

    EPZ015866; GSK3203591

    A chemical probe for PRMT5
  38. GC16397 OICR-9429 OICR-9429是一种有效的高亲和力的WD repeat domain 5(WDR5)抑制剂,与WDR5结合的Kd值为93±28nM。
  39. GC10905 Amodiaquine dihydrochloride dihydrate

    阿莫地喹盐酸盐; Amodiaquin dihydrochloride dihydrate

    A prodrug form of N-desethyl amodiaquine
  40. GC16509 Adox

    腺苷二醛

    An irreversible inhibitor of SAH hydrolase
  41. GC16261 LLY507 A SMYD2 inhibitor
  42. GC15102 EPZ020411 EPZ020411是一种具有高效选择性,且口服生物利用度高的蛋白质精氨酸甲基转移酶6(PRMT6)抑制剂,IC50值为10nM。
  43. GC17546 AMI5

    水溶伊红,Acid Red 87

    曙红 Y(二钠)是一种可溶性酸性红色染料分子。
  44. GC16224 EPZ031686 EPZ031686是一种有效且具有口服活性的SMYD3抑制剂,其IC50值为3nM,EPZ031686能够以非竞争性方式同时抑制SAM和MEKK2,其Ki值分别约为1.2nM和1.1nM。
  45. GC12874 SGC707 A potent allosteric inhibitor of PRMT3
  46. GC17207 UNC3866 An inhibitor of CBX7
  47. GC12005 C7280948 A PRMT1 inhibitor
  48. GC11414 GSK503 A potent, selective EZH2 inhibitor
  49. GC15302 EPZ015666

    GSK3235025

    EPZ015666是一种新型的选择性蛋白精氨酸甲基转移酶5(PRMT5)抑制剂,IC50值< 10nM。
  50. GC14763 WDR5 0103

    WD-Repeat Protein 5-0103

    An inhibitor of WDR5 peptide binding
  51. GC15652 UNC 2400 UNC 2400 与 UNC1999 非常相似,作为细胞研究的阴性对照,其效力比 UNC1999 低 1,000 倍以上。

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