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
- Cat.No. 产品名称 Information
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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。
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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。
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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。
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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。
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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。
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GC33184
LLY-283
A PRMT5 inhibitor
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GC32988
BRD9539
An inhibitor of EHMT2/G9a and PRC2 in enzyme assays
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GC32977
PF-06726304
PF-06726304是有效,选择性的EZH2抑制剂,Ki值为0.7nM。
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GC32861
A-196
A selective inhibitor of SUV420H1 and SUV420H2
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GC32693
GSK3326595 (EPZ015938)
EPZ015938
A PRMT5 inhibitor -
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。
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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。
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GC19465
JNJ-64619178
Onametostat
A PRMT5 inhibitor -
GC19388
XY1
N-2-萘基-N'-[2-氧代-2-(1-吡咯烷基)乙基]脲
A negative control for SGC707 -
GC19329
SGC2085
A PRMT4/CARM1 inhibitor
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GC19211
JQEZ5
An EZH2 inhibitor
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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。
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GC19149
EZM 2302
GSK3359088
A PRMT4 inhibitor -
GC19141
EPZ011989
An orally bioavailable EZH2 inhibitor
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GC19130
EED226
A potent and allosteric inhibitor of PRC2
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GC18949
CAY10677
Icmt Inhibitor 15
An inhibitor of protein prenylation -
GC18650
S-(5'-Adenosyl)-L-methionine (tosylate)
S-腺苷蛋氨酸对甲苯磺酸盐,S-Adenosyl methionine tosylate; Ademetionine tosylate; AdoMet tosylate
A methyl donor and cofactor -
GC18642
SW155246
A DNA methyltransferase 1 inhibitor
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GC18577
CID-2818500
Α-硝基茋
An inhibitor of PRMT1 -
GC18428
SGC2085 (hydrochloride)
A PRMT4/CARM1 inhibitor
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GC18161
BCI-121
An inhibitor of SMYD3
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GC18159
BAY-598
An inhibitor of SMYD2
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GC12530
PFI-2 (hydrochloride)
(R)-PFI-2 hydrochloride
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GC12367
CM-272
An inhibitor of G9a, GLP, and DNA methyltransferases
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GC13634
(S)-PFI-2 (hydrochloride)
(+)-PFI-2
Negative control of (R)-PFI 2 -
GC14240
MS049 (hydrochloride)
A selective, dual PRMT4/PRMT6 inhibitor
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GC16432
MS023 (hydrochloride)
An inhibitor of type I PRMTs
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GC16298
CPI-1205
EZH2抑制剂
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GC17023
HLCL-61
A PRMT5 inhibitor
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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。 -
GC14585
GSK591
EPZ015866; GSK3203591
A chemical probe for PRMT5 -
GC16397
OICR-9429
A probe for WDR5
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GC10905
Amodiaquine dihydrochloride dihydrate
阿莫地喹盐酸盐; Amodiaquin dihydrochloride dihydrate
A prodrug form of N-desethyl amodiaquine -
GC16509
Adox
腺苷二醛
An irreversible inhibitor of SAH hydrolase -
GC16261
LLY507
A SMYD2 inhibitor
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GC15102
EPZ020411
A PRMT6 inhibitor
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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。 -
GC16224
EPZ031686
EPZ031686 是一种有效且具有口服活性的 SMYD3 抑制剂,IC50 值为 3 nM。 EPZ031686 可用于癌症研究。
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GC12874
SGC707
A potent allosteric inhibitor of PRMT3
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GC17207
UNC3866
An inhibitor of CBX7
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GC12005
C7280948
A PRMT1 inhibitor
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GC11414
GSK503
A potent, selective EZH2 inhibitor
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GC15302
EPZ015666
GSK3235025
A bioavailable PRMT5 inhibitor -
GC14763
WDR5 0103
WD-Repeat Protein 5-0103
An inhibitor of WDR5 peptide binding -
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。