Chromatin/Epigenetics(染色质/表观遗传学)
Epigenetics
Epigenetics means above genetics. It determines how much and whether a gene is expressed without changing DNA sequences. Epigenetic regulations include, 1. DNA methylation: the addition of methyl group to DNA, converting cytosine to 5-methylcytosine, mostly at CpG sites; 2. Histone modifications: posttranslational modificationEpigeneticss of histone proteins including acetylation, methylation, ubiquitylation, phosphorylation and sumoylation; 3. miRNAs: non-coding microRNA downregulating gene expression; 4. Prions: infectious proteins viewed as epigenetic agents capable of inducing a phenotype without changing the genome.
Products for Chromatin/Epigenetics
- Bromodomain(47)
- Aurora Kinase(57)
- DNA Methyltransferase(32)
- HDAC(176)
- Histone Acetyltransferases(71)
- Histone Demethylases(99)
- Histone Methyltransferase(204)
- HIF(91)
- JAK(154)
- MBT Domains(1)
- PARP(104)
- Pim(27)
- Protein Ser/Thr Phosphatases(31)
- RNA Polymerase(6)
- Sirtuin(70)
- Sphingosine Kinase-2(1)
- Polycomb repressive complex(2)
- SUMOylation(3)
- PAD(21)
- Epigenetic Reader Domain(205)
- MicroRNA(20)
- Chromodomain(1)
- Citrullination(20)
- DNA/RNA Demethylation(2)
- DNA/RNA Methylation(8)
- Histone Deacetylation(42)
- Histones/Histone Peptides(62)
- PHD Domains(1)
- Tandem Tudor & Tudor-like Domains(1)
- PRMT(2)
- Readers(1)
- Cat.No. 产品名称 Information
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GC12821
Oltipraz
奥替普拉; RP 35972; NSC 347901
A Nrf2 and CAR activator - GC12074 BG45 A selective HDAC3 inhibitor
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GC10417
ACY-241
西他司他,Citarinostat
An HDAC6 inhibitor -
GC10770
Decernotinib(VX-509)
迪西替尼
A selective JAK3 inhibitor -
GC16042
Chidamide
西达本胺,Chidamide impurity
An HDAC inhibitor - GC12005 C7280948 A PRMT1 inhibitor
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GC16299
BET bromodomain inhibitor
BET抑制剂,CPI-0610; CPI0610; CPI 0610
BET 溴结构域抑制剂是从专利 WO/2015/153871A2 化合物实施例 11 中提取的一种有效的 BET 抑制剂。 - GC11578 GSK2879552 An LSD1 inhibitor
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GC10046
Molidustat (BAY85-3934)
BAY 85-3934
A pan-HIF-PH inhibitor - GC11641 Boc-Lys(Ac)-AMC A fluorogenic HDAC substrate
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GC12997
GSK J4 free base
N-[2-(2-吡啶基)-6-(1,2,4,5-四氢-3H-3-苯并氮杂卓-3-基)-4-嘧啶基]-BETA-丙氨酸乙酯
GSK J4 free base 是 H3K27me3/me2-去甲基化酶 JMJD3/KDM6B 和 UTX/KDM6A 的有效双重抑制剂,IC50 分别为 8.6 和 6.6 μM。 GSK J4 游离碱抑制 LPS 诱导的 TNF-α;在人原代巨噬细胞中产生,IC50 为 9 μM. GSK J4 是 GSK-J1 的细胞渗透性前药。 GSK J4 free base 诱导内质网应激相关的细胞凋亡。 - GC14857 LFM-A13 A BTK inhibitor
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GC16638
FG2216
IOX3; YM311
An inhibitor of HIF-PH2 - GC11414 GSK503 A potent, selective EZH2 inhibitor
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GC13541
G007-LK
Tankyrase 1/2 Inhibitor VI
A TNKS1/2 inhibitor -
GC15049
MCB-613
4-乙基-2,6-双(吡啶-3-基亚甲基)环己酮
A small molecule stimulator of SRCs -
GC15302
EPZ015666
GSK3235025
A bioavailable PRMT5 inhibitor - GC12484 BRD73954 A dual inhibitor of HDAC6 and HDAC8
- GC15368 GSK-LSD1 2HCl 不可逆的、选择性的 LSD1 抑制剂
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GC12498
Sephin1
(E/Z)-Sephin1; (E/Z)-IFB-088
A selective inhibitor of the phosphatase regulatory subunit PPP1R15A -
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。
- GC16015 A 366 A potent inhibitor of G9a
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GC13474
Garcinol
山竹子素
Garcinol是组蛋白乙酰转移酶p300和PCAF的非特异性抑制剂,IC50分别为7μM和5μM。
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GC15836
IWP 12
Inhibitor of Wnt Production-12
A PORCN inhibitor -
GC10319
TC-E 5002
N-(9-环丙基-1-氧代壬基)-N-羟基-Β-丙氨酸
A KDM2/7 inhibitor - GC14655 OXF BD 02 OXF BD 02 是 BRD4(1)(BRD4 的第一个溴结构域)的选择性抑制剂,IC50 值为 382 nM。
- GC10727 Ischemin sodium salt CBP bromodomain inhibitor
- GC12440 GSK 5959 An inhibitor of the BRPF1 bromodomain
- GC15175 BAZ2-ICR A BAZ2A/B bromodomain inhibitor
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GC17126
EX-527 R-enantiomer
(R)-EX-527
EX-527 R-对映异构体 ((R)-EX-527) 是 Selisstat 的 R-对映异构体。 Selisistat (EX-527) 是一种有效的选择性 SIRT1 抑制剂,IC50 为 98 nM。 -
GC13417
EX-527 S-enantiomer
(1S)-6-氯-2,3,4,9-四氢-1H-咔唑-1-甲酰胺,(S)-EX-527
EX-527 S-对映异构体 ((S)-EX-527) 是一种有效的选择性 SIRT1 抑制剂,IC50 为 98 nM。 - GC17482 OF-1 A bromodomain probe for BRPF proteins
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GC14631
SP2509
HCI-2509, LSD1 Inhibitor VII
A reversible inhibitor of LSD1 -
GC12557
ML324
CID-44143209
A cell-permeable inhibitor of JMJD2 demethylases - GC11574 HPOB A potent and selective inhibitor of HDAC6
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GC12971
CAY10603
BML-281
An exceptionally potent inhibitor of HDAC6 - GC12189 LB-100 A PP2A inhibitor with anticancer activity
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GC10259
BRD4770
HMTase Inhibitor VI
An inhibitor of EHMT2/G9a - GC10021 CPI-360 A selective EZH2 inhibitor
- GC11430 Remodelin Remodelin 是 N-乙酰转移酶 10 (NAT10) 的小分子抑制剂。
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GC17956
PFI-2
(R)-PFI-2
PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride 是一种有效的选择性 SET 结构域,含有赖氨酸甲基转移酶 7 (SETD7) 抑制剂。 -
GC14439
Santacruzamate A (CAY10683)
HDAC抑制剂,CAY-10683
A histone deacetylase inhibitor -
GC16611
GW841819X
BET bromodomain inhibitor
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GC11209
Cerdulatinib (PRT062070)
赛度替尼,PRT062070; PRT2070
A dual inhibitor of Syk and JAKs - GC16741 UNC0379 A selective SET8 inhibitor
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GC13249
Rucaparib (free base)
瑞卡帕布; AG014699; PF-01367338
A PARP1 inhibitor -
GC11990
TCS-PIM-1-4a
5-[[3-(三氟甲基)苯基]亚甲基]-2,4-噻唑烷二酮,SMI-4a
TCS-PIM-1-4a (SMI-4a) 是一种泛 Pim 激酶抑制剂,通过激活 AMPK 来阻断 mTORC1 的活性。 TCS-PIM-1-4a 可杀死多种髓系和淋巴系细胞系(IC50 值范围为 0.8 μM 至 40 μM)。 - GC17222 GLPG0634 analogue GLPG0634 类似物 (Compoun 176) 是一种广谱 JAK 抑制剂,对 JAK1、JAK2 和 JAK3 的 IC50 值 <100 nM。
- GC16314 TC-E 5001 TC-E 5001 是一种 Wnt 通路抑制剂,通过新的腺苷口袋结合抑制 tankyrase 1/2 (TNKS1/2),Kd 分别为 79 nM 和 28 nM。 TC-E 5001 还抑制 Axin2 和 STF,IC50 分别为 0.709 μM 和 0.215 μM。