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(45)
- Aurora Kinase(62)
- DNA Methyltransferase(35)
- HDAC(201)
- Histone Acetyltransferases(77)
- Histone Demethylases(104)
- Histone Methyltransferase(238)
- HIF(101)
- JAK(162)
- MBT Domains(1)
- PARP(118)
- Pim(31)
- Protein Ser/Thr Phosphatases(31)
- RNA Polymerase(6)
- Sirtuin(74)
- Sphingosine Kinase-2(1)
- Polycomb repressive complex(2)
- SUMOylation(3)
- PAD(21)
- Epigenetic Reader Domain(243)
- MicroRNA(24)
- 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)
- Small Interfering RNA (siRNA)(1)
- METTL3(2)
- WDR5(1)
- TET Protein(2)
- HuR(1)
- SF3B1(1)
- Cat.No. 产品名称 Information
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GC11576
Tranylcypromine (2-PCPA) HCl
(1S,2R)-2-苯基-环丙胺盐酸盐,(1S,2R)-SKF 385 hydrochloride
(1S,2R)-Tranylcypromine ((1S,2R)-SKF 385) hydrochloride 是一种有效的抗抑郁剂。 -
GC17314
OG-L002
An LSD1 inhibitor
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GC15259
EPZ004777 HCl
EPZ004777 HCl 是一种有效的选择性 DOT1L 抑制剂,IC50 为 0.4 nM。
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GC12733
C646
C646是一种有效的选择性p300/CBP组蛋白乙酰转移酶抑制剂(Ki 400 nM),已被证明具有多效性,包括神经保护、抗癌和抗上皮间质转化(anti-EMT)作用。
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GC15410
Bufexamac
丁苯羟酸; Bufexamic acid
An NSAID and a class IIb HDAC inhibitor -
GC16290
Nafamostat hydrochloride
盐酸萘莫司他
Nafamostat hydrochloride 是一种合成丝氨酸蛋白酶抑制剂,是一种抗凝剂。 -
GC17676
Nafamostat
萘莫司他
A serine protease inhibitor -
GC14490
Donepezil HCl
盐酸多奈哌齐; E2020
An AChE inhibitor
-
GC12579
GLPG0634
非戈替尼,GLPG0634
A JAK1 inhibitor -
GC10154
ABC294640
3-(4-氯苯基)-N-(4-吡啶基甲基)金刚烷-1-甲酰胺,ABC294640
An inhibitor of SPHK2 -
GC14699
CPI-203
A bioavailable inhibitor of BET bromodomains
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GC12698
BAY 87-2243
A mitochondrial complex I inhibitor and inducer of ferroptosis
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GC14756
EI1
6-氰基-N-[(1,2-二氢-4,6-二甲基-2-氧代-3-吡啶基)甲基]-1-(1-乙基丙基)-1H-吲哚-4-甲酰胺,KB-145943
A selective inhibitor of EZH2 -
GC14151
CBB1007
CBB1007 是一种细胞可渗透的脒基胍化合物,可作为一种有效的、可逆的和底物竞争性 LSD1 选择性抑制剂(hLSD1 的 IC50 = 5.27 μM)。
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GC13103
AZ505 ditrifluoroacetate
N-环己基-3-[[2-(3,4-二氯苯基)乙基]氨基]-N-[2-[[2-(3,4-二氢-5-羟基-3-氧代-2H-1,4-苯并恶嗪-8-基)乙基]氨基]乙基]丙酰胺二(2,2,2-三氟乙酸盐)
An inhibitor of SMYD2 -
GC13744
AZ505
N-环己基-3-(3,4-二氯苯乙基氨基)-N-[2-[[2-[5-羟基-3-氧代-3,4-二氢-2H-苯并[B][1,4]恶嗪-8-基]乙基]氨基]乙基]丙酰胺
An inhibitor of SMYD2 -
GC14063
GSK1324726A
I-BET726
A selective inhibitor of BET family proteins -
GC13148
MS436
MS436 是一类新的溴结构域抑制剂,对 BRD4 BrD1 具有估计的 Ki=30-50 nM 的强亲和力,对 BrD2 的选择性是 10 倍。
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GC12548
UNC 0631
An inhibitor of G9a/GLP methyltransferases
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GC15747
I-BET151 (GSK1210151A)
7-(3,5-二甲基异噁唑-4-基)-8-甲氧基-1-((R)-1-(吡啶-2-基)乙基)-1H-咪唑并[4,5-C]喹啉-2(3H)-酮,GSK1210151A
A BRD2, BRD3, and BRD4 inhibitor -
GC17073
I-BET-762
(4S)-6-(4-氯苯基)-N-乙基-8-甲氧基-1-甲基-4H-[1,2,4]三唑并[4,3-A][1,4]苯并二氮杂卓-4-乙酰胺,I-BET762; GSK525762; GSK525762A
Inhibitor of BET proteins -
GC11537
MK-4827 tosylate
尼拉帕尼对苯甲磺酸盐; MK-4827 tosylate
An orally bioavailable PARP1/2 inhibitor -
GC12756
MK-4827 hydrochloride
MK-4827 hydrochloride
MK-4827 hydrochloride (MK-4827 hydrochloride) 是一种高效且具有口服生物利用度的 PARP1 和 PARP2 抑制剂,IC50 分别为 3.8 和 2.1 nM。 MK-4827 hydrochloride 抑制 DNA 损伤的修复,激活细胞凋亡并显示出抗肿瘤活性。 -
GC11424
Valproic acid
丙戊酸; VPA; 2-Propylpentanoic Acid
A class I HDAC inhibitor -
GC16143
Varenicline Hydrochloride
6,7,8,9-四氢-6,10-甲桥-6H-吡嗪并[2,3-H][3]苯并氮杂卓盐酸盐,CP 526555 hydrochloride
Varenicline Hydrochloride (CP 526555 hydrochloride) 是一种高亲和力、选择性的 α4β2 尼古丁乙酰胆碱受体 (nAChR) 部分激动剂和完整的 α7 nAChR 激动剂。 -
GC11439
MG 149
Tip60 HAT inhibitor
A HAT inhibitor -
GC12891
CCT007093
(2E,5E)-2,5-二(2-噻吩基亚甲基)环戊酮
An inhibitor of PPM1D -
GC14755
Inauhzin
INZ
A selective SIRT1 inhibitor -
GC14364
SGI-1027
DNA Methyltransferase Inhibitor II
A DNA methyltransferase inhibitor -
GC14676
Pacritinib (SB1518)
帕克替尼
An equipotent inhibitor of FLT3 and JAK2 -
GC11375
UNC1999
A selective, cell-permeable EZH2 inhibitor
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GC14652
MM-102
HMTase Inhibitor IX
An inhibitor of WDR5/MLL interactions -
GC15603
JIB-04
5-氯-2(1H)-吡啶酮(2E)-(苯基-2-吡啶基亚甲基)腙
A pan Jumonji histone demethylase inhibitor -
GC14199
RVX-208
阿帕他隆; RVX-208; RVX000222
A selective BET bromodomain antagonist -
GC18096
UNC669
A selective MBT inhibitor
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GC13419
ME0328
A selective PARP3 inhibitor
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GC10442
MK-8745
An Aurora A kinase inhibitor
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GC17703
TMP269
TMP 269;TMP-269
A selective class IIa HDAC inhibitor -
GC14285
RGFP966
RGFP 966;RGFP-966
RGFP966是一种N-(o-aminophenyl)carboxamide HDAC抑制剂,对HDAC3的IC50为0.08 μM,是一类针对HDAC3的慢开/慢关竞争性紧密结合抑制剂。 -
GC11548
Tankyrase Inhibitors (TNKS) 49
TNKS 49;TNKS49;TNKS-49
Tankyrase inhibitor -
GC15041
Tankyrase Inhibitors (TNKS) 22
TNKS 22;TNKS22;TNKS-22
Tankyrase inhibitor -
GC12337
Tenovin-3
Tenovin 3;Tenovin3
A small molecule activator of p53 -
GC10322
Tubastatin A HCl
TubastatinA盐酸盐,TSA HCl;Tubastatin A hydrochloride
A potent HDAC6 inhibitor -
GC16436
Tenovin-6
A small molecule activator of p53
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GC12781
XAV-939
3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-D]嘧啶-4-酮
XAV-939 选择性抑制 β-连环蛋白介导的转录。 -
GC10555
Splitomicin
斯普利特麻一辛
Inhibitor of yeast Sir2p -
GC17455
TAK-632
A selective pan-Raf inhibitor
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GC15718
CID 2011756
An inhibitor of protein kinase D
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GC14062
EPZ-6438
E-7438,Tazemetostat
EPZ-6438 是一种有效且具有生物利用度的 EZH2 抑制剂,EZH2 是多梳抑制复合物 2 (PRC2) 的催化亚基,可催化组蛋白 H3 (H3K27) 的赖氨酸 27 甲基化,从而抑制含有人 PRC2 的活性抑制常数 Ki 值为 2.5 nM 的野生型 EZH2。
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GC14562
Nanaomycin A
七尾霉素,Nanafrocin, Nanafrocine, Nanafrocinum, Rosanomycin A
A bacterial metabolite