Chromatin/Epigenetics
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.
- Bromodomain(50)
- Aurora Kinase(63)
- DNA Methyltransferase(35)
- HDAC(210)
- Histone Acetyltransferases(78)
- Histone Demethylases(110)
- Histone Methyltransferase(240)
- HIF(102)
- JAK(173)
- MBT Domains(1)
- PARP(122)
- Pim(32)
- Protein Ser/Thr Phosphatases(34)
- RNA Polymerase(7)
- Sirtuin(77)
- Sphingosine Kinase-2(1)
- Polycomb repressive complex(2)
- SUMOylation(3)
- PAD(21)
- Epigenetic Reader Domain(246)
- MicroRNA(24)
- Protein Arginine Deiminase(7)
- Chromodomain(1)
- Citrullination(20)
- DNA/RNA Demethylation(2)
- DNA/RNA Methylation(8)
- Histone Deacetylation(44)
- 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)
Chromatin/Epigenetics 相关产品(1617)
- GC17836ITF2357 (Givinostat)CAS: 732302-99-7纯度: >98.00%
HDAC inhibitor with anti-inflammatory and antineoplastic activities
- GC11572Bardoxolone methylCAS: 218600-53-4纯度: >98.50%
Bardoxolone methyl是核因子红细胞2相关因子2(Nrf2)介导的抗氧化和抗炎反应的有效激活剂,也是NF-κB通路的抑制剂。
- GC11576Tranylcypromine (2-PCPA) HClCAS: 4548-34-9
(1S,2R)-Tranylcypromine ((1S,2R)-SKF 385) hydrochloride 是一种有效的抗抑郁剂。
- GC17162MK-5108 (VX-689)CAS: 1010085-13-8纯度: >98.00%
MK-5108 (VX-689)是一种有效的ATP竞争性Aurora A激酶抑制剂,IC 50 值为0.064nM。
- GC17783Veliparib dihydrochlorideCAS: 912445-05-7纯度: >99.50%
An orally bioavailable inhibitor of PARP1 and PARP2
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17050 | CYT387 | 1056634-68-4 | >98.50% | |
A potent inhibitor of JAK1 and JAK2 | ||||
| GC13433 | AZ 960 | 905586-69-8 | >98.00% | |
A JAK2 inhibitor | ||||
| GC13558 | PIM-1 Inhibitor 2 | 477845-12-8 | - | |
A potent PIM-1 kinase inhibitor | ||||
| GC14936 | Chaetocin | 28097-03-2 | >98.00% | |
据报道毛壳素是组蛋白甲基转移酶 (HMT)(例如 SUV39H1)的非特异性抑制剂,从而影响基因表达。 | ||||
| GC17836 | ITF2357 (Givinostat) | 732302-99-7 | >98.00% | |
HDAC inhibitor with anti-inflammatory and antineoplastic activities | ||||
| GC10035 | TG101209 | 936091-14-4 | >99.50% | |
An inhibitor of JAK2, FLT3, RET, and JAK3 | ||||
| GC11572 | Bardoxolone methyl | 218600-53-4 | >98.50% | |
Bardoxolone methyl是核因子红细胞2相关因子2(Nrf2)介导的抗氧化和抗炎反应的有效激活剂,也是NF-κB通路的抑制剂。 | ||||
| GC11576 | Tranylcypromine (2-PCPA) HCl | 4548-34-9 | - | |
(1S,2R)-Tranylcypromine ((1S,2R)-SKF 385) hydrochloride 是一种有效的抗抑郁剂。 | ||||
| GC12548 | UNC 0631 | 1320288-19-4 | >99.00% | |
An inhibitor of G9a/GLP methyltransferases | ||||
| GC13103 | AZ505 ditrifluoroacetate | 1035227-44-1 | >99.50% | |
An inhibitor of SMYD2 | ||||
| GC13488 | R8-T198wt | 2305815-72-7 | - | |
R8-T198wt 是一种细胞可渗透的羧基末端 p27Kip1 肽,通过抑制 Pim-1 激酶表现出抗肿瘤活性。 | ||||
| GC13744 | AZ505 | 1035227-43-0 | >99.50% | |
An inhibitor of SMYD2 | ||||
| GC14490 | Donepezil HCl | 120011-70-3 | >99.50% | |
An AChE inhibitor | ||||
| GC15002 | Sodium Phenylbutyrate | 1716-12-7 | >99.50% | |
Sodium Phenylbutyrate是一种组蛋白去乙酰化酶(HDAC)抑制剂。 | ||||
| GC15315 | Scriptaid | 287383-59-9 | >98.50% | |
HDAC inhibitor | ||||
| GC16290 | Nafamostat hydrochloride | 80251-32-7 | - | |
Nafamostat hydrochloride 是一种合成丝氨酸蛋白酶抑制剂,是一种抗凝剂。 | ||||
| GC16518 | UNC 0646 | 1320288-17-2 | >99.50% | |
An inhibitor of G9a/GLP methyltransferases | ||||
| GC17162 | MK-5108 (VX-689) | 1010085-13-8 | >98.00% | |
MK-5108 (VX-689)是一种有效的ATP竞争性Aurora A激酶抑制剂,IC 50 值为0.064nM。 | ||||
| GC17314 | OG-L002 | 1357302-64-7 | >99.50% | |
An LSD1 inhibitor | ||||
| GC17783 | Veliparib dihydrochloride | 912445-05-7 | >99.50% | |
An orally bioavailable inhibitor of PARP1 and PARP2 | ||||
| GC11491 | SGC 0946 | 1561178-17-3 | >99.50% | |
A potent inhibitor of DOT1L | ||||
| GC12083 | CEP-33779 | 1257704-57-6 | >99.00% | |
A potent, orally available inhibitor of JAK2 | ||||
| GC13383 | EPZ004777 | 1338466-77-5 | >98.00% | |
EPZ004777 作为一种有效的表观遗传调节剂,可以逆转 TGF-β1 诱导的 T 调节细胞,可用于治疗多种免疫疾病。 | ||||
| GC14151 | CBB1007 | 1379573-92-8 | - | |
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)。 | ||||
