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)
- GC12743Calcineurin Autoinhibitory PeptideCAS: 148067-21-4
Calcineurin autoinhibitory peptide 是 Ca2+/calmodulin-dependent protein phosphatase (calcineurin) 的选择性抑制剂,IC50 为 ~10 μM。
- GC13139FG-4592 (ASP1517)CAS: 808118-40-3纯度: >99.50%
FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。
- GC131453-Deazaneplanocin,DZNepCAS: 102052-95-9纯度: >98.00%
An inhibitor of lysine methyltransferase EZH2
- GC13154Pim1/AKK1-IN-1CAS: 1093222-27-5纯度: >98.00%
Pim1/AKK1-IN-1是一种有效的多靶点抑制剂,对Pim1、AKK1(AAK1)、LKB1和MST2等激酶具有抑制作用。
- GC14191Ruxolitinib (INCB18424)CAS: 941678-49-5纯度: >98.00%
Ruxolitinib (INCB18424)作为一种抑制剂,能够抑制Janus相关激酶(JAKs)JAK1和JAK2, IC50 分别为 3.3 nM 和 2.8 nM,Ruxolitinib介导对造血和免疫功能重要的若干细胞因子和生长因子信号。
- GC14366ThioguanineCAS: 154-42-7纯度: >99.00% / >98.00%
Thioguanine是一种抗白血病和免疫抑制剂,对重组USP2和冠状病毒PLpro的IC 50 值分别为40μM和25μM。
- GC14395Fostriecin sodium saltCAS: 87860-39-7纯度: >95.00%
A potent inhibitor of protein phosphatases 2A and 4
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12743 | Calcineurin Autoinhibitory Peptide | 148067-21-4 | - | |
Calcineurin autoinhibitory peptide 是 Ca2+/calmodulin-dependent protein phosphatase (calcineurin) 的选择性抑制剂,IC50 为 ~10 μM。 | ||||
| GC12781 | XAV-939 | 284028-89-3 | >98.50% / >98.00% | |
XAV-939 选择性抑制 β-连环蛋白介导的转录。 | ||||
| GC12932 | EPZ5676 | 1380288-87-8 | >99.50% | |
EPZ5676是一种新型的、高效的、选择性DOT1L组蛋白甲基转移酶抑制剂,K i 值小于80pM,对DOT1L的IC 50 为0.8nM,选择性比作用于其他多种蛋白甲基转移酶高37000倍。 | ||||
| GC12961 | Apicidin | 183506-66-3 | >98.00% / >90.00% | |
A cell-permeable HDAC inhibitor | ||||
| GC13018 | IOX2(Glycine) | 931398-72-0 | >99.50% | |
A selective PHD2 inhibitor | ||||
| GC13055 | Mocetinostat (MGCD0103, MG0103) | 726169-73-9 | >99.00% | |
An orally available HDAC inhibitor | ||||
| GC13056 | CX-6258 | 1202916-90-2 | >99.50% | |
A pan-Pim kinase inhibitor | ||||
| GC13139 | FG-4592 (ASP1517) | 808118-40-3 | >99.50% | |
FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。 | ||||
| GC13141 | KC7F2 | 927822-86-4 | >99.00% / >98.00% | |
KC7F2是转录因子HIF-1(缺氧诱导因子-1)的抑制剂,其IC₅₀分别为20μM ,KC7F2常被用于肿瘤发育和血管形成的研究中 | ||||
| GC13145 | 3-Deazaneplanocin,DZNep | 102052-95-9 | >98.00% | |
An inhibitor of lysine methyltransferase EZH2 | ||||
| GC13154 | Pim1/AKK1-IN-1 | 1093222-27-5 | >98.00% | |
Pim1/AKK1-IN-1是一种有效的多靶点抑制剂,对Pim1、AKK1(AAK1)、LKB1和MST2等激酶具有抑制作用。 | ||||
| GC13398 | RG 108 | 48208-26-0 | >99.50% | |
RG 108是一种强效的DNA甲基转移酶抑制剂,IC 50 值为115nM。 | ||||
| GC13878 | EPZ005687 | 1396772-26-1 | >99.00% | |
A potent, selective inhibitor of EZH2 | ||||
| GC14024 | DL-AP3 | 5652-28-8 | >95.00% | |
A metabotropic glutamate receptor antagonist | ||||
| GC14165 | Tenovin-1 | 380315-80-0 | >99.50% | |
A small molecule activator of p53 | ||||
| GC14191 | Ruxolitinib (INCB18424) | 941678-49-5 | >98.00% | |
Ruxolitinib (INCB18424)作为一种抑制剂,能够抑制Janus相关激酶(JAKs)JAK1和JAK2, IC50 分别为 3.3 nM 和 2.8 nM,Ruxolitinib介导对造血和免疫功能重要的若干细胞因子和生长因子信号。 | ||||
| GC14245 | ZM 39923 HCl | 1021868-92-7 | >99.50% | |
A potent inhibitor of JAK3 | ||||
| GC14319 | ML 228 | 1357171-62-0 | >98.00% | |
A HIF pathway activator | ||||
| GC14321 | Sal 003 | 1164470-53-4 | >99.50% | |
An inhibitor of eIF2α dephosphorylation | ||||
| GC14366 | Thioguanine | 154-42-7 | >99.00% / >98.00% | |
Thioguanine是一种抗白血病和免疫抑制剂,对重组USP2和冠状病毒PLpro的IC 50 值分别为40μM和25μM。 | ||||
| GC14395 | Fostriecin sodium salt | 87860-39-7 | >95.00% | |
A potent inhibitor of protein phosphatases 2A and 4 | ||||
| GC14409 | ZM 447439 | 331771-20-1 | >98.00% | |
Selective inhibitor of Aurora B kinase | ||||
| GC14553 | Resveratrol | 501-36-0 | >99.50% | |
白藜芦醇(转-白藜芦醇;SRT501)是一种植物抗菌素。 | ||||
| GC14562 | Nanaomycin A | 52934-83-5 | >98.00% | |
A bacterial metabolite | ||||
