Histone Acetyltransferases
Histone Acetyltransferases(组蛋白乙酰转移酶)
Histone acetyltransferases (HATs) are a diverse group of enzymes catalyzing a posttranslational modification of acetylation in which the acetyl group from the acetyl-CoA cofactor is transferred to the Nζ nitrogen of the target lysine side chain within histones. Based on the sequence divergence within the HAT domain, HATs is classified into at least five distinct families, including HAT1 family, Gcn5/PCAF family, MYST family, p300/CBP family and Rtt109 family. Despite the sequence divergence, a structurally conserved core region has been identified within each of the protein families, which contains a three-stranded β-sheet with a α—helix corresponding to the A and D regions of the Gcn5-related N-acetyltransferases (GNAT) proteins.
Histone Acetyltransferases 相关产品(77)
- GC10226Butyrolactone 3CAS: 778649-18-6纯度: >95.00% / >98.00%
Butyrolactone 3是组蛋白乙酰转移酶GCN5的小分子抑制剂(IC 50 = 100μM)。
- GC15104(R)-(+)-Etomoxir sodium saltCAS: 828934-41-4纯度: >99.00%
(R)-(+)-Etomoxir sodium salt(Etomoxir; ETO)是一种用于代谢和心血管疾病的小分子,经酶转化为活性抑制剂乙托莫西里尔辅酶a (IC50 约为0.01-0.70 µM)后,对CPT-1a和CPT-1b的抑制表现出纳摩尔效价。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12733 | C646 | 328968-36-1 | >98.00% | |
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。 | ||||
| GC18153 | WM-8014 | 2055397-18-5 | >99.50% | |
An inhibitor of KAT6A and KAT6B | ||||
| GC18154 | WM-1119 | 2055397-28-7 | >99.50% | |
WM-1119是一种强效KAT6抑制剂,IC 50 值为6.3μM,对KAT6A、KAT5和KAT7的K D 值分别为0.002μM、2.2μM和0.5μM。 | ||||
| GC10174 | SGC-CBP30 | 1613695-14-9 | >99.50% | |
A potent inhibitor of CREBBP/EP300 bromodomains | ||||
| GC10226 | Butyrolactone 3 | 778649-18-6 | >95.00% / >98.00% | |
Butyrolactone 3是组蛋白乙酰转移酶GCN5的小分子抑制剂(IC 50 = 100μM)。 | ||||
| GC10382 | CPI-637 | 1884712-47-3 | >99.50% | |
An inhibitor of CBP/EP300 bromodomains | ||||
| GC10931 | VULM 1457 | 228544-65-8 | - | |
VULM 1457 是一种有效的胆固醇酰基转移酶 (acyl-CoA) 抑制剂。 | ||||
| GC11430 | Remodelin | 1622921-15-6 | >98.00% | |
Remodelin 是 N-乙酰转移酶 10 (NAT10) 的小分子抑制剂。 | ||||
| GC11439 | MG 149 | 1243583-85-8 | >99.50% / >98.00% | |
MG 149是一种组蛋白乙酰转移酶(HAT)抑制剂,对Tip60和MOF的IC 50 值分别为74μM和47μM。 | ||||
| GC11539 | CI 976 | 114289-47-3 | - | |
An inhibitor of ACAT-1 | ||||
| GC11972 | NU 9056 | 1450644-28-6 | >98.00% | |
NU 9056(1,2-双(异噻唑-5-基)二硫烷)是一种有效且选择性的Tip60(KAT5) 组蛋白乙酰转移酶(HAT)抑制剂,IC 50 值为2μM,具有抗肿瘤活性。 | ||||
| GC12009 | HAT Inhibitor II | 932749-62-7 | >99.00% | |
An inhibitor of HAT p300 | ||||
| GC12917 | Acetaminophen | 103-90-2 | >99.00% | |
An analgesic and antipyretic compound | ||||
| GC12934 | YM 750 | 138046-43-2 | >98.00% | |
YM 750 是一种有效的 acyl-CoA:cholesterol acyltransferase (ACAT) 抑制剂 (IC50\u003d0.18 μM)。 | ||||
| GC13474 | Garcinol | 78824-30-3 | >95.00% | |
Garcinol是组蛋白乙酰转移酶p300和PCAF的非特异性抑制剂,IC 50 分别为7μM和5μM。 | ||||
| GC14103 | NSC228155 | 113104-25-9 | >98.00% | |
An EGFR activator and inhibitor of KID-KIX interactions | ||||
| GC14428 | CPTH2 (hydrochloride) | 2108899-91-6 | - | |
A HAT inhibitor | ||||
| GC14524 | CTPB | 586976-24-1 | >98.00% | |
A selective activator of p300 HAT | ||||
| GC14787 | Curcumin | 458-37-7 | >98.00% | |
A yellow pigment with diverse biological activities | ||||
| GC15049 | MCB-613 | 1162656-22-5 | >99.50% | |
A small molecule stimulator of SRCs | ||||
| GC15104 | (R)-(+)-Etomoxir sodium salt | 828934-41-4 | >99.00% | |
(R)-(+)-Etomoxir sodium salt(Etomoxir; ETO)是一种用于代谢和心血管疾病的小分子,经酶转化为活性抑制剂乙托莫西里尔辅酶a (IC50 约为0.01-0.70 µM)后,对CPT-1a和CPT-1b的抑制表现出纳摩尔效价。 | ||||
| GC15731 | L002 | 321695-57-2 | >98.50% | |
A p300 acetyltransferase inhibitor | ||||
| GC15836 | IWP 12 | 688353-45-9 | - | |
A PORCN inhibitor | ||||
| GC17284 | Anacardic acid | 16611-84-0 | >98.00% | |
A histone acetyltransferase inhibitor | ||||
