n-acetyltransferase

Remodelin hydrobromide (Remodelin HBR) 是一种新型有效的选择性乙酰转移酶蛋白 NAT10 抑制剂，能改善早衰综合征细胞表型。

MeAIB 是一种n -乙酰转移酶抑制剂，抑制SNAT2相关信号通路。MeAIB 是氨基酸转运系统a (ATA1)的特异性底物。氨基酸转运系统a (ATA1）以Na+流动调控短链中性氨基酸的摄取。

N-Acetyl-5-hydroxytryptamine (O-Demethylmelatonin) 是褪黑激素的直接前体，能够有效激活TrkB 受体。

N-Acetyl-L-phenylalanine (N-Ac-Phenylalanine) 是一种大肠杆菌中的主要酰基氨基酸，由 L-苯丙氨酸和乙酰辅酶 A 合成。

4-Acetamidophenyl acetate, an impurity of Acetaminophen, which is a selective COX-2 inhibitor (IC50: 25.8 μM) and a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor.

AK-968-11563024 是一种作用于海洋V. vulnificus NAT [(VIBVN)NAT] 的抑制剂，具有18.86 µM的IC50。海洋V. vulnificus中的NAT（芳香胺 N-乙酰转移酶）在药物代谢中扮演着重要角色，并促进药物耐受性的形成。因此，AK-968-11563024 可用于与药物耐受性相关的研究。

Monosodium N-acetylglutamate is the sodium salt of N-acetylglutamate, biosynthesized from glutamate and acetylornithine by ornithine acetyltransferase, and from glutamic acid and acetyl-CoA by the enzyme N-acetylglutamate synthase.

MeIQx (MeIQx) is a food-derived carcinogen that has been found in high temperature-cooked fish and meats.1It is activated by hydroxylation and subsequent O-acetylationviathe cytochrome P450 (CYP) isoform CYP1A2 and N-acetyltransferase 2, respectively, in UV5 cells expressing the human enzymes to a metabolite that reacts with DNA to form adducts.2MeIQx (200 and 400 ppm in the diet) induces tumor formation in rats.3

CAY10685 is a cell-active analog of the lysine acetyltransferase inhibitor CPTH2 that contains an alkyne moiety for use in click chemistry reactions. Its ability to inhibit N-acetyltransferase 10 activity has been used to modulate chromatin organization in order to study changes in nuclear architecture associated with cancer and certain laminopathies.

ANAT Inhibitor-1 serves as an inhibitor of human aspartate N-acetyltransferase (ANAT), targeting Canavan disease.

NSC 694621是一种PCAF和组蛋白乙酰转移酶（ histone acetyltransferase，HAT）抑制剂，与PCAF的活性位点Cys574形成共价键，从而不可逆地抑制其乙酰转移酶活性，能够抑制SK-N-SH 和HCT116细胞增殖，具有抗癌潜力。

NAT2-IN-1 (APA) 是药物代谢酶 N-乙酰转移酶 2 (NAT2) 的抑制剂。NAT2-IN-1 可以选择性地杀死慢速 NAT2 细胞。

Diethylnorspermine, also known as DENSPM, BE-333, DE-333 and N(1),N(11)-Diethylnorspermine, is a highly potent known inducer of the polyamine catabolic enzyme, spermidine spermine N1-acetyltransferase (SSAT). A designed polyamines (PAs) analog which induces cell cycle arrest, inhibits proliferation and induces apoptosis in melanoma, breast, prostate, lung and colon cancer cells..

GlmU-IN-5175178 is an inhibitor of the acetyltransferase activity of Escherichia coli N-acetylglucosamine-1-phosphate-uridyltransferase glucosamine-1-phosphate-acetyltransferase (GlmU).

N-acetylglucosamine-1-P uridyltransferase (AGX1) (GlcNAc1pUT) 是具有双功能乙酰转移酶 尿苷转移酶活性的原核生物专有酶。该酶能结合GlcNAc-1-P与UTP，催化合成UDP-GlcNAc的尿苷酰转移反应。

Naa50-IN-1 (化合物 4a)，作为N-α-Acetyltransferase 50 (Naa50) 的特异性抑制剂，展现出IC50为7 mM的活性，并具备作为癌症研究潜力候选物的特征。

Compound 350 (NAT1-IN-1) 为一种针对 N-乙酰转移酶 1 (NAT1) 的高效抑制剂,其半抑制浓度 (IC50) 为 44 nM.该化合物适用于肌萎缩侧索硬化症、癌症恶病质及脓毒症等代谢亢进疾病的研究.