nascent

Fosbretabulin Disodium (CA 4P) 是一种微管蛋白去稳定剂，是 Combretastatin A4 前药，可选择性靶向内皮细胞，诱导新生肿瘤新血管消退，减少肿瘤血流量并引起中央肿瘤坏死。

5-Ethynyluridine 可用于标记新合成的 RNA。这种方法称为使用点击化学 (RICK) 捕获新转录的 RNA 相互作用组，系统地捕获与多种 RNA 结合的蛋白质，包括新生 RNA 和传统上被忽视的非多腺苷酸化 RNA。

GJ071 oxalate 是一种无义抑制剂。无义抑制剂（NonSups）诱导“读出”，即在提前终止密码子处选择近同源tRNA，并将相应的氨基酸插入新生多肽中。

MU147 是一种具有抗癌活性的 MRE11 核酸酶抑制剂和化学探针，对体内外的 Ehrlich 腹水肿瘤细胞具有致死性。MU147 消除依赖于 MRE11 核酸酶活性的双链断裂修复机制，而不影响 ATM 的激活。它还损害停滞复制 FOX 的新生链降解，并选择性影响 brca2 缺陷细胞。

QD325 is a potent redox modulator for the Treatment of Pancreatic Ductal Adenocarcinoma. Nascent RNA sequencing following treatments with QD325 revealed induction of stress responses in the nucleus, endoplasmic reticulum, and mitochondria of pancreatic ca

GJ-072 is a Nonsense suppressor. Nonsense suppressors (NonSups) induce “readthrough”, i.e., the selection of near cognate tRNAs at premature termination codons and insertion of the corresponding amino acid into nascent polypeptide.

Z-Hpg is a novel bortac-gj enabled selective probe for labeling of nascent proteomes, thus recording translation, in cell networks connected by gap junctions, leaving unconnected cells not labeled

4-Thiouridine (4-TU) 是一种光活化核糖核苷类似物，广泛用于RNA 分析。

Erythromycin A N-oxide is a potential impurity found in commercial preparations of erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains. It is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus (MIC90s = 0.015-2.0 mg/l). Erythromycin is known to potently inhibit the cytochrome P450 isoform CYP3A4, which can affect the metabolism of numerous clinically relevant medications. Erythromycin A N-oxide is also a precursor in the synthesis of clarithromycin .

Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains.[1] It is effective against a host of bacterial genera, including Streptococcus, Staphylococcus, and Haemophilus (MIC90s range from 0.015-2.0 mg/l).[2] Erythromycin is known to potently inhibit the cytochrome P450 isoform CYP3A4, which can affect the metabolism of numerous clinically relevant medications.[3],[4] Erythromycin lactobionate is a soluble salt of erythromycin that is typically used for intraperitoneal or intravenous injections.[5],[6]

Api137是一种抗生肽，其作用机制为通过抑制翻译干预细菌生长。具体来说，Api137在新生多肽链水解后，通过俘获释放因子于70S核糖体，从而抑制了蛋白质的合成。

Lamivudine triphosphate (3TCTP)是Lamivudine(核苷类似物)的磷酸化形式.该化合物能够抑制HIV或HBV的逆转录酶,通过链终止机制防止病毒复制.此外,Lamivudine triphosphate亦作为HCVNS5B RdRp亚基的抑制剂,且可被SARS-CoV-2 RdRp整合入新合成的RNA中,有效阻断新生SARS-CoV-2 RNA的突变.

Cotransin 是一种 Sec61 易位抑制剂，能以信号序列辨别的方式阻止新生链插入 Sec61 易位通道中，通过抑制 VCAM-1 和 p-selectin 蛋白跨内质网 (ER) 膜的共翻译易位 (IC50=0.5-5 µM) 来选择性抑制这些蛋白的表达，有用于研究炎症及免疫的潜力。