IMT1B是一种口服活性的线粒体RNA聚合酶(POLRMT) 抑制剂，能够抑制线粒体DNA表达，对抗肿瘤具有潜力。

Methylproamine is a DNA-binding radioprotector which, on the basis of published pulse radiolysis studies, acts by repair of transient radiation-induced oxidative species on DNA.

MM41是一种四聚体 DNA 稳定剂，对 MIA PaCa-2 胰腺癌细胞具有显著的抑制作用，IC₅₀ 值低于 10 nM，具有潜在的抗癌应用。

Werner syndrome RecQ helicase-IN-3是一种口服活性的 WRN 抑制剂，IC₅₀ 为 0.06 µM。它能够显示出显著的抗增殖活性，适用于癌症治疗中针对 WRN 的研究，尤其在与抗增殖相关的肿瘤治疗中具有潜力。

Quarfloxin是一种氟喹诺酮类衍生物，具有抗肿瘤活性，其通过干扰核糖体DNA和G-四重螺旋结构相互作用，靶向抑制RNA聚合酶 I 的活性。

3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) is an improved dopamine analog cytotoxic and inhibits DNA polymerase activity in melanoma cells. 3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) displays growth inhibitory activity in melanoma cell lines with varying degrees of tyrosinase activity.

Remdesivir nucleoside monophosphate是 Remdesivir 的代谢产物，Remdesivir 是一种抗病毒药物，能够有效抑制 SARS-CoV 和 MERS-CoV 的复制，适用于抗病毒药物及新冠病毒治疗的研究。

2'-O-Methylguanosine is a modified nucleoside that is produced in tRNAs by the action of tRNA guanosine-2’-O-methyltransferase, using S-adenosyl-L-methionine as a substrate.

3'-O-Acetylthymidine is a useful modified nucleoside.

HAMNO is a potent and selective inhibitor of replication protein A (RPA) interactions with proteins involved in the replication stress response. It has shown to significantly inhibits colony formation when combined with etoposide.

FEN1 inhibitor C2 is an inhibitor of flap endonuclease 1 (FEN1) which is required for proficient DNA replication and the repair of DNA damage.

LMI070 is a highly potent, selective and orally active small molecule SMN2 splicing modulator.

5-Bromouridine is used to label RNA in measurement of RNA production.

BMVC-8C3O is a DNA G-quadruplexes (G4s) ligand. It can induce topological conversion of non-parallel to parallel forms in human telomeric DNA G4s.

BVDV-IN-1 is a non-nucleoside inhibitor (NNI) of bovine viral diarrhea virus (BVDV) with EC50 value of 1.8μM. It directly binds to a hydrophobic pocket of the BVDV RdRp. BVDV-IN-1 has antiviral activity against BVDV resistant to NNI thiosemicarbazone (TSC).

Triapine is a ribonucleotide reductase inhibitor and a CDK inhibtor.

2'-Deoxyguanosine HCl is composed of the purine nucleoside guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose.

NSAH是一种非核苷类的核糖核苷酸还原酶（RNR)抑制剂，具有在细胞增殖和癌症治疗中的应用潜力。

3'-O-(TBDMS)Thymidine is a useful modified nucleoside.

FEN1 inhibitor C3 is an inhibitor of flap endonuclease 1 (FEN1) which is required for proficient DNA replication and the repair of DNA damage.