Aphidicolin是一种 DNA 聚合酶 α 和 δ 的抑制剂，通过抑制 DNA 合成来阻止细胞有丝分裂。Aphidicolin 来源于 Cephalosporium aphidicola，具有抗病毒和增强阿拉伯糖基核苷诱导细胞凋亡的作用，广泛用于抗癌及抗病毒研究。

Isookanin可用于多种疾病研究，包括肿瘤、皮疹、蛇和昆虫叮咬、糖尿病、腹泻，且具有抗HSV和水痘带状疱疹病毒 (VZV) 的抗病毒活性，具备抗氧化特性。

5-Hydroxymethyl-2'-deoxyuridine是一种核苷类似物，能够有效抑制多种人类白血病细胞系的增殖，IC₅₀ 范围为 1.7-5.8 μM。该化合物在白血病模型中延长了小鼠的存活时间，适用于白血病和细胞增殖的相关研究。

SIBA selectively inhibits spermine synthase, IC50=8 μM.

BAY 57-1293 represents a potent inhibitor of herpes simplex virus (HSV) that target the virus helicase primase complex.

TL4-12是一种选择性MAP4K2/GCK抑制剂，能下调IKZF1和BCL-6，抑制MM细胞增殖（IC50=37 nM），并诱导凋亡。TL4-12可用于克服多发性骨髓瘤（MM）中的免疫调节药物耐药性。

Presatovir is a novel inhibitor of respiratory syncytial virus (RSV) fusion F protein with potent antiviral activity against a broad range of strains, working by binding to F protein on the viral surface.

Pritelivir, also known as AIC-316 and BAY 57-1293, is a potent helicase primase inhibitor. BAY 57-1293 inhibits replication of herpes simplex virus (HSV) type 1 and type 2 in the nanomolar range in vitro by abrogating the enzymatic activity of the viral primase-helicase complex. In various rodent models of HSV infection the antiviral activity of BAY 57-1293 in vivo was found to be superior compared to all compounds currently used to treat HSV infections. The compound shows profound antiviral activity in murine and rat lethal challenge models of disseminated herpes, in a murine zosteriform spread model of cutaneous disease, and in a murine ocular herpes model. It is active in parenteral, oral, and topical formulations.

Adenosine 5'-monophosphate monohydrate是一种腺苷A1受体(adenosine A1 receptor) 激动剂，具有显著的抗病毒活性，对HSV-1和HSV-2病毒有抑制作用。

Edoxudine 是一种抗病毒分子，胸苷类似物，对单纯疱疹病毒有效。

Valacyclovir HCl is a Herpes Simplex Virus and Herpes Zoster Virus nucleoside analog DNA polymerase inhibitor as it is a synthetic purine nucleoside analogue.

Oxytetracycline HCI是一种四环素类抗生素，能有效抑制革兰氏阳性和阴性细菌的生长。它通过阻断aminoacyl-tRNA与核糖体RNA的结合来抑制蛋白质的合成。此外，Oxytetracycline hydrochloride还显示出对HSV-1的抗病毒活性。

Vidarabine is an antiviral drug effects by interfering with the synthesis of viral DNA, which is used in treatment of herpes simplex and varicella zoster viruses.

Penciclovir is a guanosine analogue antiviral drug as a DNA polymerase inhibitor.

Famciclovir is a guanine analogue antiviral drug as it is a competitive inhibitor of herpes simplex 2 DNA polymerase.

Acyclovir is a highly potent inhibitor of herpes simplex virus (HSV), types 1 and 2, and varicella zoster virus as it is an acrylic purine nucleoside analog.

1-Docosanol is an inhibitor of lipid-enveloped viruses which can inhibit replication of herpes simplex virus and respiratory syncytial virus.

Diacetylacyclovir is an impurity constitute of Aciclovir.

N-Carbobenzyloxy-L-valinyl-ganciclovir is the impurity of ganciclovir , which is used for the treatment of Hepatitis B.