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.

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.

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.

2-Deoxy-D-glucose 是一种葡萄糖类似物，通过作用于己糖激酶 (hexokinase) 来抑制糖酵解 (glycolysis) 的葡萄糖代谢抑制剂。

Floxuridine is an oncology drug that belongs to antimetabolites with an GI50 of 5.1 μM for the inhibition of PEPT1.

Diacetylacyclovir is an impurity constitute of Aciclovir.