Remdesivir (GS-5734) 是一种核苷类似物，具有抗病毒活性，在 HAE 细胞中，对 SARS-CoV 和 MERS-CoV 的 EC50 值为 74 nM，在延迟脑肿瘤细胞中，对鼠肝炎病毒的 EC50 值为 30 nM。Remdesivir 有潜力用于 2019-nCoV (COVID-19) 研究。

Peramivir trihydrate (RWJ-270201 trihydrate;BCX-1812 trihydrate) 是一种高效、选择性和口服有效的流感病毒神经氨酸酶 (NA) 抑制剂，对 9 个亚型 NA 抑制作用的 IC50 值为 0.9-4.3 nM。

GS-441524 对猫传染性腹膜炎病毒 (FIPV) 有较强的抑制作用，对应的 EC50 值为 0.78 μM。

Telaprevir (VX-950) is an HCV NS3-4A serine protease inhibitor with IC50 of 0.35 μM.

Nelfinavir(AG-1341) is a potent and orally bioavailable human immunodeficiency virus HIV-1 protease inhibitor (Ki=2 nM) and is widely prescribed in combination with HIV reverse transcriptase inhibitors for the treatment of HIV infection.

A novel anti-TB agent that has an MIC range of 0.06-0.5 ug/mL..

R enantiomer of Hydroxychloroquine. Hydroxychloroquine is a potent drug for the COVID-19 trement.

NHC-triphosphate is an intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a triphosphate form.

Nelfinavir(AG-1341) is a potent and orally bioavailable human immunodeficiency virus HIV-1 protease inhibitor (Ki=2 nM) and is widely prescribed in combination with HIV reverse transcriptase inhibitors for the treatment of HIV infection.

Ritonavir is an inhibitor of HIV protease used to treat HIV infection and AIDS,showed potent activity against COVID-19(SARS-COV-2) .

Darunavir(TMC114) is an HIV protease inhibitor,showed potent activity against COVID-19(SARS-COV-2) .

Atazanavir is a HIV protease inhibitor with Ki of 2.66 nM.

PF 1022A is a N-methylated cyclooctadepsipeptides (CODPs) with strong anthelmintic properties; acts as an ionophore.

Erythromycin Cyclocarbonate, derivative of Erythromycin, inhibits protein synthesis of bacteria by binding to the 50S ribosome.

Minocycline is a tetracycline antibiotic with neuroprotective, antiapoptotic, anti-inflammatory and antimicrobial effects.

Doravirine (MK-1439) is a non-nucleoside reverse transcriptase inhibitor.

Cidofovir(Vistide)

Voriconazole is an ergosterol biosynthesis inhibitor, as well as systemic antifungal. This compound, like many antifungal agents, is an inhibitor of CYP2C9, an enzyme involved in the oxidative metabolism of many xenobiotics.

Raltegravir Salt is a potent human immunodeficiency virus (HIV) integrase inhibitor and a novel anti-AIDS drug.