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Antiviral activity of phenanthrenes from the medicinal plant Bletilla striata against influenza A virus


Influenza viruses are responsible for seasonal epidemics and occasional pandemics, which cause significant morbidity and mortality. The vaccines need to be reformulated almost every year owing to antigenic drift, and the timely production of pandemic vaccines remains problematic because of the limitations of current technology [1–4]. Antiviral drugs play a significant role in controlling the spread of the disease, but the emergence of drug-resistant viral strains has been reported occasionally [5, 6], which has become a serious public health concern globally. Therefore, safe and effective new antiviral drugs need to be developed urgently to combat viral infections for either therapeutic or prophylactic purposes.

Two surface glycoproteins are present on the envelope of the influenza virus: hemagglutinin (HA) and neuraminidase (NA). The life cycle of the influenza virus begins with viral HA binding to sialic acid (SA) receptors on the host cell surface, followed by internalization of the virus by receptor-mediated endocytosis [7, 8]. Subsequently, endosomal acidification alters the conformation of HA and leads to the fusion of the host and viral membranes, which allows the release of the viral nucleoproteins (NPs) into the cytoplasm. In the nucleus of the infected cells, the viral RNAs are transcribed into mRNAs and replicated. Finally, the newly synthesized viral ribonucleoproteins (vRNPs) are exported into the cytoplasm, and after packaging, mature virions are released from the cell surface depending on the cleaving of SA receptors by sialidase. Therefore, HA plays a key role in initiating viral infection by binding to SA-containing receptors on the host cells, thus mediating the subsequent viral entry and membrane fusion [9–11]. The NA cleaves the specific linkage of the SA receptor, resulting in the release of the newly formed virions from the infected cells [12, 13]. Oseltamivir, marketed under the trade name Tamiflu, was the first orally administered commercially developed NA inhibitor. It was discovered using shikimic acid as a starting point for synthesis. Shikimic acid was originally available as an extract of Chinese star anise. Oseltamivir is on the World Health Organization’s list of essential medicines, a list of the most important medications needed in a basic health system. However, it was found that a substantial number of patients might become oseltamivir-resistant as a result of oseltamivir use and that oseltamivir resistance might be significantly associated with pneumonia [14, 15].

The tuber of Bletilla striata (Orchidaceae family) is a well-known traditional Chinese herb (known as Baiji in Chinese). The Chinese Pharmacopoeia states that B. striata supports hemostasis and detumescence and promotes recovery. Phytochemical research revealed that Bletilla contains polysaccharides, bibenzyl, phenanthrene, dihydrophenanthrene, flavonoids, and phenolic compounds [16–19]. In addition, it was reported to have antimicrobial, antioxidant, and anti-inflammatory activities. The chemical components of B. striata and its 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical-scavenging, ferric-reducing antioxidant, and tyrosinase-inhibitory activities were studied. Furthermore, six biphenanthrenes were separated, and their antibacterial activities were reported. In the present study, the anti-influenza viral activity of 12 phenanthrenes was investigated, and the antiviral mechanisms, such as inhibition of the activity of NA or HA, were explored.

Preparation of the compounds

The rhizomes of B. striata (Orchidaceae family) were collected from Tuankou Town, Zhejiang Province, People’s Republic of China, and authenticated by Prof. ZS Ding (one of the authors). A voucher specimen was deposited at the Zhejiang Chinese Medical University with specimen number BS-2012-I. The organic extract of B. striata was prepared via maceration in 95% ethanol under reflux four times (each time, 100 min). After removal of the solvent under reduced pressure, the residual was suspended in 1 L of H2O and partitioned with EtOAc (1 L × 4) to yield an EtOAc-soluble fraction. The fraction was purified on a silica gel column eluted with a gradient CHCl3-MeOH solvent system (100:1, 75:1, 50:1, 25:1, 5:1, and 1:1) and then purified using a high-performance liquid chromatography (HPLC) system (260 nm, 1 mL/min) on a Venusil XBP C18 column (Bonna-Agela, USA) (250 × 10 mm2, 5 μM) eluted with a gradient mixture of acetonitrile in water with 0.1% formic acid [22, 23]. The structures were determined using an extensive spectroscopic analysis including UV, LC-MS, 1H–NMR, and 13C–NMR.

Virus propagation and titration

The influenza virus strain A/Sydney/5/97 (H3N2) used in this study was obtained from Zhejiang Provincial Center for Disease Control and Prevention, propagated in the allantoic cavity of 9- to 11-day-old chicken eggs at 34 °C, and harvested 48 h after inoculation as the pooled allantoic fluid [24, 25]. After a brief centrifugation (3000 rpm at 4 °C for 20 min) and hemagglutination titer measured by a hemagglutination test (WHO, 2002), the virulence of the virus was determined by a 50% egg infective dose (EID50) analysis in chicken eggs [24, 26] and a 50% tissue culture infective dose (TCID50) analysis in Madin-Darby canine kidney (MDCK) epithelial cells [26, 27].

A series of tenfold dilutions of the virus were inoculated into the chick allantoic cavity (0.2 mL/embryo), each dilution with 10 embryos, at 34 °C for 48 h, and then harvested. A hemagglutination test was performed, and the positive rate of each dilution was recorded. EID50 was evaluated using the method of Reed and Muench [24, 26]. Approximately 5 × 104 cells/well were seeded in 96-well microplates in minimum essential medium (MEM) with 10% fetal bovine serum (FBS) at 37 °C in a humidified 5% CO2 incubator. When the monolayer was confluent, the cells were washed twice with phosphate-buffered saline (PBS) and then infected with a series of tenfold virus dilutions (no-virus used as a control and each dilution with 10 replicates). The maintenance medium (MEM containing 100 U/mL penicillin G and 100 μg/mL streptomycin) was supplemented with 10 μg/mL L-1-(tosyl-amido-2-phenyl) ethyl chloromethyl ketone-treated trypsin (Sigma-Aldrich Company Ltd, UK) and then incubated at 37 °C with 5% CO2. The development of cytopathic effect (CPE) in the host cells was observed daily until no further CPE was observed and all no-virus control cells remained normal. CPE was recorded as five grades: ++++ (75–100% rounding of cells, increased refractility, or loss of adherence/detachment); +++ (50–74%); ++ (25–49%); + (1–24%); − (no morphologic changes in all the cells) (Fig. 1). The TCID50 was evaluated using the method of Reed and Muench [26, 27].

Antiviral activity in embryonated eggs

Various concentrations of the compounds were prepared by diluting with PBS and mixed with equal volumes of influenza virus at 100 EID50. The compound-virus mixture was incubated for 1 h at 37 °C. The 9-day-old swabbed eggs were punched and inoculated with the compound-virus mixture via the allantoic route. PBS and the virus without treatment were used as controls. The positive control was oseltamivir phosphate. Triplicate tests were performed for each compound against the virus. The eggs were incubated at 34 °C for 48 h. The allantoic fluid was harvested, and the virus titer was measured using a hemagglutination test. The logarithmic transformation (log 2 calculations) was done for HA titers of the influenza virus, and the inhibitory activity was calculated. Inhibition (%) = (X - Y)/X × 100%, where X is the log 2 HA titer of the viral control, and Y is the log 2 HA titer of the tested samples [24, 25].

Cytotoxicity to MDCK cells

An MTS-based assay was performed to evaluate the cytotoxic effects of the test compounds on MDCK cells. Approximately 5 × 104 cells/well were seeded in 96-well microplates in MEM with 10% FBS at 37 °C in a humidified 5% CO2 incubator. When the monolayer was confluent, the cells were washed twice with PBS and then treated with compounds diluted in serum-free MEM. After incubation at 37 °C for 48 h, 20 μL of MTS was added to each well, and the cells were incubated for 2 h. The absorbance at 490 nm was determined using a microplate reader. The cell viability was calculated using the following formula: cell viability (%) = (drug treatment – background)/(control – background) × 100%. The half-maximal cytotoxic concentration (CC50) of the compounds was defined as the concentration that reduced the A490 of compound-treated cells to 50% of that of untreated cells [27, 28].

Reduction of CPE in MDCK cells

Three tests were developed, and the non-cytotoxic concentration of each compound was determined using the cytotoxicity test. (1) Pretreatment: non-cytotoxic concentrations of the compounds were added to the cells, incubated for 18 h, and then removed. The cells were washed and infected with the influenza A/Sydney/5/97 (H3N2) at 100 TCID50 for 1 h. The virus was removed, and the medium was replaced with serum-free MEM as the maintenance medium. (2) Simultaneous treatment: non-cytotoxic concentration of the compounds and the virus at 100 TCID50 were added to the cell monolayers simultaneously at 37 °C for 1 h, and then supplemented with the maintenance medium. (3) Post-treatment: MDCK cells were infected with the virus at 37 °C for 1 h. Then the test compounds were added for 1 h and then supplemented with the maintenance medium. Cells without any treatment were used as not-infected control. PBS instead of the compounds was used as the infected control and oseltamivir phosphate as the positive control. Each test was performed in triplicate. All cultures were incubated for 72 h at 37 °C under 5% CO2 atmosphere until the infected control showed complete CPE: almost 100% of the cells were affected and most of the cell sheet came off the wall of the culture well as observed under a light microscope. Then, 20 μL of MTS was added to each well, and the cells were incubated for 2 h. The absorbance at 490 nm was determined using a microplate reader. CPE Inhibition (%) = (A

drug treatment – A

infected control)/(A

not-infected control – A

infected control) × 100%. The 50% inhibition concentration (IC50) was calculated using the Reed-Muench analysis [26–28].

Hemagglutination inhibition assay

The hemagglutination inhibition assay was used to study whether the compound could block the SA-containing receptors. The phenanthrenes from B. striata and oseltamivir phosphate were all tested Fresh guinea pig blood was collected at the Laboratory Animal Research Center of the Zhejiang Chinese Medical University, supplemented with 1.6% sodium citrate in sterile water. Then, red blood cells (RBC) were separated by centrifugation (800×g for 10 min at room temperature), washed three times with sterile PBS, and then suspended at a concentration of 1.5%. The least number of virus particles able to agglutinate the guinea pig RBC was determined in a serial virus dilution as four hemagglutination units (HAU). PBS instead of the compounds was used as the hemagglutinating positive control and no-virus RBC as the hemagglutinating negative control. Then, 50 μL of the compounds in serial twofold dilutions in PBS were mixed with 50 μL of 4 HAU influenza virus suspension, incubated for 1 h at 37 °C, mixed with an equal volume of 1.5% guinea pig RBC suspension for 1 h at room temperature, and then monitored for agglutination [10, 11].

Neuraminidase inhibition assay

The neuraminidase inhibition assay was used to evaluate the effects of each compound on the neuraminidase activity of the influenza virus, according to the instructions of the Neuraminidase Inhibitors Screen Kit (Beyotime, China). Inhibition = [(C− S) / (C − C

0)] × 100%, where C is the fluorescence of the control (enzyme, buffer, and substrate) after 30 min of incubation, and C

0 is the fluorescence of the control (buffer and substrate). S is the fluorescence of the tested samples (enzyme, sample solution, and substrate) after incubation. Standard curves were made by plotting the percentage of fluorescence inhibition relative to the activity of virus controls against the log2 of concentrations. In addition, 10 μg/mL oseltamivir phosphate was used as the positive control. Then, 10 μL of NA in 70 μL of reaction buffer was mixed with equal volumes of twofold dilutions of the compounds. After a 2-min incubation at 37 °C, equal volumes (10 μL) of the substrate solution [2-(4-methylumbelliferyl)-α-D-N-acetylneuraminic acid sodium (4-MU-NANA)] were added, and the mixtures were further incubated for 30 min at 37 °C. The fluorescence intensity was measured using a fluorescence plate reader at an excitation wavelength of 322 nm and an emission wavelength of 450 nm. The 50% inhibitory concentration (IC50) was calculated by regression analysis with r

2 ≥ 0.9, representing the mean values of three independent experiments [13, 29].

Evaluation of the expression levels of matrix protein mRNA of the influenza virus using quantitative real-time polymerase chain reaction (RT-PCR)

The expression level of matrix protein mRNA of the influenza virus was determined by reverse transcription and quantitative RT-PCR to evaluate the effects of each compound on virus replication. MDCK cells were grown to approximately 90% confluence in 24-well plates with 4 × 105 cells per well at 37 °C under 5% CO2, infected with the influenza virus at 100 TCID50, and cultured in the presence of the compounds at a concentration of 8 μM. PBS and the virus without treatment were used as controls, and the positive control was oseltamivir phosphate. The medium was removed after 18 h. The cells were scraped off, washed twice with PBS, and collected by centrifugation (500×g for 3 min). Total RNA was isolated using an RNeasy Mini Kit (Qiagen, Germany) according to the manufacturer’s instructions. RT-PCR was performed using a One-Step PrimeScript RT-PCR Kit (TaKaRa Biotech, Dalian, China). The primer sequences used for quantitative real-time PCR of viral matrix protein mRNA were 5′-GAC CRA TCC TGT CAC CTC TGA C-3′ (sense) and 5′-AGG GCA TTY TGG ACA AAK CGT CTA-3′ (antisense). Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as an internal control of cellular RNAs, with primer sequences of 5′-CAA CGG ATT TGG CCG TAT TGG-3′ (sense) and reverse: 5′-TGA AGG GGT CAT TGA TGG CG-3′ (antisense). RT-PCR was conducted in a 25-μL reaction system: 2× One-Step RT-PCR Buffer III, 12.5 μL; TaKaRa Ex Taq HS (5 U/μL), 0.5 μL; PrimeScript RT Enzyme Mix II, 0.5 μL; PCR Forward Primer (20 μM) 0.6 μL; PCR Reverse Primer (20 μM), 0.6 μL; SYBR Green Dye, 1 μL; total RNA, 3 μL; and RNase-Free dH2O, 6.3 μL. The amplification conditions were as follows: 40 °C for 30 min, 95 °C for 2 min, 95 °C for 5 s, and 55 °C for 35 s (40 cycles). The data were analyzed using the mode for normalized expression (2–ΔΔCt).

Statistical analysis

Data was presented as mean ± standard deviation (SD). Comparisons for all pairs were performed by the Student t test using SPSS version 17.0 (SPSS, IL, USA). A P value of <0.05 was considered to be significant. The IC50 and CC50 values were calculated using GraphPad Prism (GraphPad Software Inc., San Diego, CA, USA).

Antiviral activity in embryonated eggs

The influenza virus A/Sydney/5/97 (H3N2) was propagated in 9-day-old chicken eggs; the dose was evaluated as 107.8 EID50/mL. The suitable dilutions of all the compounds were set according to their solubility and toxicity. Then, 9-day-old swabbed eggs were inoculated with the compound-100 EID50 virus mixture via the allantoic route at 34 °C for 48 h. The virus titer of the allantoic fluid was measured by the hemagglutination test. The result showed that the B. striata compounds had significant antiviral activity against the influenza virus in the embryonated hen egg model. Compared with the control, nine compounds could significantly decrease the titers of viruses, with inhibition rates of 20.7% (compound 1), 79.3% (compound 2), 17.2% (compound 3), 34.5% (compound 4), 34.5% (compound 6), 34.5% (compound 9), 44.8% (compound 10), 75.9% (compound 11), and 34.5% (compound 12), at a concentration of 0.08 mmol/egg (Table 2). Compounds 2 and 11 were the best, although they seemed less efficient than oseltamivir, which showed a 100% inhibition rate at 0.01 mmol/egg. The results for other concentrations are presented (Table 2).

CPE reduction in MDCK cells

In the first set of experiments, the cytotoxicity of the compounds was measured using the MTS-based assay. It was found that each compound reduced the viability of MDCK cells with the CC50 values (corresponding to a 50% cytotoxic effect after 48 h of the inhibitor treatment) lower than oseltamivir (Table 3). No morphological alternations, loss of cell viability, or modification of cell multiplication rates could be observed in the cells treated with B. striata compounds with selected working doses of each compound.

The MTS-based CPE reduction assay of the MDCK model was used to confirm the antiviral activity. The antiviral effect of the compounds was quantified using the selectivity index (SI), which was the ratio of CC50mean versus IC50mean values (Table 3). The data from the CPE reduction assay demonstrated that B. striata compounds exhibited inhibitory antiviral effects in two groups: simultaneous treatment and post-treatment. In the simultaneous treatment assay, compounds 2, 3, 4, 6, 7, 10, and 11 exhibited inhibitory activities against the influenza virus with IC50 values ranging from 14.6 ± 2.4 to 43.3 ± 5.3 μM, and compound 4 showed the maximum inhibitory activity (Fig. 3). The IC50 values of B. striata compounds ranged from 18.4 ± 3.1 to 42.3 ± 3.9 μM in the post-treatment assay (Fig. 3). The compound 4 showed the most potent activity with the SI of 5.5, though it was lower than the value of oseltamivir at 122.2.

Hemagglutination inhibition of phenanthrenes from Bletilla striata

The simultaneous treatment assay results indicated that treatment with B. striata compounds on virus entry abrogated virus infectivity. Hence, the hemagglutination inhibition assay was used to test the hypothesis that B. striata compounds interfere with viral attachment. However, the results showed that the compounds could not inhibit hemagglutination by the influenza virus, neither do oseltamivir (Fig. 4).

Neuraminidase inhibition of phenanthrenes from Bletilla striata

The NA activity assay (NA standard curve and the detailed data are shown in Additional file 1, Fig. 5 and Table 4) was performed to detect any antiviral effect of B. striata compounds and to determine the mechanisms. The results (Table 5) showed that compounds 1, 3, 4, 6, 10, and 11 exhibited an inhibitory effect on the NAs in a dose-dependent manner with IC50 values ranging from 16.8 ± 1.6 to 87.5 ± 10.1 μM. Compounds 3, 4, and 6 displayed a higher inhibitory activity against the NAs. As a known NA inhibitor, oseltamivir showed a much lower IC50 of 0.3 ± 0.02 μM.

Inhibition of viral RNA synthesis in MDCK cells

The synthesis of influenza viral matrix protein mRNA was compared between untreated infected cells and infected cells treated with the compounds to identify any inhibitory effect of the compounds on influenza virus replication. RNA extraction was performed 18 h after influenza virus infection, and the levels of intracellular influenza RNA were measured. Quantitative RT-PCR showed a reduction in matrix protein mRNA transcription in cell treated with the B. striata compounds (8 μM) compared with the untreated infected cells (Fig. 6). Compounds 1, 2, 3, 4, 6, 7, 9, 10, and 11 showed a stronger inhibitory effect, with the compound 4 most efficient, even more powerful than oseltamivir. These results indicated that the blockage of virus replication was one of the mechanisms by which B. striata compounds exerted antiviral effects.


Influenza remains a serious problem in many countries, with a long history of outbreaks, epidemics, and recent pandemic [1–4]. With developments in viral biology, more novel antiviral strategies targeting these viruses, such as HA, M2 ion channel protein, RNA-dependent RNA polymerase (RdRp), NP, NS, and NA, have been developed. The two main classes of antiviral drugs clinically used against influenza are inhibitors of the viral M2 protein, such as amantadine (Symmetrel) and rimantadine (Flumadine), or neuraminidase inhibitors, such as zanamivir (Relenza) and oseltamivir (Tamiflu) (Fig.7).

M2 protein inhibitor amantadine consists of an adamantane backbone that has an amino group substituted at one of the four methyne positions, and rimantadine is a closely related derivative of adamantane with similar biological properties (Fig. 8). According to the US Centers for Disease Control and Prevention, 100% of seasonal H3N2 and 2009 pandemic flu samples tested have shown resistance to adamantanes, and amantadine is no longer recommended for the treatment of influenza in the United States. A new M2 protein inhibitor is urgently needed.

The M2 channel transports protons from the vacuolar space into the interior of the virion. Acidification of the interior results in the dissociation of ribonucleoproteins and the onset of viral replication. Amantadine and rimantadine function in a mechanistically identical fashion in entering the barrel of the tetrameric M2 channel and blocking the pore function (i.e., proton translocation) [32, 33]. Resistance to the drug class is a consequence of mutations to the pore-lining residues of the channel, leading to the inability of the sterically bulky adamantane ring that both share in entering in their usual way into the channel.

Neuraminidase inhibitor serves as a competitive inhibitor of the activity of the viral neuraminidase (NA) enzyme on SA found in glycoproteins on the surface of normal host cells. By blocking the activity of the enzyme, oseltamivir prevents new viral particles from being released through the cleaving of terminal SA on glycosylated hemagglutinin (Fig. 7, Wikipedia). The discovery of the first designed influenza virus neuraminidase inhibitor and anti-influenza drugs zanamivir and, subsequently, oseltamivir has now inspired a number of continuing efforts toward the discovery of next-generation anti-influenza drugs.

Phenanthrene is a polycyclic aromatic hydrocarbon composed of three fused benzene rings. The name “phenanthrene” is a composite of phenyl and anthracene. Most natural phenanthrenes originate biosynthetically from stilbenoids via oxidative coupling of the aromatic rings. They have demonstrated a variety of pharmacological effects, such as antiallergic, anti-inflammatory, antimicrobial, cytotoxic, and spasmolytic activities. Further C-C coupling of two phenanthrenes by 1–1′, 1–3′, 1–8′, or 3–3′ linkages produces rarely occurring biphenanthrenes, which show interesting atropisomeric features due to the hindered rotation of the linkage bond when -OH or -OMe groups are present nearby. Some synthetic chiral biphenanthrenes have been applied as effective enantioselective catalysts and ligands, while the atropisomeric features of many natural biphenanthrenes are not always discussed fully in scientific publications. The optically active naturally occurring biphenanthrene blestriarene C was shown to undergo rapid racemization even in daylight [35, 36].

Some compounds used to fight viral infections are based on the phenanthrene core, including compounds against plant viruses [37, 38] and human viruses [39, 40]. The secretion of phenanthrenes is a natural defense mechanisms of plants against fungal infection. Phenanthrenes from B. striata have some efficacy against Gram-positive bacteria, but only weak efficace against fungi. The phenanthrenes of Taxol communis have some efficacy against the vesicular stomatitis virus and the human rhinovirus serotype 1B. A phenanthrene derivative showed some efficacy against coronaviruses. The antiviral property of phenanthrenes from B. striata against the influenza A virus was investigated in this study using embryonated hen eggs, and it was confirmed that compounds 1, 2, 3, 4, 6, 9, 10, 11, and 12 exerted significant inhibitory effects. In MDCK models, compounds 2, 3, 4, 6, 7, 10, and 11 exhibited CPE reduction activities. The study showed that phenanthrenes from B. striata had strong anti-influenza viral activity. Furthermore, the HA, matrix protein, and NA were employed as targets for the study of possible mechanisms.

B. striata compounds 2, 3, 4 6, 7, 10, and 11 served as matrix protein inhibitors and resulted in the reduction of mRNA transcription. The function-structure relationship of these compounds and whether they interfere with the M2 proton channel need further exploration.

Compounds 1, 3, 4, 6, 10, and 11 exhibited an inhibitory effect on NA; compounds 3, 4, and 6 displayed a higher inhibitory activity. NA is an exoglycosidase that destroys the HA receptor by cleaving the α(2,6)- or α(2,3)-ketosidic linkage that exists between a terminal SA and a sugar residue of the N-acetylneuraminic acid (Neu5Ac)-containing receptor on the surface of the host cells. Neuraminidase inhibitors commonly interfere with the enzyme activity by mimicking the natural substrate and fitting into the active site of the neuraminidase enzyme. The binding efficiency of the compound with the neuraminidase is the major determinant of the inhibitory activity. The structure-activity relationship of new neuraminidase inhibitors should be proved for better molecular properties and higher efficiency against neuraminidase receptor compared with zanamivir or oseltamivir.

In the present study, compounds 4, 6, 9, and 12 showed the same efficacy in the egg model. The reasons for the similar efficacy are presently unknown. Indeed, these four compounds do not share the same molecular structure. The results could have been biased by the small number of eggs used in the experiments. There is also a possibility that these compounds share a mechanism that has not been studied here. In addition, some compounds inhibited the influenza virus through two mechanisms, but the reasons for this dual inhibition are currently unknown. Additional studies are necessary to better characterize these compounds.


This study indicated that diphenanthrenes (compounds 2–8 and 11) had stronger inhibitory activity compared with monophenanthrenes (compounds 1, 9, 10, and 12). In MDCK models, the antiviral effects of most monophenanthrenes were less than 50% except compound 10, while the effects of diphenanthrenes were all higher than 50% and IC50 could be calculated. This might be because of the hydroxyl group, which impacts the hydrophilicity/hydrophobicity of the compound. All diphenanthrenes share more hydroxyl groups. However, how the hydroxyl group affects the antiviral activity still needs further investigation. Compounds 2, 3, 4 6, 7, 10, and 11 served as matrix protein inhibitors and resulted in the reduction of mRNA transcription. Compounds 1, 3, 4, 6, 10, and 11 exhibited an inhibitory effect on NA. Additional studies are required to elucidate the exact mechanisms of these compounds.