Sesquiterpenoids with anti-influenza virus activity and application thereof
1. A compound having any one of the general structural formulas of formula (I) to formula (IV):
wherein R is1-R11Each independently selected from:
(1)-H、-CH3、-CH2CH3、-CH2CH2CH3、-CH2-CH2-CH2CH3、-CH-(CH3)2、-C(OH)(CH3)2、-CH2-CH(CH3)2、-CH2-(C(OH)(CH3)2、-CH2-(C(OH)(CH3)2(ii) a Or
(2)＝O、-OH、-F、-Cl、-Br、-OCH3、-OCH2CH3、-OCH2CH2CH2CH3、-O-CH2(ii) a Or
(3) Benzene ring, aromatic ring.
2. The compound of claim 1, wherein the compound is selected from any one of formulas 1-14:
3. use of a compound as claimed in claim 1 or 2 or a derivative thereof for the manufacture of a medicament for the prophylaxis and/or treatment of influenza virus.
4. Use of a compound according to claim 1 or 2 or a derivative thereof for the manufacture of an influenza virus infection inhibitor/blocker.
5. Use according to claim 3 or 4, wherein the derivative comprises a compound according to claim 1 or 2, or a pharmaceutically acceptable salt, hydrate, solvate, polymorph, tautomer, stereoisomer, isotopic derivative or prodrug thereof.
6. The use according to any one of claims 3 to 5, wherein the influenza virus is an influenza A virus.
7. The use according to claim 6, wherein the influenza virus is influenza A virus subtype H1N1 or H3N 2.
8. The use of claim 7, wherein the medicament further comprises a pharmaceutically acceptable carrier or excipient.
9. The use of claim 8, wherein the medicament is in the form of a powder, pill, tablet, capsule, oral liquid, paste, granule, mixture, suppository, aerosol or injection.
10. A pharmaceutical composition, the active ingredient of which is the compound or the derivative of claim 1 or 2, the pharmaceutical composition being an anti-influenza virus, an influenza treatment or an influenza prevention drug.
Background
Influenza viruses (IAVs) are a major pathogenic microorganism that can spread among humans, birds, dogs, pigs, and other animals, are the main cause of seasonal epidemics and opportunistic epidemics, often cause death of millions of people worldwide, and have serious effects on human health and economic development. Due to the mixing of virus genes, influenza viruses are easy to rapidly mutate to generate new influenza virus strains, which often causes the failure of the existing clinical medicines and the pandemics of the influenza viruses with great destructive power. Therefore, there is a need to develop a novel anti-influenza virus drug having a different action mechanism from existing drugs for preventing and treating infection of influenza virus.
Disclosure of Invention
The invention aims to provide a sesquiterpene compound and application thereof in preparation of anti-influenza virus drugs.
The technical scheme adopted by the invention is as follows:
in a first aspect of the invention, there is provided a compound having any one of the general structural formulas (I) - (IV):
wherein R is1-R11Each independently selected from:
(1)-H、-CH3、-CH2CH3、-CH2CH2CH3、-CH2-CH2-CH2CH3、-CH-(CH3)2、-C(OH)(CH3)2、-CH2-CH(CH3)2、-CH2-(C(OH)(CH3)2、-CH2-(C(OH)(CH3)2(ii) a Or
(2)＝O、-OH、-F、-Cl、-Br、-OCH3、-OCH2CH3、-OCH2CH2CH2CH3、-O-CH2(ii) a Or
(3) Benzene ring, aromatic ring.
In some preferred embodiments of the present invention, the compound is selected from any one of formula 1 to formula 14:
in a second aspect of the present invention there is provided the use of a compound according to the first aspect of the present invention or a derivative thereof in the manufacture of a medicament for the prophylaxis and/or treatment of influenza virus.
In a third aspect of the invention, there is provided the use of a compound according to the first aspect of the invention or a derivative thereof in the manufacture of an inhibitor/blocker of influenza virus infection.
In some embodiments of the invention, the derivative comprises a compound of the first aspect of the invention, a pharmaceutically acceptable salt, hydrate, solvate, polymorph, tautomer, stereoisomer, isotopic derivative or prodrug thereof.
In some embodiments of the invention, the influenza virus is an influenza a virus.
In some preferred embodiments of the invention, the influenza virus is influenza a virus subtype H1N1 or H3N 2.
In some embodiments of the present invention, the pharmaceutical composition further comprises a pharmaceutically acceptable carrier or excipient.
In some embodiments of the present invention, the medicament is formulated as a powder, pill, tablet, capsule, oral liquid, paste, granule, mixture, suppository, aerosol, or injection.
In a fourth aspect of the present invention, there is provided a pharmaceutical composition, the active ingredient of which is the compound according to the first aspect of the present invention or a derivative thereof, wherein the pharmaceutical composition is an anti-influenza virus, influenza treatment or influenza prevention medicament.
In some embodiments of the invention, the derivative comprises a compound of the first aspect of the invention, a pharmaceutically acceptable salt, hydrate, solvate, polymorph, tautomer, stereoisomer, isotopic derivative or prodrug thereof.
In some embodiments of the invention, the virus is an influenza a virus.
In some preferred embodiments of the invention, the influenza virus is preferably an influenza a virus subtype H1N1 or H3N 2.
In some embodiments of the present invention, the pharmaceutical composition further comprises a pharmaceutically acceptable carrier or excipient.
In some embodiments of the present invention, the medicament is formulated as a powder, pill, tablet, capsule, oral liquid, paste, granule, mixture, suppository, aerosol, or injection.
The invention has the beneficial effects that:
the invention provides a new sesquiterpene compound, the structural formula is shown in formula 1-formula 14, and the application of the compound or the derivative thereof in preparing products such as influenza virus prevention medicines, influenza virus treatment medicines, influenza virus infection inhibitors/blockers and the like is provided. The compound is obtained by separating from an ethyl acetate extract of Streptomyces sp XM17 fermentation liquor, and antiviral activity researches show that the sesquiterpene compounds have good anti-influenza virus activity, and the selectivity index of partial compounds for resisting the influenza virus is more than 500, so that good research and application prospects are shown.
Drawings
FIG. 1 is a key to Compounds 1-51H-1H COSY, HMBC and NOESY are related.
FIG. 2 is a CD spectrum of compound 1 and (4aS,5R) -4,4a,5,6,7,8-Hexahydro-5-hydroxy-4a-methyl-2(3H) -nalenone.
FIG. 3 is an X single crystal diffractogram of Compounds 2-4.
FIG. 4 is a graph showing the change in the HA gene expression level of influenza virus (PR8) after treatment with compounds 3 and 14.
(***p<0.001)。
Detailed Description
The concept and technical effects of the present invention will be clearly and completely described below in conjunction with the embodiments to fully understand the objects, features and effects of the present invention. It is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments, and those skilled in the art can obtain other embodiments without inventive effort based on the embodiments of the present invention, and all embodiments are within the protection scope of the present invention.
Experimental materials and methods:
an experimental instrument: the melting point was measured by using a melting point measuring instrument X-5 from Scorzon instruments Ltd. The ultraviolet spectrum measurement adopts UV-5500(PC) type ultraviolet-visible spectrophotometer of Shanghai Yuan analysis Co., Ltd. Nuclear magnetic resonance1H and 2D NMR spectra (400MHz),13C NMR spectrum (100MHz) is measured by Bruker AVANCED III 400NMR instrument, deuterated reagent is CDCl3Or CD3OD. Chemical shift values refer to the deuterated reagent peak (CDCl)3Is 7.26/77.23, CD3OD 3.31/49.15). The optical rotation was measured by using an automatic polarimeter of WZZ-2S type (Shanghai Shenguan instrument Co., Ltd.) and methanol as a solvent. High resolution mass spectrometry HRESI MS was performed using an Orbitrap fusion Tribridge mass spectrometer (Seimerfet). The low-resolution mass spectrum is an APITOF-5000 type mass spectrometer (Hexin Mass Spectrometry, China). Single crystal diffractograms were obtained using a XtaLAB PRO MM007HF type diffractometer (Rigaku) using copper palladium (Cu K α).
Statistical analysis: the data histograms are statistically analyzed by prism5 software, two groups of comparison adopt t-test and the multiple groups of comparison adopt Tukey-Kramer of one-way ANOVA for significance test statistics, and the statistical significance is achieved when P is less than 0.05; the data from the qRT-PCR was analyzed using ABI7500PCR analysis software and plotted against Prism 5.
The strain is as follows: the XM17 strain is collected from zoos of Guangzhou city in Guangdong province in 2013, fresh panda (Ailuropoda melanoleuca) feces is collected before the zoos are opened in the early morning, and the obtained product is obtained by sampling the feces, gradually diluting the feces, and separating and purifying the feces for multiple times. The mycelium of the strain is white and is dispersed in a solid culture medium in a dotted manner. The strain is identified as Streptomyces sp after 16S rRNA gene sequencing by Guangzhou Aiji biotechnology, and is preserved in glycerol frozen stock solution at the temperature of-80 ℃ and preserved in polypeptide and natural product research groups of southern medical university college.
Strain culture and extraction: the strain XM17 was first removed from the cryopreservation tube at-80 ℃ and placed in a culture dish containing # 32 medium for resuscitation. After the strain grew well, it was transferred to a flask (250mL) containing 50mL of the No. 302 medium, and placed in a shaker for 2 days (200rpm, 28 ℃ C.). Then, the seed culture was added to a flask (2L) containing 500mL of 400# medium and cultured on a shaker for 7 days (200rpm, 28 ℃).
By adopting the method, 28L of fermentation liquor is cultured in total. The mycelium and the bacterial solution were separated. Soaking the mycelia in equal volume of 95% ethanol for three times, mixing soaking solutions, drying under reduced pressure, dispersing with pure water, extracting with equal volume of dichloromethane and ethyl acetate for three times, mixing extractive solutions, and drying under reduced pressure. And (3) allowing the bacterial liquid to flow through a D-101 macroporous resin column, eluting with a large amount of pure water, eluting with 95% ethanol, collecting ethanol eluates, mixing, drying under reduced pressure, and extracting with dichloromethane and ethyl acetate with the same volume for three times respectively. The dichloromethane and ethyl acetate extracts were combined and subjected to the next separation to yield a total of 7.1g of dark brown extract.
Wherein the 32# culture medium comprises glucose 4g/L, yeast extract 4g/L, malt extract powder 5g/L, and trace salt (1mL trace amount)Saline solution/1L of culture medium), agar 20g/L, 1mol/L NaOH to adjust the pH value to 7.0; 302 the components of the culture medium are 20g/L of soluble starch; 10g/L of glucose; peptone 10 g/L; 10g/L of beef extract; 5g/L of yeast extract; CaCO3Adjusting the pH value to be 7.0 by 10g/L and 1mol/L NaOH; 400 the components of the culture medium are 30g/L of mannitol; 10g/L of glucose; 5g/L of yeast extract; 1g/L of sodium citrate; MgSO (MgSO)40.5g/L；K2HPO40.5 g/L; trace salt (1mL of trace salt solution/1L of fermentation broth), and pH is adjusted to 7.5 by 1mol/L NaOH; the trace salt component is FeSO4·7H2O 0.2％，MnCl2·2H2O 0.1％，ZnSO4·7H20.1 percent of O, and is prepared by dissolving in pure water.
And (3) separating and purifying a compound: the extract (7.1g) was completely dissolved with a small amount of methanol and dichloromethane, stirred with 5.5g of 200-300 mesh silica gel in a fume hood, and then subjected to column packing after drying. 55g of 200-300 mesh silica gel is stirred with petroleum ether and packed into a silica gel column (30 cm. times.3.5 cm, column volume about 150 mL). And (3) loading the mixed silica gel into a column, eluting by adopting a gradient elution method (petroleum ether: ethyl acetate 15: 1-0: 1; dichloromethane: methanol 9: 1-1: 1), checking eluent by TLC, combining similar fractions, and drying under reduced pressure to obtain 13 components (Fr.1-Fr.13). Fr.3(260mg) was completely dissolved in methanol and separated with Sephadex LH-20, and eluted with 100% methanol to give 5 major components. Fr.3-5(75mg) was further purified by silica gel column (1 cm. times.35 mm, petroleum ether: ethyl acetate 15:1 to 1:1) to give 2 fractions, Fr.3-5-1(11mg) was separated by reverse phase C-18 column (2 cm. times.35 cm), and eluted with 60% methanol/water solution to give compound 3(2.32 mg); fr.3-5-2(6.6mg) was separated on a reverse phase C-18 column (2 cm. times.35 cm) eluting with 60% methanol/water solution to give compound 7(1.9 mg).
Fr.4(267mg) was completely dissolved in methanol and separated on Sephadex LH-20 column, eluting with 100% methanol to give 5 major components. Fr.4-2(95mg) was further purified with a silica gel column (1 cm. times.35 mm, petroleum ether: ethyl acetate 12:1 to 1:1) to give nine fractions, Fr.4-2-5(17.73mg) as a white solid, which was separated with a reverse phase C-18 column (2 cm. times.35 cm) and eluted with 80% methanol/water to give compounds 14(1.0mg) and 13(9.1 mg). Fr.4-3(95mg) was further purified with a silica gel column (1 cm. times.35 mm, petroleum ether: ethyl acetate 10:1 to 1:1) to give five fractions, and Fr.4-3-3(10.24mg) was eluted twice with reverse phase C-18 column separation (55% methanol/water) to give compound 10(4.3 mg); fr.4-3-4(9.56mg) was eluted twice over reverse phase C-18 column (55% methanol/water) to give compound 8(3.2 mg); fr.4-3-5(17.17mg) was eluted twice over reverse phase C-18 column (50% methanol/water) to give compound 5(4.8mg), 9(3.2 mg).
Fr.5(775mg) dissolved completely with methanol and Sephadex LH-20 separation, 100% methanol elution, obtained 7 main components. Fr.5-2(140mg) was separated on a reverse phase C-18 column (2 cm. times.35 cm) and eluted with 50% methanol/water solution to give 6 fractions, and Fr.5-2-5(50mg) was purified on a C-18 preparative column (2.5 cm. times.35 mm, 50% methanol/water) to give Compound 6(3.5 mg).
Fr.6(472mg) was completely dissolved in methanol and separated with Sephadex LH-20, and eluted with 100% methanol to give 5 major components. Fr.6-3(55.3mg) was further purified by silica gel column (1 cm. times.35 mm, methylene chloride: ethyl acetate 3.5:1) to give 6 fractions, and Fr.6-3-3(17.5mg) was separated by reverse phase C-18 column (2 cm. times.35 cm) and eluted with 40% to 60% methanol/water solution to give compound 4(1.9 mg).
Fr.7(232mg) was dissolved completely in methanol and separated with Sephadex LH-20, eluting with 100% methanol to give 6 major components. Fr.7-2(102mg) was further purified by a silica gel column (1 cm. times.35 mm, petroleum ether: ethyl acetate 1:1, methylene chloride: ethyl acetate 4:1) to give 6 fractions, Fr.7-2-1(43mg) was separated by a reverse phase C-18 column (2 cm. times.35 cm) and eluted with 60% to 100% methanol/water solution to give 6 fractions of the compound, Fr.7-2-1-3(7.2mg) was separated by a reverse phase C-18 column (2 cm. times.35 cm) and eluted with 40% methanol/water solution to give compound 1(3.3 mg).
Fr.8(308mg) was completely dissolved in methanol and separated with Sephadex LH-20, and eluted with 100% methanol to give 7 major components. Fr.8-5(31mg) was further purified by a silica gel column (1 cm. times.35 mm, dichloromethane: ethyl acetate 50:1 to 15:1) to obtain 10 fractions. Fr.8-5-7(5mg) was separated by reverse phase C-18 column (2 cm. times.35 cm) and eluted with 60% -100% methanol in water to give 2(2.29 mg).
Meanwhile, the compound 10 was also isolated from a culture broth of Streptomyces sp HTL 16.
Cell culture: the MDCK cell strain is preserved by liquid nitrogen in the laboratory, and is used for experiments after two generations to three generations after the cells are recovered. The cells were cultured in DMEM medium containing 100U/ml penicillin/streptomycin and 10% south American Fetal Bovine Serum (FBS), and placed at 37 deg.C and 5% CO2The culture medium is cultured and grown in a culture box, and the culture medium is grown to be full of T25 cell culture bottles according to the ratio of 1: 4 and subcultured and recorded as good passage number.
Virus strain: influenza A virus A/Puerto/8/34(H1N1) and A/Aichi/2/68(H3N2) strains were amplified using allantoic fluid from 9-day-old SPF-grade chick embryos and stored at-80 ℃ in the laboratory.
MTT assay for compounds cytotoxic to MDCK: MDCK cells in logarithmic growth phase were digested with trypsin at a concentration of 0.25%, and the cells were digested at 2X 10 cells per well4Inoculating into 96-well plate, and adding 5% CO at 37 deg.C2The incubator was overnight. Discarding the supernatant, adding compounds with different series concentrations (the compound dissolved in DMSO is diluted by DMEM basic culture solution to ensure that the final content of DMSO is less than or equal to 5 thousandths), setting a solvent control group (the basic culture solution containing 5 thousandths of DMSO and no medicine) and a blank control group (the basic culture solution and no medicine), continuously placing the cells in an incubator for culturing for 48 hours, discarding the supernatant, adding 100 mu L of MTT (0.5mg/mL) into each hole, and incubating for 4 hours in a dark place. After termination of the culture, the supernatant was carefully aspirated, 150. mu.L of DMSO was added to dissolve formazan crystals formed by the culture, and the solution was sufficiently dissolved by shaking on a low-speed shaker for 10 min. And detecting the OD value at the position of 570nm of wavelength by using an enzyme-labeled detector, and calculating the cell survival rate.
Cell survival (%) ═ a570nm]Drug combination/[ A570nm]Blank group × 100%.
Determination of viral titres: MDCK cells were seeded in 96-well plates at a cell density of 2X 104Individual cells/well at 5% CO2Culturing for 18-22 h in a cell culture box at 37 ℃, removing supernatant after cells grow to be a monolayer, washing with PBS for 2 times, adding 100 mu L of influenza virus diluted by 10 times of DMEM into each hole, wherein the virus dilution concentration is 10-2～10-8Setting 8 multiple wells for each concentration, and setting cell control group without influenza virus. The cells added with the virus are placed in an incubator and incubated for 1h, then the virus solution is discarded, the cells are washed with PBS for 2 times, and 200 mu L of cell maintenance solution (DMEM containing 1 mu g/mL TPCK pancreatin) is added into each hole for continuous culture for 48 h. Cell morphology was observed under a microscope. When the cells have the pathological phenomena (cytopathic effect, CPE) such as atrophy, rounding, shedding and the like, recording the CPE generation condition, and calculating the TCID of the virus on MDCK cells according to a Reed-Muench two-kind method50. The formula is as follows:
distance scale ═ (above 50% variability-50%)/(above 50% variability-below 50% variability);
TCID50viral dilution log + distance ratio above 50% morbidity rate;
anti-influenza virus activity IC50And (3) determination: MDCK cells were seeded in 96-well plates at 2X 104Individual cells/well at 5% CO2Culturing for 18-22 h in a cell culture box at 37 ℃, discarding supernatant after the cells grow to a monolayer, and washing for 2 times by PBS. Assay of compound anti-influenza virus activity using a Pretreatment virus model (Pretreatment of viruses): 100TCID50The virus diluent and the compound diluted by equal amount in a gradient way are evenly mixed and incubated for 30min at 37 ℃; adding the virus-compound mixture into the cells washed with PBS, 100 μ L per well, and incubating in an incubator for 1 h; the mixture was removed, washed twice with PBS, and cultured for another 48h by adding 200. mu.L of DMEM medium containing 1. mu.g/mL TPCK pancreatin. After 48h, the supernatant was discarded, MTT (0.5mg/mL) was added at 100. mu.L/well, mixed well, and incubated for 4h in the dark. After termination of the culture, the supernatant was discarded, 150. mu.L of DMSO was added to dissolve formazan crystals formed by the culture, and the solution was shaken for 10min on a low-speed shaker to dissolve them sufficiently. Detecting OD value with enzyme-labeled detector at 570nm wavelength, and calculating cell survival rate.
Fluorescent real-time quantitative PCR: MDCK cells were seeded in 6-well plates, 2X 105Individual cells/well at 5% CO2Culturing for 18-22 h in a cell culture box at 37 ℃, discarding supernatant after the cells grow to a monolayer, and washing for 2 times by PBS. Effect of Compounds on HA expression Using Pretreatment Virus model (Pretreatment of viruses) 100TCID50The virus solution of (4) was mixed with Compound No. 3(5 ng/mL and 1ng/mL) and Compound No. 14 (5ng/mL and 1ng/mL), respectivelyPositive control (arbidol) (5. mu.g/mL and 1. mu.g/mL) were mixed well, incubated at 37 ℃ for 30min, added to the cells washed with PBS, 1mL per well, and incubated in an incubator for 1 h; the supernatant was removed, washed twice with PBS, and cultured for 24 hours by adding 1mL of DMEM medium containing 1. mu.g/mL of TPCK pancreatin.
And (3) RNA extraction: after 24h, the supernatant was discarded, and cellular RNA was extracted by Trizol. The specific operation is as follows: discarding the culture medium, washing twice with PBS, adding 1mL Trizol per well, standing for 5min, lightly blowing with a gun head, transferring into a 1.5mL centrifuge tube, adding 0.2mL chloroform, shaking vigorously for 15s, standing at room temperature for 10min, centrifuging at 12000g/min for 15min, separating the solution into three layers, carefully sucking the upper layer (about 0.4mL) and transferring into another clean EP tube, adding equal amount of isopropanol, standing at room temperature for 10min after turning upside down and mixing, centrifuging at 12000g/min for 10min, discarding the supernatant, adding 1mL 75% ethanol, centrifuging at 7500g/min for 10min, discarding the supernatant, drying the precipitate at room temperature, adding 30-50 μ L DEPC water to dissolve the precipitate, measuring the concentration and purity of mRNA, OD of mRNA with a micro ultraviolet spectrophotometer260/OD280Can be used for subsequent experiments within the range of 1.8-2.0.
Reverse transcription: the procedure was performed according to the PrimeScript RT kit protocol, with a reverse transcription system of 20. mu.L, in a 2720Thermal Cycler PCR instrument, programmed as follows: the first step is as follows: maintaining at 37 deg.C for 15 min; maintaining at 85 deg.C for 5 s; maintaining at 4 deg.C for 60 min.
Fluorescent quantitative PCR experiment: the operation was performed according to SYBR Premix Ex Taq kit instructions, the amplification system was 10. mu.L, the apparatus ABI7500PCR (Applied Biosystems, US) was performed, and the parameters were set as follows according to the apparatus instructions: the first step is as follows: 95 ℃, 30s, 1 cycle; the second step is that: 94 ℃,5s, 60 ℃, 34s, 40 cycles; the third step: dissolution profile. Analyzing by ABI7500PCR analysis software, calculating CT values of all samples, calculating average CT value of the samples by CT value of multiple wells, normalizing by using GAPDH gene as reference gene, and normalizing by using 2-△△CTThe relative expression amounts of the genes of the respective experimental groups were counted and then plotted by Prism 5.
HA forward primer: 5'-TTCCCAAGATCCATCCGGCAA-3' (SEQ ID NO: 1);
HA reverse primer: 5'-CCTGCTCGAAGACAGC CACAACG-3' (SEQ ID NO: 2).
GAPDH forward primer: 5'-AGGGCAATGCCAGCCCCAGCG-3' (SEQ ID NO: 3);
GAPDH reverse primer: 5'-AGGCGTCGGAGGGCCCCCTC-3' (SEQ ID NO: 4).
The experimental results are as follows:
(1) isolation and purification of Compounds
Streptomyces sp XM17 was isolated from fresh faeces of healthy pandas (Ailuropoda melanoleuca) from Guangzhou zoos. 14 sesquiterpene compounds are separated from the ethyl acetate extract of the fermentation liquor of the strain, and are respectively as follows: (2R,4S,8aR) -8,8a,1,2,3,4-hexahydro-2-hydroxy-4,8a-dimethyl-2(2H) -naphthalone (1); (1S,3S,4S,4aS,8aR) -4,8 a-dimethylhydroaphtalene-1, 3,4a (3H) -triol (2); (4S,4aS,8aS) -octahydro-4a-hydroxy-4,8a-dimethyl-1(2H) -naphthalone (3); ganodermanol L (4); and 4 α,15-epoxy-eudesmane-1 β,6 α,11-triol (5); cybellol (6); (3 beta, 4 alpha beta, 8 alpha) -4,8 a-dimethyl-octahydroaphthalene-3, 4a (2H) -diol (7); (1S,4S,4aS,8aR) -4,8 a-dimethylnectahydronaphthalene-1, 4a (2H) -diol (8); (4 β,4a β,8 α,8a α) -4,8 a-dimethylnectahydronaphthalene-4 a,8(2H) -diol (9); (2 α,4 β,4a β,8a α) -4,8 a-dimethylnectahydronaphthalene-2, 4a (2H) -diol (10); (1 β,4 β,4a β,8a α) -4,8 a-dimethylcyclohydroaphtalene-1, 4a (2H) -diol (11); eudsm-1 β,6 α,11-triol (12), rel- (+) - (2aR,5S,5aR,8S,8aS,8bR) -decahydro-2,2,5, 8-tetramethyll-2H-naptho [1,8-bc ] furan-5-ol (13); caryolane-1,7 α -diol (14). Various broad-spectrum means such as single crystal diffraction (X-ray), nuclear magnetic resonance (one-dimensional and two-dimensional spectrums) and the like are adopted to analyze the chemical structures of the new compounds 1 to 14, which are respectively shown as follows:
1: white needles. mp 265.5-267.0 ℃.(c＝0.013MeOH).UV(MeOH)λmax(logε)212(3.39),233(3.57)nm.ECD(MeOH)λmax(Δε),201(+11.46),233(+29.93)nm.1H and13c NMR data, see Table 1. HRESIMS M/z 217.1201[ M + Na ]]+(theoretical value C)12H18O2Na 217.1199)。
2: white needles. mp 167.0-168.2 ℃.(c＝0.015MeOH).1H and13c NMR data, see Table 1. HRESIMS M/z 237.1466[ M + Na ]]+(theoretical value C)12H22O3Na 237.1461). X single crystal diffractogram is shown in figure 3.
3: white needles. mp 110.7-111.4 deg.C.(c＝0.02MeOH).1H and13c NMR data, see Table 1. ESIMS M/z 219.15[ M + Na ]]+.HRESIMS m/z 219.1359[M+Na]+(theoretical value C)12H20O2Na 219.1356). X single crystal diffractogram is shown in figure 3.
4: white needles. mp 172.9-176.1 ℃.(c＝0.019MeOH).1H and13c NMR data, see Table 2.HRESIMS M/z 277.1780[ M + Na ]]+(theoretical value C)15H26O3Na 277.1774). Single-crystal X Single crystal diffraction pattern is shown in figure 3.
5: a colorless oil.(c＝0.014MeOH).1H and13c NMR data, see Table 2 HRESIMS M/z 293.1725[ M + Na ]]+(theoretical value C)15H26O4Na 293.1723)。
The compound 1 is colorless needle-shaped substance, and the high resolution mass spectrum HRESI MS is m/z 217.1201[M+Na]+，C12H18O2The theoretical calculation value of Na is 217.1199, and the molecular formula is determined to be C by combining the hydrocarbon spectrum data12H18O2The unsaturation degree Ω is 4.1H NMR data show that compound 1 contains 2 methyl signals, 1 single-peak methyl hydrogen proton signal 1.26, and 1 methyl hydrogen proton signal delta split into two peaksH1.14, 1 oxygen-linked methine Signal 4.11, 1 methine Signal δ which splits into two peaksH5.82，13C NMR and DEPT spectra show that compound 1 contains 12 carbon atoms, including 3 quaternary carbons, 3 methine carbons, 4 methylene carbons, 2 methyl carbon signals.
1H-1The H COSY spectra show that there is a correlation between H-1 (delta 1.99 and 1.31) and H-2 (delta 4.11), H-2 and H-3 (delta 02.17 and 1.19), H-3 and H-4 (delta 12.48), H-4 and H-10 (delta 21.14), H-7 (delta 32.52) and H-8 (delta 41.89). The HMBC spectra show that H-9 (delta 51.26) correlates with C-1 (delta 650.4), C-8a (delta 737.2), C-4a (delta 8171.0), and C-8 (delta 924.0), suggesting that a methyl group (C-9, delta 24.0) is attached to C-8 a. HMBC spectra show that H-5 (delta 05.82) and C-4 (delta 32.8), C-8a, H-7 (delta 2.52 and 2.35) have correlation with C-8a, C-6 (delta 200.0), H-8 (delta 1.89) and C-1, C-4a, C-8 and C-8a, and partial compound structures can be deduced by combining the correlation of the spectra. Meanwhile, the HMBC spectrum shows that H-1 is related to C-2 (delta 66.2), C-3 (delta 44.8), C-8a, C-9, H-3 and C-1, C-2, C-4a, C-10 (delta 18.0), and H-4 is related to C-8a, H-10 and C-4a, C-3 and C-4, and further partial structure of the compound 1 can be verified. Through the derivation of the one-dimensional and two-dimensional nuclear magnetic resonance spectra of the compound 1, the compound 1 can be deduced to be the sesquiterpene compound.
As can be seen from FIG. 1, the NOESY spectrum shows that H-2 has a long-range correlation with H-4, H-2 has a long-range correlation with H-9, and H-4 has a long-range correlation with H-9, indicating that H-2, H-4, and H-8a have cis-configuration. Meanwhile, proton coupling constants for H-1(Δ 1.99, dt, J ═ 4.08,12.44Hz,. delta.1.31, br t, J ═ 12.12Hz), H-2(Δ 4.11, br tt, J ═ 4.30,11.28Hz) suggest that the 2-position contains a hydroxyl signal. Compound 1 has a structural backbone of α, β -unsaturated cyclohexenone, which has been reported in the literature to have a characteristic optical rotation (CD) due to its specific steric structure. Therefore, the absolute steric structure of compound 1 can be deduced by CD spectroscopy, and determining the pi → pi transition signal at the wavelength of 220-260 nm. As can be seen in FIG. 2, compared with the known compound (4aS,5R) -4,4a,5,6,7,8-Hexahydro-5-hydroxy-4a-methyl-2(3H) -nalenone, compound 1 showed a positive Ketton Effect (Cotton Effect) at 235nm, suggesting that the chiral carbon atom at position 8a of the compound should be in the R configuration. This structure is also consistent with the data reported in the literature. Therefore, it is concluded that the structure of compound 1 should be (2R,4S,8aR) -8,8a,1,2,3,4-hexahydro-2-hydroxy-4,8a-dimethyl-2(2H) -naphthalone.
Compound 2 was a colorless needle. The high resolution mass spectrum of the compound 2 shows that the molecular ion peak is M/z 237.1466[ M + Na ]]+(C12H22O3Theoretical calculation of Na 237.1461), suggesting that the chemical structural formula of the compound is C12H22O3The unsaturation degree is 2.1H NMR spectral data showed that compound 2 contained 2 methyl signals, including 1 single peak signal δ 0.94 and 1 bimodal signal δ 1.02; the signals delta 3.97 and delta 3.86 of 2 methylene hydrogen protons containing oxygen linking groups.13C NMR and DEPT spectral data show that Compound 2 contains 12 carbon atom signals, including 2 quaternary carbons (1 of which is attached to a hydroxyl group), 3 methine carbons (two of which are attached to a hydroxyl group), 5 methylene carbons, and two methyl carbon signals.
Of compounds 1 to 3 of Table 11H and13c NMR spectral data
ain CDCl3；bin CD3OD；c400MHz,δin ppm；d100 MHz,δin ppm；eThese data partially overlap.
1H-1H COSY data show that H-1 (delta 3.97) is related to H-2 (delta 1.97 and 1.85), H-2 is related to H-3 (delta 3.86), and H-3 is related to H-4 (delta 1.71). HMBC spectra show that H-1 is associated with C-2 (delta 39.1), C-8 (delta 31.8), C-8a (delta 44.0), C-9 (delta 14.4); h-2 and C-1 (. delta.70.5) C-3 (. delta.74.8), C-4 (. delta.37.5), C-8 a; h-3 and C-1, C-2, C-4a (delta 79.5), C-10 (delta 12.0); and H-4 has correlation with C-3, C-4a, C-8a, C-5 (delta 21.5) and C-10 (figure 1). The HMBC spectra also show the correlation between H-9 (. delta.0.94) and C-1, C-4a, C-8 a; h-10 (. delta.1.02) is associated with C-3, C-4 a. At the same time, the user can select the desired position,1H-1h COSY shows that H-4 has a correlation with H-10. Thus, from the above spectra data, it was deduced that the planar structure of Compound 2 is similar to the known compound, geosmin, except that Compound 2 contains two methine carbon signals (δ) linked to the hydroxyl groupC 70.5,δH 3.97andδC 74.8,δH3.86). In combination with the above NMR experimental data, the two hydroxyl groups are located at the C-1 and C-3 positions, respectively. By measuring the X single crystal diffraction pattern of compound 2 (fig. 3), the Flack constant was [ χ ═ 0.0(2)]Further determining the chemical structural formula and the three-dimensional structure thereof. Thus, the compound is (1S,3S,4S,4aS,8aR) -4,8 a-dimethylthiocyanilene-1, 3,4a (3H) -triol.
Compound 3 was a colorless needle. The high resolution mass spectrum HRESI MS shows that the molecular ion peak of the compound is M/z 219.1359[ M + Na ]]+(theoretical calculation value is C)12H20O2Na 219.1356) suggesting that the compound has the formula C12H20O2The unsaturation degree is 3.1The H NMR spectrum shows that compound 3 contains two methyl signals, with δ 1.23(3H) being a single peak and δ 0.89(3H) being a double peak; two methylene hydrogen proton signals, δ 2.72(1H) and δ 2.23(1H), both linked to oxygen; and a methine signal δ 2.16(1H) (table 1).13C NMR and DEPT spectra show that compound 3 contains 12 carbon atoms, of which 3 quaternary carbons (1 quaternary carbon to hydroxyl, 1 quaternary carbon to carbonyl), 1 tertiary carbon, 6 secondary carbons, and 2 methyl carbons are signaled (table 1).
The HMBC spectrum of compound 3 shows that H-2 (delta 2.72 and 2.23), H-3 (delta 1.78), H-9 (delta 1.24) are correlated with the carbonyl carbon signal delta 215.9, indicating that C-1 is the carbonyl carbon. The HMBC spectra show that H-9 correlates with C-1, C-8a (Δ 52.0), C-4a (Δ 78.0), and C-8(Δ 27.7), suggesting that the methyl group at C-9 is attached to the quaternary carbon at C-8 a. Thus, another quaternary carbon (C-4a) should be attachedOne hydroxyl group. Meanwhile, the HMBC spectra also show that H-10 (delta 0.89) is associated with C-4 (delta 33.8), C-4a, and C-3 (delta 29.9), suggesting that C-10, (delta 14.5) is associated with C-3, C-4, and C-4 a.1H-1The inference is further verified by the correlation of H-2 with H-3, H-3 with H-4 (delta 2.16), and H-4 with H-10 (delta 0.89) in the H COSY spectra. Therefore, it is deduced that the structural formula of the compound 3 is shown in the above, and the compound is a sesquiterpene compound.
The relative configuration of compound 3 can be deduced by NOESY spectroscopy and further verified by X single crystal diffraction spectroscopy. From the X single crystal diffractogram (fig. 3) of the compound, the Flack parameter is [ χ ═ 0.08(7) ], and the compound is (4S,4aS,8aS) -octahydro-4a-hydroxy-4,8a-dimethyl-1(2H) -naphthalone.
Compound 4 was white needles. The high resolution mass spectrum HRESI MS shows that the molecular ion peak of the compound is M/z 277.1780[ M + Na ]]+(theoretical calculation value is 277.1774), and the molecular formula is presumed to be C15H26O3Na, unsaturation degree is 3.1The H NMR spectrum showed that the compound contained 4 methyl hydrogen proton signals, including 3 single peaks δ 1.05(3H) and δ 1.33(6H), 1 double peak δ 0.96(3H), 2 hydrogen proton signals connected to hydroxyl groups δ 3.95(1H) and δ 3.58(1H), and 1 methine hydrogen proton signal δ 2.28 (1H).13The C NMR and DEPT spectral data show that 4 contains 15 carbon signals, of which 2 quaternary carbon signals (1 hydroxyl linkage), 6 methine carbon signals (2 hydroxyl linkages), 3 methylene signals, and 4 methyl signals (Table 2).
Process for preparation of Compound 41H-1The H COSY spectra show that H-1 (delta 3.95) is associated with H-2 (delta 1.88 and 1.59), H-10 (delta 01.45), H-2 is associated with H-3 (delta 12.28), H-3 is associated with H-4 (delta 23.58), H-15 (delta 30.96), H-4 is associated with H-5 (delta 41.29), H-6 (delta 51.52 and 1.67) is associated with H-7 (delta 61.22), and H-7 is associated with H-8 (delta 71.81 and 1.57). The HMBC spectrum shows that H-4 is related to C-5 (delta 842.4), C-6 (delta 952.3) and C-15 (delta 11.7), H-12 (delta 01.05) is related to C-6, C-11 (delta 183.7) and C-13 (delta 229.2), H-13 (delta 31.33) is related to C-6, C-11 and C-12 (delta 424.8), H-14 (delta 1.33) is related to C-8 (delta 42.8) and C-9 (delta 73.9), and H-15 (delta 0.96) is related to C-2 (delta 39.8), C-3 (delta 31.3) and C-4 (delta 81.0). These data allow the derivation of the chemical structures of Compound 4 and Compound 13Similarly, 13 is a known compound isolated from the culture of Ptychanthus striatus and mycelium Garoderma capense. The biggest difference between the two is that compound 4 has one more hydroxyl group. By analyzing the HMBC spectrum of 4, H-1 is related to C-2, C-5, C-9 and C-10 (delta 53.8), H-10 is related to C-1 (delta 68.0), C-2, C-4, C-5, C-9 and C-14 (delta 22.3), so that the hydroxyl group is presumed to be positioned at the C-1 position. NOESY spectra showed significant remote correlations between H-1 and H-14/15, and between H-4 and H-6/13, suggesting that the relative conformations of 4 and 13 are similar. The compound was further measured for its X single crystal diffraction pattern and found to have a Flack constant [ χ ═ 0.06(8)]The absolute configuration of compound 4 was determined to be 1S,3S,4S,5R,6R,9S,10R, compound 4 was named ganodermanol L.
TABLE 2 preparation of compounds 4 to 51H and 13C NMR Spectroscopy (deuterated reagent is CDCl)3)
a100 MHz,δ(ppm)；b400 MHz,δ(ppm)；cThese data partially overlap.
Compound 5 was a colorless oil. The high resolution mass spectrum HRESI MS shows that the molecular ion peak of the compound is M/z 293.1725[ M + Na ]]+ (theoretical calculation C)15H26O4Na 293.1723), suggesting that the compound has the formula C15H26O4The unsaturation degree is 3.1The H NMR spectral data showed that compound 5 contained three monomodal methyl signals δ 1.21(3H), 1.15(3H), and 0.88(3H), 2 methylene hydrogen proton signals δ 3.23(1H) and 2.82(1H) with oxygen, 2 methylene hydrogen proton signals δ 3.81(1H) and 3.44(1H) with hydroxyl.13The C NMR and DEPT spectra showed that 5 contained 15 carbon signals, of which 3 quaternary carbons (two linked hydroxyl groups), 4 methine carbons (two linked hydroxyl groups), and 5 methylene groups (one linked hydroxyl group)) And three methyl carbon signals (fig. 1).
Process for preparation of Compound 51H-1The H COSY spectra show that H-1 (delta 3.44) correlates with H-2 (delta 1.94 and 1.75), H-2 correlates with H-3 (delta 02.10 and 1.33), H-5 (delta 11.79) correlates with H-6 (delta 23.91), H-6 correlates with H-7 (delta 31.52), and H-7 correlates with H-8 (delta 41.68 and 1.11). HMBC spectra show that H-1 (delta 53.44) correlates with C-2 (delta 629.6), C-5 (delta 749.3), C-9 (delta 37.2), C-10 (delta 142.2), C-14 (delta 212.4), H-15 (delta 33.23 and 2.82) correlates with C-3 (delta 433.5), C-4 (delta 62.1), C-5, and H-14 (delta 0.88) correlates with C-1 (delta 78.2), C-5, C-9, and C-10. From these spectral data, it can be deduced that Compound 5 is similar in chemical structure to a known compound 4. delta.8, 15-epoxyyeudemane-1. delta.9, 6. delta.0-diol isolated from fruits of Torilis japonica. Careful analysis of the HMBC spectrum of 5 revealed that H-12 (delta 1.21) is associated with C-7, C-11, C-13 (delta 29.4), and H-13 (delta 1.15) is associated with C-7, C-11, C-12 (delta 24.5), thus the greatest difference between these two compounds was deduced to be that compound 5 has one more hydroxyl group at the C-11 position.
NOESY spectra show that H-14 of 5 is related remotely to H-15/6, H-15 is related remotely to H-12/13, while the coupling constants of H-1[ delta 3.44, dd (2.72,11.48) ], H-5[ delta 1.79, dd (2.72,6.76) ] and H-7[ delta 1.52, dd (4.00,9.92) ] are similar to 4 alpha, 15-epoxyyeudesmane-1 beta, 6 alpha-diol, indicating that the relative configuration of 5 is similar to this known compound. Thus, 5 was named 4 α, 15-epoxyyeudesmane-1 β,6 α, 11-triol.
(2) Detection of antiviral Effect
The antiviral effects of compounds 1-14 on influenza strains A/Puerto Rico/8/34(H1N1) and A/Aichi/2/68(H3N2), as well as the neocoronavirus SARS-CoV-2, were determined using the "pretreatment virus" model. As a result, as shown in Table 3, it can be seen that these compounds have no inhibitory activity against SARS-CoV-2 virus strain in the range of 25. mu.M, but have a strong inhibitory activity against influenza virus in the range of 4.8 to 48.7nM, suggesting that these compounds may act at an early stage of viral infection by inhibiting the entry of influenza virus. Meanwhile, the cytotoxicity of the compounds is measured by adopting an MTT method, and the cytotoxicity range is found to be in a micromolar level, which indicates that the selectivity index of the compounds is more than 500, and shows that the compounds have the potential to be further studied.
TABLE 3 antiviral Effect of Compounds 1-14
aCytotoxicity to canine kidney cells (MDCK);b influenza A/PR/8/34(H1N1)virus；cinfluenza A/Aichi/2/68(H3N2)virus：dμM.。
subsequently, compounds 3 and 14 were arbitrarily selected and their anti-influenza virus activity was further confirmed by RT-PCR. As shown in FIG. 4, when the virus was pretreated with the concentrations of 1ng/mL and 5ng/mL of the compounds, respectively, significant decrease in the expression level of the hemagglutinin enzyme (HA) gene was observed in the RT-PCR experiment, and further confirmed their antiviral activity.
The present invention is not limited to the above embodiments, and various changes can be made without departing from the spirit of the present invention within the knowledge of those skilled in the art. Furthermore, the embodiments of the present invention and the features of the embodiments may be combined with each other without conflict.
SEQUENCE LISTING
<110> southern medical university
<120> sesquiterpene compound with anti-influenza virus activity and application thereof
<130>
<160> 4
<170> PatentIn version 3.5
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