CN111233814A - Terpene phenolic compound ZKYY-057 and preparation method and application thereof - Google Patents
Terpene phenolic compound ZKYY-057 and preparation method and application thereof Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
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Abstract
The invention discloses a terpene phenolic compound ZKYY-057, a preparation method and application thereof, wherein the compound has a structure shown in a formula I:
the compound shown in the formula I can be obtained by extracting the inflorescence of the hemp plant to obtain a crude extract, and then separating the crude extract, and cell experiments show that the compound shown in the formula I has better anti-tumor cell proliferation activity, and particularly has obvious effect of inhibiting cell proliferation in liver cancer cells and lung cancer cells.
Description
Technical Field
The invention relates to the technical field of biological medicines, and particularly relates to a terpene phenolic compound ZKYY-057 and a preparation method and application thereof.
Background
The hemp plant is a plant with a complex chemical type, mainly because the hemp plant contains many natural chemical components. By 1980, there were 432 species of compounds isolated from hemp plants, increasing to 483 species by 1995 and 490 species by 2005. The biological activity of cannabis is well known and, following the discovery of receptors, there is an opportunity to explore the source of physiologically active compounds in cannabis as new therapeutic agents. There are also an increasing number of patients suffering from severe diseases such as cancer who seek natural drugs as an alternative or complementary therapy, and there is a continuing need for new treatments for cancer or other symptoms.
The incidence rate of cancer is gradually high due to different living habits, environmental factors and other reasons, the malignant tumor is found in a late stage, the disease is difficult to cure once the malignant tumor is found, and the cancer incidence rate is high and the malignant tumor is difficult to cure at present, so the method has important significance for screening active ingredients in the hemp plants.
Disclosure of Invention
In view of the above, the invention provides an application of a terpene phenolic compound ZKYY-057 with a molecular formula of C21H31O3And the molecular weight is 330.47, and the compound has good anti-tumor cell proliferation activity.
The invention provides a terpene phenolic compound ZKYY-057, which has a structure shown in a formula I:
the invention also provides a preparation method of the compound shown in the formula I, which comprises the following steps:
(1) sequentially performing carbon dioxide supercritical extraction and ethanol extraction on the hemp plant inflorescence to obtain a crude extract;
(2) dissolving the obtained crude extract, and separating by normal phase silica gel column chromatography, macroporous adsorption resin column chromatography, first-stage medium pressure normal phase silica gel column chromatography, second-stage medium pressure normal phase silica gel column chromatography, third-stage medium pressure normal phase silica gel column chromatography, and high pressure reverse phase HPLC chromatography to obtain compound shown in formula I.
Preferably, the method of preparation comprises any one or more of the following features: firstly, the supercritical carbon dioxide extraction conditions are as follows: pExtraction kettle＝20-30MPa，TExtraction kettle＝35-60℃；PSeparation kettle I＝8-11MPa，TSeparation kettle I＝35-65℃；PSeparation kettle II＝3-6MPa，TSeparation kettle II30-40 ℃; secondly, the usage amount of ethanol in the ethanol extraction is 15-25% of the weight of the hemp plant inflorescence, and the extraction time is 30-60 min; thirdly, fully dissolving the crude extract by using petroleum ether; fourthly, the normal phase silica gel column chromatography is carried out with n-hexane/ethyl acetate 98:2 as an eluent for isocratic elution; fifthly, performing gradient elution by using a D101 macroporous adsorption resin column and 30-100% ethanol/water as an eluent through macroporous adsorption resin column chromatography; sixthly, performing gradient elution on the first-stage medium-pressure normal-phase silica gel column chromatography by using dichloromethane/ethyl acetate as an eluent; seventhly, performing gradient elution on the secondary medium-pressure positive-phase silica gel column chromatography by using n-hexane/diethyl ether as an eluent; eighthly, carrying out gradient elution on the three-stage medium-pressure normal-phase silica gel column chromatography by using n-hexane/diethyl ether as an eluent; and ninthly, carrying out gradient elution by using acetonitrile/water solution as an eluent by the high-pressure reversed-phase HPLC chromatography.
The invention also provides application of the compound shown in the formula I in preparing a tumor cell proliferation inhibitor.
Correspondingly, the invention provides a tumor cell proliferation inhibitor drug which is characterized by comprising an active ingredient and pharmaceutically acceptable auxiliary materials, wherein the active ingredient comprises a compound shown in a formula I.
The invention also provides application of the compound shown in the formula I in preparing a medicament for treating tumor diseases.
Correspondingly, the invention provides an anti-tumor medicament which comprises an active ingredient and a pharmaceutically acceptable auxiliary material, wherein the active ingredient comprises a compound shown in a formula I.
Preferably, the tumor disease is liver cancer or lung cancer.
Preferably, the medicament comprises an effective dose of the compound shown in the formula I, and the effective dose is 660ng per dose.
Preferably, the medicine is an oral preparation or an injection preparation, and the oral preparation is one of dripping pills, tablets, capsules, granules or oral liquid; the injection preparation is selected from injection or powder injection.
The invention has the beneficial effects that: the terpene phenolic compound ZKYY-057 shown in the formula I is high in purity, good in stability and good in biological activity, and the compound shown in the formula I has good anti-tumor cell proliferation activity through cell experiments, and particularly has an obvious effect of inhibiting cell proliferation in liver cancer cells and lung cancer cells.
Drawings
FIG. 1 is a graph showing the effect of compounds of formula I on the survival rate of human hepatoma cells (HepG 2);
FIG. 2 shows the effect of compounds of formula I on the survival of human lung cancer cells (A549);
FIG. 3 shows the effect of compounds of formula I on the survival of human hepatoma cells (HepG 2);
FIG. 4 shows the effect of compounds of formula I on the survival of human lung cancer cells (A549);
FIG. 5 shows a microscopic image of cell colonies after treatment of human hepatoma cells (HepG2) with a compound of formula I;
FIG. 6 shows the effect of compounds of formula I on the colony formation of human hepatoma cells (HepG 2);
FIG. 7 shows a microscopic image of a cell colony obtained after treatment of human lung cancer cells (A549) with a compound of formula I;
FIG. 8 shows the effect of compounds of formula I on colony formation of human lung cancer cells (A549);
FIG. 9 shows the effect of compounds of formula I on the mobility of human hepatoma cells (HepG 2);
FIG. 10 shows the effect of compounds of formula I on the mobility of human lung cancer cells (A549).
Detailed Description
To explain technical contents, structural features, and objects and effects of the technical solutions in detail, the following detailed description is given with reference to the accompanying drawings in conjunction with the embodiments.
The invention provides a terpene phenolic compound ZKYY-057, which has a structure shown in a formula I:
example 1
The preparation method of the terpene phenolic compound ZKYY-057 shown in the formula I comprises the following steps:
(1) taking a hemp plant inflorescence as a raw material, crushing 500g of a dried sample, and performing supercritical extraction by using carbon dioxide. The extraction conditions were: pExtraction kettle＝30MPa，TExtraction kettle＝45℃；PSeparation kettle I＝8MPa，TSeparation kettle I＝45℃； PSeparation kettle II＝6MPa，TSeparation kettle IIThe temperature is 35 ℃; adding 20 wt% ethanol as carrier, and extracting for 45 min. Extracting to obtain 101.031g of crude extract.
(2) And (2) fully dissolving 50g of crude extract by using petroleum ether, performing normal-phase silica gel column chromatography by using a Changzhou trite medium-pressure rapid preparation chromatograph, performing gradient elution by using n-hexane/ethyl acetate 98:2 and the like until the peak value of the sixth peak of online detection is lower than 100mAU and the flow rate is 80mL/min, analyzing by using thin-layer chromatography, and combining the sixth peaks of online detection maps to obtain a first-stage component containing the target compound. And (3) taking 7.8g of first-grade component, further separating by using D101 macroporous adsorption resin column chromatography, carrying out gradient elution by using 30-100% ethanol/water in an elution system, and regulating the flow rate until the eluent flows down in a strand. And (4) carrying out thin-layer chromatography analysis, and combining the elution parts of 45% ethanol solution to obtain a secondary component containing the target compound. And taking 1.62g of the secondary component, and further performing medium-pressure normal-phase silica gel column chromatography separation, wherein an elution system is a dichloromethane/ethyl acetate system for gradient elution, and the elution is carried out until the peak value of the eighth peak detected on line is lower than 50mAU, and the flow rate is 15 mL/min. And (3) carrying out thin-layer chromatography analysis, combining the second peaks of the online detection spectra to obtain a third-level component containing the target compound, taking 0.313g of the third-level component, further carrying out medium-pressure normal-phase silica gel column chromatography separation, carrying out gradient elution by using n-hexane/diethyl ether until the peak value of the thirteenth peak of online detection is lower than 30mAU, and carrying out flow rate of 15 mL/min. And (3) carrying out thin-layer chromatography analysis, combining the ninth peak of the online detection spectrum to obtain a fourth-stage component containing the target compound, taking 0.064g of the fourth-stage component, further adopting medium-pressure normal-phase silica gel chromatography for separation, carrying out gradient elution by using n-hexane/diethyl ether until the peak value of the second peak of the online detection is lower than 10mAU, and carrying out flow rate of 10 mL/min. And (3) carrying out thin-layer chromatography analysis, combining the first peaks of the online detection maps to obtain a five-level component containing the target compound, taking 0.048g of the five-level component, further adopting HPLC high-pressure reversed-phase preparation, carrying out gradient elution by acetonitrile/water and the like in an elution system, wherein the peak-out time of the target compound is 18.29min, the detection wavelength is 228nm, and finally obtaining 32mg of a compound ZKYY-057 shown in the formula I.
Example 2
Identification of antitumor activity of terpene phenolic compound ZKYY-057 shown in formula I
Medicine preparation: the terpene phenolic compound ZKYY-057 of formula I prepared in example 1.
(1) MTT colorimetric method for detecting influence of compound shown as formula I on tumor cell survival performance
Taking human liver cancer cells (HepG2) in a logarithmic growth phase, using a DMEM culture medium, adjusting the cell concentration to 7000 cells, inoculating 100 mu L of DMEM culture medium in each hole to a 96-well plate, culturing the DMEM culture medium in the 96-well plate in an incubator until the cells adhere to the wall, using 100 mu L of DMSO as a solvent to respectively prepare compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into experimental groups for treatment, adding 100 mu L of DMSO into blank groups, and acting for 24 hours under the culture medium; detecting cell survival rate with MTT reagent by using 20ug/ml antitumor drug cisplatin (DDP) as control, repeating for 3 times, and averaging;
as shown in FIG. 1, the survival rate of the human liver cancer cell (HepG2) is lower with the increase of the concentration, i.e. the inhibition effect of the compound ZKYY-057 shown in the formula I on the survival performance of the human liver cancer cell (HepG2) is stronger; when the concentration is 40ug/ml, the inhibition effect is stronger than that of the antitumor drug DPP with the dosage of 20 ug/ml.
Taking human lung cancer cells (A549) in logarithmic growth phase, adjusting the number of the cells to 7000 by using a DMEM medium, inoculating 100 mu L of the DMEM medium in each well into a 96-well plate, culturing the 96-well plate in an incubator until the cells adhere to the wall, respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml by using 100 mu L of DMSO as solvents, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into an experimental group for treatment, adding 100 mu L of DMSO into a blank group, and acting for 24 hours in the culture medium; using 20ug/ml of cisplatin (DDP) as a control, detecting the cell survival rate by using MTT reagent, and repeating for 3 times to obtain an average value;
as shown in fig. 2, the survival rate of the human lung cancer cell (a549) is lower with the increase of the concentration, i.e., the inhibition effect of the compound ZKYY-057 shown in formula I on the survival of the human lung cancer cell (a549) is stronger; when the concentration is 40ug/ml, the inhibition effect is stronger than that of the antineoplastic drug cisplatin (DDP) with the dosage of 20 ug/ml.
(2) CKK8 cell proliferation toxicity detection method for detecting influence of compound shown in formula I on survival performance of tumor cells
Taking human liver cancer cells (HepG2) in a logarithmic growth phase, adjusting the cell concentration to 7000 cells by using a DMEM medium, inoculating 100 mu L of DMEM medium into each well to a 96-well plate in an incubator, culturing in the incubator at 37 ℃ until the cells adhere to the walls, respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml by using 100 mu L of DMSO as a solvent, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into experimental groups for treatment, adding 100 mu L of DMSO into blank groups, and acting for 24 hours in the culture medium; detecting cell survival rate with CCK8 kit with 20ug/ml antitumor drug cisplatin (DDP) as control, repeating for 3 times, and averaging;
as shown in FIG. 3, the survival rate of human liver cancer cells (HepG2) is lower with the increase of concentration, i.e. the inhibiting effect of the compound shown in formula I on the survival of human liver cancer cells (HepG2) is stronger; when the concentration is 40ug/ml, the inhibition effect is basically equivalent to that of the antitumor drug cisplatin (DDP) with the dosage of 20 ug/ml.
Taking human lung cancer cells (A549) in logarithmic growth phase, adjusting the number of the cells to 7000 by using a DMEM medium, inoculating 100 mu L of the DMEM medium in each well into a 96-well plate, culturing the 96-well plate in an incubator until the cells adhere to the wall, respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml by using 100 mu L of DMSO as solvents, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into an experimental group for treatment, adding 100 mu L of DMSO into a blank group, and acting for 24 hours in the culture medium; using 20ug/ml of cisplatin (DDP) as a control, detecting the cell survival rate by using a CCK8 kit, and repeating the steps for 3 times to obtain an average value;
as shown in fig. 4, the survival rate of human lung cancer cell (a549) is lower with the increase of the concentration, i.e., the compound of formula I has stronger inhibition effect on the survival of human lung cancer cell (a 549); when the concentration is 40ug/ml, the inhibition effect is stronger than that of the antineoplastic drug cisplatin (DDP) with the dosage of 20 ug/ml.
(3) Cell clone colony forming method for detecting influence of compound shown as formula I on proliferation performance of tumor cells
Taking human liver cancer cells (HepG2) in a logarithmic growth phase, digesting the cells into single cells, inoculating the single cells to a 6-well plate, adding 350 cells in each well, adding a human DMEM culture medium 3ML, culturing the cells to an adherent position in an incubator, using 100 mu L DMSO as a solvent to prepare compound solutions shown in a formula I with the concentrations of 20ug/ML and 40ug/ML respectively, adding the prepared compounds shown in the formula I with the concentrations of 20ug/ML and 40ug/ML respectively into experimental groups, adding 100 mu L DMSO into blank groups, replacing fresh culture medium and medicaments every 2-3 days, and continuously culturing for one week until macroscopic clones are formed; after each well is treated, a proper amount of 0.1% crystal violet is added for staining, then the staining solution is slowly washed away by running water, the cells are dried in the air, the clone number of the cells is counted, a picture is taken under a microscope (figure 5), and the cell colony forming rate is calculated. As shown in fig. 6, the higher the concentration, the lower the colony formation rate of the human hepatoma cells (HepG2), i.e., the stronger the inhibition of the proliferation of the human hepatoma cells (HepG2) by the compound of formula I.
Taking human lung cancer cells (A549) in a logarithmic growth phase, digesting the cells into single cells, inoculating the single cells to a 6-well plate, adding 350 cells in each well, adding 3ML of a human DMEM culture medium, culturing the cells to adhere to the wall in an incubator, respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ML and 40ug/ML by taking 100 muL of DMSO as a solvent, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ML and 40ug/ML into an experimental group, respectively adding 100 muL of DMSO into a blank group, replacing fresh culture medium and medicament every 2-3 days, and continuously culturing for one week until macroscopic clones are formed; after each well is treated, a proper amount of 0.1% crystal violet is added for staining, then the staining solution is slowly washed away by running water, the cells are dried in the air, the clone number of the cells is counted, a picture is taken under a microscope (figure 7), and the cell colony forming rate is calculated. As shown in fig. 8, the lower the colony formation rate of human lung cancer cell (a549) with the increase in concentration, i.e., the stronger the inhibition effect of the compound represented by formula I on the proliferation performance of human lung cancer cell (a 549).
(4) Detecting the influence of the compound shown as the formula I on the migration performance of tumor cells
Taking tumor cells in logarithmic growth phase as human liver cancer cells (HepG2), adjusting the cell concentration to 70000 cells/ML by using a DMEM culture medium, inoculating 2ML of DMEM culture medium in each hole into a 12-hole plate, culturing until the DMEM culture medium is fully paved at the bottom of the 12-hole plate, and drawing a line from top to bottom by using culture holes of a sterile gun head; respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml by taking 100 mu L of DMSO as a solvent, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into an experimental group for treatment, adding 100 mu L of DMSO into a blank group, taking different time points within 0-24 h for observation and photographing, and counting the cell migration condition by calculating the area of a cell-free area in a scratch area.
As shown in FIG. 9, the compound of formula I can inhibit the migration ability of human liver cancer cells (HepG2), and the tumor cell migration rate decreases with increasing concentration, showing a decreasing relationship.
Taking tumor cells in logarithmic growth phase as human lung cancer cells (A549), adjusting the cell concentration to 70000 cells/ML by using a DMEM medium, inoculating 2ML of DMEM medium in each hole into a 12-hole plate, culturing until the DMEM medium is fully paved at the bottom of the 12-hole plate, and drawing a line from top to bottom by using culture holes of a sterile gun head; respectively preparing compound solutions shown in the formula I with the concentrations of 20ug/ml and 40ug/ml by taking 100 mu L of DMSO as a solvent, respectively adding the prepared compounds shown in the formula I with the concentrations of 20ug/ml and 40ug/ml into an experimental group for treatment, adding 100 mu L of DMSO into a blank group, taking different time points within 0-24 h for observation and photographing, and counting the cell migration condition by calculating the area of a cell-free area in a scratch area.
As shown in fig. 10, the compound of formula I can inhibit the migration ability of human lung cancer cell (a549), and the tumor cell migration rate decreases with increasing concentration, showing a decreasing relationship.
It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or terminal apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or terminal apparatus. Without further limitation, an element defined by the phrases "comprising … …" or "comprising … …" does not exclude the presence of additional elements in a process, method, article, or terminal that comprises the element. Further, in this document, "greater than", "less than", "more than", and the like are understood to not include the present numbers; the terms "above", "below", "within" and the like are to be understood as including the number.
Although the embodiments have been described, once the basic inventive concept is obtained, other variations and modifications of these embodiments can be made by those skilled in the art, so that the above embodiments are only examples of the present invention, and not intended to limit the scope of the present invention, and all equivalent structures or equivalent processes that can be used in the present specification and drawings, or used directly or indirectly in other related fields are encompassed by the present invention.
Claims (10)
1. A terpene phenolic compound ZKYY-057 has a structure shown in formula I:
2. a process for the preparation of a compound of formula I according to claim 1, comprising the steps of:
(1) sequentially performing carbon dioxide supercritical extraction and ethanol extraction on the hemp plant inflorescence to obtain a crude extract;
(2) dissolving the obtained crude extract, and separating by normal phase silica gel column chromatography, macroporous adsorbent resin column chromatography, primary medium pressure normal phase silica gel column chromatography, secondary medium pressure normal phase silica gel column chromatography, tertiary medium pressure normal phase silica gel column chromatography, and high pressure reverse phase HPLC chromatography to obtain compound shown in formula I.
3. The method of claim 2, comprising any one or more of the following features: firstly, the supercritical carbon dioxide extraction conditions are as follows: pExtraction kettle＝20-30MPa，TExtraction kettle＝35-60℃；PSeparation kettle I＝8-11MPa，TSeparation kettle I＝35-65℃；PSeparation kettle II＝3-6MPa，TSeparation kettle II30-40 ℃; secondly, the usage amount of ethanol in the ethanol extraction is 15-25% of the weight of the hemp plant inflorescence, and the extraction time is 30-60 min; thirdly, fully dissolving the crude extract by using petroleum ether; fourthly, the normal phase silica gel column chromatography is carried out with n-hexane/ethyl acetate 98:2 as an eluent for isocratic elution; fifthly, performing gradient elution on the macroporous adsorption resin column by adopting a D101 macroporous adsorption resin column and using 30-100% ethanol/water as an eluent; sixthly, washing the first-stage medium-pressure normal-phase silica gel column chromatography by using dichloromethane/ethyl acetate as washing agentGradient elution is carried out by removing agent; seventhly, performing gradient elution on the secondary medium-pressure normal-phase silica gel column chromatography by using n-hexane/diethyl ether as an eluent; eighthly, carrying out gradient elution on the three-stage medium-pressure normal-phase silica gel column chromatography by using n-hexane/diethyl ether as an eluent; and ninthly, carrying out gradient elution by using acetonitrile/water solution as an eluent by the high-pressure reversed-phase HPLC chromatography.
4. The application of the compound shown in the formula I in preparing a tumor cell proliferation inhibitor.
5. The tumor cell proliferation inhibitor medicine is characterized by comprising an active ingredient and pharmaceutically acceptable auxiliary materials, wherein the active ingredient comprises a compound shown in a formula I.
6. The use of a compound of formula I in the manufacture of a medicament for the treatment of a neoplastic disease.
7. An antitumor drug is characterized by comprising an active ingredient and pharmaceutically acceptable auxiliary materials, wherein the active ingredient comprises a compound shown as a formula I.
8. The use according to claim 4 or 6, wherein the neoplastic disease is liver cancer or lung cancer.
9. Antineoplastic drug according to claim 5 or 8, characterized in that said drug comprises an effective dose of compound represented by formula I, preferably an effective dose of 660 ng/dose.
10. The antitumor drug as claimed in claim 5 or 8, wherein the drug is an oral preparation or an injection preparation, and the oral preparation is one selected from dripping pills, tablets, capsules, granules or oral liquid; the injection preparation is selected from injection or powder injection.
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| CN111548332A (en) * | 2020-05-15 | 2020-08-18 | 福建省中科生物股份有限公司 | Terpene phenolic compound NO95, and preparation method and application thereof |
| CN111560001A (en) * | 2020-05-15 | 2020-08-21 | 福建省中科生物股份有限公司 | Phenolic compound NO84, and preparation method and application thereof |
| CN111574531A (en) * | 2020-05-15 | 2020-08-25 | 福建省中科生物股份有限公司 | Terpene phenolic compound NO85, and preparation method and application thereof |
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| US6448288B1 (en) * | 2000-05-17 | 2002-09-10 | University Of Massachusetts | Cannabinoid drugs |
| GB2494461A (en) * | 2011-09-12 | 2013-03-13 | Gw Pharma Ltd | Phytocannabinoids for use in the treatment of invasive cancers or metastases |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN111548332A (en) * | 2020-05-15 | 2020-08-18 | 福建省中科生物股份有限公司 | Terpene phenolic compound NO95, and preparation method and application thereof |
| CN111560001A (en) * | 2020-05-15 | 2020-08-21 | 福建省中科生物股份有限公司 | Phenolic compound NO84, and preparation method and application thereof |
| CN111574531A (en) * | 2020-05-15 | 2020-08-25 | 福建省中科生物股份有限公司 | Terpene phenolic compound NO85, and preparation method and application thereof |
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