CN115160347B - Glycosyl white vine zinc (II) complex and application - Google Patents
Glycosyl white vine zinc (II) complex and application Download PDFInfo
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- CN115160347B CN115160347B CN202210962695.6A CN202210962695A CN115160347B CN 115160347 B CN115160347 B CN 115160347B CN 202210962695 A CN202210962695 A CN 202210962695A CN 115160347 B CN115160347 B CN 115160347B
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- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 title claims abstract description 19
- 125000003147 glycosyl group Chemical group 0.000 title claims abstract description 18
- 241000219108 Bryonia dioica Species 0.000 title description 5
- INYYVPJSBIVGPH-QHRIQVFBSA-N Sinomenine Chemical compound C([C@@H]1N(CC2)C)C3=CC=C(OC)C(O)=C3[C@@]32[C@@H]1C=C(OC)C(=O)C3 INYYVPJSBIVGPH-QHRIQVFBSA-N 0.000 claims abstract description 10
- INYYVPJSBIVGPH-UHFFFAOYSA-N 14-episinomenine Natural products C1CN(C)C2CC3=CC=C(OC)C(O)=C3C31C2C=C(OC)C(=O)C3 INYYVPJSBIVGPH-UHFFFAOYSA-N 0.000 claims abstract description 9
- RARWEROUOQPTCJ-RBUKOAKNSA-N cepharamine Natural products C1CC2=CC=C(OC)C(O)=C2[C@@]2(CCN3C)[C@]13C=C(OC)C(=O)C2 RARWEROUOQPTCJ-RBUKOAKNSA-N 0.000 claims abstract description 9
- 229930002966 sinomenine Natural products 0.000 claims abstract description 9
- 239000000126 substance Substances 0.000 claims abstract description 5
- 239000003814 drug Substances 0.000 claims description 10
- 206010033128 Ovarian cancer Diseases 0.000 claims description 8
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 8
- 229940079593 drug Drugs 0.000 claims description 7
- 238000002626 targeted therapy Methods 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 abstract description 7
- 229940041181 antineoplastic drug Drugs 0.000 abstract description 7
- 238000000338 in vitro Methods 0.000 abstract 1
- 230000005918 in vitro anti-tumor Effects 0.000 abstract 1
- 230000005917 in vivo anti-tumor Effects 0.000 abstract 1
- 230000008685 targeting Effects 0.000 abstract 1
- 239000011701 zinc Substances 0.000 description 24
- 230000000694 effects Effects 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 20
- 210000004027 cell Anatomy 0.000 description 19
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 18
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 16
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- 239000003446 ligand Substances 0.000 description 12
- 229910052697 platinum Inorganic materials 0.000 description 10
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229960004316 cisplatin Drugs 0.000 description 8
- 238000001228 spectrum Methods 0.000 description 8
- 230000000259 anti-tumor effect Effects 0.000 description 7
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 235000005074 zinc chloride Nutrition 0.000 description 5
- 239000011592 zinc chloride Substances 0.000 description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 235000007082 baiteng Nutrition 0.000 description 4
- 244000290660 baiteng Species 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 238000001819 mass spectrum Methods 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 230000004060 metabolic process Effects 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 230000001093 anti-cancer Effects 0.000 description 2
- 244000309466 calf Species 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 230000010261 cell growth Effects 0.000 description 2
- 239000006285 cell suspension Substances 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000009982 effect on human Effects 0.000 description 2
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 2
- 210000005260 human cell Anatomy 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 210000004881 tumor cell Anatomy 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 108091005461 Nucleic proteins Proteins 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 239000012980 RPMI-1640 medium Substances 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 230000003698 anagen phase Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 230000011712 cell development Effects 0.000 description 1
- 239000013553 cell monolayer Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 239000012738 dissolution medium Substances 0.000 description 1
- 230000000857 drug effect Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- -1 platinum metals Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- YAYGSLOSTXKUBW-UHFFFAOYSA-N ruthenium(2+) Chemical class [Ru+2] YAYGSLOSTXKUBW-UHFFFAOYSA-N 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- 229910021654 trace metal Inorganic materials 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/003—Compounds containing elements of Groups 2 or 12 of the Periodic Table without C-Metal linkages
-
- 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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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention relates to a glycosyl sinomenine zinc (II) complex, the chemical structural formula of which is shown as the following formula:the invention also discloses application of the glycosyl sinomenine zinc (II) complex. The glycosyl sinomenine zinc (II) complex has excellent in-vitro and in-vivo antitumor activity and targeting property, has potential medicinal value, and is expected to be used for preparing various antitumor drugs.
Description
Technical Field
The invention relates to a complex, in particular to a high-activity glycosyl white vine zinc (II) complex. Meanwhile, the invention also relates to application of the complex.
Background
Since cisplatin was found to have antitumor activity, metal antitumor drugs have been rapidly developed, and several compounds other than platinum metals have been sequentially found to have certain antitumor activity (Chao, H.; et al, the development of anticancer ruthenium (II) complexes: from single molecule compounds to nanomaterials, chem. Soc. Rev.2017, 46:5771-5804.). Compared with platinum-based metal drugs, the non-platinum-based metal antitumor drugs have relatively slow development, but have certain achievements and have great application prospects.
Non-platinum anticancer drugs are mainly concentrated on trace metal elements such as copper and zinc which have biological activity and are necessary for life. Among them, zinc plays an important role in physiological activities of cells, and is an active center of many enzymes, participating in various metabolic processes. Therefore, there is an urgent need to develop an anticancer complex of zinc metal with high efficiency and low toxicity.
Cisplatin anti-cancer drugs have significant toxic and side effects during the course of treatment, limiting the application of these platinum drugs (Talcum, et al. Chemical progress, 2006, 18:107-112). In order to overcome the defects of platinum drugs, researchers are working on developing non-platinum metal antitumor drugs with better drug effect and smaller toxic and side effects besides further developing new platinum drugs.
Zinc is one of essential trace elements of human body, is related to metabolism of various enzyme activities in the human body, participates in the metabolic processes of nucleic acid and protein, can promote cell growth and development and tissue regeneration, can influence the immunity of the human body, and can also enhance the resistance of the human body. Thus, the design of efficient, targeted, water-soluble novel zinc complexes is one of the hot spots in the chemical, pharmaceutical chemistry and biology industries.
Disclosure of Invention
The invention aims at providing a high-activity glycosyl sinomenine zinc (II) complex.
Specifically, a high-activity glycosyl white vine zinc (II) complex has a chemical structural formula shown as follows:
the second purpose of the invention is to provide the application of the high-activity glycosyl sinomenine zinc (II) complex. In particular to an application of the sinomenine zinc (II) complex in preparing antitumor drugs. More specifically, the application of the high-activity glycosyl sinomenine zinc (II) complex in preparing the medicine for targeted treatment of ovarian cancer is provided.
The invention has the beneficial effects that:
compared with the prior art, the invention synthesizes the novel white leaf vine derivative by self and takes the white leaf vine derivative as an active ligand T to synthesize 1 novel high-activity glycosyl white leaf vine zinc (II) complex Zn (T); and the activity and toxicity experiments of the anti-cisplatin-resistant SK-OV-3 and anti-cisplatin-resistant SK-OV-3cis and normal HL-7702 cells of the anti-ovarian cancer are examined. Experimental results show that Zn (T) has good inhibition effect on human ovarian cancer and cisplatin-resistant cells thereof, especially SK-OV-3cis has the best inhibition effect, and IC 50 The value is as low as 1.01+/-0.11 mu M, the activity is far greater than that of cisplatin, metallic zinc (II) chloride and ligand T, and the toxicity to normal HL-7702 cells is very small; it is illustrated that the novel high-activity glycosyl white rattan zinc (II) complex Zn (T) can target proliferation of cis-platinum resistant cells SK-OV-3cis of human ovarian cancer. In a word, the novel high-activity glycosyl white rattan zinc (II) complex Zn (T) shows excellent anti-tumor activity and tumor selectivity, has potential medicinal value, and is expected to be used for preparing various anti-tumor medicaments.
Drawings
FIG. 1 is an electrospray mass spectrum of a compound T prepared in example 1 of the present invention;
FIG. 2 is a nuclear magnetic resonance hydrogen spectrum of the compound T prepared in example 1 of the present invention;
FIG. 3 is a nuclear magnetic resonance carbon spectrum of the compound T prepared in example 1 of the present invention;
FIG. 4 is an electrospray mass spectrum of the compound Zn (T) prepared in example 1 of the present invention;
FIG. 5 is a nuclear magnetic resonance carbon spectrum of the compound Zn (T) prepared in example 1 of the present invention;
FIG. 6 is a nuclear magnetic resonance carbon spectrum of the compound Zn (T)) produced in example 1 of the present invention.
Detailed Description
The present invention will be further illustrated by the following specific examples, but the present invention is not limited to these examples.
Example 1
The synthetic route is as follows:
1. the preparation of the sinomenine derivative, ligand T, is carried out in accordance with the literature (T.—M.ou; et al J.Med. Chem.2017,60, 5407-5423.).
The characterization data are as follows:
(1) Electrospray mass spectrum of ligand T is shown in FIG. 1.
ESI-MS m/z:478.2[M+H] + Wherein M is the molecular weight of ligand T.
(2) The nuclear magnetic resonance hydrogen spectrum of the ligand T is shown in FIG. 2.
1 H NMR(400MHz,DMSO-d6)δ8.41(d,J＝8.5Hz,1H),8.13-8.25(m,2H),8.00(d,J＝8.5Hz,1H),7.74-7.84(m,2H),7.61-7.69(m,2H),7.46(t,J＝7.6Hz,2H),5.46(d,J＝9.3Hz,1H),5.21-5.29(m,3H),5.19(d,J＝4.9Hz,1H),5.08(d,J＝5.5Hz,1H),4.52(t,J＝5.4Hz,1H),3.68-3.77(m,1H),3.62(br dd,J＝5.8,10.1Hz,1H),3.33-3.41(m,2H),3.25-3.31(m,1H),3.15(dt,J＝5.7,8.9Hz,1H).
(3) The nuclear magnetic resonance carbon spectrum of the ligand T is shown in FIG. 3.
13 C NMR(101MHz,DMSO-d6)δ157.89,147.26,146.69,146.52,135.10,133.15,130.69,129.48,128.41,123.82,123.55,122.88,122.76,121.97,118.57,112.90,87.76,80.39,77.51,72.34,70.00,61.15.
(4) The elemental analysis results are shown in table 1.
Table 1 results of elemental analysis of ligand T in the examples
Thus, the resulting yellow ligand T can be determined as follows:
2. in a high temperature pressure-resistant tube of 15.0mL, 1.00mol of ligand T and 1.00mol of zinc (II) chloride are weighed, 2.5mL of methanol solution is added, after the reaction is carried out for 72.0 hours at 80.0 ℃, the product is washed 3 times by 5.0mL of diethyl ether solution, and the yellow target product Zn (T) is obtained by drying in a vacuum drying oven at 45 ℃, and the yield is 89.7%.
(1) Electrospray mass spectrum of the compound Zn (T) is shown in FIG. 4.
ESI-MS:m/z＝701.80for[M-Cl+4(CH 3 OH)] + Wherein M is the molecular weight of the compound Zn (T).
(2) The nuclear magnetic resonance hydrogen spectrum of the compound Zn (T) is shown in FIG. 5.
1 H NMR(500MHz,DMSO-d6)δ8.43(d,J＝8.7Hz,1H),8.24(d,J＝7.6Hz,1H),8.21(s,1H),8.04(d,J＝8.4Hz,1H),7.84(t,J＝6.7Hz,1H),7.77(d,J＝8.4Hz,1H),7.67(t,J＝7.6Hz,2H),7.48(q,J＝7.2,6.6Hz,2H),5.51(d,J＝9.3Hz,1H),5.36(d,J＝6.0Hz,1H),5.27(d,J＝5.6Hz,3H),5.16(d,J＝5.6Hz,1H),4.62(t,J＝5.6Hz,1H),3.79(td,J＝9.2,5.6Hz,1H),3.67(dd,J＝10.6,5.4Hz,1H),3.43-3.34(m,3H),3.21(dd,J＝9.8,4.7Hz,2H).
(3) The nuclear magnetic resonance carbon spectrum of the compound Zn (T) is shown in FIG. 6.
13 C NMR(126MHz,DMSO)δ157.87,147.18,146.66,146.55,135.14,133.14,130.69,129.41,128.45,123.84,123.78,123.46,122.83,122.77,122.02,118.54,112.84,87.80,80.37,77.52,72.38,70.01,61.16,49.12,40.41,40.25,40.08,39.91,39.75,39.58,39.41.
(4) Elemental analysis results are shown in table 2.
TABLE 2 elemental analysis results of Compound Zn (T) in examples
Thus, the resulting yellow Zn (T) can be determined, and has the following structural formula:
example 2
In a high temperature pressure-resistant tube of 15.0mL, 1.00mol of ligand T and 1.00mol of zinc (II) chloride are weighed, 0.5mL of methanol solution is added, after the reaction is carried out for 72.0 hours at 80.0 ℃, the product is washed 3 times by 5.0mL of diethyl ether solution, and the yellow target product Zn (T) is obtained by drying in a vacuum drying oven at 45 ℃, and the yield is 79.5%.
Example 3
In a high temperature pressure-resistant tube of 15.0mL, 1.00mol of ligand T and 1.00mol of zinc (II) chloride are weighed, 3.0mL of methanol solution is added, after the reaction is carried out for 72.0 hours at 80.0 ℃, the product is washed 3 times by 5.0mL of diethyl ether solution, and the yellow target product Zn (T) is obtained by drying in a vacuum drying oven at 45 ℃, and the yield is 71.1%.
Test example 1
In order to fully explain the application of the 1 novel high-activity glycosyl white vine zinc (II) complex Zn (T) in pharmacy, the applicant carries out an anti-tumor activity experiment.
1. Cell strain and cell culture
The experiment selects 3 human cell lines such as human ovarian cancer SK-OV-3 and cisplatin-resistant strain SK-OV-3cis and normal HL-7702 cells.
All the human cell lines are cultured in RPMI-1640 culture solution containing 100U/mL penicillin, 10wt% calf blood and 100U/mL streptomycin, and the culture solution is placed at 37 ℃ and contains CO with the volume concentration of 5% 2 Culturing in incubator.
2. Preparation of test Compounds
All compounds used were > 95% pure and their DMSO stock was diluted with physiological buffer to 20 μmol/L final solution (DMSO final concentration 1%) at which the extent of inhibition of growth of normal or selected tumor cells by each compound was tested.
3. Cell growth inhibition experiment (MTT method)
(1) Taking normal cells or tumor cells in logarithmic growth phase, preparing a cell suspension with the concentration of 5000 cells/mL by using a culture solution containing 10% calf serum after trypsin digestion, and inoculating 190 mu L of the cell suspension into a 96-well culture plate for each well to enable the density of cells to be detected to 1000-10000 wells (the edge wells are filled with sterile PBS);
(2)5％ CO 2 incubating at 37 ℃ for 24 hours until cell monolayers are fully paved at the bottom of the wells, adding 10 mu L of a drug with a certain concentration gradient into each well, and setting 4 compound wells for each concentration gradient;
(3)5％ CO 2 incubating at 37 ℃ for 48 hours, and observing under an inverted microscope;
(4) mu.L of MTT solution (5 mg/mL PBS, i.e., 0.5% MTT) was added to each well and incubation was continued for 4h;
(5) Stopping culturing, carefully sucking out the culture solution in the holes, adding 150 mu L of DMSO into each hole to fully dissolve formazan precipitate, uniformly mixing by using a shaker, measuring the optical density value of each hole at the wavelength of 570nm for an enzyme-labeling instrument and the reference wavelength of 450 nm;
(6) At the same time, zeroing wells (medium, MTT, DMSO) and control wells (cells, medium, MTT, drug dissolution medium of the same concentration, DMSO) were set.
(7) The number of living cells is judged based on the measured optical density value (OD value), and the greater the OD value, the stronger the cell activity. Using the formula:
calculating the inhibition rate of each compound on the growth of the selected cells, and calculating the IC of each tested compound on each selected cell strain by using a Bliss method 50 Values. The results are shown in Table 3 below.
TABLE 3 IC of compounds against various cell lines 50 Value (mu M)
Slave IC 50 The result of activity screening shows that Zn (T) has good inhibition effect on human ovarian cancer and cis-platinum-resistant cells thereof, especially SK-OV-3cis, has the best inhibition effect, and is IC 50 The value is as low as 1.01+/-0.11 mu M, and the activity is far higher than that of cisplatin, metallic zinc (II) chloride and a complexBody T, and it has little toxicity to normal HL-7702 cells; it is illustrated that the novel high-activity glycosyl white rattan zinc (II) complex Zn (T) can target proliferation of cis-platinum resistant cells SK-OV-3cis of human ovarian cancer. In a word, the novel high-activity glycosyl white rattan zinc (II) complex Zn (T) shows excellent anti-tumor activity and tumor selectivity, has potential medicinal value, and is expected to be used for preparing various anti-tumor medicaments.
Claims (2)
1. A glycosyl sinomenine zinc (II) complex is characterized in that the chemical structural formula is shown as the following formula:
2. use of the glycosyl sinomenine zinc (II) complex of claim 1 for preparing a drug for targeted therapy of ovarian cancer.
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| CN111187303A (en) * | 2020-01-17 | 2020-05-22 | 玉林师范学院 | Novel platinum (II) complex with high antitumor activity of cryptolepine, and synthetic method and application thereof |
| CN111205311A (en) * | 2020-01-17 | 2020-05-29 | 玉林师范学院 | Novel high-antitumor-activity white leaf vine zinc (II) complex and synthesis method and application thereof |
| CN111253418A (en) * | 2020-01-17 | 2020-06-09 | 玉林师范学院 | Novel white leaf vine zinc (II) complex and synthesis method and application thereof |
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| CN114573598A (en) * | 2022-03-21 | 2022-06-03 | 玉林师范学院 | White leaf vine zinc (II) complex with high activity in vivo and in vitro and synthesis method and application thereof |
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