CN109081801A - The indoles alcohol derivative of acidic amino acid modification, synthesis, activity and application - Google Patents

The indoles alcohol derivative of acidic amino acid modification, synthesis, activity and application Download PDF

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CN109081801A
CN109081801A CN201710442553.6A CN201710442553A CN109081801A CN 109081801 A CN109081801 A CN 109081801A CN 201710442553 A CN201710442553 A CN 201710442553A CN 109081801 A CN109081801 A CN 109081801A
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obzl
indoles
ethoxyacetyl
acetyl
tumor
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CN109081801B (en
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赵明
彭师奇
王玉记
吴建辉
吴晨
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Capital Medical University
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Capital Medical University
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12—Radicals substituted by oxygen atoms

Abstract

The invention discloses the 1- of following formula (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue in formula), it discloses their preparation method, disclose their anti-tumor activity, disclose their activity of resisting tumor metastasis, and disclose their anti-inflammatory activity activity, anti-tumor drug thus is being prepared the invention discloses them, the application in medicine for anti transfer of tumor and anti-inflammatory drug.

Description

The indoles alcohol derivative of acidic amino acid modification, synthesis, activity and application
Technical field
The present invention relates to 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles, are related to their preparation Method is related to their anti-tumor activity, is related to their activity of resisting tumor metastasis, and is related to their anti-inflammatory activity work Property, thus anti-tumor drug is being prepared the present invention relates to them, the application in medicine for anti transfer of tumor and anti-inflammatory drug.The present invention Belong to biomedicine field.
Background technique
Malignant tumour seriously threatens human health.Wherein lung cancer is one of most invasive human cancer.For lung cancer The patient in patient's advanced stage, the people of usual 10%-15% can only survive 5 years.The situation of this difficulty is not yet in past 30 years Significantly make moderate progress.In many clinical cases, lung cancer is transferred into surrounding tissue before being diagnosed.Metastases, especially It is the greateset risk that neoplasm lung metastasis is tumor patient death.So far, the antineoplastic of metastases still can not prevented Object is for clinic.Inflammation then can further deteriorate the prognosis of tumour and metastases patient.So far, more not can prevention of inflammation and The anti-tumor drug of metastases is for clinic.Invention have it is antitumor, the drug of anti-tumor metastasis and anti-inflammatory triple role is The forward position of anti-tumor drug research.The early period of inventor invents (patent application publication CN 106349148A, application number CN 201510409682.6) it once discloses, double heteroauxin alcohol that amino-acid benzyl ester replaces under 0.2 μm of ol/kg dosage have anti- Tumour, anti-tumor metastasis and anti-inflammatory triple role (levoform).Inventor has two o'clock to this class double-indole alcohol amido acid acid benzyl ester It is dissatisfied.First point dissatisfied be MTT model show their anti-tumor activity from cytotoxicity (in addition to 1 compound, Remaining all compound inhibits the IC of 5 kinds of tumor cell proliferations50It is 8.2-62.2 μM).Clinical application shows, cytotoxic drug There is biggish toxic side effect.That is, this class double-indole alcohol amido acid acid benzyl ester faces the wind of biggish toxic side effect Danger.Dissatisfied second point is that their performances are antitumor, and the minimum effective dose of anti-tumor metastasis and anti-inflammatory triple role is 0.2 μ Mol/kg, it is higher.In past 2 years, inventor always searches for the minimum effective dose acellular lower than 0.2 μm of ol/kg Malicious class has antitumor, the compound of anti-tumor metastasis and anti-inflammatory triple role.Finally inventors have found that acidic amino acid benzyl The indoles ethyl alcohol (right formula) of ester (Glu (OBzl)-OBzl and Asp (OBzl)-OBzl) modification has under 0.02 μm of ol/kg dosage It is antitumor, anti-tumor metastasis and anti-inflammatory triple role.It disappears because the toxic side effect of drug can be reduced with dosage, 10 times of effective dose reduction, which shows this structural modification, technical effect outstanding.In addition, MTT model shows them to tumour The IC of cell Proliferation50It is all larger than 200 μM.That is, acidic amino acid benzyl ester (Glu (OBzl)-Obzl and Asp (OBzl)- OBzl) there are no the toxic side effects of cell toxicant class compound for the indoles ethyl alcohol modified.According to both sides advantage, inventor is proposed The present invention.
Summary of the invention
First content of the invention is to provide 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) of following formula Indoles (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue).
Second content of the invention is to provide 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles The preparation method of (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue), this method are made of following steps:
1) indoles ethyl alcohol reacts for 80 DEG C in tetrahydrofuran with bromoacetate under sodium hydride catalysis, is generated as 1- ethoxy Carbonyl methyl -3- ethoxy carbo methoxy group Ethyl-indole (1)；
2) saponification of compound 1 obtains 1- carboxymethyl -3- carboxymethoxyl ethylindole in the NaOH aqueous solution that concentration is 2N (2)；
3) in the presence of dicyclohexylcarbodiimide and N- hydroxy benzo triazole compound 2 in anhydrous tetrahydro furan with The reaction of l-amino acid benzyl ester, generates 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles (AA L-Asp (OBzl) residue and L-Glu (OBzl) residue).
Third content of the invention is evaluation 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles The activity of resisting tumor metastasis of (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue).
4th content of the invention is evaluation 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles The anti-tumor activity of (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue).
5th content of the invention is evaluation 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles The anti-inflammatory activity of (AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue).
Detailed description of the invention
The synthetic route .i of Fig. 1 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles) bromoacetic acid second Ester, NaH, 80 DEG C；Ii) concentration is the NaOH aqueous solution of 2N；Iii) dicyclohexylcarbodiimide, N- hydroxy benzo triazole, N- Methyl morpholine；AA=Asp (OBzl) residue in 3a, AA=L-Glu (OBzl) residue in 3b.
Specific embodiment
In order to which the present invention is further explained, a series of embodiments are given below.These embodiments be entirely it is illustrative, it Only be used to the present invention is specifically described, be not construed as limitation of the present invention.
Embodiment 1 prepares 1- ethoxycarbonymetyl -3- ethoxy carbo methoxy group Ethyl-indole (1)
It is slowly added at room temperature into 5.00g (31mmol) indoles ethyl alcohol and the solution of 50mL anhydrous tetrahydro furan (THF) 17.22mL (5mmol) bromoacetate, 80 DEG C of heating are slowly added dropwise in 2.98g (4mmol, 60%) NaH, stirring after 30 minutes 48 hours.TLC (petrol ether/ethyl acetate, 3/1) display reaction is completed.Stop heating, reaction mixture is cooled to room temperature.Filter Remove solid, filtrate decompression concentration.Residue is purified with silica gel column chromatography (petrol ether/ethyl acetate, 3/1), obtains 1.54g (15%) title compound is yellow syrup.ESI-MS(m/e):334[M+H]+。
Embodiment 2 prepares 1- carboxymethyl -3- carboxymethoxyl ethylindole (2)
By 1.31g (3.9mmol) 1- ethoxycarbonymetyl -3- ethoxy carbo methoxy group Ethyl-indole (1) 10mL first under ice bath Alcohol dissolution.The NaOH aqueous solution that concentration is 2N is added dropwise into obtained solution, adjusts the pH to 12 of solution, TLC after stirring 5 hours (petrol ether/ethyl acetate, 3/1) display reaction is completed.Reaction mixture saturation KHSO4Aqueous solution section pH to 7 is depressurized dense Contracting, residue object are extracted 3 times with 15mL ethyl acetate, water layer saturation KHSO4Aqueous solution adjusts pH to 4, with 15mL acetic acid second Ester extracts 3 times.The water layer separated continues with saturation KHSO4Aqueous solution adjusts pH to 2, is extracted 3 times and is closed with 15mL ethyl acetate And isolated ethyl acetate layer, it is washed 3 times with 15mL saturation NaCl aqueous solution, uses anhydrous Na2SO4It is 12 hours dry.Filtering, filtrate It is concentrated under reduced pressure, obtains 0.68g (62%) title compound, be yellow syrup.ESI-MS(m/e):276[M-H]-；Mp 97-100 ℃；(C=0.1, ethyl alcohol)；IR(KBr,cm-1):3196,3051,2892,1651,1469,1435,1175, 1124,840,901,724；1H NMR(300MHz,DMSO-d6) δ/ppm=12.731 (s, 2H), 7.549 (d, J=7.8Hz, 1H), 7.324 (d, J=6.9Hz, 1H), 7.172 (s, 1H), 7.114 (t, J=6.9Hz, 1H), 7.021 (t, J=6.9Hz, 1H), 4.937 (s, 2H), 4.053 (s, 2H), 3.725 (t, J=7.2Hz, 2H), 2.947 (t, J=7.2Hz, 2H).
Embodiment 3 prepares 1- (acetyl-Asp (OBzl)-OBzl) -3- (Ethoxyacetyl-Asp (OBzl)-OBzl) indoles (3a)
By 0.55g (2.0mmol) 1- carboxymethyl -3- carboxymethoxyl Ethyl-indole (2), 0.54g (4.0mmol) N- hydroxyl The solution of benzotriazole and the anhydrous THF of 10mL stir 30 minutes, obtain reaction solution A.By two hexamethylene of 0.82g (4.0mmol) The base carbodiimide anhydrous THF of 5mL dissolves, and obtains reaction solution B.Under ice bath, reaction solution B is slowly added dropwise to reaction solution In A, stir 30 minutes.Then inward in plus the anhydrous THF of 2.79g (8.0mmol) HClAsp (OBzl)-OBzl and 15mL it is molten Liquid.Reaction mixture adjusts pH to 9 with N-methylmorpholine, is stirred at room temperature 10 hours.TLC(CH2Cl2/CH3OH, 30/1, add 3 drops Acetic acid) display reaction completion.Reaction mixture filtering, filtrate decompression concentration, residue 30mL ethyl acetate dissolve.It obtains Solution is successively saturated NaHCO with 20mL3Aqueous solution is washed 3 times, and 20mL saturation NaCl aqueous solution washes 3 times, 20mL5%KHSO4Aqueous solution It washes 3 times, 20mL saturation NaCl aqueous solution is washed 3 times, and 20mL is saturated NaHCO3Aqueous solution is washed 3 times and 20mL saturation NaCl aqueous solutions and is washed 3 times.Ethyl acetate layer adds anhydrous Na2SO4It is 12 hours dry, filtering, filtrate decompression concentration, residue silica gel column chromatography (CH2Cl2/CH3OH, 30/1, add 3 drop acetic acid) purifying, 0.50g (29%) title compound is obtained, is colourless syrup.ESI-MS (m/e):868[M+H]+；(C=0.1, ethyl alcohol)；IR(KBr,cm-1):3407,3033,2929,1732, 1679,1517,1170,967,738,696；1H NMR(300MHz,DMSO-d6) δ/ppm=8.793 (d, J=8.1Hz, 1H), 8.183 (d, J=8.4Hz, 1H), 7.537 (d, J=1.5Hz, 1H), 7.339 (m, 20H), 7.231 (d, J=4.8Hz, 1H), 7.051 (s, 1H), 7.023 (m, 2H), 5.089 (m, 8H), 4.821 (m, 4H), 3.941 (s, 2H), 3.669 (t, J=6.3Hz, 2H),2.926(m,6H)。
Embodiment 4 prepares 1- (acetyl-Glu (OBzl)-OBzl) -3- (Ethoxyacetyl-Glu (OBzl)-OBzl) indoles (3b)
Using the method for embodiment 3 from 0.55g (2.0mmol) 1- carboxymethyl -3- carboxymethoxyl Ethyl-indole (2) and 2.91g (8.0mmol) HClGlu (OBzl)-OBzl obtains 0.53g (30%) title compound, is colourless syrup.ESI-MS (m/e):896[M+H]+；(C=0.1, ethyl alcohol)；IR(KBr,cm-1):3361,3033,2934,1732, 1678,1518,1454,1164,738,696；1H NMR(300MHz,DMSO-d6) δ/ppm=8.726 (d, J=7.8Hz, 1H), 8.067 (d, J=7.8Hz, 1H), 7.545 (d, J=7.5Hz, 1H), 7.340 (m, 20H), 7.247 (d, J=7.2Hz, 1H), 7.116(s,1H),7.004(m,2H),5.081(m,8H),4.803(m,2H),4.398(m,2H),3.947(s,2H),3.678 (m, 2H), 2.957 (t, J=6.9Hz, 2H), 2.439 (m, 4H), 2.112 (m, 2H), 1.903 (m, 2H).
Embodiment 5 measures compound 3a, the activity of resisting tumor metastasis of b
Lewis murine lung cancer cell (LLC the is purchased from ATCC) inoculation of this rating model, selects DMEM culture medium (to contain 10% Fetal calf serum through inactivating, 1 × 105U/L penicillin and 100mg/L streptomysin), it was passed according to attached cell cultural method every two days In generation, is primary, enrichment of cell.Vitellophag when cell growth state is good and is in logarithmic growth phase, is adjusted thin with physiological saline Born of the same parents' density is to 1 × 107A/mL.The dyeing of placenta indigo plant, makes viable count > 95%.Take inbred strais C57BL/6 male mice (SPF Grade, 20 ± 2g of weight), the fixed mouse of left hand.It is sterilized with 75% Mice Hepatocytes Injured by Ethanol right fore skin of axillary fossa.It is sterile that the right hand holds 1mL LLC tumor cell suspension is subcutaneously injected toward mouse armpit in syringe, and every mouse injects 0.2mL.After mouse inoculation 10 days, grow The tumour of diameter about 4-5mm is knurl source.The Lewis lung cancer tumor-bearing mice etherization of inoculation 10 days, cervical dislocation are put to death.With 75% ethyl alcohol impregnates 10min, and knurl is removed in disinfection on superclean bench.Select well-grown tumor tissues sterile flat It shreds, is placed in the tissue homogenizer of glass manufacture in ware.The ratio for being again 1 to 3 (g ratio mL) than physiological saline volume in tumor mass The physiological saline that heating degree is 4 DEG C, is lightly ground and cell suspension is made.Cell suspension crosses 200 mesh cell sieve single cell suspensions. With the cell density of physiological saline tune single cell suspension to 1.5 × 107A/mL.The dyeing of placenta indigo plant, makes viable count > 95%. Left hand fixes inbred strais C57BL/6 male mice, is sterilized with 75% Mice Hepatocytes Injured by Ethanol right fore skin of axillary fossa.The right hand holds 1mL Tumor cell suspension, every injection 0.2mL is subcutaneously injected in mouse armpit in asepsis injector.Mouse grows diameter 4- after inoculation 10 days Mice Inoculated is grouped by the tumour of 5mm at random by the gross tumor volume measured.Every group of 12 mouse.The 11st day of inoculated tumour is small (dosage is 20 μm of ol/ to the normal saline solution of mouse or oral generally acknowledged anti tumor translocation peptide Arg-Gly-Asp-Ser (RGDS) Kg/ days) or oral administration of compound 3a, b normal saline solution (dosage be 0.02 μm ol/kg/ days) or oral administration of compound 2 physiology Saline solution (dosage be 2 μm ol/kg/ days) or oral normal saline (dosage is 10mL/kg/ days) give 1 medicine, continuously daily Administration 12 days, measures and records gross tumor volume every three days.The next day measurement knurl product of last time administration, etherization take off neck Vertebra is put to death, and the tumour of mouse is taken to weigh, and is taken the lung of mouse and is calculated the burrknot number of tumour lung transfer.With t examine to data into Row statistical analysis.It the results are shown in Table 1.Neoplasm lung metastasis is not only effectively inhibited in 0.02 μm of ol/kg dosages for Compound 3a, b, and And activity does not have significant difference with their high 1000 times of RGDS of dose ratio and their high 100 times compounds 2 of dose ratio.These Statistics indicate that the present invention has significant technical effect.
The activity of resisting tumor metastasis of table 1 compound 3a, b
B) p<0.01 compared with physiological saline, with RGDS and compound 2 than p>0.05；N=10
Embodiment 6 measures compound 3a, the neoplasm growth activity of b
By adriamycin physiological saline solution, compound 2 and compound 3a, b physiological saline solution before measurement, it is used for The administration of S180 mouse.It is taken in gnotobasis and is inoculated in male ICR mouse 10 days eugonic S180 ascitic tumor fluids, use physiology The liquid that salt water is diluted to (1:2) is sufficiently mixed, and 0.2% Trypan Blue of tumor cell suspension Fresh mixes It is counted afterwards by white blood cell count(WBC) method, dye blue person is dead cell, and tinter is not living cells.By cell concentration=4 block plaids Interior viable count/4 × 104× extension rate=cell number/mL calculates cell density, by cell survival rate=viable count/(work Cell number+dead cell number) × 100% calculating cell survival rate.Density is made with homogenate method in tumor liquid by survival rate greater than 90% It is 2.0 × 107The cell suspension of a/mL.The cell suspension inoculation is subcutaneous (0.2mL/ is only) in mouse right axillary, manufactures S180 lotus knurl Mouse.Inoculation for 24 hours after S180 tumor-bearing mice be injected intraperitoneally daily adriamycin normal saline solution (dosage be 2 μm ol/kg/ days Or the normal saline solution of daily oral administration of compound 2 (dosage be 5 μm ol/kg/ days) or the life of oral administration of compound 3a, b daily g) Manage saline solution (dosage be 0.02 μm ol/kg/ days).It is administered once a day, successive administration 12 days.The next day of last time administration Knurl product is measured, etherization cervical dislocation puts to death, then fixes mouse right axillary tumor location with tweezers, cut off skin passivity Removing tumour is simultaneously weighed.Curative effect is indicated with knurl weight (mean value ± SD g), and data are examined with t and variance analysis.It the results are shown in Table 2.? 0.02 μm of ol/kg dosages for Compound 3a, b not only effectively inhibit tumour growth, but also they are 100 times high for activity and dose ratio Compound 2 do not have significant difference.These statistics indicate that, the present invention has significant technical effect.
The influence of table 2 compound 3a, 3b to S180 mice tumors grew
A) p<0.05 compared with physiological saline, with compound 2 than p>0.05；N=12.
Embodiment 7 measures compound 3a, the anti-inflammatory activity of b
Because mouse ear swelling caused by dimethylbenzene is acknowledged as acute inflammation model, the present invention causes in dimethylbenzene Mouse ear swelling model on measure compound 3a, the therapeutic effect of b.Because aspirin is the positive for treating acute inflammation Medicine, so the present invention selects aspirin for positive control drug.The ring that ICR male mice (20 ± 2g of weight) is 22 DEG C in temperature Border tranquillization 2 days, free water and feed.Later, physiological saline group (dosage is 0.2mL/), aspirin group are randomly divided into (dosage 1.11mmol/kg), (dosage is 0.02 μm of ol/ for 2 groups of compound (dosage is 2 μm of ol/kg) and compound 3a, b group Kg), every group of 12 mouse.Mouse is by place group or oral normal saline or oral aspirin or oral administration of compound when measurement 2 or oral administration of compound 3a, b.After 30min is administered, the left auricle toward mouse uniformly smears 30 μ L dimethylbenzene, and mouse receives after 2h Etherization, the neck that breaks are put to death, and are cut two ears of left and right, are taken round auricle in the same position of two ears with the punch of 7mm, weigh, Two ear swelling differences are found out as swelling.That is swelling=auris dextra disk weight-left ear disk weight.It the results are shown in Table 3.? 0.02 μm of ol/kg dosages for Compound 3a, b not only effectively inhibit mouse ear swelling caused by dimethylbenzene, but also activity is better than Its high 100 times compound 2 of dose ratio, its high 55500 times aspirin does not have significant difference with dose ratio.These data Show that the present invention has significant technical effect.
The influence of mouse ear swelling caused by 3 compound 3a, b paraxylene of table
A) p<0.01 compared with physiological saline and compound 2, with aspirin ratio p>0.05；N=12.

Claims (5)

1. 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles of following formula,
AA is L-Asp (OBzl) residue and L-Glu (OBzl) residue in formula.
2. the preparation method of 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles of claim 1, this method Include:
1) indoles ethyl alcohol reacts for 80 DEG C in tetrahydrofuran with bromoacetate under sodium hydride catalysis, is generated as 1- ethoxy carbonyl first Base -3- ethoxy carbo methoxy group Ethyl-indole (1)；
2) saponification of compound 1 obtains 1- carboxymethyl -3- carboxymethoxyl ethylindole (2) in the NaOH aqueous solution that concentration is 2N；
3) in the presence of dicyclohexylcarbodiimide and N- hydroxy benzo triazole compound 2 in anhydrous tetrahydro furan with L- ammonia The reaction of base acid benzyl ester, generates 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles.
3. 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles of claim 1 is in preparation anti-tumor metastasis Application in drug.
4. 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles of claim 1 is preparing anti-tumor drug In application.
5. 1- (acetyl-AA-OBzl) -3- (Ethoxyacetyl-AA-OBzl) indoles of claim 1 is in preparing anti-inflammatory drug Application.
CN201710442553.6A 2017-06-13 2017-06-13 Acidic amino acid modified indoloethanol derivative, and synthesis, activity and application thereof Expired - Fee Related CN109081801B (en)

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