CN101723903B - 4-carbonyl diaryl pyrimidine derivatives and its preparation method and use - Google Patents
4-carbonyl diaryl pyrimidine derivatives and its preparation method and use Download PDFInfo
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Abstract
The invention belongs to the technical field of medicines, in particular to 4-carbonayl diaryl pyridine derivatives (CO-DAPYs) shown as a general formula I as well as preparation methods and applications thereof. The compounds of the 4-carbonyl diaryl pyridine derivatives also comprise medicinal salts, stereochemical isomers, hydrates, solvates, polycrystals and eutectics, precursors with same biological functions and derivatives thereof. A pharmacological test result shows that the compounds have remarkable anti-HIV-1 virus activity and show better inhibiting effect to common mutated virus strains in clinic, therefore, the compositions containing one or a plurality of compounds can be used for preparing related medicines for treating Aids, and the like.
Description
Technical field
The invention belongs to medical technical field, be specifically related to a kind of 4-carbonyl diaryl pyridine derivatives.
Background technology
AIDS (AIDS) is that AIDS (Acquired immune deficiency syndrome) is by human immunodeficiency virus (Human immunodeficiency virus, the epidemic infectious diseases that HIV) is caused.
(Reverse transcriptase RT) has become the process of DNA decisive role at HIV to reversed transcriptive enzyme from the mRNA rt, therefore become one of important target spot of anti-AIDS drug design.
In existing inverase research, non-nucleoside reverse transcriptase inhibitor (NNRTIs) becomes one of focus of various countries' Pharmaceutical Chemist concern because of advantages such as its high-efficiency low-toxicities.At present, the anti-hiv reverse transcriptase inhibitor that goes on the market through drugs approved by FDA has four kinds: how Wella is put down (Nevirapine), De Laweiding (Delavirdine), Yi Feiweilun (Efavirenz),
Etravirine(TMC-125), α-APA089439, HBY097 in addition, TMC278 etc. are carrying out clinical study.
Summary of the invention
The objective of the invention is to propose a kind of RTI 4-carbonyl diaryl miazines (CO-DAPYs) verivate.
Another purpose of the present invention is to propose the preparation method of above-claimed cpd.
Still a further object of the present invention is the application that proposes above-claimed cpd.
Diarylmiazines derivatives (DAPYs) is the one type of NNRTIs with higher HIV-resistant activity that found in recent years, through a series of structure of modification, has developed a series of compounds with better prospect.The present invention adopts the means of area of computer aided SARS drug design to simulate the mode of action and the structure activity relationship of such suppressor factor and HIV-1RT, instructs further structure of modification with this.Carbonylate replaces in the α position of pyrimidine ring 4-position, in the hope of adding potent inhibitor and amino-acid residue Tyr188 on every side, the π between the Tyr181～pi accumulation effect; In the C5-position of pyrimidine ring, substituting group is introduced in the C6-position simultaneously, with the synergy of reinforcement and carbonyl, disturbs the katalysis of amino-acid residue Asp; A series of 4-carbonyl diaryl miazines (CO-DAPYs) verivate has been synthesized in design, and it has been carried out biological activity test, and the result shows that majority of compounds has stronger anti-HIV-1 virus function, higher SI.
The present invention has designed and synthesized 4-carbonyl diaryl miazines (CO-DAPYs) verivate of a series of brand news according to the analytical results of area of computer aided SARS drug design.
Above-claimed cpd provided by the invention has following general structure:
Wherein, R
1And R
2Be selected from hydrogen respectively, hydroxyl, halogen, substituted C
1-4Alkyl, substituted C
2-6Thiazolinyl, substituted C
2-6Alkynyl, C
1-6Alkoxyl group, cyanic acid, nitro, amino ,-NH (OH)-, or-N (R
4) p-.
R
3Be selected from hydrogen, hydroxyl, halogen, by cyanic acid or-C (=O) R
5Substituted C
1-6Alkyl, C
3-7Naphthenic base is by one or more halogen atoms or the substituted C of cyanic acid
2-6Thiazolinyl is by one or more halogen atoms or the substituted C of cyanic acid
2-6Alkynyl, C
1-6Alkoxyl group, C
1-6Carbalkoxy, carboxyl, cyanic acid, nitro, amino ,-NR
5-, many halogenated methyls, many halogenated methoxies, many halos methylthio group ,-S (=O)
pR
5,-NH-S (=O)
pR
5,-C (=O) R
5,-NHC (=O) H ,-C (=O) NHNH
2,-NHC (=O) R
5, or-C (=NH) R
5
Ar is selected from aryl, substituted aryl, and naphthyl, substituted naphthyl, anthryl replaces anthryl, and phenanthryl replaces phenanthryl, pyrryl; The substituted azole base, pyrazolyl, substituted pyrazolecarboxylic base, imidazolyl, substituted imidazole base, triazolyl, substituted triazole base, tetrazyl; Replace tetrazyl, benzimidazolyl-, the substituted benzimidazole base, the benzotriazole base replaces the benzo triazolyl, furyl, substituted furan base, oxazolyl; The substituted oxazoline base, isoxazolyl replaces isoxazolyl, and benzoxazolyl replaces benzoxazolyl, thienyl, substituted thiophene base, thiazolyl; Substituted thiazolyl, benzothiazolyl, substituted benzene benzothiazolyl, pyridyl, substituted pyridinyl, quinolyl, substd quinolines base, isoquinolyl; The substituted isoquinoline base, acridyl replaces acridyl, and pyridazinyl replaces pyridazinyl, pyrimidyl, substituted pyrimidyl, pyrazinyl; Replace pyrazinyl, triazinyl, purine radicals, substituted purinyl, other five yuan or hexa-atomic aromatic heterocyclic, the hexa-atomic aromatic heterocyclic of benzo five-membered or benzo replaces benzo five-membered or the hexa-atomic aromatic heterocyclic of replacement benzo, C
1-6Carbalkoxy, aryloxy carbonyl, or replace aryloxy carbonyl.
X is selected from-NR
4-,-NH-NH-,-N=N-,-O-,-C (=O)-, C
1-4Alkane two bases ,-CH (OH)-,-S-,-S (=O) p-,-X
1-C
1-4Alkane two bases-or-C
1-4Alkane two bases-X
1-, or-CH (CN)-.
X
1For-NR
4-,-NH-NH-,-N=N-,-O-,-C (=O)-,-CH (OH)-, or-S (=O) p-.
R
4Be selected from hydrogen, aryl, formyl radical, C
1-6Alkyl-carbonyl, C
1-6Alkyl, C
1-6Carbalkoxy is by formyl radical, C
1-6Alkyl-carbonyl, C
1-6Carbalkoxy or C
1-6The substituted C of alkyl carbonyl oxy
1-6Alkyl is by C
1-6The substituted C of carbalkoxy
1-6Alkoxyl group or C
1-6Carbalkoxy.
R
5Be C
1-4Alkyl, amino, single or two (C
1-4Alkyl) amino or many halos C
1-4Alkyl.
M is the integer of 0-5, and n is the integer of 0-6.
P is 1 or 2.
The preparation method of this compounds is following:
Under protection of inert gas, be reactant with the itrile group Diarylmiazines derivatives, react acquisition product of the present invention down in alkali (like Lithamide (sodium), sodium hydride, n-Butyl Lithium, diisobutyl amido lithium, or potassium tert.-butoxide) effect, its reaction expression is as follows:
Wherein:
The concrete operations step is following: the itrile group Diarylmiazines derivatives is joined in the dry polar aprotic solvent, stir and make it dissolving, add alkali (like Lithamide (sodium); Sodium hydride, n-Butyl Lithium, diisobutyl amido lithium; Or potassium tert.-butoxide), in 20-35 ℃, stirring reaction 24～36h.After TLC showed that reaction finishes, reaction solution poured in the cold water, ethyl acetate extraction, drying.Remove solvent under reduced pressure, obtain bullion.Re-crystallizing in ethyl acetate gets pure article.Wherein:
(1) alkali (Lithamide (sodium), sodium hydride, n-Butyl Lithium, diisobutyl amido lithium, potassium tert.-butoxide) is excessive, is about about 1.8～2.3 times of itrile group Diarylmiazines derivatives.
(2) used solvent is THF (THF), 2-methyltetrahydrofuran, ether, MTBE (MTBE), N, dinethylformamide (DMF), DMAC N,N (DMA), or acetonitrile.1mmol 4-chloropyrimide verivate need add aprotic solvent 5～8mL.
(3) rare gas element is nitrogen, argon gas or helium.
This compounds class can be made hydrochloride, vitriol, tartrate, Citrate trianion, fumarate, malate and pharmaceutically acceptable prodrug and verivate use.
Compound of the present invention is a kind of synthetic simple brand-new anti HIV-1 virus reagent, can be used as the drug candidates of anti-HIV.The biological activity test of cell levels shows:
(1) this compounds generally has good anti-HIV-1 virus activity, and wherein part of compounds not only demonstrates other biological activity of nmole level, and demonstrates higher SI.
(2) in institute's synthetic compound, part of compounds demonstrates good inhibitory effect to clinical common mutations virus strain.
The The compounds of this invention novel structure has anti-preferably HIV biological activity, and cytotoxicity is less; Compounds process for production thereof is simple, can be used to develop anti-AIDS medicine.
Embodiment
The present invention will be helped to understand through following embodiment, but content of the present invention can not be limited.
Synthesizing of embodiment 1:4-carbonyl diaryl miazines (CO-DAPYs) verivate
Under the protection of rare gas element, 4-(4-(cyanic acid (phenyl) methyl) pyrimidine-2-is amino) cyanobenzene (2.4mmol) is joined in the anhydrous aprotic solvent of 20mL, stir and make it dissolving;, add alkali (Lithamide (sodium), sodium hydride; N-Butyl Lithium; Diisobutyl amido lithium, potassium tert.-butoxide) (4.8mmol), stirring at room reaction 24～36h.TLC shows that reaction finishes, and reaction solution pours in the 60mL cold water, and ethyl acetate extraction (10mL * 3) merges organic layer, anhydrous magnesium sulfate drying.Filter, remove solvent under reduced pressure, obtain bullion.Re-crystallizing in ethyl acetate gets pure article.
Yellow powdery solid, yield 70.1%; Fusing point: 220.0-223.8 ℃;
1H NMR (DMSO-d
6) δ (ppm) 7.34 (d, 1H, J=4.8Hz, H
5), 7.58 (d, 2H, J=7.2Hz, Ar`H
3,5), 7.67 (d, 2H, J=8.8Hz, ArH
2,6), 7.71 (d, 2H, J=7.2Hz, Ar`H
4), 7.92 (d, 2H, J=8.8Hz, ArH
3,5), 7.98 (d, 2H, J=7.2Hz, Ar`H
2,6), 8.85 (d, 1H, J=4.8Hz, H
6), 10.45 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 103.4,112.2,119.0 (2C), 119.9,129.1 (2C), 130.9 (2C), 133.5 (2C), 134.5,135.3,144.9,159.2,160.9,162.8,193.2.MS (EI) m/z 300 (M
+).
4-itrile group Diarylmiazines derivatives with different is a raw material, makes target compound respectively with aforesaid method, and partial results is following:
Yellow powdery solid, yield 70.8%; Fusing point: 193.6-194.9 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.41 (s, 3H, CH
3), 7.29 (d, 1H, J=4.8Hz, H
5), 7.38 (d, 2H, J=8.0Hz, Ar`H
3,5), 7.68 (d, 2H, J=8.8Hz, ArH
2,6), 7.89 (d, 2H, J=8.0Hz, Ar`H
2,6), 7.93 (d, 2H, J=8.8Hz, ArH
3,5), 8.82 (d, 1H, J=4.8Hz, H
6), 10.45 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 21.8,103.4,112.1,119.0 (2C), 119.9,129.7 (2C), 131.1 (2C), 132.6,133.5 (2C), 145.0,145.3,159.2,160.7,163.2,192.6.MS (ESI) m/z 315 (M
++ 1).
Yellow powdery solid, yield 75.5%; Fusing point: 196.8-197.4 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.37 (s, 3H, CH
3), 7.31 (d, 1H, J=4.8Hz, H
5), 7.44-7.55 (m, 2H, Ar`H
3,5), 7.67 (d, 2H, J=8.8Hz, ArH
2,6), 7.75-7.79 (m, 2H, Ar`H
2,6), 7.93 (d, 2H, J=8.8Hz, ArH
3,5), 8.83 (d, 1H, J=4.8Hz, H
6), 10.48 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 21.3,103.4,112.2,119.0 (2C), 119.9,128.3,129.0,131.1,133.4 (2C), 135.1,135.2,138.6,159.2,160.8,162.9,193.3.MS (EI) m/z 314 (M
+).
Yellow powdery solid, yield 62.8%; Fusing point: 176.3-176.8 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.33 (s, 3H, CH
3), 7.33-7.55 (m, 5H, H
5+ Ar`H), 7.58 (d, 2H, J=8.8Hz, ArH
2,6), 7.81 (d, 2H, J=8.8Hz, ArH
3,5), 8.86 (d, 1H, J=4.8Hz, H
6), 10.43 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 20.6,103.3,111.7,118.9 (2C), 119.9,126.0 (2C), 130.8,131.6,132.1,133.3 (2C), 136.6,137.9,144.9,159.5,161.2,196.7.MS (ESI) m/z 315 (M
++ 1).
Light yellow crystal, yield 77.2%; Fusing point: 226.2-226.8 ℃;
1H NMR (DMSO-d
6) δ (ppm) 7.35 (d, 1H, J=4.8Hz, H
5), 7.64-7.70 (m, 4H, ArH
2,6+ Ar`H
3,5), 7.91 (d, 2H, J=8.8Hz, ArH
3,5), 8.03 (d, 2H, J=8.8Hz, Ar`H
2,6), 8.86 (d, 1H, J=4.8Hz, H
6), 10.47 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 103.5,112.3,119.0 (2C), 119.9,129.3 (2C), 132.9 (2C), 133.5 (2C), 134.0,139.5,144.9,159.2,161.0,162.2,192.0.MS (EI) m/z 334 (M
+).
The light green crystal, yield 68.4%; Fusing point: 215.6-216.3 ℃;
1H NMR (DMSO-d
6) δ (ppm) 7.35 (d, 1H, J=4.8Hz, H
5), 7.68 (d, 2H, J=8.4Hz, ArH
2,6), 7.80 (d, 2H, J=8.0Hz, Ar`H
3,5), 7.89-7.94 (m, 4H, ArH
3,5+ Ar`H
2,6), 8.86 (d, 1H, J=4.8Hz, H
6), 10.46 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 103.5,112.3,119.0 (2C), 119.9,128.7,132.2 (2C), 132.9 (2C), 133.5 (2C), 134.3,144.9,159.2,161.0,162.1,192.3.MS (ESI) m/z 379 (M
++ 1).
Yellow powdery solid, yield 67.4%; Fusing point: 200.8-201.2 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.53 (s, 3H, CH
3), 7.25 (s, 1H, H
5), 7.58 (d, 2H, J=7.6Hz, Ar`H
3,5), 7.64 (d, 2H, J=8.8Hz, ArH
2,6), 7.71 (t, 1H, J=7.6Hz, Ar`H
4), 7.92 (d, 2H, J=8.8Hz, ArH
3,5), 7.97 (d, 2H, J=7.6Hz, Ar`H
2,6), 10.39 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 24.5,103.2,111.8,118.9 (2C), 119.9,129.1 (2C), 130.9 (2C), 133.4 (2C), 134.4,135.4,145.2,159.1,162.4,170.8,193.5.MS (ESI) m/z 315 (M
++ 1).
The white powdery solid, yield 73.0%; Fusing point: 219.9-220.5 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.41 (s, 3H, CH
3), 2.51 (s, 3H, CH
3), 7.20 (s, 1H, H
5), 7.38 (d, 2H, J=8.0Hz, Ar`H
3,5), 7.66 (d, 2H, J=8.4Hz, ArH
2,6), 7.88 (d, 2H, J=8.0Hz, Ar`H
2,6), 7.94 (d, 2H, J=8.4Hz, ArH
3,5), 10.38 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 21.8,24.5,103.1,111.7,118.8 (2C), 119.9,129.7 (2C), 131.0 (2C), 132.7,133.5 (2C), 145.1,145.2,159.0,162.8,170.7,192.9.MS (EsI) m/z 329 (M
++ 1).
Yellow powdery solid, yield 62.3%; Fusing point: 135.6-136.1 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.38 (s, 3H, CH
3), 2.53 (s, 3H, CH
3), 7.25 (s, 1H, H
5), 7.45-7.56 (m, 2H, Ar`H
3,5), 7.66 (d, 2H, J=8.8Hz, ArH
2,6), 7.76-7.80 (m, 2H, Ar`H
2,6), 7.94 (d, 2H, J=8.8Hz, ArH
3,5), 10.42 (s, 1H, NH).
13CNMR (DMSO-d
6) δ (ppm) 21.3,24.5,103.1,111.7,118.8 (2C), 119.9,128.2,129.0,131.1,133.4 (2C), 135.1,135.4,138.6,145.2,159.1,162.6,170.7,193.6.MS (EI) m/z 328 (M
+).
Yellow powdery solid, yield 62.5%; Fusing point: 146.7-147.2 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.32 (s, 3H, CH
3), 2.54 (s, 3H, CH
3), 7.33-7.52 (m, 5H, H
5+ Ar`H), 7.55 (d, 2H, J=8.8Hz, ArH
2,6), 7.80 (d, 2H, J=8.8Hz, ArH
3,5), 10.39 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 20.5,24.5,103.1,111.3,118.8 (2C), 119.9,125.9,130.6,131.5,131.9,133.3 (2C), 136.9,137.7,145.1,159.4,161.7,171.2,197.0.MS (EI) m/z 328 (M
+).
Yellow powdery solid, yield 70.3%; Fusing point: 226.1-226.7 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.54 (s, 3H, CH
3), 7.29 (s, 1H, H
5), 7.66-7.69 (m, 4H, ArH
2,6+ Ar`H
3,5), 7.93 (d, 2H, J=8.4Hz, ArH
3,5), 8.03 (d, 2H, J=8.4Hz, Ar`H
2,6), 10.42 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 23.9,102.7,111.3,118.4 (2C), 119.4,128.7 (2C), 132.3 (2C), 132.9 (2C), 133.6,138.9,144.6,158.5,161.3,170.4,191.8.MS (EI) m/z 348 (M
+).
Yellow powdery solid, yield 64.9%; Fusing point: 236.2-236.5 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.54 (s, 3H, CH
3), 7.29 (s, 1H, H
5), 7.68 (d, 2H, J=8.8Hz, ArH
2,6), 7.81 (d, 2H, J=8.4Hz, Ar`H
3,5), 7.91-7.95 (m, 4H, ArH
3,5+ Ar`H
2,6), 10.42 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 24.0,102.7,111.3,118.4 (2C), 119.4,128.1,131.7 (2C), 132.3 (2C), 132.9 (2C), 133.0,133.9,144.6,158.5,170.4,192.0.MS (EI) m/z 394 (M
+).
Yellow powdery solid, yield 62.5%; Fusing point: 195.2-195.9 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.53 (s, 3H, CH
3), 3.89 (s, 3H, CH
3O), 7.11 (d, 2H, J=8.8Hz, Ar`H
3,5), 7.20 (s, 1H, H
5), 7.69 (d, 2H, J=8.4Hz, ArH
2,6), 7.95-8.02 (m, 4H, J=8.0Hz, ArH
3,5+ Ar`H
2,6), 10.41 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 24.5,56.2,103.1,111.7,114.6 (2C), 118.8 (2C), 120.2,127.9,133.4 (2C), 133.5 (2C), 145.2,159.0,163.3,164.4,170.6,191.6.MS (ESI) m/z 344 (M
++ 1).
The cotton-shaped solid of white, yield 42%; Fusing point: 231.4-232.1 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.55 (s, 3H, CH
3), 7.43 (s, 1H, H
5), 7.45-7.84 (m, 8H, ArH
2,6+ Ar`H), 8.08-8.25 (m, 3H, ArH
3,5+ Ar`H), 10.34 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 24.5,103.0,111.6,118.7 (2C), 119.9,125.2,125.7,127.1,128.4,129.2,130.8,130.9,133.1 (2C), 133.2,133.7,134.0,145.0,159.4,162.2,171.2,196.5.MS (ESI) m/z 365 (M
++ 1).
Yellow powdery solid, yield 72.0%; Fusing point: 164.7-166.3 ℃;
1H NMR (DMSO-d
6) δ (ppm) 2.54 (s, 3H, CH
3), 7.30 (s, 1H, H
5), 7.55-8.09 (m, 10H, ArH+Ar`H), 8.65 (s, 1H, Ar`H
1), 10.43 (s, 1H, NH).
13C NMR (DMSO-d
6) δ (ppm) 24.5,103.1,111.9,118.9 (2C), 119.9,125.4,127.6,128.3,128.9,129.7,130.3,132.3,132.6,133.4 (2C), 133.9,135.8,145.1,159.1,162.7,170.7,193.3.MS (ESI) m/z 365 (M
++ 1).
Embodiment 2 anti-HIV biological activity tests
The anti HIV-1 virus activity of cell in vitro level is measured by the Rega institute of materia medica of Belgian Katholleke university, mainly comprises: MT-4 cell inhibiting activity and cytotoxicity two aspects that HIV is infected.Method is described below: make compound in the MT-4 cell that HIV infects; In the infected by HIV different time; Measure the cytopathic provide protection of medicine with mtt assay, calculate and make 50% cell avoid the required concentration medium effective concentration IC of HIV inductive cytopathy HIV mutagenesis
50, parallel the carrying out of toxicity test and HIV-resistant activity experiment also is in the MT-4 cell cultures, measures with mtt assay to make 50% non-infected cells that cytopathic concentration (CC take place
50), and calculate SI SI=CC
50/ IC
50
Materials and methods:
The HIV-resistant activity of each compound is monitored the cytopathic restraining effect efficient that HIV causes in cell by medicine.Adopt the MT-4 cell to carry out cell cultures.The virus strain that adopts has: HIV-1 virus strain IIIB and HIV-2 virus strain ROD.
Concrete operations are following: with compound with DMSO or water dissolution after with phosphate-buffered common salt aqueous solution dilution, with 3 * 10
5The MT-4 cell is cultivated 1h with each this solution of compound different concns of 100 μ L at 37 ℃ in advance, in this compound, adds the suitable viral dilution liquid of 100 μ L then, and cell is cultivated 1h in 37 ℃.After washing three times, cell is suspended in respectively once more contains or do not contain in the developing medium of compound.Follow cell at 5%CO
2In the atmosphere, under 37 ℃, cultivated again 7 days, and in infecting back the 3rd day with the additional nutrient solution of developing medium replacement that contains or do not contain compound.All twice of the repetitive operations of every kind of nutrient solution condition.Cytopathic effect to virus all uses reverse opticmicroscope to monitor every day.The typical case, used viral dilution liquid usually can be behind virus infection causes cytopathy on the 5th day in this experiment.The medicine inhibition concentration with medicine to the virocyte pathology effect produce 50% restraining effect and simultaneously pair cell do not have direct toxic concentration (CC
50) expression.It is emphasized that when compound water soluble relatively poorly, when needing could to dissolve with DMSO, the DMSO specific concentration generally is lower than 10% with respect to water, (DMSO in the MT-4 cell culture medium ultimate density less than 2%).Because DMSO can influence the antiviral activity of test compounds, also should parallelly carry out containing same concentrations DMSO solution antiviral activity contrast blank assay.In addition, DMSO ultimate density (1/1000) is duplicated required concentration well below influencing HIV-1 in the T cell.
The present invention uses nevirapine, and delavirdine and efavirenz compare article, and the part target compound is seen table 1 to the active result of the inhibition of HIV.
Table?1.Anti-HIV?Activity?and?Cytotoxicity?of?Compounds?1-32?in?MT-4?Cells
aEC
50: make 50% normal cell avoid the required concentration of HIV-1 inductive cytopathy.
bCC
50: make 50% non-infected cells that cytopathic concentration take place.
cSI: SI SI=CC
50/ EC
50
Experimental result shows that the compound that is comprised in the chemical structure of general formula generally has stronger anti-HIV-1 virus activity, less cytotoxicity and higher SI.
The invention is not restricted to above-mentioned instance.
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2009101993735A CN101723903B (en) | 2009-11-26 | 2009-11-26 | 4-carbonyl diaryl pyrimidine derivatives and its preparation method and use |
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| CN102153517B (en) * | 2011-03-03 | 2014-04-02 | 复旦大学 | Diaryl pyrimidone hydrazone derivatives and preparation method and application of diaryl pyrimidone hydrazone derivatives |
| CN104876880A (en) * | 2015-04-27 | 2015-09-02 | 复旦大学 | Diaryl ether derivatives as well as preparation method and application thereof |
| CN110483417B (en) * | 2018-03-06 | 2022-07-15 | 云南大学 | DACOs NNRTIs amino acid ester derivative, preparation method, pharmaceutical composition and application thereof |
| CN114539162B (en) * | 2022-02-17 | 2023-05-30 | 复旦大学 | Substituted aryl urea imine group containing diaryl pyrimidine derivatives and its preparation method and use |
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