CN100497363C - Lactose with first anti-adhesion activity and its fluorescent mark - Google Patents

Lactose with first anti-adhesion activity and its fluorescent mark Download PDF

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CN100497363C
CN100497363C CNB200610078665XA CN200610078665A CN100497363C CN 100497363 C CN100497363 C CN 100497363C CN B200610078665X A CNB200610078665X A CN B200610078665XA CN 200610078665 A CN200610078665 A CN 200610078665A CN 100497363 C CN100497363 C CN 100497363C
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glucopyranosyl
galactopyranose base
ethanoyl
lactose
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CN1834104A (en
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李中军
李庆
赵致辉
孟祥豹
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Peking University
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Peking University
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Abstract

This invention relates to a kind of new lactose homologues, their fluorescence-labeled compounds, their preparation methods and their applications in the preparation of anti-adhesion and anti-shock drugs and as molecular probes in biological research. These kinds of compounds are effectively inhibitory to the adhesion of endothelial cells and leucocytes; they can alleviate shock degree and lengthen the survival time and thus can be used in salvage and therapy of serious-shock patients as anti-inflammation and anti-shock drugs. The fluorescence-labeled compounds of some of the homologues can be used in research of adhesion sites as molecular probes.

Description

The lactose of one class anti-adhesion activity bunch and fluorescent marker thereof
Technical field:
The present invention relates to the new lactose of a class bunch and its fluorescent marker, and preparation method thereof and in preparation anti-adhesive, anti-shock medicament and as the purposes of molecular probe in biological study.This compounds can suppress endotheliocyte and leukocytic adhesion effectively, alleviates the degree of shock, prolongs the survival time, can be used as rescue and treatment that anti-inflammatory, anti-shock medicament are used for the severe hemorrhagic shock patient.Its fluorescent marker can be used as the research that molecular probe is used for attachment sites.
Background technology:
The interaction of white corpuscle-endotheliocyte plays an important role in many physiology and pathologic process, for example, and inflammatory reaction, thrombus, atherosclerotic plaque formation etc.And sticking in the hemorrhagic shock of white corpuscle-endotheliocyte plays an important role equally [1-9]Wound, the severe hemorrhagic shock that causes of burn be at ordinary times with war common pathological process, be the one of the main reasons that causes patient death and army to cut personnel wartime.Research to the shock genesis mechanism at present enters molecular level by cell, subcellsular level; Studies confirm that leukocyte adhesion not only can reduce the organ of tissue and volume of blood flow but also can swim out of and cause further damage in capillary blood vessel, is to cause the irreversible one of the main reasons of shock.Therefore, adhere to microvascular quantity of leucocyte when reducing shock, shock is alleviated, be the comprehensive treatment create openings [10-12]Had report to show that lactose has anti-adhesion activity, the derivative of some lactose also has been proved the function of inhibition white corpuscle-endothelial cell adhesion.For the further influence of the length antagonism adhesion effect of sugared cluster effect cui of research and connecting arm, some polyvalent lactose are synthetic, and in addition, fluorescently-labeled multivalence lactose derivative also has been synthesized and is used for the research of adhesive mechanism as the fluorescence probe.
Summary of the invention:
The present invention has prepared the lactose puted together with different connecting arms and bunch has been used for anti-adhesive, antishock activity research, and these connecting arms comprise polyoxyethylene glycol, 2-amino-1, ammediol and polycarboxylic acid.Reserve amino at corresponding sugared cluster compound, sew, it is used for white corpuscle-endotheliocyte as the small molecules probe adheres to Its Mechanisms such as site with fluorescein.
The synthetic compound can be used following general formula:
Figure C200610078665D00031
R 1Be selected from polyoxyethylene glycol, 2-amino-1, one or more in ammediol and the polycarboxylic acid.
Wherein m is 2,4,6.
Figure C200610078665D00032
R 1Be selected from polyoxyethylene glycol, 2-amino-1, one or more in ammediol and the polycarboxylic acid.
Wherein m is 2,4,6.
Bromo-2,3,4,6-four-O-ethanoyl-β-D-galactopyranose-(1 → 4)-2,3,6-three-O-ethanoyl-α-D-Glucopyranose and polyoxyethylene glycol (PEG, n=4,5,6) are at anhydrous CH 2Cl 2In, Ag 2CO 3Be catalyzer, reaction promptly obtains corresponding divalence lactose 1,2,3, yield 60-70% under the room temperature.
By 2,3,4,6-four-O-ethanoyl-β-D-galactopyranose-(1 → 4)-2,3,6-three-O-ethanoyl-α-D-Glucopyranose and 2-nitrine glycerine are at anhydrous CH 2Cl 2In, BF 3OEt 2Be catalyzer, reaction makes divalence lactose 4, yield 86% under the room temperature.In EtOAc-EtOH (1:1), use Pd (OH) then 2/ C catalytic hydrogenation obtains compound 5,5 and is used for sugared bunch synthesizing as sugar unit.
Figure C200610078665D00042
5 with connecting arm reaction, Succinic Acid for example, suberic acid, trimesic acid are in anhydrous tetrahydro furan, coupling obtains four in the presence of HOBt and DCC, sexavalence lactose 6,7,8.Yield 70-88%.
Figure C200610078665D00043
Figure C200610078665D00051
Tetravalence lactose 9 makes with the L-glutamic acid reaction of Cbz protection by 5, and compound 9 is at CH 3Obtain 10 with the Pd/C catalytic hydrogenation with 94% yield among the OH.5 or 10 and FITC (fluorescein-5-isothiocyanic acid) at anhydrous CH 2Cl 2In DMF, 40 ℃ were reacted 6～8 hours, had just successfully introduced the fluorescent functional group, yield 95～96% in sugared bunch.
Figure C200610078665D00061
With sugar bunches 1,2,3,5,6,7,8,9,10,11 and 12 use CH 3ONa/CH 3OH handles and obtains target compound 13,14, and 15,16,17,18,19,20,21 and 22, yield 94-98%.
Description of drawings
The influence that Fig. 1 compound 16 and the 20 pairs of Burn shock rat leukocytes and endotheliocyte adhere to
The influence of Fig. 2 compound 16 and 20 pairs of Burn shock survival of rats times
The adhesion results of Fig. 3 compound 21
The adhesion results of Fig. 4 compound 22
Embodiment
Embodiment 1.3,6,9-trioxa-1,11-two O-two-[2,3,4,6-four-O-ethanoyl-β-D-galactopyranose-(1 → 4)-2,3,6-three-O-ethanoyl-α-D-glucopyranosyl] dodecane-1
1-bromo-2,3,4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3,6-three-O-ethanoyl-α-D-Glucopyranose (0.2g, 0.29mmol) and PEG (n=4,0.02g 0.10mmol) are dissolved in anhydrous CH 2Cl 2(10mL), add Ag 2CO 3(0.08g and 4
Figure C200610078665D0007173104QIETU
Molecular sieve (0.1g), stirring at room 20 hours.Filtering mixt is used CH 2Cl 2Dilution, washing, anhydrous Na 2SO 4Drying, steaming desolventizes.Thick product column chromatography purification, sherwood oil (60-90 ℃): ethyl acetate=1:3.Get colourless syrup.Yield 70%.[α] D＝+30.3°(c＝0.66，CH 3Cl)； 1HNMR(CD 3Cl)δ：5.35(d，1H，H-4′)，5.16(t，1H，H-3)，5.09(dd，1H，H-2′)，4.97(dd，1H，H-3′)，4.86(t，1H，H-2)，4.56(d，1H，J 1，2＝7.80Hz，H-1)，4.49(d，1H，J 1′，2′＝9.00Hz，H-1′)，4.51，4.22～4.08(m，4H，H-6a，b，H-6a′，b′)，3.90～3.61(m，11H，H-4，5，H-5′，-CH 2O-)，2.15～1.97(7s，21H，7CH 3CO-)； 13CNMR(CD 3Cl)δ：170.4～169.0(7C，CH 3C＝O)，101.0(C-1′)，100.5(C-1)，76.2(C-4)，72.7(C-3)，72.5(C-5)，71.5(C-2)，71.0(C-5′)，70.6(C-3′)，70.5(-CH 2O-)，70.1(-CH 2O-)，69.9(-CH 2O-)69.0(-CH 2O-)，68.7(C-2′)，66.5(C-4′)，63.5(C-6′)，60.7(C-6)，20.9～20.4(7C，7CH 3CO-)
Embodiment 2.3,6, and 9; 12-four oxa-s-1; 14-two-O-two-[2,3,4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2; 3,6-three-O-ethanoyl-α-D-glucopyranosyl] preparation of n-Hexadecane-2 compound 2 is with 1, is connecting arm with PEG (n=5); thick product column chromatography purification, sherwood oil (60-90 ℃): ethyl acetate=2:7.Get colourless syrup.Yield 63%.
Embodiment 3.3,6, and 9; 12,15-five oxa-s-1,17-two-O-two-[2; 3; 4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3; 6-three-O-ethanoyl-α-D-glucopyranosyl] preparation of eicosane-3 compound 3 is with 1; with PEG (n=6) is connecting arm, thick product column chromatography purification, sherwood oil (60-90 ℃): ethyl acetate=1:4.Get colourless syrup.Yield 60%.
Embodiment 4.2-azido--1,3-two-O-two-[2,3; 4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3; 6-three--O-ethanoyl-α-D-glucopyranosyl] and propane 4-2,3,4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-1,2,3; 6-four-O-ethanoyl-α-D-Glucopyranose (5.1g; 7.52mmol) and 2-nitrine-1, (0.4g 3.42mmol) is dissolved in anhydrous CH to ammediol 2Cl 2(10mL), add BF 3OEt 2(0.2mL), stirring at room is 24 hours.Mixture CH 2Cl 2(20mL) after the dilution, use saturated sodium bicarbonate aqueous solution and water washing successively, anhydrous Na 2SO 4Drying, steaming desolventizes.Thick product column chromatography purification, sherwood oil (60-90 ℃): acetone 3:2 gets colourless syrup.Yield 86%.
Embodiment 5.2-amino-1; 3-two-O-two-[2; 3; 4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3; 6-three--O-ethanoyl-α-D-glucopyranosyl] and propane 5---compound 4 (1g; 0.74mmol) (1:1 20mL), adds Pd (OH) to be dissolved in ethyl acetate-ethanol 2(100mg), catalytic hydrogenation under the room temperature (0.4MPa) 6 hours, filtration catalizer, steaming desolventizes.Thick product column chromatography purification, sherwood oil (60-90 ℃): acetone 2:3.Get colourless syrup.Yield 92%.[α] 25 D-18.65°(c?1.93，CHCl 3). 1HNMR(CD 3Cl)δ：5.35(d，1H，H-4′)，5.18(t，1H，H-3)，5.10(dd，1H，H-2′)，4.96(dd，1H，H-3′)，4.89(t，1H，H-2)，4.49(d，2H，J 1，2＝8.10Hz，H-1)，4.44(d，1H，J 1′，2′＝8.40Hz，H-1′)，4.46，4.12～4.08(m，4H，H-6a，b，H-6a′，b′)，3.91～3.43(m，6H，H-4，5，H-5′，-CH 2O-，-CHNH 2-)，2.17～1.92(7s，21H，7CH 3CO-)； 13CNMR(CD 3Cl)δ：170.2～168.9(7C，CH 3 C＝O)，100.9(C-1′)，100.7(C-1)，76.0(C-4)，72.6(C-3)，72.1(C-5)，71.5(C-2)，70.8(C-5′)，70.5(C-3′)，69.0(-CH 2O-)，68.7(C-2′)，66.5(C-4′)，61.7(C-6′)，60.7(C-6)，50.5(-CHNH 2-)，20.7～20.4(7C，7 CH 3CO-)
Embodiment 6.N-{2-[1; 3-two-O-two-[2,3,4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2; 3,6-three--O-ethanoyl-α-D-glucopyranosyl] and propyl group }-(0.02g 0.17mmol) is dissolved in anhydrous THF (3mL) to succinic diamide 6-Succinic Acid; be cooled to 0 ℃; add then HOBt (0.07g, 0.51mmol) and DCC (0.11g, 0.51mmol).0 ℃ was stirred 0.5 hour down, (0.4g, THF solution (5mL) 0.34mmol) transfer to pH=8～9 backs with the N-methylmorpholine with solution and add in the reaction flask compound 5, and mixture stirred 36 hours under room temperature after stirring 2 hours under 0 ℃, steaming desolventizes, and adds CH 2Cl 2(10mL), elimination insolubles, solution are used 10% citric acid solution, saturated sodium bicarbonate solution and water washing, anhydrous Na successively 2SO 4Drying, steaming desolventizes.Thick product column chromatography purification, sherwood oil (60-90 ℃): acetone 2:3.Get colourless syrup (0.35g), yield 85%.[α] 25 D-19.75°(c1.62，CHCl 3)； 1HNMR(CD 3Cl)δ：6.14(d，1H，-NHCO)，5.36(d，1H，H-4′)，5.20(t，1H，H-3)，5.13(dd，1H，H-2′)，4.93(dd，1H，H-3′)，4.87(t，1H，H-2)，4.49(d，2H，J 1，2＝7.80Hz，H-1)，4.45(d，1H，J 1′，2′＝7.80Hz，H-1′)，4.53，4.13～4.05(m，4H，H-6a，b，H-6a′，b′)，3.89～3.49(m，6H，H-4，5，H-5′，-CH 2O-，-CHNH 2-)，2.16～2.14(s，1H，COCH 2-)，2.14～1.97(7s，21H，7CH 3CO-)，1.84(t，1H，-CH 2-)； 13CNMR(CD 3Cl)δ：171.4～169.0(8C，CH 3 C＝O，-CONH)，101.0(C-1′)，100.8(C-1)，76.1(C-4)，72.7(C-3)，72.4(C-5)，71.7(C-2)，71.5(C-5′)，70.9(C-3′)，70.6(-CH 2O-)，69.0(C-2′)，66.6(C-4′)，61.8(C-6′)，60.7(C-6)，48.3(-CHNHCO-)，30.8(-CH 2CO)，20.9～20.5(7C，7 CH 3CO-，).
Embodiment 7.N-{2-[1; 3-two-O-two-[2; 3,4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2; 3; 6-three--O-ethanoyl-α-D-glucopyranosyl] and propyl group }-suberamide 7---preparation of compound 7 connects arm with compound 6 with suberic acid, thick product column chromatography purification; sherwood oil (60-90 ℃): acetone 2:3 gets colourless syrup.Yield 83%.
Embodiment 8.N-{2-[1,3-two-O-two-[2,3; 4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3; 6-three--O-ethanoyl-α-D-glucopyranosyl] and propyl group }-1; the preparation of 3,5 equal benzene triamide 8-compounds 8 is with compound 6, with 1; 3; the 5-trimesic acid connects arm, thick product column chromatography purification, sherwood oil (60-90 ℃): acetone 2:3.Get colourless syrup.Yield 70%.
Embodiment 9.N-{2-[1; 3-two-O-two-[2; 3; 4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2; 3,6-three--O-ethanoyl-α-D-glucopyranosyl] and propyl group }-preparation of 2-benzyloxy carbonyl amido glutaramide 9-compound 9 connects arm with compound 6 with carbobenzoxy-(Cbz)-L-L-glutamic acid.Thick product column chromatography purification, sherwood oil (60-90 ℃): acetone=2:3 gets colourless syrup, yield 88%.
Embodiment 10.N-{2-[1; 3-two-O-two-[2; 3; 4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2; 3,6-three--O-ethanoyl-α-D-glucopyranosyl] and propyl group }-(0.2g 0.07mmol) is dissolved in MeOH (10mL) to the amino glutaramide 10-compound 9 of 2-; add Pd/C; catalytic hydrogenation under the room temperature (0.4MPa) 3 hours, filtration catalizer, steaming desolventizes; thick product column chromatography purification; sherwood oil (60-90 ℃): acetone 2:5 gets colourless syrup (0.18g), yield 94%.[α] 25 D-31.58°(c1.14，CHCl 3)； 1HNMR(CD 3Cl)δ：6，21(d，1H，-NHCO)，6.18(d，1H，-NHCO)，5.35(d，1H，H-4′)，5.20(t，1H，H-3)，5.12(dd，1H，H-2′)，4.96(dd，1H，H-3′)，4.86(dd，1H，H-2)，4.46(d，2H，J 1，2＝J 1′，2′＝7.50Hz，H-1，H-1′)，4.48，4.13～4.08(m，4H，H-6a，b，H-6a′，b′)，3.90～3.53(m，7H，H-4，5，H-5′，-CH 2O-，-COCHNH-，-CHNH 2-，)，2.32～1.97(m，23H，7CH 3CO-，-COCH 2-，-CH 2CHNH 2)； 13CNMR(CD 3Cl)δ：170.3～169.0(9C，CH3C＝O，-CONH)，101.0(2C，C-1，C-1′)，76.1(C-4)，72.8(C-3)，72.6(C-5)，71.6(C-2)，71.5(C-5′)，70.9(C-3′)，70.6(-CH 2O-)，69.0(C-2′)，66.5(C-4′)，61.8(C-6′)，60.7(C-6)，48.6～48.3(2C.-CHNHCO-)，20.8～20.5(9C，7CH 3CO-，-CH 2CO，-CH 2CHNH 2).
Embodiment 11.2-FITC-1; 3-two-O-two-[2; 3; 4,6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3; 6-three--O-ethanoyl-α-D-glucopyranosyl] and propane 11-FITC (0.06g; 0.15mmol) be dissolved in dry DMF (0.2mL), drip compound 5 (0.2g, CH 0.15mmol) 2Cl 2(10mL) solution, 40 ℃ were stirred 8 hours.Steaming desolventizes, thick product column chromatography purification, CHCl 3: MeOH=10:1 obtains yellow syrup (0.25g), yield 96%.[α] 25 D-28.95 ° (c 1.52, CHCl 3); 8.02,7.93,6.72,6.58 (m, 9H, PhH), 7.15 (d, 2H ,-NHCSNH-), 5.35 (d, 1H, H-4 '), 5.14 (t, 1H, H-3), and 5.10 (dd, 1H, H-2 '), 4.92 (dd, 1H, H-3 '), 4.82 (dd, 1H, H-2), 4.55 (d, 2H, J 1,2=J 1 ', 2 '=7.80Hz, H-1, H-1 '), 4.53,4.13～4.09 (m, 4H, H-6a, b, H-6a ', b '), 3.93～3.68 (m, 6H, H-4,5, H-5 ' ,-CH 2O-,-CHNHCS-), 2.94 (1H, PhCH-), 2.18～1.97 (m, 21H, 7CH 3CO-); 13CNMR (CD 3Cl) δ: 207.3,180.7,139.9,129.4,110.6 (10C, Ph, PhCH-), 171.1～169.0 (8C, CH 3C=O ,-PhCO), 162.7 (C=S), 102.7 (C-1 '), 100.8 (C-1), 75.9 (C-4), 72.9 (C-3), 72.6 (C-5), 71.5 (C-2), 71.3 (C-5 '), 70.8 (C-3 '), 70.4 (CH 2O-), 68.9 (C-2 '), 66.5 (C-4 '), 61.7 (C-6 '), 60.6 (C-6), 52.9 (CHNHCS-), 30.7 (), 20.9～20.3 (7C, 7CH 3CO-).
Embodiment 12.N-{2-[1; 3-two-O-two-[2; 3; 4; 6-four-O-ethanoyl-β-D-galactopyranose base-(1 → 4)-2,3,6-three--O-ethanoyl-α-D-glucopyranosyl] propyl group }-preparation of 2-FITC-glutaramide 12-compound 12 is with compound 11; thick product column chromatography purification, CHCl 3: MeOH=10:1 obtains yellow syrup, yield 95%.
Embodiment 13.3,6,9-trioxa-1,11-two-O-two-[β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] dodecane 13-compound 1 (0.1g) is dissolved in methyl alcohol (10mL), the sodium that adds catalytic amount, stirring at room 12 hours is neutralized to neutrality with Zeo-karb then.The elimination resin, steaming desolventizes, and residue is dissolved in 20mL water, and lyophilize gets white solid (0.06g, 97%).[α] D＝+56.3°(c＝0.71，H 2O)； 1HNMR(D 2O)δ：4.33(d，1H，J 1′2′＝8.40Hz，H-1′)，4.26(d，1H，J 1，2＝7.50Hz，H-1)，3.85～3.47(m，19H，H-3，4，5，6a，b，H-2′，3′，4′，5′，6a′，b′，-CH 2O-)，3.36(m，1H，H-2)； 13CNMR(D 2O)δ：105.7(C-1′)，104.8(C-1)，81.0(C-4)，78.1，77.5，77.0，75.2，74.4，73.8，73.7，72.3，72.2，71.5，71.3，63.8，62.8(C-2，3，5，6，C-2′，3′，4′，5′，6′，-CH 2O-).
Embodiment 14.3,6,9,12-four oxa-s-1,14-two-O-two-[β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] n-Hexadecane 14
The preparation of-compound 14 is with compound 13, yield 97%.
Embodiment 15.3,6,9,12,15-five oxa-s-1,17-two-O-two-[β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] eicosane 15
The preparation of-compound 15 is with compound 13, yield 95%.
Embodiment 16.2-amino-1,3-two-O-two-[β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propane 16
The preparation of-compound 16 is with compound 13, yield 98%.
Embodiment 17.N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-succinic diamide 17
The preparation of-compound 17 is with compound 13, yield 97%.[α] 25 D-46.51°(c?1.29，H 2O)； 1HNMR(D 2O)δ：6.10(d，1H，-NHCO)，4.33(d，1H，J 1，2＝7.80Hz，H-1)，4.28(d，1H，J 1′.2′＝7.80Hz，H-1′)，3.83～3.18(m，13H，H-2，3，4，5，6a，b，H-2′，3′，4′，5′，6a′，b′，-CH 2O-，-CHNH 2)，2.40(s，1H，-CH 2CO)； 13CNMR(D 2O)δ：175.4(-NHC＝O)，103.5(C-1′)，103.1(C-1)，78.9(C-4)，75.9，75.3，74.8，73.3，73.1，72.3，71.5，69.1，(C-2，3，5，C-2′，3′，4′，5′，-CH 2O-)，61.6，60.6(C-6，C-6′)，49.5(-CHNH 2)，31.5(COCH 2).
Embodiment 18.N-{2-[1,3-two-O-two-[O-β-D galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-suberamide 18
The preparation of-compound 18 is with compound 13, yield 95%.
Embodiment 19.N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-1,3, the equal benzene triamide 19 of 5-
The preparation of-compound 19 is with compound 13, yield 94%.
Embodiment 20.N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-2-amino-glutaramide 20
The preparation of-compound 20 is with compound 13, yield 96%.
Embodiment 21.N-2-FITC-1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propane 21
The preparation of-compound 21 is with compound 13, yield 96%.[α] 25 D-35.82°(c1.34，H 2O)； 1HNMR(D 2O)δ：7.77，6.68，6.36(m，9H，C 6H 5)，7.10(d，2H，-NHCSNH-)，4.26(d，2H，J 1，2＝J 1′，2′＝7.50Hz，H-1，H-1′)，3.75～3.17(m，13H，H-2，3，4，5，6a，b，H-2′，3′，4′，5′，6a′，b′，-CH 2O-，-CHNH-)； 13CNMR(D2O)δ：165.5(C＝S)，155.4，152.7，141.0，131.3，119.9，117.4，113.2(10C，C 6H 5，C 6H 5CH)，103.6(C-1′)，103.3(C-1)，79.1(C-4)，78.8，75.9，75.4，74.8，73.4，73.1，71.5，69.1，68.7(C-2，3，5，C-2′，3′，4′，5′，-CH 2O-)，61.6，60.8(C-6，C-6′)，49.4(-CHNH).
Embodiment 22.N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-2-FITC-glutaramide 22
The preparation of-compound 22 is with compound 13, yield 94%.
The activity test result
Above-mentioned synthetic compound is carried out anti-adhesive and the active mensuration of antishock, all showed good anti-adhesive and shock provide protection.Fluorescently-labeled lactose conjugated material has obtained clear and definite result as bioprobe in the research that adheres to target cell.The result of concrete activity test operation and typical compound is as follows:
The anti-adhesion activity test:
(1) the granulocytic preparation of blood
After the Animal Anesthesia, separate the neck arteries intubate, get blood 3-5ml with anticoagulant heparin, and add the dilution of equivalent physiological saline, be added to the bottom behind the mixing gently the centrifugal 20min of 2000rpm is housed in the test tube of 5ml lymphocyte separation medium, get the white corpuscle on red corpuscle top layer, be added to shake up in the 5ml erythrocyte cracked liquid and place 8min, the centrifugal smin of looorpm abandons supernatant liquor again, (red corpuscle is removed not exclusively can repeat cracking 1 time again), wash 2 times with the DMEM substratum, behind the counting, be made into 1-2XIO 6The granulocyte suspension of/ml concentration is standby.
(2) cultivation of induced lung vascular endothelial cell
: the animal sacrificed by exsanguination, 75% alcohol-pickled sterilization animal skin is opened chest and is got its lung tissue under the aseptic condition, again lung perienchyma is cut a circle behind the flush away blood, and it is shredded into 1mm 3The tissue block of size adds and contains 20% calf serum DMEM nutrient solution, puts into 37 ℃ of cell culture incubators, 5%CO2 cultivated 60～72 hours, changed liquid and removed tissue block, cultivated 4～7 days again, covered with cobblestoning pulmonary vascular endothelial cell in the culturing bottle.Use 0.25% trypsin digestion and cell, it is passaged to continues on the slide glass to cultivate, treat to be used for after it covers with to adhere to experiment.
(3) enchylema stream chamber makes
The hollow flow passage is made by two-layer transparent organic glass, interior path length 6.1cm, wide 1.5cm in liquid stream chamber.Respectively there is a passage liquid stream two ends, chamber and both sides, are used to feed liquid and measuring pressure.Wherein an end connects the liquid perfusion that peristaltic pump is used to form the different shearing stress of different in flow rate.
(4) detection of GA characteristic:
The slide glass that covers with pulmonary vascular endothelial cell is put into liquid stream chamber, around rubber cradle upper-lower seal slide, build the back and be torqued-up to the absence of liquid seepage with screw.Connect the observation ward that puts into the Olympus inverted microscope behind the peristaltic pump, observation ward keeps 37 ℃ of constant temperature.The visual field is amplified 400 times, with MTV color video camera, National watch-dog and JVC video recorder synchronized video recording observed and recorded.Use the lavation of Hanks liquid to remove the bubble (committed step) in liquid stream chamber and the linking conduit thereof earlier.And then add isolating white corpuscle in the liquid stream chamber with endotheliocyte incubation 20～30min.Start peristaltic pump,, count the leukocyte count that adheres to endotheliocyte in the various shearing stress perfusion rearward visions, calculate its adhesion rate with different shearing stress perfusion 2min.
Two representative compounds 16 and 20 anti-adhesion activity (flow chamber) be as shown in Figure 1: the result shows: these two kinds of oligosaccharides have the activity that obvious inhibition Shock in Rats white corpuscle and endotheliocyte adhere to.
Burn shock protection activity test:
Animal model: 24 SD rats, body weight 180～220g, male and female are not limit, and are divided into 3 groups at random.With 133% urethane+05% glucochloral (06mL/100g body weight, ip) anesthesia.One side arteria carotis communis inserts the PE-50 conduit, is used to monitor blood pressure and blood sampling.Scald waist with 80 ℃ of hot water and cause deep ii degree burn, duplicate rat severe Burn shock model with lower limb body 30s (accounting for body surface area 35%～40%).Scald and gave oligosaccharides or physiological saline in back about 20 minutes, only be administered once.
Zooperal sample size: 40nmol/100g body weight.
Two representative compounds 16 and 20 anti-Burn shock protection active (rat model), as shown in Figure 2: the result shows that two kinds of oligosaccharides all can prolong the survival time of Burn shock rat, have the obvious treatment effect.
Fluorescent mark oligosaccharides conjugate is used to adhere to determining of target spot
Oligosaccharides is mixed with the working fluid of 10pmol/ul, and separates the white corpuscle effect that obtains flush away binding oligosaccharide not after 10 minutes, under fluorescent microscope, observe.
Compound 21,22 adhesion results are distinguished as shown in Figure 3, Figure 4:
The result shows: compound 21,22 can both combine with white corpuscle, particularly granulocyte.This may be its anti-adhesive and antishock cytology basis.
Reference
1.Nakae，H.，Endo，S.，Yamada，Y.，Inada，K.，Burns，2000，26，139-144.
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Claims (6)

1、
Lactose cluster compound with anti-adhesion activity of general formula (I),
Figure C200610078665C00021
R 1Be selected from 2-amino-1, ammediol,
Wherein m is 2 or 4 or 6.
2, the lactose cluster compound that has anti-adhesion activity is characterized in that this compound is:
2-amino-1,3-two-O-two-[β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propane;
N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-succinic diamide;
N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group]-suberamide;
N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group]-1,3, the equal benzene triamide of 5-
Or N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-2-amino-glutaramide.
3, the fluorescent mark compound that has general formula (II),
Figure C200610078665C00022
R 1Be selected from 2-amino-1, ammediol,
Wherein m is 2 or 4 or 6.
4, fluorescent mark compound is characterized in that this compound is:
N-2-FITC-1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propane or
N-{2-[1,3-two-O-two-[O-β-D-galactopyranose base-(1 → 4)-β-D-glucopyranosyl] propyl group }-the 2-FITC-glutaramide.
5, the application of any described compound in preparation anti-adhesive or antishock active medicine in the claim 1 to 2.
6, in the claim 3 to 4 any described fluorescent mark compound as the preparation molecular probe purposes.
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