CN1194007C - Separation, synthesis and application in medicine for P6A'S metabolic product - Google Patents
Separation, synthesis and application in medicine for P6A'S metabolic product Download PDFInfo
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- CN1194007C CN1194007C CN 01136780 CN01136780A CN1194007C CN 1194007 C CN1194007 C CN 1194007C CN 01136780 CN01136780 CN 01136780 CN 01136780 A CN01136780 A CN 01136780A CN 1194007 C CN1194007 C CN 1194007C
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Abstract
The present invention relates to a separation process of ultrashort peptides generated by the metabolism of a P6A metabolic product in an animal body, a synthesis process of the ultrashort peptides and an application of the ultrashort peptides used as thrombolytic drugs. Animal experiments prove that the micromolecular peptides of the present invention have higher thrombolytic action than P6A.
Description
Invention field
The present invention relates to separation, the evaluation, synthetic of the ultrashort peptide that fibrin degradation product (FDP) P6A generates through metabolism in animal body, and the application in medical science, for example as the application of thrombolytic agent.
Background technology
Belew in 1978 etc. are hatched human fibrin 60 minutes in the system of the fibre-bearing protein resolvase of pH8 at 37 ℃, make fibrin degradation become the polypeptide of small molecular weight.With Bio Gel P-6 column chromatography for separation, obtain 12 kinds of cuts.In 3 kinds of cuts that can increase vascular permeability, a kind of be named as P6A (Ala-Arg-Pro-Ala-Lys) (M.Belew, etal., Thromb.Res., 1978,13:983).The acute myocardial ischemia that hat intravascular coagulation enzyme causes usually can be alleviated by thrombolytics, and Mehta in 1989 etc. have investigated the thrombolytic effect of P6A.Electricity consumption stimulating endothelial surface produces crooked coronary embolism, and after electricity irritation stopped, thrombus was stablized 15 minutes at least, then along with giving P6A (5 μ mol/ branches in the hat, 20 minutes) or tPA (10 μ mol/ branches in the hat, 20 minutes).The dog of accepting 12 coronary artery embolisms of P6A has 6 to rebuild coronary blood flow, and the dog of accepting 10 coronary artery embolisms of tPA has 4 to rebuild coronary blood flow (J.Meht, etal., Cadiovasc.Pharmacol., 1989,13 (6): 803).The nineteen ninety contriver adopts liquid phase method to synthesize P6A (Zhao Ming etc., chemistry circular, 1990,12:29), find that P6A has a series of important activity (the pivot Tang Dynasty etc., Chinese circulation magazines such as the coronary flow of increasing, inhibition thrombosis, inhibition angiotensin-converting enzyme, 1991,6 (6): 606).
Summary of the invention
In order to investigate the pharmacokinetic property of P6A and analogue, in the tail vein injected the mouse body, sacrificed by decapitation was got whole blood with P6A in the present invention, and 0 ℃ centrifugal, and the blood plasma that obtains carries out LC/MS research after treatment.The ion that the various metabolic waies that P6A is possible produce in mass spectrum enrolls in the acquisition tables of polyion detection.The result who records shows that P6A generates Ala-Arg-Pro-Ala, Arg-Pro-Ala-Lys, four kinds of sequences of Ala-Arg-Pro, Pro-Ala-Lys through metabolism in the mouse body.In order to illustrate between P6A and its meta-bolites getting in touch aspect the thrombolytic effect, the present invention adopts liquid phase method to synthesize described 4 kinds of oligopeptides, has estimated their thrombus dissolving effect on rat arteriovenous shut intubate model.The result shows that Pro-Ala-Lys is the thrombolytic compound more outstanding than P6A.
Therefore, an object of the present invention is to provide structural formula Ala-Arg-Pro-OH, Ala-Arg-Pro-Ala-OH, the synthesized micromolecule peptide of Arg-Pro-Ala-Lys-OH and Pro-Ala-Lys-OH.
Another object of the present invention provides above-mentioned small-molecular peptides as the treatment thrombotic diseases, as the application of the medicine of diseases such as cerebral thrombosis, cerebral embolism, coronary heart disease, venous thrombosis.
The accompanying drawing summary
Fig. 1 is that P6A is at intravital pathways metabolism of mouse and product.
In order further to set forth the present invention, provide a series of embodiment below.These embodiment are illustrative fully, and they only are used for the present invention is specifically described, and not should be understood to limitation of the present invention.
Embodiment
Hereinafter, term " Boc " is a tertbutyloxycarbonyl, and " Bzl " is benzyl, and " Tos " is p-toluenesulfonyl, and " Ala " is L-Ala, and " Arg " is arginine, and " Pro " is proline(Pro), and " Lys " is Methionin.
Embodiment 1
The structure determination of P6A meta-bolites
4mg P6A is dissolved in the 0.3ml physiological saline, and the clear and bright solution that obtains is in the tail vein is expelled to the mouse body that body weight is 40g lentamente, and the mouse sacrificed by decapitation is got whole blood, 0 ℃ centrifugal 5 minutes, separated plasma.Get 100 μ l blood plasma and with 100 μ l perchloric acid (1mol/l) thorough mixing, under the rotating speed of 3500rpm centrifugal 15 minutes then, get 30 μ l supernatant liquors sample introduction on LC/MS.Other gets 100 μ l perchloric acid (1mol/l) thorough mixing, under the rotating speed of 3500rpm centrifugal 15 minutes then, get 30 μ l supernatant liquors on LC/MS sample introduction as blank.The ion that in mass spectrum all possible pathways metabolism of P6A is produced enrolls in the acquisition tables of polyion detection.The structure of detected ion, total mass number, correspondence, and peak area is listed table 1 in.
The meta-bolites of the detected P6A of table 1 LC/MS
The amount number
414 343 471 315
(m/z)
Sequence A la-Arg-Ala-Arg-Arg-Pro-Pro-Ala-
Pro-Ala Pro Ala-Lys Lys
Peak area 4.02 * 10
79.54 * 10
66.92 * 10
62.88 * 10
6
Relation between the metabolite of listing in the table, and the relation between they and the P6A can be expressed as Fig. 1.
Embodiment 2
Ala-Arg-Pro-Ala-OH's is synthetic
2.1 Boc-Pro-Ala-OCH
3Synthetic
22.0mg (0.25mmol) Boc-Pro-OH is dissolved in an amount of anhydrous THF, ice bath adds 31mg (0.27mmol) N-hydroxy-succinamide and 56mg (0.27mmol) DCC down, reaction mixture places refrigerator to place 24 hours, filtering DCU, filtrate is concentrating under reduced pressure at room temperature, residue sherwood oil crystallization obtains corresponding active ester.
35.0mg (0.25mmol) HClAlaOCH
3, 27mg (0.27mmol) N-methylmorpholine mixes with an amount of anhydrous THF, adds the active ester that obtains above, room temperature reaction 26 hours, TLC (CHCl then
3: CH
3OH, 19: 1) show that raw material point disappears.Reaction mixture is concentrated into dried, residue 10ml acetic acid ethyl dissolution.The solution that obtains is used saturated NaHCO successively
3The aqueous solution, the saturated NaCl aqueous solution, saturated aqueous citric acid solution, and saturated NaCl solution washing.Tell organic layer, use anhydrous Na
2SO
4Drying is filtered, and filtrate obtains title compound 71.3mg (95%) in 37 ℃ of concentrating under reduced pressure.FAB-MS(m/z)：301〔M+H〕
+。
2.2 HClPro-Ala-OCH
3Synthetic
75mg (0.25mmol) Boc-Pro-Ala-OCH
3Mix stirring at room 4 hours, TLC (CHCl with the anhydrous HCl/ ethyl acetate solution of an amount of 6N
3: CH
3OH, 9: 1) show that raw material point disappears.Reaction mixture room temperature concentrating under reduced pressure, residue with acetic acid ethyl dissolution after concentrating under reduced pressure at room temperature again, this operation repeatedly for several times, until eliminating free hydrogenchloride.Residue anhydrous diethyl ether crystallization, the title compound that obtains is directly used in the next step.
2.3 Boc-Arg (Tos)-Pro-Ala-OCH
3Synthetic
According to the operation under 2.1, just replaces Boc-Pro-OH, usefulness 59.4mg (0.25mmol) HClPro-Ala-OCH with 107mg (0.25mmol) Boc-Arg (Tos)-OH
3Replace HClAla-OCH
3, obtain title compound 137.5mg (90%).FAB-MS(m/z)：611〔M+H〕
+。
2.4 HClArg (Tos)-Pro-Ala-OCH
3Synthetic
According to the operation under 2.2, by 133mg (0.25mmol) Boc-Arg (Tos)-Pro-Ala-OCH
3Make title compound, be directly used in the next step.
2.5 Boc-Ala-Arg (Tos)-Pro-Ala-OCH
3Synthetic
According to the operation under 2.1, just replace Boc-Pro-OH, with 137mg (0.25mmol) HClArg (Tos)-Pro-Ala-OCH with 47mg (0.25mmol) Boc-Ala-OH
3Replace HClAla-OCH
3, obtain title compound 153mg (90%).FAB-MS(m/z)：682〔M+H〕
+。
2.6 Ala-Arg-Pro-Ala-OH's is synthetic
170.3mg (0.25mmol) Boc-Ala-Arg (Tos)-Pro-Ala-OCH
3With an amount of 1N NaOH/CH
3OH solution mixes, and ice bath stirred TLC (CHCl 2 hours down
3: CH
3OH, 9: 1) show that raw material point disappears.Reaction mixture is neutralized to pH7 with hydrochloric acid (2mol/l), and concentrating under reduced pressure is removed methyl alcohol under the room temperature, and residue uses hydrochloric acid (2mol/l) to be acidified to pH2 again, is evaporated to dried.Above-mentioned product adds 1ml dimethyl sulphide, 1ml methyl-phenoxide, and 5ml CF
3SO
3H/CF
3COOH (1: 4), 0 ℃ was reacted 2 hours, removal of solvent under reduced pressure, residue solidifies with anhydrous diethyl ether, and solids obtains 91mg (88%) title compound with Sephadex G 10 purifying.FAB-MS(m/z)：414〔M+H〕
+。
Embodiment 3
Ala-Arg-Pro-OH's is synthetic
3.1 Boc-Arg-(Tos)-Pro-OCH
3Synthetic
According to the operation under 2.1, replaces Boc-Pro-OH with 107mg Boc-Arg-(Tos)-OH, usefulness 41.4mg (0.25mmol) HClPro-OCH
3Replace HClAla-OCH
3, obtain 119.9mg (89%) title compound, FAB-MS (m/z): 540 (M+H)
+
3.2 HClArg-(Tos)-Pro-OCH
3Synthetic
According to the operation under 2.2, by 135mg (0.25mmol) Boc-Arg-(Tos)-Pro-OCH
3The title compound that obtains is directly used in the next step.
3.3 Boc-Ala-Arg-(Tos)-Pro-OCH
3Synthetic
According to the operation under 2.1, replace Boc-Pro-OH with 47mg (0.25mmol) Boc-Ala-OH, with 119mg (0.25mmol) HClArg-(Tos)-Pro-OCH
3Replace HClAla-OCH
3, obtain 140mg (92%) title compound, FAB-MS (m/z): 611 (M+H)
+
3.4 Ala-Arg-Pro-OH's is synthetic
According to the operation under 2.6, by 152mg (0.25mmol) Boc-Ala-Arg-(Tos)-Pro-OCH
3, make 77mg (90%) title compound, FAB-MS (m/z): 343 (M+H)
+
Embodiment 4
Arg-Pro-Ala-Lys's is synthetic
4.1 Boc-Ala-Lys (Cl2Bzl)-OCH
3Synthetic
According to the operation under 2.1, replace Boc-Pro-OH with 47mg (0.25mmol) Boc-Ala-OH, with 91mg (0.25mmo1) HClLys (Cl
2Bzl)-OCH
3Replace HClAla-OCH
3, obtain 120mg (96%) title compound, FAB-MS (m/z): 501 (M+H)
+
4.2 HClAla-Lys (Cl2Bzl)-OCH
3Synthetic
According to the operation under 2.2, by 125mg (0.25mmol) Boc-Ala-Lys (Cl
2Bzl)-OCH
3Make title compound.
4.3 Boc-Pro-Ala-Lys (Cl
2Bzl)-OCH
3Synthetic
According to the operation under 2.1, with 22mg (0.25mmol) Boc-Pro-OH and 109mg (0.25mmol) HClAla-Lys (Cl
2Bzl)-OCH
3Reaction obtains 135mg (90%) title compound, FAB-MS (m/z): 598 (M+H)
+
4.4 HClPro-Ala-Lys (Cl
2Bzl)-OCH
3Synthetic
According to the operation under 2.2, by 150mg (0.25mmol) BocPro-Ala-Lys (Cl
2Bzl)-OCH
3Make title compound.
4.5 Boc-Arg (Tos)-Pro-Ala-Lys (Cl
2Bzl)-OCH
3Synthetic
According to the operation under 2.1, replaces Boc-Pro-OH with 107mg (0.25mmol) Boc-Arg (Tos)-OH, usefulness 134mg (0.25mmol) HClPro-Ala-Lys (Cl
2Bzl)-OCH
3Replace HClAla-OCH
3, obtain 198mg (87%) title compound, FAB-MS (m/z): 908 (M+H)
+
4.6 the preparation of Arg-Pro-Ala-Lys-OH
According to the operation under 2.6, by 227mg (0.25mmol) Boc-Arg (Tos)-Pro-Ala-Lys (Cl
2Bzl)-OCH
3Make 99.9mg (85%) title compound, FAB-MS (m/z): 471 (M+H)
+
The preparation of embodiment 5 Pro-Ala-Lys-OH
According to the operation under 2.6, by 149.6mg (0.25mmol) Boc-Pro-Ala-Lys (Cl
2Bzl)-OCH
3Make 71mg (90%) title compound, FAB-MS (m/z): 315 (M+H)
+
Embodiment 6
The thrombolysis activity of Pro-Ala-Lys-OH and Ala-Arg-Pro-OH
6.1 the preparation of thrombus
The Glass tubing of past vertical fixing (long 15mm, internal diameter 2.5mm, external diameter 5.0mm, the pipe end, seal with plug) the middle 0.1ml of injection citron acidifying rat artery blood, the multiple calcium of this blood does not coagulate.Toward the interior thrombus standing bolt that inserts a stainless steel material rapidly of pipe.This thrombus standing bolt diameter is the Stainless Steel Wire coiled of 0.2mm, and the long 12mm of spiral part contains 15 bung flanges, and the diameter of bung flange is 1.0mm, and the holder handle links to each other with spiral, and long 7.0mm is the question mark type.After the blood coagulation 15 minutes, open the plug of Glass tubing bottom,, from Glass tubing, take out fixedly spiral of the thrombus that wrapped up by thrombus carefully, accurately weigh (mass range is 74-84mg) with the fixing fixing holder handle of spiral of thrombus of tweezers.
6.1.2 the preparation of bypass duct
Other network pipeline constitutes by 3 sections, and the stage casing is a polyethylene rubber tube, long 60.0mm, internal diameter 3.5mm, two ends are identical polyethylene tube, long 100.0mm, internal diameter 1.0mm, external diameter 2.0mm, one end of this pipe is strained to point pipe (being used to insert rat carotid artery or vein), and external diameter is 110mm, the outer cover one segment length 7.0mm of the other end, the polyethylene tube of external diameter 3.5mm is used to insert in the polyethylene tube in stage casing.The equal silanization of the inwall of 3 sections pipes.The thrombus standing bolt that the thrombus of accurately weighing wraps up is put into the stage casing polyethylene tube, and the two ends of sebific duct link to each other with the sleeve end of firm two polyethylene tubes describing respectively.With syringe by sharp pipe end with filling with heparin-saline solution (50IU/kg body weight) in the pipe, standby.
6.1.3 rat neck arteriovenous shut intubate model
(male, 250～300g) anaesthetize by 80mg/kg dosage abdominal injection Sodital sodium solution the Wistar rat.Undergo surgery after the anesthetized rat dorsal position is fixing, separate tracheae, separate right common carotid artery and left external jugular vein.On the left external jugular vein that exposes, cut an angle carefully, the sharp pipe of the bypass duct for preparing is above inserted the proximal part of left external jugular vein opening by angle, simultaneously away from the holder handle of bypass tube stage casing thrombus standing bolt.Push the heparin-saline (50Iu/kg) of accurate amount with syringe by the sharp pipe of the other end, this moment, syringe was not withdrawn polyethylene tube.Proximal part in right common carotid artery stops blooding with bulldog clamp, right common carotid artery is cut an angle carefully nearby at the calcarine artery folder.Extract syringe from the tip of polyethylene tube, the tip of polyethylene tube is inserted the proximal part of artery angle.The two ends of bypass duct all use 4 trumpeter's art sutures and arteriovenous to fix.Open bulldog clamp, make blood flow flow to vein from artery by bypass duct.So, constituted rat arteriovenous shut Thrombolysis Model.
6.1.4 the thrombolytic effect of Pro-Ala-Lys-OH and Ala-Arg-Pro-OH
With scalp acupuncture with the normal saline solution (2000IU/kg) of physiological saline (3ml/kg), urokinase, the normal saline solution (5.4mg/kg) of P6A, the normal saline solution (3.4mg/kg) of Ala-Arg-Pro-OH, and the stage casing thorn people of the normal saline solution of Pro-Ala-Lys-OH (3.1mg/kg) by bypass tube slowly is injected into (about 6 minutes) in the blood away from the fixing nearly vein place of spiral of thrombus.Make physiological saline (blank), urokinase (positive control), P6A (parent compound contrast), Ala-Arg-Pro-OH (meta-bolites) and Pro-Ala-Lys-OH (meta-bolites) by blood circulation, the sequential action of pressing vein-heart-artery is to thrombus.Pick up counting from start injection contrast liquid or drug solution, after 1 hour from bypass tube the removal of thromboses standing bolt, accurately weigh, obtain thrombus standing bolt in every rat bypass duct and enter of poor quality before and after the bypass duct, add up the thrombus quality difference (x ± S) of each treated animal, and carry out the t check, data are listed table 2 in.
The thrombolytic effect of table 2 Ala-Arg-Pro-OH and Pro-Ala-Lys-OH
Group dosage (the thrombus loss of weight of dosage/kg) (x ± S)
NS 3ml 15.31±3.57
UK 2000Iu 24.10±3.54 1)，2)，3)
P6A 5.4mg 18.84±3.18 1)
Ala-Arg-Pro- 3.4mg 18.08±2.60 1)
OH
Pro-Ala-Lys- 3.1mg 24.63±2.44 1)，2)，3)
OH
N=12,1) compare P＜0.05 with NS; 2) compare P＜0.001 with NS;
3) compare P＜0.001 with P6A and Ala-Arg-Pro-OH
The result shows that thrombolytic effect and the UK of Pro-Ala-Lys-OH are suitable, compares with parent compound P6A, shows remarkable advantages (P＜0.001).
6.1.5 the acute toxicity of Ala-Arg-Pro-OH
Press 10mg/kg, 100mg/kg, three dosage groups of 1000mg/kg, every group of 3 mouse according to the animal dead situation, are selected four dosage again, 1 mouse of each dosage.Get the geometrical mean of two or three adjacent doses according to the animal dead situation, obtain LD
50Value.
Pro-Ala-Lys-OH presses 10mg/kg, 100mg/kg and 1000mg/kg dosage, is made into the 0.2ml normal saline solution, slowly injects through the tail vein.The result is that under 10mg/kg and the 100mg/kg dosage, all mouse survives, all death of mouse under the 1000mg/kg dosage.So, selecting dosage for the second time, 140mg/kg, 225mg/kg, 370mg/kg and 600mg/kg, mouse death rate are 0/1,0/1,1/1 and 1/1.Get the mean value of 140mg/kg, 225mg/kg and three adjacent doses of 370mg/kg, LD
50Be 226mg/kg.Heavy dose of administration is after 5 minutes, mouse whole body Yong lazyness, and tic of the limbs is short of breath subsequently, and palpitating speed is dead after 30 minutes.Become celestial and find that cardia is hemorrhage, organ no abnormality seens such as brain, lung, intestines, pancreas, spleen, stomach, liver, kidney.
Middle dosed administration is after 15 minutes, and the mouse whole body is sluggish, and tic of the limbs is short of breath subsequently, and palpitating speed is dead after 40 minutes.Become celestial and find that cardia is hemorrhage, organ no abnormality seens such as brain, lung, intestines, pancreas, spleen, stomach, liver, kidney.
After the low dosage administration 30 minutes, the mouse whole body is sluggish, recovers normal after 1 hour, and becoming celestial, it is any unusual not see.
Mouse does not see the overt toxicity sign after the low dose of administration, becomes celestial each organ no abnormality seen after raising a week.
Under all dosages, all do not find the existing common phenomenon of intracranialing hemorrhage of thrombolytic drug.The result shows the LD that is tried to achieve by toxic dose
50Value is equivalent to 73 times of therapeutic dose, and more satisfactory security is arranged.
Claims (6)
1, the separation method of the meta-bolites of a kind of fibrin degradation product (FDP) P6A, comprise P6A in vein injection experiments animal body, put to death, get whole blood, centrifugal, separated plasma, mix with perchloric acid, centrifugal, be LC/MS then, isolate Ala-Arg-Pro, Arg-Pro-Ala-Lys, four kinds of sequences of Ala-Arg-Pro-Ala, Pro-Ala-Lys.
2, a kind of is the synthesized micromolecule peptide of fibrin degradation product (FDP) P6A meta-bolites, and its sequence is Ala-Arg-Pro-OH.
3, a kind of is the synthesized micromolecule peptide of fibrin degradation product (FDP) P6A meta-bolites, and its sequence is Pro-Ala-Lys-OH.
4, a kind of medicine for the treatment of thrombotic diseases is characterized in that containing the small-molecular peptides of claim 2.
5, a kind of medicine for the treatment of thrombotic diseases is characterized in that comprising the small-molecular peptides of claim 3.
6, the application of each small-molecular peptides in the medicine of preparation treatment thrombotic diseases in the claim 2 or 3.
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|---|---|---|---|
| CN 01136780 CN1194007C (en) | 2001-10-25 | 2001-10-25 | Separation, synthesis and application in medicine for P6A'S metabolic product |
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|---|---|---|---|
| CN 01136780 CN1194007C (en) | 2001-10-25 | 2001-10-25 | Separation, synthesis and application in medicine for P6A'S metabolic product |
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Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI234460B (en) * | 2002-04-03 | 2005-06-21 | Purzer Pharmaceutical Co Ltd | Cyclic pentad-peptide and its preparing method |
| CN101318992B (en) * | 2007-06-04 | 2010-09-29 | 北京大学 | All-basic amino acid oligopeptide and its copper complex, its synthesis method, self-assembly and application |
| CN102477074B (en) * | 2010-11-30 | 2013-09-25 | 首都医科大学 | Oligopeptide compound and preparation method and application thereof |
| CN102477071B (en) * | 2010-11-30 | 2013-09-25 | 首都医科大学 | Pro-Ala-Lys-Lys(Pro-Ala-Lys)-Asp[OCH2(CH2)nCH3]-OCH2(CH2)nCH3, its synthesis and application as a thrombolytic agent |
| CN102477073B (en) * | 2010-11-30 | 2013-08-28 | 首都医科大学 | Oligopeptide with thrombolytic activity, preparation method thereof, and application thereof |
| CN102898507B (en) * | 2012-09-05 | 2015-05-27 | 上海晟顺生物科技有限公司 | Thrombolysis oligopeptide-imidazolidine binary conjugate, preparation method and uses thereof |
| ES2758451T3 (en) * | 2012-09-19 | 2020-05-05 | Gemvax & Kael Co Ltd | Cell penetration peptide, conjugate comprising the same and composition comprising the conjugate |
| CN106317189B (en) * | 2015-06-23 | 2019-07-12 | 首都医科大学 | Five methoxytryptamine base carbonyl propionyl-RPAK peptides, preparation, activity and application |
| CN106279363B (en) * | 2015-06-23 | 2020-01-17 | 首都医科大学 | Pentamethoxytryptamine carbonyl propionyl-GRPAK peptide, its preparation, activity and application |
| CN107459553B (en) * | 2016-06-03 | 2021-06-08 | 首都医科大学 | L-dimensional C-2-oxyacetyl-PAK, its synthesis, activity and application |
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