EP1309611A1 - Anti-heparin peptides - Google Patents
Anti-heparin peptidesInfo
- Publication number
- EP1309611A1 EP1309611A1 EP01965326A EP01965326A EP1309611A1 EP 1309611 A1 EP1309611 A1 EP 1309611A1 EP 01965326 A EP01965326 A EP 01965326A EP 01965326 A EP01965326 A EP 01965326A EP 1309611 A1 EP1309611 A1 EP 1309611A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- heparin
- aha
- compound according
- reagent
- carboxylic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000002668 anti-heparin effect Effects 0.000 title claims description 12
- 102000004196 processed proteins & peptides Human genes 0.000 title description 4
- 108090000765 processed proteins & peptides Proteins 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 41
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 33
- 239000002607 heparin antagonist Substances 0.000 claims abstract description 17
- 238000000338 in vitro Methods 0.000 claims abstract description 9
- 239000003814 drug Substances 0.000 claims abstract description 4
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims description 31
- 229920000669 heparin Polymers 0.000 claims description 31
- 229960002897 heparin Drugs 0.000 claims description 29
- 230000015271 coagulation Effects 0.000 claims description 16
- 238000005345 coagulation Methods 0.000 claims description 16
- 239000008280 blood Substances 0.000 claims description 8
- 210000004369 blood Anatomy 0.000 claims description 8
- 238000001514 detection method Methods 0.000 claims description 5
- 150000001413 amino acids Chemical class 0.000 claims description 4
- 238000003556 assay Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 claims description 3
- 239000004475 Arginine Substances 0.000 claims description 3
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims description 3
- 239000004472 Lysine Substances 0.000 claims description 3
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 3
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 3
- NMDDZEVVQDPECF-LURJTMIESA-N (2s)-2,7-diaminoheptanoic acid Chemical compound NCCCCC[C@H](N)C(O)=O NMDDZEVVQDPECF-LURJTMIESA-N 0.000 claims description 2
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 claims description 2
- QUOGESRFPZDMMT-UHFFFAOYSA-N L-Homoarginine Natural products OC(=O)C(N)CCCCNC(N)=N QUOGESRFPZDMMT-UHFFFAOYSA-N 0.000 claims description 2
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims description 2
- QUOGESRFPZDMMT-YFKPBYRVSA-N L-homoarginine Chemical compound OC(=O)[C@@H](N)CCCCNC(N)=N QUOGESRFPZDMMT-YFKPBYRVSA-N 0.000 claims description 2
- -1 Omithine Chemical compound 0.000 claims description 2
- ODHCTXKNWHHXJC-GSVOUGTGSA-N Pyroglutamic acid Natural products OC(=O)[C@H]1CCC(=O)N1 ODHCTXKNWHHXJC-GSVOUGTGSA-N 0.000 claims description 2
- ODHCTXKNWHHXJC-UHFFFAOYSA-N acide pyroglutamique Natural products OC(=O)C1CCC(=O)N1 ODHCTXKNWHHXJC-UHFFFAOYSA-N 0.000 claims description 2
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 2
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 2
- IADUEWIQBXOCDZ-UHFFFAOYSA-N (2S)-azetidine-2-carboxylic acid Natural products OC(=O)C1CCN1 IADUEWIQBXOCDZ-UHFFFAOYSA-N 0.000 claims 1
- IADUEWIQBXOCDZ-VKHMYHEASA-N Azetidine-2-carboxylic acid Natural products OC(=O)[C@@H]1CCN1 IADUEWIQBXOCDZ-VKHMYHEASA-N 0.000 claims 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 238000002405 diagnostic procedure Methods 0.000 abstract description 3
- 230000001747 exhibiting effect Effects 0.000 abstract description 3
- PGOHTUIFYSHAQG-LJSDBVFPSA-N (2S)-6-amino-2-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S,3R)-2-[[(2S)-2-[[(2S)-2-[[(2R)-2-[[(2S)-2-[[(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-5-carbamimidamidopentanoyl]amino]propanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-4-methylpentanoyl]amino]acetyl]amino]-3-hydroxypropanoyl]amino]-4-methylpentanoyl]amino]-3-sulfanylpropanoyl]amino]-4-methylsulfanylbutanoyl]amino]-5-carbamimidamidopentanoyl]amino]-3-hydroxybutanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-3-hydroxypropanoyl]amino]-3-hydroxypropanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-4-methylpentanoyl]amino]-3-hydroxybutanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-5-carbamimidamidopentanoyl]amino]-5-oxopentanoyl]amino]-3-hydroxybutanoyl]amino]-3-hydroxypropanoyl]amino]-3-carboxypropanoyl]amino]-3-hydroxypropanoyl]amino]-5-oxopentanoyl]amino]-5-oxopentanoyl]amino]-3-phenylpropanoyl]amino]-5-carbamimidamidopentanoyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-4-oxobutanoyl]amino]-5-carbamimidamidopentanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-4-carboxybutanoyl]amino]-5-oxopentanoyl]amino]hexanoic acid Chemical compound CSCC[C@H](N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(O)=O PGOHTUIFYSHAQG-LJSDBVFPSA-N 0.000 description 11
- 108010000499 Thromboplastin Proteins 0.000 description 11
- 102000002262 Thromboplastin Human genes 0.000 description 11
- 230000000694 effects Effects 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 102000007327 Protamines Human genes 0.000 description 5
- 108010007568 Protamines Proteins 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229940127215 low-molecular weight heparin Drugs 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- 229940048914 protamine Drugs 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 3
- 230000010355 oscillation Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 108010094028 Prothrombin Proteins 0.000 description 2
- 102100027378 Prothrombin Human genes 0.000 description 2
- 230000002429 anti-coagulating effect Effects 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000013642 negative control Substances 0.000 description 2
- 230000014508 negative regulation of coagulation Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229940039716 prothrombin Drugs 0.000 description 2
- 238000004007 reversed phase HPLC Methods 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- MTDHILKWIRSIHB-UHFFFAOYSA-N (5-azaniumyl-3,4,6-trihydroxyoxan-2-yl)methyl sulfate Chemical group NC1C(O)OC(COS(O)(=O)=O)C(O)C1O MTDHILKWIRSIHB-UHFFFAOYSA-N 0.000 description 1
- 125000003088 (fluoren-9-ylmethoxy)carbonyl group Chemical group 0.000 description 1
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
- 102000004411 Antithrombin III Human genes 0.000 description 1
- 108090000935 Antithrombin III Proteins 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- 108010049003 Fibrinogen Proteins 0.000 description 1
- 102000008946 Fibrinogen Human genes 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- 229920000209 Hexadimethrine bromide Polymers 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- 101710093543 Probable non-specific lipid-transfer protein Proteins 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical group O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000001858 anti-Xa Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 229940127219 anticoagulant drug Drugs 0.000 description 1
- 229960005348 antithrombin iii Drugs 0.000 description 1
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000036471 bradycardia Effects 0.000 description 1
- 208000006218 bradycardia Diseases 0.000 description 1
- 210000004899 c-terminal region Anatomy 0.000 description 1
- 150000001720 carbohydrates Chemical group 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 229940012952 fibrinogen Drugs 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000002489 hematologic effect Effects 0.000 description 1
- 230000000004 hemodynamic effect Effects 0.000 description 1
- 230000002008 hemorrhagic effect Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000036543 hypotension Effects 0.000 description 1
- IAJILQKETJEXLJ-LECHCGJUSA-N iduronic acid Chemical compound O=C[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-LECHCGJUSA-N 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 210000004347 intestinal mucosa Anatomy 0.000 description 1
- HBEFVZMJESQFJR-UHFFFAOYSA-N isocyanatosulfanylbenzene Chemical compound O=C=NSC1=CC=CC=C1 HBEFVZMJESQFJR-UHFFFAOYSA-N 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 201000002364 leukopenia Diseases 0.000 description 1
- 231100001022 leukopenia Toxicity 0.000 description 1
- 235000018977 lysine Nutrition 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical compound S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 description 1
- 229920000729 poly(L-lysine) polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229950008679 protamine sulfate Drugs 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 235000019515 salmon Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 206010043554 thrombocytopenia Diseases 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/02—Linear peptides containing at least one abnormal peptide link
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- the present invention relates to a compound exhibiting anti-heparin activity, of the formula Z - B m - (AXA) X - B overwhelm- (AXA) y - B 0 - (AXA) Z - B p , the diagnostic reagents the comprising and the use of said compound in an in vitro diagnostic test or for the manufacture of a drug for anti-heparin purposes.
- Unfractionated heparin is a natural sulfated polysaccharide, from the glycosaminoglycan family. It is mainly extracted from the intestinal mucosa of pork or beef.
- the ionic charge of the molecule is also heterogeneous: different degree of sulfation of glucosamine sulfate units and number of different carboxylic functions at the level of iduronic and glucuronic acid units [1, 2].
- heparin The essential physical characteristics of heparin are: its polyanionicity and its high charge density. Indeed, each disaccharide carries 3 to 4 negative charges (sulfates and carboxylates).
- a particular arrangement of the different heparin units forms the pentasaccharide in a reproducible manner throughout the sequence.
- This pentasaccharide is known as the site of recognition of heparin for antithrombin III, generating between these two entities a strong affinity and consequently a high anticoagulant activity [3].
- Unfractionated heparin is a polydisperse macromolecule: commercial preparations based on NHF have a molecular weight between 12,000 and 18,000 Da.
- the NHF has an equivalent activity on factors lia and Xa.
- LMWHs keep a high anti-Xa activity and an anti- ⁇ a activity which decreases with the size of the LMWH molecule.
- LMWHs can be advantageously used as an anticoagulant instead of UFHs.
- heparins HNF or LMWH in therapy may require the administration of compounds neutralizing their anti-coagulant effects, in particular at the end of interventions on the circulatory system, such as for example the extra-corporal circulation.
- the presence of heparin in the samples can lead to erroneous interpretations of the results. It is therefore necessary to also have compounds with anti-heparin properties for the diagnosis.
- Protamine sulfate is the only known compound capable of neutralizing the anti-coagulant effects of heparin in vivo.
- Protamine belongs to the family of basic proteins rich in arginine residues, is purified from salmon sperm [6 - 7] and neutralizes heparin thanks to its positive charges [8 - 10].
- protamine causes hemodynamic and hematological side effects such as hypotension, bradycardia, thrombocytopenia and leukopenia [11 - 15].
- the positive charges of protamine are directly proportional to the neutralization efficiency of heparin, but also to the toxicity of the molecule [16].
- Poly L-Lysine and Polybrene are other compounds known to neutralize heparin. However, these polycations also appear too toxic for clinical use.
- Wakefield et al. (WO 95/13083) describe variants of the protamine which would be less toxic. These are peptides having a sequence of 20 to 40 amino acids, with a positive charge between +14 and +18 and the structure of which corresponds to clusters of positive residues interspersed with neutral amino acids. Harris et al. (EP 999219) describe linear or branched anti-heparin peptides comprising a succession of clusters of Arginine and Alanine.
- the present invention relates to new synthetic molecules useful as agents neutralizing heparin.
- the properties of the molecules of the present invention have been more particularly studied in in vitro diagnostic reagents.
- heparin which may be present in the blood samples tested
- the molecules whose general formula 1 is explained below make it possible to meet these two criteria. They therefore prove to be particularly useful for neutralizing any interference linked to the presence of heparin for both diagnostic and therapeutic purposes.
- the present invention relates to a compound exhibiting antiheparin activity, of general formula 1 below:
- * B represents a basic amino acid and can be advantageously selected from Lysine, Arginine, Ornithine, Histidine, Homolysine, Homoarginine; m, n, o and p independently of one another represent an integer between 2 and 4. Among the preferred compounds of the invention, there are more particularly the compounds in which m, n, o are equal to 4 and p equal to 2.
- AXA represents a hydrocarbon chain corresponding to the formula:
- n being an integer between 2 and 6; x, y and z independently of one another represent an integer between 1 and 6.
- Z is selected from the following compounds:
- Z is pyroglutamic acid (PGIu).
- AHA corresponds to NH - (CH 2 ) 5 - CO - that is to say amino hexanoic acid, with x equal to 2 and y, z equal to 1.
- the invention relates to the compound corresponding to the following formula: PGIu -, - (AHA) 2 - K "- AHA - I - AHA - K 2
- the compounds described above have an anti-heparin power, determined by the ⁇ relative coagulation time between a heparin plasma and a non-heparinized plasma, less than 10%, preferably less than 5%.
- the present invention therefore also relates to the use of a compound corresponding to formula 1 indicated above in an in vitro diagnostic reagent, in particular the reagents for calculating the coagulation time of a blood sample or the detection or determination of different elements of the coagulation cascade, regardless of the presence or absence of heparin in said sample.
- Said reagents in particular reagents of the TP (prothrombin time) type, advantageously have a turbidity measured by an OD at 630 nm, less than 0.5, preferably less than 0.1.
- the invention relates to an in vitro diagnostic reagent comprising a compound as defined by general formula 1 above, preferably a compound in which AXA corresponds to NH - (CH 2 ) 5 - CO - c 'is to say amino hexanoic acid, with x equal to 2 and y, z equal to 1, and more preferably the compound below of formula:
- Such a diagnostic reagent thus makes it possible to carry out tests or assays in blood samples, regardless of the presence or absence of heparin in said samples.
- a reagent according to the invention advantageously corresponds to conventional coagulation tests, that is to say tests making it possible to determine the coagulation time of a blood sample or tests allowing the detection or the assay of different elements of the cascade of coagulation, such as the assay of factor Vlla, fibrinogen, proteins C and S, the TP test. These tests are commonly used by those skilled in the art.
- a preferred in vitro diagnostic reagent according to the invention is a reagent comprising Thromboplastin, making it possible to carry out a TP test (Prothrombin time or Quick time)
- the final concentration in such reagents of the compound according to the invention defined above is advantageously between 2 and 10 ⁇ g / ml. Preferably this concentration is 5 ⁇ g / ml.
- the invention also relates to the use of a compound of general formula 1 defined above, as an anti-heparin agent for the preparation of a medicament.
- the synoptic table of figure 1 summarizes the various stages of the synthesis.
- the structural sequence is synthesized by chemistry on solid support, using an appropriate automaton (Applied Biosystems 433A).
- hydrophobic spacer arms (AXA) were added in double coupling.
- the resin used is an MBHA resin (methyl benzydrylamine), so as to recover a neutral amide C-terminal structure after cleavage of the resin.
- the chemistry used here is an Fmoc chemistry, using piperidine deprotection at each step.
- the synthesis scale on the synthesizer is 0.1 nmole, leading to approximately 100 mg of crude product.
- the product is cleaved from the resin and deprotected on the side chains by a treatment with TFA (55% trifluoroacetic acid). After concentrating the cleavage solution by 2/3 of the volume, the product is precipitated from ether.
- the crude product is then lyophilized and then purified by reverse phase HPLC, using a Cl 8 Kromasil 5 ⁇ m column (20 mm * 250 mm) with a water / acetonitrile gradient 0.1% of TFA (from 0 to 60% acetonitrile in 30 min at 15 ml / minute). The detection is made at 214 nm and the fractions are collected manually. The quantity of purified product recovered is 50 mg.
- the structure of the final product is confirmed by analysis of the sequence after hydrolysis with HCl 6N, 120 ° C, 24h; the hydrolyzate is then analyzed by reverse phase HPLC (Kromasil Cl 8 column, 5 ⁇ m, 250 mm * 4.6 mm), after derivatization with PITC (phenylthioisocyanate).
- Example 2 Test of anti-heparin agents according to the invention on a TP test:
- the objective is to analyze the performances (anti-heparin power and turbidity) of anti-heparin agents incorporated in a Thromboplastin Diagnostica Stago reagent.
- the samples to be tested are prepared from a pool of normal plasma overloaded or not with heparin (heparin plasma at 1 IU / ml in HNF (Calciparin 25,000 IU / ml, Sanofi)).
- a reagent serving as a negative control that is to say without an anti-heparin agent, is useful for checking the heparinization of the plasma.
- the automaton takes 50 ⁇ l of sample plasma, which it incubates 240 sec. at 37 ° C in a cup containing a ball; then it transfers the well to the measurement zone and adds 100 ⁇ l of Thromboplastin reagent to the sample.
- the coagulation time is determined as follows:
- the anti-heparin power is calculated as follows: determination of the relative time delta between a heparin and non-heparin plasma, that is to say:
- the turbidity must be as low as possible for a diagnostic application and more particularly in a Thromboplastin (TP) test.
- This turbidity is determined with the measurement of the OD at 630 nm on a spectrophotometer (Uvikon 940, Kontron).
- a reagent serving as a negative control that is to say without an anti-heparin agent, is useful for measuring the influence of this anti-heparin agent on the turbidity of the reagent.
- Example 3 Analysis of the performances (anti-heparin power and turbidity) of different anti-heparin agents according to the invention, introduced into a reagent of the Thromboplastin type (results compared with the control (C) having no anti-heparin agent) :
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Abstract
The invention concerns a compound exhibiting an anti-heparin activity, of formula Z Bm (AXA)x Bn (AXA)y Bo (AXA)z Bp, the diagnostic reagents comprising it and the use of said compound in an in vitro diagnostic test of a medicine for anti-heparin activity.
Description
PEPTIDES ANTI-HEPARINE ANTI-HEPARIN PEPTIDES
La présente invention concerne un composé présentant une activité anti-héparine, de la formule Z - Bm - (AXA)X - B„ - (AXA)y - B0 - (AXA)Z - Bp, les réactifs de diagnostic le comprenant et l'utilisation dudit composé dans un test de diagnostic in vitro ou pour la fabrication d'un médicament à visée anti-héparine.The present invention relates to a compound exhibiting anti-heparin activity, of the formula Z - B m - (AXA) X - B „- (AXA) y - B 0 - (AXA) Z - B p , the diagnostic reagents the comprising and the use of said compound in an in vitro diagnostic test or for the manufacture of a drug for anti-heparin purposes.
L'héparine non fractionnée (HNF) est un polysaccharide sulfaté naturel, de la famille des glycosaminoglycanes. On l'extrait essentiellement de la muqueuse intestinale de porc ou de bœuf.Unfractionated heparin (HNF) is a natural sulfated polysaccharide, from the glycosaminoglycan family. It is mainly extracted from the intestinal mucosa of pork or beef.
C'est un produit hétérogène par la composition de ses unités saccharidiques; de ce fait, la charge ionique de la molécule est également hétérogène: degré de sulfatation différent des unités glucosamine sulfate et nombre de fonctions carboxyliques différentes au niveau des unités acide iduronique et glucuronique [1, 2].It is a heterogeneous product by the composition of its saccharide units; therefore, the ionic charge of the molecule is also heterogeneous: different degree of sulfation of glucosamine sulfate units and number of different carboxylic functions at the level of iduronic and glucuronic acid units [1, 2].
Les caractères physiques essentiels de l'héparine sont: sa polyanionicité et sa forte densité de charges. En effet, chaque disaccharide porte 3 à 4 charges négatives (sulfates et carboxylates).The essential physical characteristics of heparin are: its polyanionicity and its high charge density. Indeed, each disaccharide carries 3 to 4 negative charges (sulfates and carboxylates).
Un arrangement particulier des différentes unités de l'héparine forme le pentasaccharide de manière reproductible tout au long de la séquence. Ce pentasaccharide est connu comme étant le site de reconnaissance de l'héparine à l'antithrombine III, générant entre ces deux entités une forte affinité et par voie de conséquence une activité anticoagulante élevée [3].A particular arrangement of the different heparin units forms the pentasaccharide in a reproducible manner throughout the sequence. This pentasaccharide is known as the site of recognition of heparin for antithrombin III, generating between these two entities a strong affinity and consequently a high anticoagulant activity [3].
Les chaînes ne contenant pas de pentasaccharide sont pratiquement dépourvues d'activité anticoagulante (seulement 1/3 de la molécule d'héparine présente cette affinité pour l'ATffl) [4].
L'héparine non fractionnée (HNF) est une macromolécule polydisperse: les préparations commerciales à base d'HNF ont un poids moléculaire compris entre 12000 et 18000 Da.The chains containing no pentasaccharide are practically devoid of anticoagulant activity (only 1/3 of the heparin molecule has this affinity for ATffl) [4]. Unfractionated heparin (HNF) is a polydisperse macromolecule: commercial preparations based on NHF have a molecular weight between 12,000 and 18,000 Da.
Ces préparations sont utilisées principalement dans le but d'une action préventive ou curative vis-à-vis des thromboses.These preparations are used mainly for the purpose of a preventive or curative action against thromboses.
Il est possible de fractionner l'HNF par la taille (après traitement chimique), ce qui conduit à la famille des HBPM (héparines de bas poids moléculaire) [5].It is possible to fractionate UFH by size (after chemical treatment), which leads to the family of LMWH (low molecular weight heparins) [5].
L'HNF a une activité équivalente sur les facteurs lia et Xa. Par contre, les HBPM gardent une activité anti-Xa élevée et une activité anti-ϋa qui diminue avec la taille de la molécule d'HBPM.The NHF has an equivalent activity on factors lia and Xa. On the other hand, LMWHs keep a high anti-Xa activity and an anti-ϋa activity which decreases with the size of the LMWH molecule.
Une activité anti-IIa élevée pouvant présenter des effets secondaires hémorragiques, les HBPM peuvent être utilisés de façon avantageuse comme anticoagulant à la place des HNF.Since high anti-IIa activity can have hemorrhagic side effects, LMWHs can be advantageously used as an anticoagulant instead of UFHs.
Cependant, l'utilisation des héparines HNF ou HBPM en thérapie peut requérir l'administration de composés neutralisant leurs effets anti-coagulants, notamment à la fin des interventions sur le système circulatoire, telles que par exemple la circulation extra-corporelle. Par ailleurs, dans certains tests de diagnostic in vitro, la présence d'héparine dans les échantillons peut conduire à des interprétations erronées des résultats. H s'avère donc nécessaire de disposer également de composés aux propriétés anti-héparine pour le diagnostic.However, the use of heparins HNF or LMWH in therapy may require the administration of compounds neutralizing their anti-coagulant effects, in particular at the end of interventions on the circulatory system, such as for example the extra-corporal circulation. Furthermore, in certain in vitro diagnostic tests, the presence of heparin in the samples can lead to erroneous interpretations of the results. It is therefore necessary to also have compounds with anti-heparin properties for the diagnosis.
La Protamine sulfate est le seul composé connu capable de neutraliser in vivo les effets anti-coagulants de l'héparine. La protamine appartient à la famille des protéines basiques riches en résidus arginine, est purifiée à partir du sperme de saumon [6 - 7] et neutralise l'héparine grâce à ses charges positives [8 - 10].
Toutefois, la protamine provoque des effets secondaires hémodynamiques et hématologiques tels que l'hypotension, la bradycardie, la thrombocytopénie et la leucopénie [11 - 15]. En fait, il a été démontré que les charges positives de la protamine sont directement proportionnelles à l'efficacité de neutralisation de l'héparine, mais aussi à la toxicité de la molécule [16].Protamine sulfate is the only known compound capable of neutralizing the anti-coagulant effects of heparin in vivo. Protamine belongs to the family of basic proteins rich in arginine residues, is purified from salmon sperm [6 - 7] and neutralizes heparin thanks to its positive charges [8 - 10]. However, protamine causes hemodynamic and hematological side effects such as hypotension, bradycardia, thrombocytopenia and leukopenia [11 - 15]. In fact, it has been shown that the positive charges of protamine are directly proportional to the neutralization efficiency of heparin, but also to the toxicity of the molecule [16].
La Poly L-Lysine et le Polybrène sont d'autres composés connus pour neutraliser l'héparine. Toutefois, ces polycations apparaissent également trop toxiques pour une utilisation clinique.Poly L-Lysine and Polybrene are other compounds known to neutralize heparin. However, these polycations also appear too toxic for clinical use.
Wakefield et al. (WO 95/13083) décrivent des variants de la protamine qui seraient moins toxiques. Il s'agit de peptides possédant une séquence de 20 à 40 acides aminés, avec une charge positive comprise entre +14 et +18 et dont la structure correspond à des clusters de résidus positifs entrecoupés d'acides aminés neutres. Harris et al. (EP 999219) décrivent des peptides anti-héparine linéaires ou branchés comprenant une succession de clusters d'Arginine et d'Alanine.Wakefield et al. (WO 95/13083) describe variants of the protamine which would be less toxic. These are peptides having a sequence of 20 to 40 amino acids, with a positive charge between +14 and +18 and the structure of which corresponds to clusters of positive residues interspersed with neutral amino acids. Harris et al. (EP 999219) describe linear or branched anti-heparin peptides comprising a succession of clusters of Arginine and Alanine.
Cependant, les documents précités ne comportent aucun enseignement sur la nécessité de posséder des agents anti-héparine en diagnostic.However, the aforementioned documents do not teach anything about the need for diagnostic anti-heparin agents.
La présente invention a pour objet de nouvelles molécules synthétiques utiles en tant qu'agents neutralisant l'héparine.The present invention relates to new synthetic molecules useful as agents neutralizing heparin.
Les propriétés des molécules de la présente invention ont été plus particulièrement étudiées dans des réactifs de diagnostic in vitro.The properties of the molecules of the present invention have been more particularly studied in in vitro diagnostic reagents.
Outre leur capacité à être insensibles aux effets de l'héparine éventuellement présente dans les échantillons sanguins testés, il peut être également nécessaire pour certains de ces réactifs de diagnostic de présenter une faible turbidité. Cette propriété est particulièrement importante dans le cas des réactifs contenant de la thromboplastine pour la détermination du temps de Quick, notamment sur des automates à détection optique.
Les molécules dont la formule générale 1 est explicitée ci-dessous permettent de répondre à ces deux critères. Elles se montrent donc particulièrement utiles pour neutraliser les éventuelles interférences liées à la présence d'héparine tant à des fins diagnostiques que thérapeutiques.In addition to their ability to be insensitive to the effects of heparin which may be present in the blood samples tested, it may also be necessary for some of these diagnostic reagents to exhibit low turbidity. This property is particularly important in the case of reagents containing thromboplastin for the determination of the Quick time, in particular on automated machines with optical detection. The molecules whose general formula 1 is explained below make it possible to meet these two criteria. They therefore prove to be particularly useful for neutralizing any interference linked to the presence of heparin for both diagnostic and therapeutic purposes.
Ainsi, la présente invention se rapporte à un composé présentant une activité antihéparine, de formule générale 1 suivante:Thus, the present invention relates to a compound exhibiting antiheparin activity, of general formula 1 below:
Z-Bm-(AXA)x-Bn-(AXA)y-B0-(AXA)2-Bp ZB m - (AXA) x -B n - (AXA) y -B 0 - (AXA) 2 -B p
dans laquellein which
* Z a pour formule générale:* Z has the general formula:
-N— Cx— CH— C02H avec Cy - liaison covalente \ / -CH2--N— Cx— CH— C0 2 H with Cy - covalent bond \ / -CH 2 -
Cy— Cx -CO- -CO-S- -(CH2)n-X- avec 1 < n < 2 et X = O -, S -, YJ avec Cx = - liaison covalente -(CH2)n-, 1 ≤n≤5 ouCy— Cx -CO- -CO-S- - (CH 2 ) n -X- with 1 <n <2 and X = O -, S -, YJ with Cx = - covalent bond - (CH 2 ) n-, 1 ≤n≤5 or
— CH-CH2- i avec R1 = - OH, - NH2- CH-CH 2 - i with R1 = - OH, - NH2
* B représente un acide aminé basique et peut être avantageusement sélectionné parmi la Lysine, Arginine, Ornithine, Histidine, Homolysine, Homoarginine; m, n, o et p représentent indépendamment les uns des autres un nombre entier compris entre 2 et 4.
Parmi les composés préférés de l'invention, on note plus particulièrement les composés dans lesquels m, n, o sont égaux à 4 et p égal à 2.* B represents a basic amino acid and can be advantageously selected from Lysine, Arginine, Ornithine, Histidine, Homolysine, Homoarginine; m, n, o and p independently of one another represent an integer between 2 and 4. Among the preferred compounds of the invention, there are more particularly the compounds in which m, n, o are equal to 4 and p equal to 2.
* AXA représente une chaîne hydrocarbonée correspondant à la formule:* AXA represents a hydrocarbon chain corresponding to the formula:
- NH - (CH2)n - CO - , n étant un nombre entier compris entre 2 et 6; x, y et z représentent indépendamment les uns des autres un nombre entier compris entre 1 et 6.- NH - (CH 2 ) n - CO -, n being an integer between 2 and 6; x, y and z independently of one another represent an integer between 1 and 6.
Avantageusement, Z est sélectionné parmi les composés suivants:Advantageously, Z is selected from the following compounds:
De préférence, Z est l'acide pyroglutamique (PGIu).Preferably, Z is pyroglutamic acid (PGIu).
Parmi les composés préférés de l'invention, on note plus particulièrement les composés dans lesquels AHA correspond à NH - (CH2)5 - CO - c'est à dire acide amino hexanoïque, avec x égal à 2 et y, z égaux à 1.Among the preferred compounds of the invention, there are more particularly the compounds in which AHA corresponds to NH - (CH 2 ) 5 - CO - that is to say amino hexanoic acid, with x equal to 2 and y, z equal to 1.
Avantageusement, l'invention vise le composé répondant à la formule suivante: PGIu - , - (AHA)2 - K» - AHA - I - AHA - K2 Advantageously, the invention relates to the compound corresponding to the following formula: PGIu -, - (AHA) 2 - K "- AHA - I - AHA - K 2
Les composés décrits ci-dessus présentent un pouvoir anti-héparine, déterminé par le Δ temps de coagulation relatif entre un plasma héparine et un plasma non-hépariné, inférieur à 10 %, de préférence inférieur à 5 %.The compounds described above have an anti-heparin power, determined by the Δ relative coagulation time between a heparin plasma and a non-heparinized plasma, less than 10%, preferably less than 5%.
La présente invention a donc également pour objet l'utilisation d'un composé répondant à la formule 1 indiquée ci-dessus dans un réactif de diagnostic in vitro, notamment les
réactifs pour le calcul du temps de coagulation d'un échantillon de sang ou la détection ou le dosage de différents éléments de la cascade de la coagulation, indépendamment de la présence ou l'absence d'héparine dans ledit échantillon.The present invention therefore also relates to the use of a compound corresponding to formula 1 indicated above in an in vitro diagnostic reagent, in particular the reagents for calculating the coagulation time of a blood sample or the detection or determination of different elements of the coagulation cascade, regardless of the presence or absence of heparin in said sample.
Lesdits réactifs, en particulier les réactifs de type TP (temps de prothrombine), présentent avantageusement une turbidité mesurée par une DO à 630 nm, inférieure à 0,5, de préférence inférieure à 0, 1.Said reagents, in particular reagents of the TP (prothrombin time) type, advantageously have a turbidity measured by an OD at 630 nm, less than 0.5, preferably less than 0.1.
Selon un autre aspect, l'invention concerne un réactif de diagnostic in vitro comprenant un composé tel que défini par la formule générale 1 ci-dessus, de préférence un composé dans lequel AXA correspond à NH - (CH2)5 - CO - c'est à dire acide amino hexanoïque, avec x égal à 2 et y, z égaux à 1, et plus préférentiellement le composé ci- dessous de formule:According to another aspect, the invention relates to an in vitro diagnostic reagent comprising a compound as defined by general formula 1 above, preferably a compound in which AXA corresponds to NH - (CH 2 ) 5 - CO - c 'is to say amino hexanoic acid, with x equal to 2 and y, z equal to 1, and more preferably the compound below of formula:
PGIu - K4 - (AHA)2 - K4 - AHA - K4 - AHA - K2 PGIu - K4 - (AHA) 2 - K4 - AHA - K4 - AHA - K 2
Un tel réactif de diagnostic permet ainsi la réalisation de tests ou de dosages dans des échantillons sanguins, indépendamment de la présence ou de l'absence d'héparine dans lesdits échantillons.Such a diagnostic reagent thus makes it possible to carry out tests or assays in blood samples, regardless of the presence or absence of heparin in said samples.
Un réactif selon l'invention correspond avantageusement aux tests de coagulation classiques, c'est à dire les tests permettant de déterminer le temps de coagulation d'un échantillon de sang ou aux tests permettant la détection ou le dosage de différents éléments de la cascade de coagulation, comme par exemple le dosage du facteur Vlla, du fibrinogène, des protéines C et S, le test TP. Ces tests sont utilisés de façon courante par l'homme du métier.A reagent according to the invention advantageously corresponds to conventional coagulation tests, that is to say tests making it possible to determine the coagulation time of a blood sample or tests allowing the detection or the assay of different elements of the cascade of coagulation, such as the assay of factor Vlla, fibrinogen, proteins C and S, the TP test. These tests are commonly used by those skilled in the art.
Un réactif de diagnostic in vitro préféré selon l'invention est un réactif comprenant de la Thromboplastine, permettant de réaliser un test TP (Temps de Prothrombine ou temps de Quick)
La concentration finale dans de tels réactifs du composé selon l'invention défini ci- dessus, est avantageusement comprise entre 2 et lOμg/ml. De préférence cette concentration est de 5μg/ml.A preferred in vitro diagnostic reagent according to the invention is a reagent comprising Thromboplastin, making it possible to carry out a TP test (Prothrombin time or Quick time) The final concentration in such reagents of the compound according to the invention defined above, is advantageously between 2 and 10 μg / ml. Preferably this concentration is 5μg / ml.
L'invention se rapporte également à l'utilisation d'un composé de formule générale 1 défini ci-dessus, comme agent anti-héparine pour la préparation d'un médicament.The invention also relates to the use of a compound of general formula 1 defined above, as an anti-heparin agent for the preparation of a medicament.
Exemple 1: Protocole de synthèse du composé préféré de l'invention:Example 1: Protocol for the synthesis of the preferred compound of the invention:
Le tableau synoptique de la figure 1 résume les différentes étapes de la synthèse.The synoptic table of figure 1 summarizes the various stages of the synthesis.
L'enchaînement structural est synthétisé par chimie sur support solide, utilisant un automate approprié (Applied Biosystems 433A).The structural sequence is synthesized by chemistry on solid support, using an appropriate automaton (Applied Biosystems 433A).
De manière à parfaire les rendements de synthèse, les bras écarteurs hydrophobes (AXA) ont été ajoutés en double couplage.In order to perfect the synthesis yields, the hydrophobic spacer arms (AXA) were added in double coupling.
La résine utilisée est une résine MBHA (méthyl benzydrylamine), de façon à récupérer une structure C-terminale amide neutre après clivage de la résine. La chimie mise en oeuvre ici est une chimie Fmoc, utilisant la pipéridine en déprotection à chaque étape.The resin used is an MBHA resin (methyl benzydrylamine), so as to recover a neutral amide C-terminal structure after cleavage of the resin. The chemistry used here is an Fmoc chemistry, using piperidine deprotection at each step.
Les chaînes latérales sont protégées par des groupements Boc.The side chains are protected by Boc groupings.
L'échelle de synthèse sur le synthétiseur est de 0.1 nmole, conduisant à environ 100 mg de produit brut. Le produit est clivé de la résine et déprotégé sur les chaînes latérales par un traitement au TFA (acide trifluoroacétique à 55%). Après concentration de la solution de clivage des 2/3 du volume, le produit est précipité dans l'éther.The synthesis scale on the synthesizer is 0.1 nmole, leading to approximately 100 mg of crude product. The product is cleaved from the resin and deprotected on the side chains by a treatment with TFA (55% trifluoroacetic acid). After concentrating the cleavage solution by 2/3 of the volume, the product is precipitated from ether.
Le produit brut est ensuite lyophilisé puis purifié par HPLC en phase inverse, en utilisant une colonne Cl 8 Kromasil 5 μm (20 mm * 250 mm) avec un gradient eau / acétonitrile 0.1% de TFA (de 0 à 60% d'acétonitrile en 30 min à 15 ml / minute). La détection est faite à 214 nm et les fractions sont collectées manuellement. La quantité de produit purifié récupérée est de 50 mg.
La structure du produit final est confirmée par analyse de la séquence après hydrolyse avec HC1 6N, 120°C, 24h; l'hydrolysat est ensuite analysé par HPLC phase inverse (colonne Kromasil Cl 8, 5 μm, 250 mm * 4.6 mm), après dérivatisation au PITC (phénylthioisocyanate).The crude product is then lyophilized and then purified by reverse phase HPLC, using a Cl 8 Kromasil 5 μm column (20 mm * 250 mm) with a water / acetonitrile gradient 0.1% of TFA (from 0 to 60% acetonitrile in 30 min at 15 ml / minute). The detection is made at 214 nm and the fractions are collected manually. The quantity of purified product recovered is 50 mg. The structure of the final product is confirmed by analysis of the sequence after hydrolysis with HCl 6N, 120 ° C, 24h; the hydrolyzate is then analyzed by reverse phase HPLC (Kromasil Cl 8 column, 5 μm, 250 mm * 4.6 mm), after derivatization with PITC (phenylthioisocyanate).
Exemple 2 : Test d'agents anti-héparine selon l'invention sur un test TP:Example 2: Test of anti-heparin agents according to the invention on a TP test:
L'objectif est d'analyser les performances (pouvoir anti-héparine et turbidité) d'agents anti-héparine incorporés dans un réactif Thromboplastine Diagnostica Stago.The objective is to analyze the performances (anti-heparin power and turbidity) of anti-heparin agents incorporated in a Thromboplastin Diagnostica Stago reagent.
Analyse du pouvoir anti-héparine: Il s'agit de la capacité de l'agent anti-héparine à insensibiliser le réactif vis-à-vis de l'héparine contenue dans l'échantillon de sang:Analysis of anti-heparin power: This is the capacity of the anti-heparin agent to numb the reagent vis-à-vis the heparin contained in the blood sample:
Les échantillons à tester sont préparés à partir d'un pool de plasma normal surchargé ou non en héparine (Plasma héparine à 1 Ul/ml en HNF (Calciparine 25000 Ul/ml, Sanofi)).The samples to be tested are prepared from a pool of normal plasma overloaded or not with heparin (heparin plasma at 1 IU / ml in HNF (Calciparin 25,000 IU / ml, Sanofi)).
Remarque: un réactif servant de témoin négatif, c'est-à-dire sans agent anti-héparine, est utile pour vérifier l'héparinisation du plasma.Note: a reagent serving as a negative control, that is to say without an anti-heparin agent, is useful for checking the heparinization of the plasma.
Pour la détermination du Temps de Quick, l'automate (STA Diagnostica Stago - brevet EP0325874) prélève 50 μl de plasma échantillon, qu'il laisse incuber 240 sec. à 37° C dans une cupule contenant une bille ; puis il transfère la cupule dans la zone de mesure et ajoute à l'échantillon 100 μl de réactif Thromboplastine.For the determination of the Quick Time, the automaton (STA Diagnostica Stago - patent EP0325874) takes 50 μl of sample plasma, which it incubates 240 sec. at 37 ° C in a cup containing a ball; then it transfers the well to the measurement zone and adds 100 μl of Thromboplastin reagent to the sample.
Le temps de coagulation est déterminé de la façon suivante :The coagulation time is determined as follows:
A viscosité constante, l'amplitude d'oscillation de la bille dans la cupule (oscillation entretenue grâce à un champ électromagnétique) est constante. Quand la viscosité augmente (phénomène de coagulation), l'amplitude d'oscillation de la bille diminue.
Un algorithme utilise cette variation d'amplitude pour déterminer le temps de coagulation.At constant viscosity, the amplitude of oscillation of the ball in the cup (oscillation maintained thanks to an electromagnetic field) is constant. When the viscosity increases (coagulation phenomenon), the amplitude of oscillation of the ball decreases. An algorithm uses this amplitude variation to determine the coagulation time.
Le pouvoir anti-héparine est calculé de la manière suivante : détermination du delta temps relatif entre un plasma héparine et non héparine, c'est-à-dire :The anti-heparin power is calculated as follows: determination of the relative time delta between a heparin and non-heparin plasma, that is to say:
[{TC (plasma héparine) - TC (plasma non héparine)} / TC (plasma non héparine) * 100]. avec ΥC— Temps de Coagulation Le pouvoir anti-héparine des composés selon l'invention est estimé significatif lorsque ce delta temps est inférieur à 10%.[{TC (heparin plasma) - TC (non heparin plasma)} / TC (non heparin plasma) * 100]. with ΥC— Coagulation Time The anti-heparin power of the compounds according to the invention is estimated to be significant when this time delta is less than 10%.
Analyse de la turbidité :Turbidity analysis:
La turbidité doit être la plus faible possible pour une application en diagnostic et plus particulièrement dans un test Thromboplastine (TP).The turbidity must be as low as possible for a diagnostic application and more particularly in a Thromboplastin (TP) test.
Cette turbidité est déterminée avec la mesure de la DO à 630 nm sur un spectrophotomètre (Uvikon 940, Kontron).This turbidity is determined with the measurement of the OD at 630 nm on a spectrophotometer (Uvikon 940, Kontron).
Remarque: un réactif servant de témoin négatif, c'est-à-dire sans agent anti-héparine, est utile pour mesurer l'influence de cet agent anti-héparine sur la turbidité du réactif.
Note: a reagent serving as a negative control, that is to say without an anti-heparin agent, is useful for measuring the influence of this anti-heparin agent on the turbidity of the reagent.
Exemple 3: Analyse des performances (pouvoir anti-héparine et turbidité) de différents agents anti-héparine selon l'invention, introduits dans un réactif de type Thromboplastine (résultats comparés au contrôle (C) ne possédant pas d'agent anti-héparine):Example 3: Analysis of the performances (anti-heparin power and turbidity) of different anti-heparin agents according to the invention, introduced into a reagent of the Thromboplastin type (results compared with the control (C) having no anti-heparin agent) :
Agent anti-héparine à 5112/mIAnti-heparin agent at 5112 / mI
Pouvoir anti-HNFAnti-HNF power
TurbiditéTurbidity
Delta temps 0/1 DO 630 nm ϋl/mlDelta time 0/1 DO 630 nm ϋl / ml
(en %)(in %)
99.2 0.04799.2 0.047
1415-5 PGIu - K, - (AHA)2 - K,- AHA -K,- AHA -K2 4.5 0.0691415-5 PGIu - K, - (AHA) 2 - K, - AHA -K, - AHA -K 2 4.5 0.069
1415-4 THC-Kt- AHA^-Kt-AHA-I -AHA-Kî 5.9 0.1481415-4 THC-K t - AHA ^ -K t -AHA-I -AHA-K î 5.9 0.148
1415-3 Hyp-K4-(AHA)2-K4-AHA-K4-AHA-K2 3.4 0.1341415-3 Hyp-K 4 - (AHA) 2 -K 4 -AHA-K 4 -AHA-K 2 3.4 0.134
1415-2 Thi- K - (AHA)2 - IQ - AHA - K» - AHA - K2 5.7 0.1041415-2 Thi- K - (AHA) 2 - IQ - AHA - K ”- AHA - K 2 5.7 0.104
1394 Pro-K4-AHA-K4-APA-K3-APA-K2 6.4 0.3991394 Pro-K 4 -AHA-K 4 -APA-K 3 -APA-K 2 6.4 0.399
1401 Pro-I -AHA-Kt-APA-Kt-APA-K;! 8.1 0.4881401 Pro-I -AHA-K t -APA-Kt-APA-K ;! 8.1 0.488
1403P Pro-Ks-AHA-IC-APA-ïC-APA-Ks 7.1 0.2051403P Pro-Ks-AHA-IC-APA-ïC-APA-Ks 7.1 0.205
1403PK Pro-Ks-AHA-IC-APA-Kj-APA-Krj 8.7 0.2831403PK Pro-Ks-AHA-IC-APA-Kj-APA-Krj 8.7 0.283
1404 Pro-K4-AHA-K3-APA-K3-APA-K2 7.6 0.1471404 Pro-K 4 -AHA-K3-APA-K3-APA-K 2 7.6 0.147
1405 Pro-K4-(AHA)2-K4-AHA- 4-AHA-K2 4.2 0.323 1408-2 Pro-Kt-AHA-I -APA-IC-APA-Kî 6.9 0.0401405 Pro-K 4 - (AHA) 2 -K 4 -AHA- 4 -AHA-K 2 4.2 0.323 1408-2 Pro-K t -AHA-I -APA-IC-APA-K î 6.9 0.040
1411 Pro-K4-(AHA)2- 4-AHA- 3-AHA-K2 6.5 0.0861411 Pro-K 4 - (AHA) 2 - 4 -AHA- 3 -AHA-K 2 6.5 0.086
avec APA correspondant à l'acide amino propanoïque, de formule - (CH2)2 - CO -
REFERENCESwith APA corresponding to amino propanoic acid, of formula - (CH 2 ) 2 - CO - REFERENCES
1. Casu, B. (1985) Adv. Carbohydr. Chem. 43: 51-134.1. Casu, B. (1985) Adv. Carbohydr. Chem. 43: 51-134.
2. Constanta, et al. (1993) Angewandte Chemie, vol. 32, n°12, 1671-1818.2. Constanta, et al. (1993) Angewandte Chemie, vol. 32, n ° 12, 1671-1818.
3. Lormeau, H, et al. (1995) Thromb. Haemostasis 74: 1474-1477.3. Lormeau, H, et al. (1995) Thromb. Haemostasis 74: 1474-1477.
4. Mayo, K.M., et al. (1995) BiochemJ. 312: 357-365.4. Mayo, K.M., et al. (1995) BiochemJ. 312: 357-365.
5. Mardiguian, J. (1992) Ed Doutremepuich ch. Marcel Dekker inc 7-12.5. Mardiguian, J. (1992) Ed Doutremepuich ch. Marcel Dekker inc 7-12.
6. McKay, D.J., et al. (1986) Eur; J. Biochem. 158: 361-266.6. McKay, D.J., et al. (1986) Eur; J. Biochem. 158: 361-266.
7. Kurt, F. (1973) Protamines, Institut fur Negetative Physiologie, Frankfurt, Germany.7. Kurt, F. (1973) Protamines, Institut fur Negetative Physiologie, Frankfurt, Germany.
8. Jacques, L.B. (1973) Can. Med. Assoc. J. 108: 1291-1297.8. Jacques, L.B. (1973) Can. Med. Assoc. J. 108: 1291-1297.
9. Cundall, R.B., et al. (1979) J. Chem. Soc. Perkins Trans. 11:879.9. Cundall, R.B., et al. (1979) J. Chem. Soc. Perkins Trans. 11: 879.
10. Racanelli, A, et al. (1985) Semin. Thromb. Hemostasis 11: 176-189.10. Racanelli, A, et al. (1985) Semin. Thromb. Hemostasis 11: 176-189.
11. Horrow, J.C. (1985) Anesth. Analg. 64: 348-361.11. Horrow, J.C. (1985) Anesth. Analg. 64: 348-361.
12. Cook, XL, et al. (1992) Circulation 85:1102-1109.12. Cook, XL, et al. (1992) Circulation 85: 1102-1109.
13. Weller J.M., et al. (1985) J. Allergy. Clin. Immunol. 75: 297-303.13. Weller J.M., et al. (1985) J. Allergy. Clin. Immunol. 75: 297-303.
14. Wakefield T.W., et al. (1990) Ann. Surg. 212: 387-395.
15. Telen AN., et al. (1977) Thromb. Res. 10, 399-410.14. Wakefield TW, et al. (1990) Ann. Surg. 212: 387-395. 15. Telen AN., Et al. (1977) Thromb. Res. 10, 399-410.
16. DeLucia, A, et al. (1993) J. Vase. Surg. 10: 49-58.
16. DeLucia, A, et al. (1993) J. Vase. Surg. 10: 49-58.
Claims
1. Composé présentant une activité anti-héparine de la formule générale 1 :1. Compound having an anti-heparin activity of the general formula 1:
Z-Bm-(AXA)x-Bn-(AXA)y-B0-(AXA)z-BF ZB m - (AXA) x -B n - (AXA) y -B 0 - (AXA) z -B F
dans laquelle:in which:
* Z a pour formule générale :* Z has the general formula:
-N— Cx— CH— C02H avec Cy - liaison covalente \ / -CH2--N— Cx— CH— C0 2 H with Cy - covalent bond \ / -CH 2 -
Cy— Cx -CO-Cy— Cx -CO-
- CO - S -- CO - S -
-(CH2)n-X- avec 1 < n < 2 et X = O -, S -, V_/ avec Cx = - liaison covalente -(CH2)n-, 1 <n<5 ou- (CH 2 ) n -X- with 1 <n <2 and X = O -, S -, V_ / with Cx = - covalent bond - (CH 2 ) n -, 1 <n <5 or
-CH-CH2 —-CH-CH 2 -
II
R1 avec R1 = - OH, - NH2 R 1 with R1 = - OH, - NH2
* B représente un acide aminé basique; m, n, o et p représentent indépendamment les uns des autres un nombre entier compris entre 2 et 4.* B represents a basic amino acid; m, n, o and p independently of one another represent an integer between 2 and 4.
* AXA représente une chaîne hydrocarbonée correspondant à la formule: NH - (CH2)n - CO - , n étant un nombre entier compris entre 2 et 6; x, y et z représentent indépendamment les uns des autres un nombre entier compris entre 1 et 6. * AXA represents a hydrocarbon chain corresponding to the formula: NH - (CH 2 ) n - CO -, n being an integer between 2 and 6; x, y and z independently of one another represent an integer between 1 and 6.
2. Composé selon la revendication 1 caractérisé en ce que Z est sélectionné parmi les composés suivants:2. Compound according to Claim 1, characterized in that Z is selected from the following compounds:
- acide 4-amino-pyrolidine-2 carboxylique- 4-amino-pyrolidine-2 carboxylic acid
- acide azetidine-2-carboxylique - acide 2-carboxynιorpholine- azetidine-2-carboxylic acid - 2-carboxynιorpholine acid
- acide l,3-dihydro-2H-isoindole carboxylique- 1,3-dihydro-2H-isoindole carboxylic acid
- acide 4-hydroxypyrolidine 2-carboxylique- 4-hydroxypyrolidine 2-carboxylic acid
- acide indoline-2-carboxylique- indoline-2-carboxylic acid
- acide isonipecotique - acide pyroglutamique- isonipecotic acid - pyroglutamic acid
- acide pipecolique-2-carboxylique- pipecolic-2-carboxylic acid
- acide pyrolidine 2-carboxylique- 2-carboxylic pyrolidine acid
- acide 2-oxothiazolidine 4-carboxylique- 2-oxothiazolidine 4-carboxylic acid
- acide thiazolidin carboxylique - acide tetrahydroisoquinoline 2-carboxylique- thiazolidin carboxylic acid - tetrahydroisoquinoline 2-carboxylic acid
3. Composé selon l'une des revendications 1 et 2 caractérisé en ce que Z est l'acide pyroglutamique (PGIu), de formule:3. Compound according to one of claims 1 and 2 characterized in that Z is pyroglutamic acid (PGIu), of formula:
4. Composé selon l'une des revendications 1 à 3 caractérisé en ce que B est sélectionné parmi la Lysine, 'Arginine, l'Omithine, l'Histidine, l'Homolysine et l'Homoarginine.4. Compound according to one of claims 1 to 3 characterized in that B is selected from Lysine, 'Arginine, Omithine, Histidine, Homolysine and Homoarginine.
5. Composé selon l'une des revendications 1 à 4 caractérisé en ce que B est la Lysine.5. Compound according to one of claims 1 to 4 characterized in that B is Lysine.
6. Composé selon l'une des revendications 1 à 5 caractérisé en ce que m, n, o sont égaux à 4 et p est égal à 2. 6. Compound according to one of claims 1 to 5 characterized in that m, n, o are equal to 4 and p is equal to 2.
7. Composé selon l'une des revendications 1 à 6 caractérisé en ce que AXA correspond à la formule NH - (CH2)5 - CO - (acide amino hexanoïque).7. Compound according to one of claims 1 to 6 characterized in that AXA corresponds to the formula NH - (CH 2 ) 5 - CO - (amino hexanoic acid).
8. Composé selon l'une des revendications 1 à 7 caractérisé en ce que x est égal à 2 et y, z sont égaux à 1.8. Compound according to one of claims 1 to 7 characterized in that x is equal to 2 and y, z are equal to 1.
9. Composé selon l'une des revendications 1 à 8 caractérisé en ce qu'il répond à la formule: PGIu - 4 - (AHA)2 - K - AHA - j - AHA - K2 9. Compound according to one of claims 1 to 8 characterized in that it corresponds to the formula: PGIu - 4 - (AHA) 2 - K - AHA - j - AHA - K 2
10. Composé selon l'une des revendications 1 à 9 caractérisé en ce qu'il présente un pouvoir anti-héparine, déterminé par le Δ temps de coagulation relatif entre un plasma héparine et un plasma non héparine inférieur à 10%, de préférence inférieur à 5% dans un test de coagulation.10. Compound according to one of claims 1 to 9 characterized in that it has an anti-heparin power, determined by the Δ relative coagulation time between a heparin plasma and a non-heparin plasma of less than 10%, preferably less at 5% in a coagulation test.
11. Réactif de diagnostic in vitro comprenant un composé selon l'une des revendications 1 à 10.11. In vitro diagnostic reagent comprising a compound according to one of claims 1 to 10.
12. Réactif selon la revendication 11, permettant de calculer le temps de coagulation d'un échantillon de sang, indépendamment de la présence ou de l'absence d'héparine dans ledit échantillon.12. Reagent according to claim 11, making it possible to calculate the coagulation time of a blood sample, independently of the presence or absence of heparin in said sample.
13. Réactif selon la revendication 11, permettant la détection ou le dosage de différents éléments de la cascade de la coagulation, indépendamment de la présence ou de l'absence d'héparine dans ledit échantillon.13. Reagent according to claim 11, allowing the detection or the assay of different elements of the coagulation cascade, independently of the presence or absence of heparin in said sample.
14. Réactif selon la revendication 11, caractérisé en ce qu'il s'agit d'un réactif de TP.14. Reagent according to claim 11, characterized in that it is a TP reagent.
15. Réactif selon la revendication 11, caractérisé en ce qu'il comprend le composé de formule: PGIu - * - (AHA)2 - K4 - AHA - K, - AHA - K2 15. Reagent according to claim 11, characterized in that it comprises the compound of formula: PGIu - * - (AHA) 2 - K4 - AHA - K, - AHA - K 2
16. Réactif selon la revendication 11, caractérisé en ce qu'il présente une turbidité, mesurée par une DO à 630 nm, inférieure à 0,5, de préférence inférieure à 0,1.16. Reagent according to claim 11, characterized in that it has a turbidity, measured by an OD at 630 nm, less than 0.5, preferably less than 0.1.
17. Réactif selon la revendication 11, comprenant un composé de formule générale 1 à une concentration finale comprise entre 2 et 10 μg/ml.17. Reagent according to claim 11, comprising a compound of general formula 1 at a final concentration of between 2 and 10 μg / ml.
18. Réactif selon la revendication 11, caractérisé en ce que la concentration finale du composé dans ledit réactif est de 5 μg/ml.18. Reagent according to claim 11, characterized in that the final concentration of the compound in said reagent is 5 μg / ml.
19. Utilisation d'un composé selon l'une des revendications 1 à 10 dans un réactif de diagnostic in vitro pour calculer le temps de coagulation d'un échantillon de sang, ou détecter ou doser dans un échantillon de sang différents éléments de la cascade de coagulation, indépendamment de la présence ou de l'absence d'héparine dans ledit échantillon.19. Use of a compound according to one of claims 1 to 10 in an in vitro diagnostic reagent to calculate the coagulation time of a blood sample, or to detect or measure different elements of the cascade in a blood sample coagulation, regardless of the presence or absence of heparin in said sample.
20. Utilisation d'un composé selon l'une des revendications 1 à 10 comme agent antihéparine pour la préparation d'un médicament. 20. Use of a compound according to one of claims 1 to 10 as an antiheparin agent for the preparation of a medicament.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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FR0010682A FR2813080B1 (en) | 2000-08-17 | 2000-08-17 | ANTI-HEPARIN PEPTIDES |
FR0010682 | 2000-08-17 | ||
PCT/FR2001/002610 WO2002014353A1 (en) | 2000-08-17 | 2001-08-14 | Anti-heparin peptides |
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EP01965326A Withdrawn EP1309611A1 (en) | 2000-08-17 | 2001-08-14 | Anti-heparin peptides |
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US (1) | US6835808B2 (en) |
EP (1) | EP1309611A1 (en) |
JP (1) | JP2004506651A (en) |
CN (1) | CN1447818A (en) |
FR (1) | FR2813080B1 (en) |
WO (1) | WO2002014353A1 (en) |
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AU2005288519A1 (en) * | 2004-09-27 | 2006-04-06 | Technion Research & Development Foundation Ltd. | Fatty acid modified polylysines as antimicrobial agents |
US7915223B2 (en) * | 2004-09-27 | 2011-03-29 | Technion Research & Development Foundation Ltd. | Antimicrobial agents |
US20090092574A1 (en) | 2006-12-29 | 2009-04-09 | Scott Richard W | Ophthalmic And Otic Compositions Of Facially Amphiphilic Polymers And Oligomers And Uses Thereof |
WO2008132737A1 (en) * | 2007-04-30 | 2008-11-06 | Technion Research & Development Foundation Ltd. | Novel antimicrobial agents |
US20100173832A1 (en) * | 2007-04-30 | 2010-07-08 | Technion Research & Development Foundation Ltd. | Anticancerous polymeric agents |
US8278309B2 (en) | 2008-10-27 | 2012-10-02 | Polymedix, Inc. | Synthetic mimetics of host defense and uses thereof |
KR20120106990A (en) * | 2010-01-07 | 2012-09-27 | 폴리메딕스, 인코포레이티드 | Anti-heparin compounds |
DK2709619T3 (en) | 2011-05-16 | 2018-01-15 | Cellceutix Corp | RELATIONSHIPS FOR USING THE TREATMENT OF MUCOSITIS |
CN103739674A (en) * | 2013-04-01 | 2014-04-23 | 中国人民解放军军事医学科学院野战输血研究所 | Protamine mimic peptide series with low molecular and application thereof |
GB201400292D0 (en) | 2014-01-08 | 2014-02-26 | Haemostatix Ltd | Peptide dendrimers and agents |
GB201508024D0 (en) | 2015-05-11 | 2015-06-24 | Haemostatix Ltd | Haemostatic compositions |
GB201508014D0 (en) * | 2015-05-11 | 2015-06-24 | Haemostatix Ltd | Haemostatic device |
US11771694B2 (en) | 2020-06-05 | 2023-10-03 | Innovation Pharmaceuticals Inc. | Arylamide compounds for treatment and prevention of viral infections |
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US5614494A (en) * | 1993-11-12 | 1997-03-25 | University Of Michigan, The Board Of Regents Acting For And On Behalf Of | Peptides for heparin and low molecular weight heparin anticoagulation reversal |
US6200955B1 (en) | 1996-06-11 | 2001-03-13 | Commonwealth Biotechnologies, Inc. | Heparin binding peptides |
US5877153A (en) * | 1996-06-11 | 1999-03-02 | Commonwealth Biotechnologies Inc. | Heparin-binding peptides |
-
2000
- 2000-08-17 FR FR0010682A patent/FR2813080B1/en not_active Expired - Fee Related
-
2001
- 2001-08-14 US US10/344,754 patent/US6835808B2/en not_active Expired - Fee Related
- 2001-08-14 CN CN01814258A patent/CN1447818A/en active Pending
- 2001-08-14 EP EP01965326A patent/EP1309611A1/en not_active Withdrawn
- 2001-08-14 WO PCT/FR2001/002610 patent/WO2002014353A1/en not_active Application Discontinuation
- 2001-08-14 JP JP2002519490A patent/JP2004506651A/en active Pending
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