WO1990003389A1 - Renin inhibitory peptides containing maleamide substituents - Google Patents
Renin inhibitory peptides containing maleamide substituents Download PDFInfo
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- WO1990003389A1 WO1990003389A1 PCT/US1989/003642 US8903642W WO9003389A1 WO 1990003389 A1 WO1990003389 A1 WO 1990003389A1 US 8903642 W US8903642 W US 8903642W WO 9003389 A1 WO9003389 A1 WO 9003389A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/49—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0207—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)4-C(=0), e.g. 'isosters', replacing two amino acids
Definitions
- the present invention provides novel compounds. More particularly, the present invention provides novel renin-inhibiting peptide analogs. Most particularly, the present invention provides renininhibitory peptides containing a non-cleavable transition state insert corresponding to the 10,11-position of the renin substrate (angiotensinogen) and containing a maleic acid derived moiety corresponding to the 8,9-position of the renin substrate and which is preferably at the N-terminus of the peptide.
- the renin inhibitors provided herein are useful for the diagnosis and control of renindependent hypertension, congestive heart failure, renin dependent hyperaldosterism, and other renin dependent cardiovascular disorders.
- Renin is an endopeptidase which specifically cleaves a particular peptide bond of its substrate (angiotensinogen), of which the N- terminal sequence in equine substrate is for example:
- Human renin substrate has a different sequence as recently discovered by D.A. Tewkesbury et al., Biochem. Biophys. Res. Comm. 99, 1311 (1981). It may be represented as follows:
- Renin cleaves angiotensinogen to produce angiotensin I, which is converted to the potent pressor angiotensin II.
- a number of angiotensin I converging enzyme inhibitors are known to be useful in the treatment of hypertension.
- Inhibitors of renin are also useful in the treatment of hypertension.
- Terminal disulfide cycles have also been disclosed in renin inhibiting peptides; see, e.g., U.S. patents 4,477,440 and 4,477,441.
- Aromatic and aliphatic amino acid residues at the 10,11 position of the renin substrate are disclosed in U.S. patents 4,478,827 and 4,455,303.
- C-terminal amide cycles are disclosed in U.S. patent 4,485,099 and European published applications 156,320 and 156,318.
- Certain tetrapeptides are disclosed in European publications 111,266 and 77,027. Further, European published application No.
- Isosteric bond modifications at positions 11-12 and 12-13 have been disclosed in European published application 179,352.
- Certain peptides containing 2-substituted statine analogues have been disclosed in European published application 157,409.
- Certain peptides containing 3-aminodeoxystatine have been disclosed in European published application 161,588.
- Certain peptides containing 1-amino-2-hydroxybutane derivatives at positions 10-11 have been disclosed in European published application 172,346.
- Certain peptides containing 1-amino-2-hydroxypropane derivatives at positions 10-11 have been disclosed in European published application 172,347.
- PCT patent application PCT/US89/00247 , filed 27 January 1989, discloses renin inhibitory peptides having a variety of polar end groups at the N-terminus and/or the C-terminus.
- the present invention particularly provides:
- R 22 is (a) -(CH 2 ) p -aryl, or
- n 1 to 5, inclusive
- renin inhibitory peptide is meant a compound capable of inhibiting the renin enzyme in mammalian metabolism and having three or more amino acid residues linked by peptidic or pseudo-peptidic bonds.
- a non-cleavable transition state insert is meant a transition state insert which is not cleavable by a hydrolytic enzyme in mammalian metabolism.
- a variety of such transition state inserts, corresponding to the 10,11-position of the renin substrate, are known in the art, including those disclosed in the following references, which are hereby incorporated by reference:
- the renin inhibitory peptides of the present invention are represented by formula II.
- the non-cleavable transition state insert corresponding to the 10,11-position of the renin substrate, begins at -NHCH(CH 2 ) (R 2 )-X 1 , with the variables as defined above.
- novel renin inhibitory peptides of the present invention containing a maleic acid derived moiety are potent inhibitors of human plasma renin.
- the novel non-peptidogenic nature of these inhibitory peptides alters their absorption, distribution, metabolism, and excretion characteristics.
- the new maleic acid derived moiety makes these inhibitory peptides unrecognizable to proteinases which would normally rapidly degrade a substrate based inhibitory peptide, particularly at the position corresponding to the 8,9-position of the renin substrate (angiotensinogen).
- the renin inhibitory peptides of the present invention can occur in several isomeric forms. All such isomeric forms are included within the scope of the present invention.
- Renin inhibitory peptides commonly have protecting groups at the C-terminus. These protecting groups are known in the polypeptide art. Examples of these protecting groups are given below. Any of these protecting groups are suitable for the renin inhibitory peptides of the present invention.
- non ⁇ -amino acid moieties of the formula I of the present invention preferably occur at the N-terminus of the renin inhibitory peptide.
- the present invention provides peptide inhibitors of renin which contain a non ⁇ -amino acid moiety and have a transition state insert.
- pharmaceutically acceptable acid addition salts include: acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate , ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate , hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2- hydroxyethanesulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, palmoate, pect
- the carbon atom content of various hydrocarbon-containing moieties is indicated by a prefix designating the minimum and maximum number of carbon atoms in the moiety, i.e., the prefix (C i -C j ) indicates a moiety of the integer "i" to the integer "j" carbon atoms, inclusive.
- (C 1 -C 4 )alkyl refers to alkyl of one to 4 carbon atoms, inclusive, or methyl, ethyl, propyl, butyl, and isomeric forms thereof .
- C 4 -C 7 cyclic amino indicates a monocyclic group containing one nitrogen and 4 to 7 carbon atoms.
- Examples of (C 3 -C 10 )cycloalkyl which include alkyl-substituted cycloalkyl containing a total of up to 10 total carbon atoms, are cyclopropyl. 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-diethylcyclopropyl, 2-butylcyclopropyl, cyclobutyl, 2-methylcyclobutyl, 3-propylcyclobutyl, cyclopentyl, 2,2-dimethylcyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl and isomeric forms thereof.
- aryl examples include phenyl, naphthyl, (o-, m-, or p-)tolyl, (o-, m-, or p-)ethylphenyl, 2-ethyl-tolyl, 4-ethyl-o-tolyl, 5-ethyl- m-tolyl, (o-, m-, or p-)propylphenyl, 2-propyl- (o-, m-, or p-)tolyl, 4-isopropyl-2, ⁇ -xylyl, 3-propyl-4-ethylphenyl, (2,3,4- 2,3,6-, or 2,4,5-)trimethylphenyl, (o-, m-, or p-)fluorophenyl, (o-, m-, or p-trifluoromethyl)phenyl, 4-fIuoro-2,5-xylyl, (2,4-, 2,5-, 2,6-, 3,4-
- Het examples include: 2-, 3-, or 4-pyridyl, imidazolyl, indolyl, N in -formyl-indolyl, N in -C 1 -C 5 alkyl-C(O)-indolyl, 1,2,4- triazolyl, 2-, 4-, or 5-pyrimidinyl, 2- or 3-thienyl, piperidinyl, pyrryl, pyrrolinyl, pyrrolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, pyrazinyl, piperazinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, quinoliny
- a heterocycle as defined herein for Het would not be bonded through oxygen or sulfur or through nitrogen which is within a ring and part of a double bond.
- Halo is halogen (fluoro, chloro, bromo, or iodo) or trifluoromethyl.
- Examples of pharmaceutically acceptable cations include: pharmacologically acceptable metal cations, ammonium, amine cations, or quaternary ammonium cations.
- pharmacologically acceptable metal cations are those derived from the alkali metals, e.g., lithium, sodium, and potassium, and from the alkaline earth metals, e.g., magnesium and calcium, although cationic forms of other metals, e.g., aluminum, zinc, and iron are also within the scope of this invention.
- Pharmacologically acceptable amine cations are those derived from primary, secondary, or tertiary amines.
- novel peptides herein contain both natural and synthetic amino acid residues. These residues are depicted using standard amino acid abbreviations (see, e.g., IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN) , "Nomenclature and Symbolism for Amino Acids and Peptides.” Eur. J. Biochem. 138:9-37 (1984) unless otherwise indicated.
- JCBN Biochemical Nomenclature
- the renin inhibitors of this invention are useful for treating any medical condition for which it is beneficial to reduce the levels of active circulating renin.
- examples of such conditions include renin-dependent hypertension, hypertension, hypertension under treatment with another antihypertensive and/or a diuretic agent, congestive heart failure, renin-dependent hyperaldosterism, angina, postmyocardial infarction, other renin-dependent cardiovascular disorders and ocular disorders.
- the renin-angiotension system may play a role in maintenance of intracellular ho ⁇ teostasis: see Clinical and Experimental Hypertension, 86, 1739-1742 (1984) at page 1740 under Discussion.
- the renin inhibitors of this invention may be useful in the treatment of cerebrovascular disorders and disorders of intracellular homeotasis.
- the possible role of the renin-angiotensin system in the maintenance of intracellular homeostasis is disclosed in Clinical and Experimental Hypertension, 86:1739-1742 (1984).
- the renin inhibitors of this invention potentiate the antithrombotic activity of a thromboxane antagonist (U.S. patent 4,558,037).
- the antihypertensive effect of the renin inhibitors of this invention are potentiated by combination with a thromboxane synthetase inhibitor.
- the compounds of the present invention are preferably orally administered to humans to effect renin inhibition for the purpose of favorably affecting blood pressure.
- the compounds are administered from 0.1 mg to 100 mg per kg per dose, administered from 1 to 4 times daily.
- Equivalent dosages for other routes of administration are also employed.
- renin-associated hypertension and hyperaldosteronism are effectively treated by the administration of from 0.5 to 50 milligrams of the compound per kilogram of body weight per day.
- the exact dose depends on the age, weight, and condition of the patient and on the frequency and route of administration. Such variations are within the skill of the practitioner or can readily be determined.
- the compounds of the present invention may be in the form of pharmaceutically acceptable salts both those which can be produced from the free bases by methods well known in the art and those with which acids have pharmacologically acceptable conjugate bases.
- the compounds of the present invention are preferably orally administered in the form of phanaacologically acceptable acid addition salts.
- Preferred pharmacologically acceptable salts for oral administration include the citrate and aspartate salts, although any pharmacologically acceptable salt is useful in this invention, including those listed above. These salts may be in hydrated or solvated form.
- the co ⁇ rpounds of the present invention may be administered topically, parenterally, by inhalation spray, or rectally in dosage unit for ⁇ ulations containing conventional nontoxic pharmaceutically acceptable carriers, adjuvants and vehicles.
- parenteral as used herein includes subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
- the compounds of the invention are effective in the treatment of humans.
- the pharmaceutical compositions may be in the form of a sterile injectable preparation, for example as a sterile injectable aqueous or oleagenous suspension.
- This suspension may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents.
- the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example as a solution in 1,3- butanediol.
- the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution.
- sterile, fixed oils are conventionally employed as a solvent or suspending medium.
- any bland fixed oil may be employed including synthetic mono- or digly- cerides.
- fatty acids such as oleic acid find use in the preparation of injectables.
- the peptides of this invention may also be administered in the form of suppositories for rectal administration of the drug.
- These compositions can be prepared by mixing the drug with a suitable nonirritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug.
- suitable nonirritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug.
- Such materials are cocoa butter and polyethylene glycols.
- renin-inhibiting compounds of this invention may be administered in combination with ocher agents used in antihypertensive therapy such as diuretics, a and/or 5-adrenergic blocking agents, CNS-acting agents, adrenergic neuron blocking agents, vasodilators, angiotensin I converting enzyme inhibitors, and the like as described for example in published European patent application 156,318.
- ocher agents used in antihypertensive therapy such as diuretics, a and/or 5-adrenergic blocking agents, CNS-acting agents, adrenergic neuron blocking agents, vasodilators, angiotensin I converting enzyme inhibitors, and the like as described for example in published European patent application 156,318.
- the present invention is also directed to combinations of the novel renin-inhibitory peptides of Formula II with one or more antihypertensive agents selected from the group consisting of diuretics, a and/or ⁇ -adrenergic blocking agents, CNS-acting agents, adrenergic neuron blocking agents, vasodilators, angiotensin I converting enzyme inhibitors, and other antihypertensive agents.
- one or more antihypertensive agents selected from the group consisting of diuretics, a and/or ⁇ -adrenergic blocking agents, CNS-acting agents, adrenergic neuron blocking agents, vasodilators, angiotensin I converting enzyme inhibitors, and other antihypertensive agents.
- the compounds of this invention can be given in combination with such compounds or salt or other derivative forms thereof as:
- Diuretics acetazolamide; amiloride; bendroflumethiazide; benzthiazide; bumetanide; chlorothiazide; chlorthalidone; cyclothiazide; ethacrynic acid; furosemide; hydrochlorothiazide; hydroflumethiazide; indacrinone (racemic mixture, or as either the (+) or (-) enantiomer alone, or a manipulated ratio, e.g., 9:1 of said enantiomers, respectively); metolazone; methyclothiazide; muzolimine; polythiazide; quinethazone; sodium ethacrynate; sodium nitroprusside; spironol- actone; ticrynaten; trimaterene; trichlormethiazide;
- ⁇ -Adrenergic Blocking Agents dibenamine; phentolamine; phenoxyben- zamine; prazosin; tolazoline;
- ⁇ -Adrenergic Blocking Agents atenolol; metoprolol; nadolol; propranolol; timolol;
- Other Antihypertensive Agents aminophylline; cryptenamine acetates and tannates; deserpidine; meremethoxylline procaine; pargyline; tri methaphan camsylate; and the like, as well as admixtures and combinations thereof.
- the individual daily dosages for these combinations can range from about one-fifth of the minimally recommended clinical dosages to the maximum recommended levels for the entities when they are given singly.
- Coadainistration is most readily accomplished by combining the active ingredients into a suitable unit dosage form containing the proper dosages of each. Other methods of coad- ministration are, of course, possible.
- novel peptides of the present invention possess an excellent degree of activity in treating renin-associated hypertension and hyperaldosteronism.
- Renin inhibitors have also been disclosed to control the rise in intraocular pressure associated with the use of steroidal anti- inflammatory drugs as described in PCT International Application
- PCT/US86/02291 PCT International Publication Number WO 87/02581 dated 7 May 1987.
- D-Phenylalanine of formula C-1 is esterified with methanol and gaseous hydrochloric acid to give D-phenylanine methyl ester hydrochloride of formula C-2, which is then reacted with maleic anhydride of formula C-3 in tetrahydrofuran containing triethylamine to give the compound of formula C-4.
- the compound of formula C-4 is coupled with 2HCl-LVA-Ile-Amp of formula C-5 using diethylphosphoryl cyanide and triethylamine in methylene chloride and dimethylformamide to give the compound of formula C-6.
- the compound of formula C-6 of Chart C is used as the formula D-1 starting material.
- the compound of formula D-1 is hydrolyzed with IN potassium hydroxide in methanol and then neutralized with aqueous hydrochloric acid to give the compound of formula D-2.
- Phenethylamine of formula F-1 is reacted with maleic anhydride of formula F-2 in tetrahydrofuran as solvent to give the compound of formula F-3.
- the compound of formula F-3 is then coupled with 2HC1- LVA-Ile-Amp of formula F-4 using diethylphosphoryl cyanide and triethylamine in methylene chloride and dimethylformamide to give the compound of formula F-5.
- the Boc- group of the compound of formula 1-4 is removed vith trifluoroacetic acid in methylene chloride to give N-benzylphenethylamine of formula 1-5, which is then reacted with maleic anhydride of formula 1-6 in tetrahydrofuran to give the compound of formula 1-7.
- the compound of formula 1-7 is coupled with 2HCl-LVA-Ile-Amp of formula 1-8 using diethylphosphrryl cyanide and triethyisaine in methylene chloride and dimethylformamide to give the compound of formula 1-9.
- the compound of formula J- 6 is prepared as shown in Chart J . Tryptamine hydrochloride of formula J- 1 is stirred in formic acid, and gaseous hydrochloric acid is bubbled in to give N in -formyltrypt- amine hydrochloride of formula J -2. Biochem. et Biophys . Acta , 147 :453 (1967) . N in -formyltryptamine hydrochloride of formula J-2 is stirred with maleic anhydride of formula J-3 and triethylamine in tetrahydrofuran to give the compound of formula J-4. The compound of formula J-4 is coupled with 2HCl-LVA-Ile-Amp of formula J-5 using diethylphosphoryl cyanide and triethylamine in methylene chloride and dimethylformamide to give the compound of formula J-6.
- the compound of formula K- 7 is prepared as shown in Chart K.
- Boc-Leu ⁇ [CH(O-t-BDMS)CH 2 ]Val-OH of formula K-1 (as described in U. S . patent application, Serial No . 147 , 073 , filed 20 January 1988 , and in published European patent application 0173481 , which are hereby incorporated by reference) is coupled with S-2-methylbutylamine of formula K-2 using diethylphosphoryl cyanide and triethylamine in methylene chloride to give Boc-Leu ⁇ [CH(O- t-BDHS)CH 2 ]Val-methyl- butylamide of formula K-3.
- the Boc group of the compound of formula K-3 is removed with trifluoroacetic acid in methylene chloride to give Leu ⁇ [CH(O-t-BDMS)CH 2 ]Val-methylbutylamide of formula K-4.
- the compound of formula K-4 is coupled with the compound of formula K-5 (prepared as the compound of formula A-4 in Chart A) using diethylphosphoryl cyanide and triethylamine in methylene chloride to give the compound of formula K-6 .
- the tert-butyldimethylsilyl group of the compound of formula K- 6 is removed with tetra-n-butylammonium fluoride in tetrahydrofuran zo give the compound of formula K- 7.
- the compound of formula L-5 which is named 4- [ (1 ' R- tert- Butoxycarbonyl)phenethylamido] -maleoyl-2S-amino-1-cyclohexyi-3R,4S- diol-6-methylheptane , is prepared as shown in Chart L.
- the compound of formula L-1 (as described in PCT Application International Publication Number W088/04664 , published 30 June 1988 , which is hereby incorporated by reference) is reacted with isobutylaagnesium chloride in tetrahydrofuran and ethylene oxide to give a mixrure of isomers .
- the compound of formula L-3 is coupled with the compound of formula L-4 (prepared as the compound of formula A-4 in Chart A) using diethylphosphoryl cyanide and triethylamine in methylene chloride as solvent to give the compound of formula L-5.
- the compound of formula L-5 had an IC 50 of 1.7 x 10 -6 molar and an FAB mass spec [m + H] at m/z 545.
- the renin inhibiting polypeptides may be prepared by solution phase peptide synthetic procedures analogous to those described hereinafter or to those methods known in the art.
- Appropriate protecting groups, reagents, and solvents for the solution phase method can be found in "The Peptides: Analysis, Synthesis, and Biology," Vols. 1-5, eds. E. Gross and T. Meienhofer , Academic Press , NY, 1979-1983 ; "The Practice of Peptide Synthesis", M. Bodansky and A. Bodansky, Springer-Verlag, New York, 1984; “The Principles of Peptide Synthesis", M. Bodansky, Springer-Verlag, New York, 1984.
- the carboxylic moiety of N ⁇ -t-butyloxycarbonyl (Boc) -substituted amino acid derivatives having suitable side chain protecting groups may be condensed with the amino functionality of a suitably protected amino acid or peptide using a conventional coupling protocol such as dicyclohexylcarbodiimide (DCC) and 1-hydroxybenzotriazole (HOBT) or diethylphosphoryl cyanide (DEPC) and triethylamine (Et 3 N) in methylene chloride or dimethylformamide.
- DCC dicyclohexylcarbodiimide
- HOBT 1-hydroxybenzotriazole
- DEPC diethylphosphoryl cyanide
- Et 3 N triethylamine
- N ⁇ -Boc moiety may be selectively removed with 50% trifluoroacetic acid with or without 2% anisole (v/v) in methylene chloride.
- Neutralization of the resultant trifluoroacetate salt may be accomplished with 10% diisopropyl- ethylamine or sodium bicarbonate in methylene chloride.
- the compounds of the present invention may be in either free form or in protected form at one or more of the remaining (not previously protected) peptide, carboxyl, amino, hydroxy, or other reactive groups.
- the protecting groups may be any of those known in the polypeptide art. Examples of nitrogen and oxygen protection groups are set forth in T.W. Greene, Protecting Groups in Organic Synthesis, Wiley, New York, (1981); J.F.W. McOmie, ed. Protective Groups in Organic Chemistry, Plenum Press (1973); and J. Fuhrhop and G. Benzlin, Organic Synthesis, Verlag Chemie (1983).
- nitrogen protective groups include t-butoxycarbonyl (Boc), benzyloxycarbonyl, acetyl, allyl, phthalyl, benzyl, benzoyl, trityl and the like.
- the most preferred compound is 4-[(1'R-tert-Butoxycarbonyl)phen- ethylamido]maleoyl-Leu ⁇ [CH(OH)C2]Val-lle-2-(amidomethyl)pyridine.
- 2-Pya is 3-(2-pyridinyl)alanine
- Bn is benzylester
- BOC is t-butoxycarbonyl
- CDCI 3 is deuteriochlorofora
- Celite is a filter aid.
- C p TSA is p-toluenesulfonic acid
- C p VA is Cpa[CH(OH)CH 2 ]Val
- Dap is 2,4-diaminopyrimidin-6-yl
- DCC is dicyclohexylcarbodiimide
- DEPC diethylphosphoryl cyanide
- FAB fast atom bombardment, a technique for obtaining mass spectra of large molecules.
- FTrp is N in- formyl-Trp
- HOBT is 1-hydroxybenzotriazole
- HPLC high performance liquid chromatography
- Iba is isobutylamine
- K 2 CO 3 is potassium carbonate
- LVA is Leu ⁇ (CH(OH)CH 2 )Val with the S configuration at C4 (the hydroxyl-bearing carbon atom).
- MPLC medium pressure liquid chromatography
- Ph is phenyl Phe is phenylalanine
- RIP means a compound having the formula H-Pro-His-Phe-His-Phe- Phe-Val-Tyr-Lys-0H.2(CH 3 C(O)OH).XH 2 O which is a known renin- inhibiting peptide.
- Sta is statine
- TBS is tert-butyldimethylsilyl
- TBDMS is tert-butyldimethylsilyl
- TEA is triethylamine
- TFA is trifluoroacetic acid
- THF is tetrahydrofuran
- THP is tetrahydropyranyl
- TsOH is p-toluenesulfonic acid.
- the wedge-shape line indicates a bond which extends above the plane of the paper relative to the plane of the compound thereon.
- the dotted line indicates a bond which extends below the plane of the paper relative to the plane of the compound thereon.
- HPLC is performed using Altex Model 110A pumps, an LDC Spectro Monitor III detector, Altex Model 420 Programmer, and a Hewlett Packard 3390A integrator.
- the column used is a Brownlee RP-18 Sphere-10, 250 mm x 4.0 mm.
- the solvent system is solvent A, 50 mM NaH 2 PO 4 (6.9 g/L), 1% H 3 PO 4 (1 ml/L), and 1% CH 3 CN (10 ml/L) in H 2 O, and solvent B, 12.5 mM NaH 2 PO 4 (1.7 g/L), 0.25% H 3 PO 4 (0.25 ml/L), 25% H 2 O (250 ml/L), and 75% CH 3 CN (750 ml/L).
- 1 H- NMR spectra are recorded on a Bruker 300 MHz instrument.
- the in vitro IC 50 is measured in nano- molars.
- the in vitro test is performed as described in U.S. patent application, Serial No. 147,073, filed 20 January 1988, and in published European patent application 0173481, which are hereby incorporated by reference.
- Example 1 4- [l'R-tert-Butoxycarbonyl)phenethylamido]maleoyl- Leu ⁇ CH(HOKH 2 ]Val-Ile-2(amidomethynpyridine (Formula A-6) Refer to Chart A.
- Leutf [CH(OH)CH 2 ]Val-2S-methylbutyla mide Refer to Chart K.
- 0.0644 g of the compound of formula K-5 and 0.0836 g of Leutf[CH(O-t-BDMS)CH 2 ]Val- NHCH 2 CH(CH 3 )CH 2 CH 3 of formula K-4 are converted to 0.1341 g of the compound of formula K-6 (chromatography with 4% methanol-methylene chloride).
- the material is then stirred with 0.5 ml of 1 M (in tetrahydrofuran) tetra-n-butyl ammonium fluoride and 0.5 ml of tetrahydrofuran overnight.
- the solvent is removed in vacuo and the residue is chromatographed with 4% methanol-methylene chloride to give 0.0714 g of the title product.
- Example 3 4-(Phenethylamido)maleoyl-Leu ⁇ [CH(OH)CH 2 ]Val-Ile-2- (amidomethyl)pyridine (Formula F-5) Refer to Chart F. According to the general coupling method, 0.04406 g of the title product of Preparation 2 and 0.0847 g of LVA-Ile-Amp-2HCl in 10 ml of dimethylformamide and 1 ml of methylene chloride are coupled to give 0.0546 g of the title product after chromatography with 4% methanol- methylene chloride (ammonium hydroxide).
- Example 4 4-[(2'-Pyridyl)ethylamido]maleoyl-Leutf[CH(OH)CH 2 ]Val- Ile-2-(amidomethyl)pyridine (Formula G-5) Refer to Chart G.
- the filtrate is partitioned two times between methylene and aqueous sodium bicarbonate and the organic layers are filtered through sodium sulfate, concentrated, and chromatographed using 4% methanol-methylene chloride (ammonium hydroxide) to give 0.1183 g of the title product.
- Example 6 4- (N in -formyltryptamido)maleoyl-Leu ⁇ [CH(OH)CH 2 ]Val- Ile-2-(amidomethyl)pyridine (Formula J-6) Refer to
- Example 7 4-(N-Benzyl-N-phenethylamido)maleoyl-Leu ⁇ [CH(OH)CH 2 ]- Val-Ile-2-(amidomethyl)pyridine (Formula 1-9) Refer to Chart I.
- Example 8 4-(Benzylamido)maleoyl-Leutf[CH(OH)CH 2 ]Val-Ile-2- (amidomethyl)pyridine (Formula H-5) Refer to Chart H. Using standard coupling conditions, 0.0404 g of the title product of Preparation 9 and 0.0829 g of LVA-Ile-Amp-2HCl are coupled to give 0.0139 g of the title product with chromatography with 5% methanol-methylene chloride-ammonium hydroxide.
- Example 10 4-[(1'R-Carboxy)phenethylamido]maleoyl-Leu ⁇ [CH(OH)- CH 2 jVal-Ile-2-(amidomethyl)pyridine (Formula D-2) Refer to Chart D. To 0.0524 g of the title product of Example 5 in 2 ml of methanol is added dropwise 0.163 ml of 1 N potassium hydroxide. After stirring for 2-1/2 hrs, the solvent is removed in vacuo and the residue is partitioned between ethyl acetate and 0.087 ml of 2 N hydrochloric acid with 0.5 ml of water added. (After several extractions, solid is still visible floating in the aqueous layer). The organic layers are dried over magnesium sulfate and taken to dryness to give 0.020 g of the title product.
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Abstract
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24896388A | 1988-09-26 | 1988-09-26 | |
US248,963 | 1988-09-26 |
Publications (1)
Publication Number | Publication Date |
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WO1990003389A1 true WO1990003389A1 (en) | 1990-04-05 |
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ID=22941461
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Application Number | Title | Priority Date | Filing Date |
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PCT/US1989/003642 WO1990003389A1 (en) | 1988-09-26 | 1989-08-28 | Renin inhibitory peptides containing maleamide substituents |
Country Status (4)
Country | Link |
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EP (1) | EP0435887A1 (en) |
JP (1) | JPH04500963A (en) |
AU (1) | AU4197189A (en) |
WO (1) | WO1990003389A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0461546A2 (en) * | 1990-06-12 | 1991-12-18 | Bio-Mega/Boehringer Ingelheim Research Inc. | Antiherpes peptide derivatives having a 1,4-dioxo-C4 N-terminus |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989001488A1 (en) * | 1987-08-07 | 1989-02-23 | The Upjohn Company | Renin inhibiting peptides with nonpeptide linkages |
-
1989
- 1989-08-28 JP JP1509265A patent/JPH04500963A/en active Pending
- 1989-08-28 WO PCT/US1989/003642 patent/WO1990003389A1/en not_active Application Discontinuation
- 1989-08-28 EP EP89909979A patent/EP0435887A1/en not_active Ceased
- 1989-08-28 AU AU41971/89A patent/AU4197189A/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989001488A1 (en) * | 1987-08-07 | 1989-02-23 | The Upjohn Company | Renin inhibiting peptides with nonpeptide linkages |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0461546A2 (en) * | 1990-06-12 | 1991-12-18 | Bio-Mega/Boehringer Ingelheim Research Inc. | Antiherpes peptide derivatives having a 1,4-dioxo-C4 N-terminus |
EP0461546A3 (en) * | 1990-06-12 | 1993-03-24 | Bio-Mega Inc. | Antiherpes peptide derivatives having a 1,4-dioxo-c4 n-terminus |
Also Published As
Publication number | Publication date |
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AU4197189A (en) | 1990-04-18 |
JPH04500963A (en) | 1992-02-20 |
EP0435887A1 (en) | 1991-07-10 |
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