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WO1999052877A1 - Ligands de recepteur - Google Patents

Ligands de recepteur Download PDF

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Publication number
WO1999052877A1
WO1999052877A1 PCT/US1998/007389 US9807389W WO9952877A1 WO 1999052877 A1 WO1999052877 A1 WO 1999052877A1 US 9807389 W US9807389 W US 9807389W WO 9952877 A1 WO9952877 A1 WO 9952877A1
Authority
WO
WIPO (PCT)
Prior art keywords
receptor
trans
cis
multimeric
independently
Prior art date
Application number
PCT/US1998/007389
Other languages
English (en)
Inventor
Martin Rosenberg
Katherine Louisa Widdowson
Original Assignee
Smithkline Beecham Corporation
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Smithkline Beecham Corporation filed Critical Smithkline Beecham Corporation
Priority to JP2000543439A priority Critical patent/JP2002511569A/ja
Priority to EP98918154A priority patent/EP1071667A4/fr
Priority to PCT/US1998/007389 priority patent/WO1999052877A1/fr
Priority to CA002328252A priority patent/CA2328252A1/fr
Publication of WO1999052877A1 publication Critical patent/WO1999052877A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/18—Dibenzazepines; Hydrogenated dibenzazepines
    • C07D223/22—Dibenz [b, f] azepines; Hydrogenated dibenz [b, f] azepines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C61/12—Saturated polycyclic compounds
    • C07C61/125—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system
    • C07C61/13—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system having two rings

Definitions

  • This invention relates to multimeric receptor ligands, methods for making and identifying them and their use as agonist or antagonists of multimeric biological receptors.
  • receptors of the single transmembrane class appear to respond to ligand binding by some form of aggregation. Aggregation can be in the form of homodimerization or homotrimerization in the case of identical receptor subunits or in the form of heterodimerization or heterotrimerization in the case of different receptor subunits. It has become clear in several systems that receptor aggregation is part of the signal for the target cell to respond biologically. See review by Young, P.R. entitled "Protein hormones and their receptors" in Curr . Opin . Biotech . 3 , 408-421 (1992) .
  • monoclonal antibodies Despite the success of monoclonal antibodies in producing an agonist response in certain dimeric receptors, they are not considered ideal candidates for development of pharmaceutical compositions. Lack of oral bioavailability and a limited serum half-life limit the desirability and efficacy of monoclonal antibodies as pharmaceutical agents. Consequently, a need exists for non-antibody ligands which have agonist or antagonist properties towards dimeric or trimeric receptors .
  • one aspect of the present invention is a method for agonizing or antagonizing a multimeric receptor comprising contacting the multimeric receptor with a non-antibody multimeric receptor ligand.
  • Another aspect of the invention is a method for identifying agonists and antagonists of multimeric receptors . The method comprises the steps of contacting a multimeric receptor with non-antibody multimeric receptor ligand candidates and selecting ligand candidates which bind to the receptor .
  • a third aspect of the invention is isolated non- antibody multimeric receptor agonists or antagonists.
  • a fourth aspect of the invention is a method for making non-antibody multimeric receptor ligands. The method comprises the steps of reacting a bifunctional monomer bound to a solid support with a receptor binding moiety and cleaving the reaction product from the solid support wherein the two functional groups are identical and symmetrically placed after cleavage.
  • aspects of the present invention are non-antibody multimeric receptor agonists or antagonists and a method for agonizing or antagonizing a multimeric receptor by contacting the multimeric receptor with a non-antibody multimeric receptor ligand.
  • a multimeric receptor is a receptor entity which is agonized or antagonized only when two or more subunits of the entity are aggregated on the same cell surface through binding to a common ligand.
  • Multimeric receptors which appear to signal by heterodimerization include granulocyte-macrophage- colony-stimulating factor (GM-CSF) receptor, the interleukins -3, -4, -5, -6, -12 and -13 (IL-3, 4, 5, 6, 12, and 13) receptors, oncostatin M, ciliary neurotropic factor (CNTF) receptor, leukemia inhibitory factor (LIF) receptor, nerve growth factor (NGF) receptor, fibroblast growth factor (FGF) receptor, the interferons ⁇ , ⁇ and ⁇ (IFN- , ⁇ and ⁇ ) receptors and TGF ⁇ l,2 receptor.
  • Heterotrimeric signaling receptors include interleukin-2 (IL-2) receptor and tissue necrosis factor (TNF) receptor.
  • erythropoietin EPO
  • G-CSF granulocyte-colony- stimulating fetor
  • M-CSF macrophage-colony- stimulating factor
  • TGF ⁇ tissue growth factor ⁇
  • EGF ⁇ epidermal growth factor
  • GRF epidermal growth factor
  • GH epidermal growth factor
  • GH epidermal growth factor
  • GH epidermal growth factor
  • GH epidermal growth factor
  • prolactin receptor prolactin receptor
  • placental lactogen receptor c-kit
  • tissue necrosis factor oc and ⁇ TNF ⁇ , ⁇
  • fas receptor CD40 receptor and CD27 receptor.
  • the non-antibody multimeric receptor ligand of the present invention serves as the common ligand through which two or more multimeric receptor subunits aggregate.
  • the multimeric receptor ligand includes a spacer which is substituted with two or more receptor binding moieties .
  • the spacer can be any molecule having a di- or trisubstituted center capable of substitution with the receptor binding moieties.
  • the spacer provides for spatial separation and steric orientation of the receptor binding moieties which is sufficient to effectively induce aggregation while not sterically preventing such association.
  • the spacer will provide spatial separation and steric orientation of the binding moieties which mimic the binding moieties of the natural ligand.
  • Exemplary disubstituted spacers include compounds represented by the formula (I) :
  • -4- A is independently N, 0, S, dithio, carbonyl, 0
  • Z is independently N, 0, S or carbonyl
  • R is independently - or 1-amino acid; alkyl of 1 to 10 carbons; cis, trans-2-butenyl; cis, trans-1 ,2- cyclopropyl; cis, trans-1, 2-cyclobutyl ; cis, trans-1 ,3- cyclobutyl; cis, trans-1 , 3-cyclopentyl ; cis, trans-1 ,2- cyclopentyl; cis, trans-1, 2-cyclohexyl; cis, trans-1,3- cyclohexyl; cis, trans-1 , 4-cyclohexyl; endo, exo-2,3- norbornane ; 1,5-naphthyl ; 2,6-naphthyl ; 1 , 8-anthrylene; 1, 5-anthrylene; 2 , 6-anthrylene;
  • X is independently N, 0 or S
  • M is independently C or N; p is 0, 1, 2, or 3; and m is 0 or 1; and n is 0, 1, 2 or 3.
  • Preferred compounds of formula (I) are those where
  • Exemplary trisubstituted spacers include compounds represented by the formula (II) :
  • Q is C; N; B; 1 , 3 , 5-phenyl ; 1 , 3 , 5-cyclohexyl ;
  • J is independently H or alkyl of 1 to 10 carbons ;
  • Z is independently N, 0, S or carbonyl; R is independently d- or 1-amino acid; alkyl of 1 to 10 carbons; cis, trans- 2-butenyl; cis, trans-1 ,2- cyclopropyl; cis, trans-1, 2-cyclobutyl ; cis, trans-1,3-
  • X is independently N, O or S
  • M is independently C or N; p is 0, 1, 2, or 3; and m is 0 or 1; and n is 0, 1, 2 or 3.
  • Preferred compounds of formula (II) are those where
  • HGH a 4-helix bundle protein
  • HGHBP HGHBP
  • the spacers derived from examination of HGH may be useful in designing ligands for other hematopoietic receptors, since it is known that dimeric receptor ligands share common structural features which lead to aggregation of the receptor subunits. It is expected that this method could also be generalized to other receptor-ligand complexes when their crystal structures become available.
  • the receptor binding moieties which attach to these spacers can be either peptides or small molecules from a natural or synthetic source.
  • the peptide sequences could be chosen from but not limited to linear and cyclic sequences known to be important for binding of hematopoietic proteins to their receptors .
  • Particularly interesting are those sequences found in helices one and four of the four ⁇ -helix bundle class of protein ligands, since these helices are important for binding and seem optimally situated for dimerization.
  • the helices unlike the loop regions of these receptors, are very similar in orientation throughout this class of
  • -10- proteins The identity of the possible small molecules could be chosen from but not limited to agonists and antagonists derived from database screens and peptide mimetics .
  • the receptor binding moieties of the non-antibody multimeric receptor ligands of the present invention can be identical, yielding homomultimeric compounds, or they can be different, yielding heteromultimeric compounds.
  • non-antibody multimeric receptor ligands could be synthesized by reacting a bifunctional monomer bound to a solid support with a receptor binding moiety to form a reaction product followed by cleaving the reaction product from the solid support, wherein the two functional groups are identical and symmetrically placed after cleavage.
  • Those of ordinary skill in this art would recognize that any single peptide or small organic molecule could be coupled to the spacer substitution centers to provide homomultimeric receptor ligand candidates.
  • Heteromultimeric compounds can be produced through combinatorial chemistry methods in which a library of compounds is synthesized. Combinatorial synthetic methods known to those skilled in the art can produce library members simultaneously as a mixture or individually. Diverse sets of biopolymers such as peptides containing naturally occurring and non- naturally occurring oc- and ⁇ -amino acids, oligonucleotides and oligosaccharides as well as small organic molecules can be produced.
  • Linear peptide and oligonucleotide libraries can be produced by synthesis on a solid support, such as synthesis beads, followed by cleavage from their supports . Solution synthetic methods could also be employed.
  • the core structure is
  • Non-antibody heteromultimeric receptor ligand candidates are provided by substitution of library members onto the spacer.
  • the spacer is coupled to a solid support such as a synthesis bead and the combinatorial library members are built out from the substitution centers present on the spacer.
  • the resulting ligand candidates are cleaved from the support by techniques well known to those skilled in the art.
  • Another aspect of the present invention is a method for identifying agonists and antagonists of multimeric receptors and the multimeric receptor ligands identified thereby.
  • a multimeric receptor is contacted with non-antibody multimeric receptor ligand candidates .
  • Ligand candidates which bind to the multimeric receptor are selected by receptor binding assays well known to those skilled in the art.
  • a target receptor in isolated, immobilized or cell-bound form is contacted with a plurality of receptor ligand candidates and those candidates which bind to and interact with the receptor are selected. Binding or interaction can be measured directly by using radioactively labeled ligand candidates or by measuring any second messenger effect resulting from the interaction or binding of the ligand candidate.
  • the ligand candidates can be subjected to competitive binding assays in which a known receptor ligand, labeled preferably with an analytically
  • -12- detectable reagent most prefereably radioactivity, is included with the ligand candidates and a candidate's ability to inhibit the binding of the labeled ligand is measured.
  • Positive multimeric receptor ligand binding candidates are screened for biological function by any one of the receptor function assays well known to those skilled in the art. It is expected that a positive ligand binding candidate will exhibit agonist or antagonist activity in receptor function assays. Any agonist or antagonist compounds identified can be isolated by affinity chromatography . Other isolation techniques for multimeric small organic molecules include labeling the receptor binding moieties as they are being synthesized with coding agents such as oligonucleotides and peptides or tagging the moieties with structurally related molecules that can be analyzed by electron capture capillary gas chromatography.
  • COMPETITIVE BINDING ASSAY EXAMPLE A Tissue containing the appropriate target receptor is homogenized, filtered through cheesecloth and centrifuged at 1500 x g for 10 minutes. Alternatively, cell membrane preparations from cells transfected or transformed with the target receptor gene may be employed. The supernatant is decanted and the pellet is resuspended in an appropriate incubation buffer, e.g., 75 mM Tris.HCl, pH 7.4 containing 12.5 mM MgCl 2 and 1.5 mM EDTA.
  • an appropriate incubation buffer e.g., 75 mM Tris.HCl, pH 7.4 containing 12.5 mM MgCl 2 and 1.5 mM EDTA.
  • Membranes equivalent to 100 ⁇ g protein are incubated with 50 p ol radiolabeled receptor ligand and an appropriate amount of the ligand binding candidate in a total volume of 500 ⁇ l for 1 hr at 37°C.
  • the binding reaction is terminated by dilution with the addition of 5 ml of cold incubation buffer and the bound tracer is
  • the diacids produced by the methods of Examples 1 and 2 and other diacids within the scope of the invention can serve as a spacer by attachment through an amide or ester bond. They can also be reduced to the corresponding alcohols using a reducing agent such as borane, LiAlH4 or diisobutylaluminum hydride; this alcohol can be converted to a leaving group using mesyl chloride, triphenylphosphine and CCI4 or tosyl chloride. This leaving group can be used to attach the linker to the binding moieties through an ether, amine, sulfide or hydrocarbon linkage.
  • a reducing agent such as borane, LiAlH4 or diisobutylaluminum hydride
  • the diamines produced can be attached to the binding moieties through an amide, urea, carbamate or amine linkage. These diacids and diamines can be elaborated further to create other linkers or attached to a resin used in creating combinatorial libraries .
  • CO 2 H CO 2 H 4 a) n-butyllithium, CO2 ; b) CH2N2 , ethyl ether; c) C1COCOC1, ethyl ether; d) CS2 , AICI3 ; e) H 2 0 , OH-; f) diphenylphosphorylazide, triethylamine, t-butanol; g) trifluoroacetic acid
  • the monoester 2 is available in two steps from iminodibenzyl 1 (available from Aldrich Chemical Co., Milwaukee, WI . ) .
  • the iminodibenzyl is first dilithiated with two equivalents of an alkyl lithium, such as n- butyllithium, to form the dianion which is subsequently treated with carbon dioxide to form the carboxylic acid.
  • This monocarboxylic acid can then be esterified by standard techniques, such as diazomethane in ether.
  • the monoester 2 can be acylated at the 4-position by a two step procedure.
  • the iminodibenzyl 2 is first treated with oxalyl chloride to form the amide; this intermediate cyclizes to the ⁇ -ketoamide upon treatment with a Lewis acid such as AICI3, TiCl4 or FeCl3.
  • a Lewis acid such as AICI3, TiCl4 or FeCl3.
  • the ⁇ - ketoamide 3 can be converted to the diacid by treatment with an oxidizing agent such as H2O2 or NaI ⁇ 4 and hydrolysis with hydroxide anion (Hess, B.A. et al . J.
  • the diacid can also be converted to the diamine using standard Curtius conditions (diphenylphosphorylazide and triethylamine or NaN3 and ClCOCOCl) and the t-butyl carbamate produced can be hydrolyzed with trifluoroacetic acid.
  • the diol 7 is synthesized in two steps from trans- 1, 5-decalindione (available from Aldrich Chemical Co.,
  • the first-step conversion to the ⁇ , ⁇ - unsaturated ketones involves conversion to the ⁇ -phenyl selenide using a sequential addition of a strong base, such as lithium diisopropylamide or bis [trimethylsilyl] amide, and phenylselenenyl chloride, oxidation of the selenium using hydrogen peroxide or m- chloroperoxybenzoic acid followed by a quench of the oxidant and basic elimination.
  • a strong base such as lithium diisopropylamide or bis [trimethylsilyl] amide
  • phenylselenenyl chloride oxidation of the selenium using hydrogen peroxide or m- chloroperoxybenzoic acid followed by a quench of the oxidant and basic elimination.
  • the ⁇ , ⁇ -unsaturated ketones are then reduced to the corresponding axial alcohols using a bulky hydride, such as L-Selectride® (1.0 M lithium tri-sec-butylborohydride in tetrahydrofuran) or K-Selectride® (1.0 M potassium tri- sec-butylborohydride in tetrahydrofuran) , which prefer equatorial attack.
  • L-Selectride® 1.0 M lithium tri-sec-butylborohydride in tetrahydrofuran
  • K-Selectride® 1.0 M potassium tri- sec-butylborohydride in tetrahydrofuran
  • the allylic amide is then reduced to the amide by hydrogenation using Pd, Wilkinson's catalyst (tris [triphenylphosphine] rhodium[1] chloride) or Pt as a catalyst and the amide is hydrolyzed using basic hydrolysis such as NaOH, KOH or LiOOH to form the diamine 8.
  • the diol 7 can also be converted to the diacid 10 in five steps .
  • the carbonate is formed using methylchloroformate and a base such as pyridine or triethylamine.
  • the carbonate is then methylenated using Tebbe reagent and the enol ether undergoes an allylic rearrangement.
  • the ester is then hydrogenated using Pd, Wilkinson's catalyst or Pt as a catalyst to form 9.
  • the ester is then enolized using a strong base such as lithium diisopropylamide or sodium bis [trimethylsilyl] amide and the enolate is cleaved with ozone.
  • the dialdehyde produced is treated with silver oxide to form the diacid.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)

Abstract

L'invention concerne des ligands de récepteur multimères, non anticorps, leurs procédés de fabrication et d'identification et leur utilisation comme récepteurs multimères antagonistes ou agonistes.
PCT/US1998/007389 1998-04-14 1998-04-14 Ligands de recepteur WO1999052877A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2000543439A JP2002511569A (ja) 1998-04-14 1998-04-14 受容体リガンド
EP98918154A EP1071667A4 (fr) 1998-04-14 1998-04-14 Ligands de recepteur
PCT/US1998/007389 WO1999052877A1 (fr) 1998-04-14 1998-04-14 Ligands de recepteur
CA002328252A CA2328252A1 (fr) 1998-04-14 1998-04-14 Ligands de recepteur

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1998/007389 WO1999052877A1 (fr) 1998-04-14 1998-04-14 Ligands de recepteur

Publications (1)

Publication Number Publication Date
WO1999052877A1 true WO1999052877A1 (fr) 1999-10-21

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ID=22266829

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/007389 WO1999052877A1 (fr) 1998-04-14 1998-04-14 Ligands de recepteur

Country Status (4)

Country Link
EP (1) EP1071667A4 (fr)
JP (1) JP2002511569A (fr)
CA (1) CA2328252A1 (fr)
WO (1) WO1999052877A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001025277A1 (fr) * 1999-10-07 2001-04-12 Maxygen Aps Polypeptides antagonistes a chaine unique
WO2003062276A3 (fr) * 2002-01-25 2003-10-16 Asterion Ltd Variantes de polypeptides
WO2003102207A3 (fr) * 2002-05-30 2004-04-08 Centre Nat Rech Scient Nouvelles molecules multimeriques, leur procede de preparation, et leur utilisation pour la preparation de medicaments
WO2006018429A1 (fr) * 2004-08-16 2006-02-23 Novo Nordisk A/S Mutlimeres de peptides
FR2879202A1 (fr) * 2004-12-15 2006-06-16 Centre Nat Rech Scient Nouveaux ligands multimeriques de cd40, leur procede de preparation et leur utilisation pour la preparation de medicaments
US7998481B2 (en) 2004-04-05 2011-08-16 The Regents Of The University Of California Modulation of NKG2D for treating or preventing solid organ allograft rejection

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3271365A (en) * 1962-11-05 1966-09-06 Du Pont Polyesters of decahydronaphthalenedicarboxylic acid and dihydric phenols
US3361716A (en) * 1962-02-01 1968-01-02 Du Pont Polyesters of decahydro-bis-(hydroxy-methyl)-naphthalene

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT885242E (pt) * 1995-06-07 2008-06-18 Glaxo Group Ltd Péptidos e compostos que se ligam a um receptor de trombopoietina
NZ332823A (en) * 1996-05-22 2000-05-26 Smithkline Beecham Corp ,5-Diimino-3a,6a-diaryl-1,2,3,3a,4,5,6,6a-octahydroimi dazo[4,5-d]imidazoles as non-peptide G-CSF mimetics
CA2308135A1 (fr) * 1997-10-31 1999-05-14 John G. Gleason Nouveaux complexes metalliques

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3361716A (en) * 1962-02-01 1968-01-02 Du Pont Polyesters of decahydro-bis-(hydroxy-methyl)-naphthalene
US3271365A (en) * 1962-11-05 1966-09-06 Du Pont Polyesters of decahydronaphthalenedicarboxylic acid and dihydric phenols

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1071667A4 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001025277A1 (fr) * 1999-10-07 2001-04-12 Maxygen Aps Polypeptides antagonistes a chaine unique
WO2003062276A3 (fr) * 2002-01-25 2003-10-16 Asterion Ltd Variantes de polypeptides
WO2003102207A3 (fr) * 2002-05-30 2004-04-08 Centre Nat Rech Scient Nouvelles molecules multimeriques, leur procede de preparation, et leur utilisation pour la preparation de medicaments
US7741280B2 (en) 2002-05-30 2010-06-22 Centre National De La Recherche Scientifique Multimeric molecules, the preparation method thereof and use of same for the preparation of medicaments
US7998481B2 (en) 2004-04-05 2011-08-16 The Regents Of The University Of California Modulation of NKG2D for treating or preventing solid organ allograft rejection
US8637011B2 (en) 2004-04-05 2014-01-28 The Regents Of The University Of California Modulation of NKG2D
US9211328B2 (en) 2004-04-05 2015-12-15 The Regents Of The University Of California Modulation of NKG2D for prolonging survival of a hematopoietic graft
WO2006018429A1 (fr) * 2004-08-16 2006-02-23 Novo Nordisk A/S Mutlimeres de peptides
FR2879202A1 (fr) * 2004-12-15 2006-06-16 Centre Nat Rech Scient Nouveaux ligands multimeriques de cd40, leur procede de preparation et leur utilisation pour la preparation de medicaments
WO2006064133A2 (fr) 2004-12-15 2006-06-22 Centre National De La Recherche Scientifique Nouveaux ligands multimeriques de cd40, leur procede de preparation et leur utilisation pour la preparation de medicaments
WO2006064133A3 (fr) * 2004-12-15 2006-08-31 Centre Nat Rech Scient Nouveaux ligands multimeriques de cd40, leur procede de preparation et leur utilisation pour la preparation de medicaments
US8357654B2 (en) 2004-12-15 2013-01-22 Centre National De La Recherche Scientifique Multimeric CD40 ligands, method for preparing same and use thereof for preparing drugs

Also Published As

Publication number Publication date
CA2328252A1 (fr) 1999-10-21
EP1071667A1 (fr) 2001-01-31
JP2002511569A (ja) 2002-04-16
EP1071667A4 (fr) 2004-10-20

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