US2005209192A1PendingUtilityA1

Therapeutic agents - II

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Assignee: PEPLIN RESEARCH PTY LTDPriority: Jun 7, 2000Filed: Dec 1, 2004Published: Sep 22, 2005
Est. expiryJun 7, 2020(expired)· nominal 20-yr term from priority
A61P 37/04A61P 7/00A61P 37/08A61P 43/00A61P 9/00A61P 9/10A61P 39/00A61P 39/02A61P 37/06A61P 9/12A61P 3/10A61P 25/28A61P 31/00A61P 31/14A61P 31/12A61P 25/00A61P 31/18A61P 31/04A61P 35/00A61P 25/24A61P 31/22A61P 33/10A61P 29/00A61P 31/20A61P 31/16A61P 33/00A61P 31/02A61K 31/22A61K 36/47A61K 31/455A61P 17/04A61P 17/00A61P 19/02A61P 19/00C07C 69/533A61P 17/06A61P 11/06A61P 17/10Y02A50/30Y02A90/10
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Claims

Abstract

The present invention relates generally to chemical agents useful in the treatment and prophylaxis of inflammatory conditions or in the amelioration of symptoms resulting from or facilitated by an inflammatory condition in a mammalian animal including human and primate, non-mammalian animal and avian species. More particularly, the present invention provides a chemical agent of the macrocyclic diterpene family obtaining from a member of the Euphorbiaceae family of plants or botanical or horticultural relatives thereof or derivatives or chemical analogues or chemically synthetic forms of the agents for use in the treatment or prophylaxis of an inflammatory condition or in the amelioration of symptoms resulting from or facilitated by an inflammatory condition in a mammal, animal or avian species. The present invention further contemplates a method for the prophylaxis or treatment of mammalian, animal or avian subjects for inflammatory conditions including chronic or transitory inflammatory conditions or for ameliorating. the symptoms of an inflammatory condition by the topical or systemic administration of a macrocyclic diterpene obtainable from a member of the Euphorbiaceae family or botanical or horticultural relatives thereof or a derivative, chemical analogue or chemically synthetic form of the agent. The chemical agent of the present invention may be in the form of a purified compound, mixture of compounds, a precursor form of one or more of the compounds capable of chemical transformation into a therapeutically active agent or be in the form of a chemical fraction, sub-fraction or preparation or extract of the plant.

Claims

exact text as granted — not AI-modified
1 .- 118 . (canceled)  
     
     
         119 . A method for the treatment or prophylaxis of a condition associated with protein kinase C (PKC) in a subject, said method comprising administering to said subject a symptom-ameliorating effective amount of a chemical compound represented by formulae VI:  
       
         
           
           
               
               
           
         
       
       wherein: 
 R 24 , R 25  and R 26  are independently selected from hydrogen, hydroxy, R 27 , R 28 , F, Cl, Br, I, CN, OR 27 , SR 27 , NR 27 R 28 , N(═O) 2 , NR 27 OR 28 , ONR 27 R 28 , SOR 27  , SO 2 R 27 , SO 3 R 27 , SONR 27 R 28 , SO 2 NR 27 R 28 , SO 3 NR 27 R 28 , P( 27 ), P(═O)(R 27 ) 3 , Si(R 27 ) 3 , B(R 27 ) 2 , (C═X)R 29  or X(C═X)R 29  where X is selected from sulfur, oxygen and nitrogen;  
 R 27  and R 28  are each independently selected from C 1 -C 20  alkyl (branched and/or straight chained), C 1 -C 10  arylalkyl, C 3 -C 8  cycloalkyl, C 6 -C 14  aryl, C 6 -C 14  heteroaryl, C 1 -C 14  heterocycle, C 2 -C 10  alkenyl (branched and/or straight chained), C 2 -C 10  alkynyl (branched and/or straight chained), C 1 -C 10  heteroarylkyl, C 1 -C 10  alkoxyalkyl, C 1 -C 10  dihaloalkyl, trihaloalkyl, haloalkoxy, C 1 -C 10  alkyl which is unsubstituted or substituted by CN, OR 27 , SR 27 , NR 27 R 28 , N(═O) 2 , NR 27 OR 28 , ONR 27 R 28 ,SOR 27 , SO 2 R 27 ,SONR 27 R 28 ,SO 2 NR 27 R 28 , SO 3 NR 27 R 28 , P(R 27 ) 3 , P(═O)(R 27 ) 3 , Si(R 27 ) 3 , and B(R 27 ) 2 ; and  
 R 29  is selected from R 27 , R 28 CN, COR 27 , CO 2 R 27  , OR 27 , SR 27 , NR 27 R 28 , N(═O) 2 , NR 27 OR 28 , ONR 27 R 28 , SOR 27 , SO 2 R 27 , SO 3 R 27 , SONR 27 R 28 , SO 2 NR 27 R 28 , SO 3 NR 27 R 28 , P(R 27 ) 3 , P(═O)(R 27 ) 3 , Si(R 27 ) 3 , and B(R 27 ) 2 , wherein said compound is capable of modulating PKC activity, PKC dependent expression or PKC enzyme turnover and wherein said compound is administered for a time and under conditions sufficient to ameliorate one or more symptoms associated with a PKC associated condition.  
 
     
     
         120 . The method according to  claim 119  wherein R 24  is H.  
     
     
         121 . The method according to  claim 119  wherein R 24  is OAcetyl.  
     
     
         122 . The method according to  claim 119  wherein R 24  is OH.  
     
     
         123 . The method according to  claim 119  wherein R 5  and R 26  are OH.  
     
     
         124 . The method according to  claim 119  wherein the PKC-associated condition is alcoholism, Alzheimer's disease, asthma, atherosclerosis, dermatitis, autoimmune disease, bipolar disorder, blood disorder, cardiac hypertrophy, depression, diabetes, hypertension, hyperplastic dermatosis, multiple sclerosis, myocardial ischemia, osteoarthritis, psoriasis, rheumatoid arthritis, transplantation, or latent virus.  
     
     
         125 . The method according to  claim 119  wherein said chemical compound of Formula VI is obtainable from a species of  Euphorbia.    
     
     
         126 . The method according to  claim 125  wherein the species of  Euphorbia  is selected from  Euphorbia aaron - rossii, Euphorbia abbreviata, Euphorbia acuta, Euphorbia alatocaulis, Euphorbia albicaulis, Euphorbia algomarginata, Euphorbia aliceae, Euphorbia alta, Euphorbia anacampseros, Euphorbia andromedae, Euphorbia angusta, Euphorbia anthonyi, Euphorbia antiguensis, Euphorbia apocynifolia, Euphorbia arabica, Euphorbia ariensis, Euphorbia arizonica, Euphorbia arkansana, Euphorbia arteagae, Euphorbia arundelana, Euphorbia astroites, Euphorbia atrococca, Euphorbia baselicis, Euphorbia batabanensis, Euphorbia bergeri, Euphorbia bermudiana, Euphorbia bicolor, Euphorbia biformis, Euphorbia bifurcata, Euphorbia bilobata, Euphorbia biramensis, Euphorbia biuncialis, Euphorbia blepharostipula, Euphorbia blodgetti, Euphorbia boerhaavioides, Euphorbia boliviana, Euphorbia bracei, Euphorbia brachiata, Euphorbia brachycera, Euphorbia brandegee, Euphorbia brittonii, Euphorbia caesia, Euphorbia calcicola, Euphorbia campestris, Euphorbia candelabrum, Euphorbia capitellata, Euphorbia carmenensis, Euphorbia carunculata, Euphorbia cayensis, Euphorbia celastroides, Euphorbia chalicophila, Euphorbia chamaerrhodos, Euphorbia chamaesula, Euphorbia chiapensis, Euphorbia chiogenoides, Euphorbia cinerascens, Euphorbia clarionensis, Euphorbia colimae, Euphorbia colorata, Euphorbia commutata, Euphorbia consoquitlae, Euphorbia convolvuloides, Euphorbia corallifera, Euphorbia creberrima, Euphorbia crenulata, Euphorbia cubensis, Euphorbia cuspidata, Euphorbia cymbiformis, Euphorbia darlingtonii, Euphorbia defoliata, Euphorbia degeneri, Euphorbia deltoidea, Euphorbia dentata, Euphorbia depressa, Euphorbia dictyosperma, Euphorbia dictyosperma, Euphorbia dioeca, Euphorbia discoidalis, Euphorbia dorsiventralis, Euphorbia drumondii, Euphorbia duclouxii, Euphorbia dussii, Euphorbia eanophylla, Euphorbia eggersii, Euphorbia eglandulosa, Euphorbia elata, Euphorbia enalla, Euphorbia eriogonoides, Euphorbia eriophylla, Euphorbia esculaeformis, Euphorbia espirituensis, Euphorbia esula, Euphorbia excisa, Euphorbia exclusa, Euphorbia exstipitata, Euphorbia exstipulata, Euphorbia fendleri, Euphorbia filicaulis, Euphorbia filiformis, Euphorbia florida, Euphorbia fruticulosa, Euphorbia garber, Euphorbia gaumerii, Euphorbia gerardiana, Euphorbia geyeri, Euphorbia gyptosperma, Euphorbia gorgonis, Euphorbia gracilior, Euphorbia gracillima, Euphorbia gradyi, Euphorbia graminea, Euphorbia graminiea, Euphorbia grisea, Euphorbia guadalajarana, Euphorbia guanarensis, Euphorbia gymnadenia, Euphorbia haematantha, Euphorbia hedyotoides Euphorbia heldrichii, Euphorbia helenae, Euphorbia helleri, Euphorbia helwigii, Euphorbia henricksonii, Euphorbia heterophylla, Euphorbia hexagona, Euphorbia hexagonoides, Euphorbia hinkleyorum, Euphorbia hintonii, Euphorbia hirtula, Euphorbia hirta, Euphorbia hooveri, Euphorbia humistrata, Euphorbia hypericifolia, Euphorbia inundata, Euphorbia involuta, Euphorbia jaliscensis, Euphorbia jejuna, Euphorbia johnston, Euphorbia juttae, Euphorbia knuthii, Euphorbia lasiocarpa, Euphorbia lata, Euphorbia latazi, Euphorbia latericolor, Euphorbia laxiflora, Euphorbia lecheoides, Euphorbia ledienii, Euphorbia leucophylla, Euphorbia lineata, Euphorbia linguiformis, Euphorbia longecornuta, Euphorbia longepetiolata, Euphorbia longeramosa, Euphorbia longinsulicola, Euphorbia longipila, Euphorbia lupulina, Euphorbia lurida, Euphorbia lycioides, Euphorbia macropodoides, macvaughiana, Euphorbia manca, Euphorbia mandoniana, Euphorbia mangleti, Euphorbia mango, Euphorbia marylandica, Euphorbia mayana, Euphorbia melanadenia, Euphorbia melanocarpa, Euphorbia meridensis, Euphorbia mertonii, Euphorbia mexiae, Euphorbia microcephala, Euphorbia microclada, Euphorbia micromera, Euphorbia misella, Euphorbia missurica, Euphorbia montana, Euphorbia montereyana, Euphorbia multicaulis, Euphorbia multiformis, Euphorbia multinodis, Euphorbia multiseta, Euphorbia muscicola, Euphorbia neomexicana, Euphorbia nephradenia, Euphorbia niqueroana, Euphorbia oaxacana, Euphorbia occidentalis, Euphorbia odontodenia, Euphorbia olivacea, Euphorbia olowaluana, Euphorbia opthalmica, Euphorbia ovata, Euphorbia pachypoda, Euphorbia pachyrhiza, Euphorbia padifolia, Euphorbia palmeri, Euphorbia paludicola, Euphorbia parciflora, Euphorbia parishii, Euphorbia parryi, Euphorbia paxiana, Euphorbia pediculifera, Euphorbia peplidion, Euphorbia peploides, Euphorbia peplus, Euphorbia pergamena, Euphorbia perlignea, Euphorbia petaloidea, Euphorbia petaloidea, Euphorbia petrina, Euphorbia picachensis, Euphorbia pilosula, Euphorbia pilulifera, Euphorbia pinariona, Euphorbia pinetorum, Euphorbia pionosperma, Euphorbia platysperma, Euphorbia plicata, Euphorbia poeppigii, Euphorbia poliosperma, Euphorbia polycarpa, Euphorbia polycnemoides, Euphorbia polyphylla, Euphorbia portoricensis, Euphorbia portulacoides, Euphorbia portulana, Euphorbia preslii, Euphorbia prostrata, Euphorbia pteroneura, Euphorbia pycnanthema, Euphorbia ramosa, Euphorbia rapulum, Euphorbia remyi, Euphorbia retroscabra, Euphorbia revoluta, Euphorbia rivularis, Euphorbia robusta, Euphorbia romosa, Euphorbia rubida, Euphorbia rubrosperma, Euphorbia rupicola, Euphorbia sanmartensis, Euphorbia saxatilis  M. Bieb,  Euphorbia schizoloba, Euphorbia sclerocyathium, Euphorbia scopulorum, Euphorbia senilis, Euphorbia serpyllifolia, Euphorbia serrula, Euphorbia setiloba  Engelm,  Euphorbia sonorae, Euphorbia soobyi, Euphorbia sparsiflora, Euphorbia sphaerosperma, Euphorbia syphilitica, Euphorbia spruceana, Euphorbia subcoerulea, Euphorbia stellata, Euphorbia submammilaris, Euphorbia subpeltata, Euphorbia subpubens, Euphorbia subreniforme, Euphorbia subtrifoliata, Euphorbia succedanea, Euphorbia tamaulipasana, Euphorbia telephioides, Euphorbia tenuissima, Euphorbia tetrapora, Euphorbia tirucalli, Euphorbia tomentella, Euphorbia tomentosa, Euphorbia torralbasii, Euphorbia tovariensis, Euphorbia trachysperma, Euphorbia tricolor, Euphorbia troyana, Euphorbia tuerckheimii, Euphorbia turczaninowii, Euphorbia umbellulata, Euphorbia undulata, Euphorbia vermiformis, Euphorbia versicolor, Euphorbia villifera, Euphorbia violacea, Euphorbia whitei, Euphorbia xanti  Engelm,  Euphorbia xylopoda  Greenm.,  Euphorbia yayalesia  Urb.,  Euphorbia yungasensis, Euphorbia zerayschanica  and  Euphorbia zinniiflora.    
     
     
         127 . The method according to  claim 125  wherein the species of  Euphorbia  is  Euphorbia peplus.    
     
     
         128 . The method according to  claim 119  wherein said chemical compound is an angeloyl-substituted ingenane or a derivative thereof represented by Formula VI or a pharmaceutically acceptable salt of these.  
     
     
         129 . The method according to  claim 128  wherein said derivative is an ester derivative.  
     
     
         130 . The method according to  claim 129  wherein said derivative is an acetylated derivative.  
     
     
         131 . The method according to  claim 119  wherein said compound is 20-O-acetyl-ingenol-3-angelate or a derivative thereof represented by Formula VI or a pharmaceutically acceptable salt of these.  
     
     
         132 . The method according to  claim 131  wherein said derivative is an ester derivative.  
     
     
         133 . The method according to  claim 132  wherein said ester derivative is an acetylated derivative.  
     
     
         134 . The method according to  claim 119  wherein said chemical compound is ingenol-3-angelate, or a derivative thereof represented by Formula VI or a pharmaceutically acceptable salt of these.  
     
     
         135 . The method according to  claim 119  wherein said chemical agent is 20-hydroxy-ingenol-3-angelate or a derivative thereof represented by Formula VI or a pharmaceutically acceptable salt of these.  
     
     
         136 . The method according to  claim 134  or  135  wherein said derivative is an ester derivative.  
     
     
         137 . The method according to  claim 119  wherein said subject is human.  
     
     
         138 . The method according to  claim 119  wherein both R 24  and R 25  are OH.

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