WO2013117789A2 - Análogos formilados de xantocilinas como neuroprotectores - Google Patents
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- WO2013117789A2 WO2013117789A2 PCT/ES2013/070065 ES2013070065W WO2013117789A2 WO 2013117789 A2 WO2013117789 A2 WO 2013117789A2 ES 2013070065 W ES2013070065 W ES 2013070065W WO 2013117789 A2 WO2013117789 A2 WO 2013117789A2
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- 0 *C(C1)=C(*)C=C[C@]1C=C(C(NC=O)=Cc1cc(*)ccc1)NC=O Chemical compound *C(C1)=C(*)C=C[C@]1C=C(C(NC=O)=Cc1cc(*)ccc1)NC=O 0.000 description 11
- XRROQZTZOUCWGV-KNBRTIFXSA-N O=CN/C(/C(/NC=O)=C/c(cc1)cc2c1OCO2)=C\c(cc1)cc2c1OCO2 Chemical compound O=CN/C(/C(/NC=O)=C/c(cc1)cc2c1OCO2)=C\c(cc1)cc2c1OCO2 XRROQZTZOUCWGV-KNBRTIFXSA-N 0.000 description 2
- OETZACYEPUZRPJ-DUGOVBPYSA-N Oc1ccc(/C=C(/C(/NC=O)=C/c(cc2)cc(O)c2O)\NC=O)cc1 Chemical compound Oc1ccc(/C=C(/C(/NC=O)=C/c(cc2)cc(O)c2O)\NC=O)cc1 OETZACYEPUZRPJ-DUGOVBPYSA-N 0.000 description 2
- RPXBDFLKYKJUEK-UHFFFAOYSA-N C=[O][Sn]/C(/C(N)=O)=C/[AlH2] Chemical compound C=[O][Sn]/C(/C(N)=O)=C/[AlH2] RPXBDFLKYKJUEK-UHFFFAOYSA-N 0.000 description 1
- OJZOPGITQYWEDA-UHFFFAOYSA-N C=[O][Sn]/C(/N=C=O)=C/[AlH2] Chemical compound C=[O][Sn]/C(/N=C=O)=C/[AlH2] OJZOPGITQYWEDA-UHFFFAOYSA-N 0.000 description 1
- IHFDJDSEJZOERU-UHFFFAOYSA-N [H][Sn]/C(/N=C=O)=C/C(CC1)CC2=C1OCO2 Chemical compound [H][Sn]/C(/N=C=O)=C/C(CC1)CC2=C1OCO2 IHFDJDSEJZOERU-UHFFFAOYSA-N 0.000 description 1
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- C07C233/18—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 singly-bound oxygen atoms 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 hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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- C12R2001/82—Penicillium chrysogenum
Definitions
- the invention relates to the use of formulated analogs of xanthocycins and their derivatives for the treatment of neurodegenerative diseases, cognitive deficits, dementias and especially Alzheimer's disease.
- AD Alzheimer's disease
- acetylcholinesterase (AChE) inhibitors and memantine, an inhibitor of the NMDA glutamatergic receptor (N-methyl-D-aspartic acid).
- Current therapeutic options against AD are based on the inhibition of acetylcholinesterase with drugs such as donepezil, galantamine or rivastigmine, or on the ability of memantine to antagonize the NMDA receptor.
- drugs such as donepezil, galantamine or rivastigmine
- memantine an inhibitor of the NMDA glutamatergic receptor
- MCI also known as incipient dementia or isolated memory impairment
- MCI is one of the previous stages associated with AD and other dementias.
- MCI is recognized as a risk factor for AD, and affects about 30 million people worldwide, and is considered as a previous step to AD, where between 10 and 15% of individuals with MCI progress to AD every year (Grundman et al. Arch. Neurol 2004; 61 [1]: 59-66).
- the activity of one of the two compounds was evaluated against Escherichia coli, Candida albicans, Staphylococcus aureus, Burkholderia thailandersis and Fusarium pallidoroseum, but showed no activity in these trials.
- the authors of the present invention have identified a series of compounds corresponding to formylated xanthocycline analogs, obtained from an extract produced by a strain of the Penicillium chrysogenum species, which have demonstrated a surprising neuroprotective effect against neuronal death caused Oxidative damage, which gives them beautiful properties as neuroprotective compounds.
- the in vitro antioxidant capacity analysis of these compounds has surprisingly shown that these compounds are antioxidants.
- the experimental results obtained show the potential use of the formulated analogs of xanthocycins in the prevention and / or treatment of neuronal death associated with neurodegenerative diseases, cognitive deficits, dementias, diseases associated with aging, pathological processes associated with age and progeria .
- the results obtained can be extrapolated for prophylactic or therapeutic purposes for application to the population at risk.
- a first aspect of the present invention is constituted by a compound of formula (I):
- Ri is selected from alkyl, OH, O-alkyl, SH, S-alkyl, NH 2 , H-alkyl, N (alkyl) 2 and halogen
- R 2 , R 3 and R 4 are independently selected from hydrogen, alkyl, OH , O-alkyl, SH, S-alkyl, H 2 , NH-alkyl, N (alkyl) 2 and halogen
- Ri and R 2 and / or R 3 and R 4 form a group -O-alkylene-O-, or a pharmaceutically acceptable salt, solvate or prodrug thereof, for use in the prevention and / or treatment of neurodegenerative diseases.
- the invention is directed to compounds of formula (II):
- Ri is selected from alkyl, OH, O-alkyl, SH, S-alkyl, NH 2 , NH-alkyl, N (alkyl) 2 and halogen
- R 2 , R 3 and R 4 are independently selected from hydrogen, alkyl, OH , O-alkyl, SH, S-alkyl, NH 2 , NH-alkyl, N (alkyl) 2 and halogen
- Ri and R 2 and / or R 3 and R 4 form a group -O-alkylene-O-, or a pharmaceutically acceptable salt, solvate or prodrug thereof, with the proviso that formula (II) does not include:
- R 2 and R 4 are hydrogen and Ri and R 3 are independently selected from OH and methoxy.
- the invention is directed to a pharmaceutical formulation comprising a compound of formula (II) and a pharmaceutically acceptable carrier.
- the invention is also directed to a compound of formula (II) for use in medicine.
- the invention is directed to a process for the preparation of a compound of formula (II) from an extract produced by the Penicillium chrysogenum species.
- the invention is directed to a process for the preparation of a compound of formula (II) comprising:
- R represents an alkyl group
- SE means a protective group
- the invention is directed to a strain of microorganism of the species Penicillium chrysogenum deposited in the CECT with the registration number CECT 20783.
- Figure 1 is the photograph of the sample M082-08, which belongs to a marine sponge taken in Cabo de Gata (Almer ⁇ a).
- Figure 2 is the photograph of the isolate as pure culture of the sample M082-08 inoculated on a petri dish with PD A-marine medium, the isolate strain was designated 0882_08.
- Figure 3 is a bar chart showing the protection of different dilutions of extract 08 055 C08 against cell death caused by xanthine 10 ⁇ 7 xanthine oxidase 60 mU / mL (XXO).
- the figure shows the percentage of cell death (taking 100% produced by XXO) of cultures treated with dilutions 1/100, 1/400, 1 / 1,000, 1 / 4,000 and 1 / 10,000 of the extract in the presence of XXO , representing the means ⁇ SD of an experiment in triplicate.
- * Significant difference with respect to XXO treatment according to the Student test (p ⁇ 0.05).
- Figure 4 is a list of the lethal, sublethal, teratogenic and toxicological parameters observed at 48 hours post-treatment in zebrafish embryos exposed to extract 08_055 C08 at dilutions 1/100, 1/200 and 1/400.
- Figure 5 is the sequencing of the fragment obtained by PCR of the 28 S gene of strain 0882_08.
- Figure 6 is the chromatogram of the low resolution FIPLC / MS analysis of compounds with molecular weights of m / z 340 (corresponding to peak G27) and m / z 324 (peak G28) obtained from fractionation of extract 08 055 C08 .
- Figure 7 is the mass spectrum (ESI-TOF) of peak G28 and corresponding to compound PS0156.
- Figure 8 is the 1 H NMR spectrum of the G28 peak and corresponding to compound PS0156.
- Figure 9 is the 13 C NMR spectrum of peak G28 and corresponding to compound NPS0156.
- Figure 10 shows the chemical shifts of 1H (500 MHz) and 13 C (125 MHz) for compound PS0156 in DMSO-d6.
- Figure 11 is the mass spectrum (ESI-TOF) of peak G27 and corresponding to compound PS0155.
- Figure 12 is the 1 H NMR spectrum of the G27 peak and corresponding to compound PS0155.
- Figure 13 is a diagram showing the correlations observed in the COZY (red) and FIMBC (blue) spectra for the aromatic protons of the 3,4-dihydroxyphenyl substituent.
- Figure 14 shows the chemical shifts of 1H (500 MHz) and 13 C (125 MHz) for compound PS0155 in DMSO-d6.
- Figure 15 shows in (A) the normalized cell index of SK-N-MC human neuroblastoma cells treated for 24 h with XXO and various concentrations of PS0155 (from 10 to 4,000 ng / ml).
- the XY scatter plot shows the real-time measurement of a representative test, in duplicate measurements; and in (B) the percentage of the normalized cell index referred to the cells treated with XXO and with PS0155 at the indicated concentrations at 20 h post treatment.
- the results are the mean ⁇ SEM of two tests performed in duplicate. * Significant difference with respect to XXO treatment according to the Student test (p ⁇ 0.05).
- Figure 16 shows in (A) the normalized cellular index of SK-N-MC human neuroblastoma cells treated for 24 h with XXO and various concentrations of NPS0156 (10 to 4,000 ng / ml).
- the XY scatter plot shows the real-time measurement of a representative test, in duplicate measurements; and in (B) the percentage of the normalized cellular index referred to the cells treated with XXO and with NPS0156 at the indicated concentrations at 20 h post treatment.
- the results are the mean ⁇ SEM of two tests performed in duplicate. * Significant difference with respect to XXO treatment according to the Student test (p ⁇ 0.05).
- Figure 17 shows in (A) the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA, for the carrier cells of the wild-type APP variant (APPwt) treated with camptothecin (CPT) 50 ⁇ during 6 h and for pre-treatment for 24 h with NPS0155 at 4 and 10 ⁇ g / ml followed by treatment with CPT (the percentage of apoptosis indicated is measured on the sub- region Gl of each of the conditions.); and in (B) the representative histograms showing the percentage of DNA fragmentation referred to APPwt cells treated with CPT and with pre-treatment with NPS0155 at 4 and 10 ⁇ g / ml, representing the means ⁇ SD of two independent experiments by sixfold.
- A the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA
- Figure 18 shows in (A) the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA, for the carrier cells of the Swedish APP variant (APPswe) treated with 50 ⁇ CPT for 6 h and for pre-treatment for 24 h with NPS0155 at 4 and 10 ⁇ g / ml followed by treatment with CPT (the percentage of apoptosis indicated is measured on the sub-Gl region of each of the conditions.); and in (B) the representative histograms showing the percentage of DNA fragmentation referred to APPswe cells treated with CPT and with pre-treatment with NPS0155 at 4 and 10 ⁇ g / ml, representing the means ⁇ SD of two independent experiments by sixfold. * Significant difference with respect to the treatment with CPT according to the Student test (p ⁇ 0.05).
- Figure 19 shows in (A) the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA, for the carrier cells of the wild-type APP variant (APPwt) treated with 50 ⁇ CPT for 6 h and for pretreatment for 24 h with NPS0156 at 4 and 10 ⁇ g / ml followed by treatment with CPT (the percentage of apoptosis indicated is measured on the sub-Gl region of each of the conditions.); and in (B) representative histograms showing the percentage of DNA fragmentation referred to APPwt cells treated with CPT and with pre-treatment with NPS0156 at 4 and 10 ⁇ g / ml, representing the means ⁇ SD of two independent experiments by sixfold. * Significant difference with respect to the treatment with CPT according to the Student test (p ⁇ 0.05).
- Figure 20 shows in (A) the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA, for the carrier cells of the Swedish APP variant (APPswe) treated with 50 ⁇ CPT for 6 h and for pretreatment for 24 h with NPS0156 at 4 and 10 ⁇ g / ml followed by treatment with CPT (the percentage of apoptosis indicated is measured on the sub-Gl region of each of the conditions.); and in (B) representative histograms showing the percentage of DNA fragmentation referred to APPswe cells treated with CPT and with the pre treatment with PS0156 at 4 and 10 ⁇ g / ml, representing the means ⁇ SD of two independent experiments per sextuplicate. * Significant difference with respect to the treatment with CPT according to the Student test (p ⁇ 0.05).
- Figure 21 shows the synthesis scheme of an xanthocillin X derivative, as an example of the synthesis route to generate the analogs of compound PS0155.
- the steps indicated consist of: a. H 3 ac, THF, ta., 3 days; b. N-Bu 3 SnH, Pd (PPh 3 ) 4 , THF, 0 ° C, 0.5 h; C. Pb (OAc) 4 , TMS (CH 2 ) 2 OH, DMF, 0 ° C to 50 ° C, 8 h; d. Pb (OAc) 2 , CuCL 2 , THF, 0 ° C, 0.5 h; and.
- Figure 22 shows the nature of groups A to P representing Ar 1 and Ar 2 on the schematic structure in (II), which defines a family of xanthocycline derivatives.
- Figure 23 is a matrix showing the value of the CLOGP, defined as the log P of a compound, which is the partition coefficient between n-octanol and water, log (c oc tanoi / cagua), of the different combinations of substituents of the molecule of formula (II).
- Figure 24 shows the synthesis scheme of compounds PS0158 (G + G), PS0159 (F + F), PS0160 (P + P), NPS0161 (H + H) and PS0163 (J + J).
- Figures 25-28 show in (A) the normalized cell index of SK-N-MC human neuroblastoma cells treated for 24 h with XXO and various concentrations of the synthesized analogs (100 to 1000 ng / ml).
- the XY scatter plot shows the real-time measurement of a representative test, in duplicate measurements; and in (B) the percentage of the normalized cell index referred to the cells treated with XXO and with the analogues synthesized at the indicated concentrations at 20 h post treatment.
- Figures 25-28 correspond respectively to the results of analogs PS0158 (G + G), PS0159 (F + F), PS0160 (P + P) and PS0161 (H + H). The results are the mean ⁇ SD of 2-3 trials performed in duplicate. * Significant difference with respect to XXO treatment according to the Student test (p ⁇ 0.05).
- Figure 29 shows the results obtained with analogs PS0158, PS0159, PS0160 and PS0161 on the production of Reactive Oxygen Species (ROS) corrected for LDH (lactate dehydrogenase activity), as a measure of cell viability, with respect to XXO treatment of each analog in a dose response curve.
- ROS Reactive Oxygen Species
- LDH lactate dehydrogenase activity
- Figure 30 shows in (A) the flow cytometry analysis of the propidium iodide fluorescence against the amount of DNA, for pre-treated SK-N-MC cells for 24 h with NPS0158 and NPS0159 at 10 ⁇ g / ml, NPS0160 at 1 ⁇ g / ml and NPS0161 at 0.4 ⁇ g / ml followed by treatment with camptothecin (CPT) 50 ⁇ for 6 h (the percentage of apoptosis indicated is measured on the sub-Gl region of each of the conditions.) ; and in (B) representative histograms showing the percentage of DNA fragmentation referred to SK-N-MC cells treated with CPT. Z-VAD-fmk is used as a commercial apoptosis inhibitor. The results represent the means ⁇ SD of two independent experiments in quadruplicate. * Significant difference with respect to the treatment with CPT according to the Student test (p ⁇ 0.05).
- a "neurotoxic substance” as used herein is chemical substances that produce functional, structural and biochemical alterations of the central nervous system. These adverse effects involve changes that cause deregulation or alteration of the nervous system. The nature of such change may be neurochemical, morphological, or behaviorally related and may manifest itself temporarily or permanently.
- neurodegenerative disease includes diseases that result from degeneration or deterioration of nerve tissue, particularly neurons, which leads, over time, to dysfunction or inability;
- degeneration includes loss of cell viability, loss of cell function and / or loss of cell numbers (neurons and others).
- Illustrative, non-limiting examples of neurodegenerative diseases include Alzheimer's disease, mild cognitive impairment, Huntingon's disease, Parkinson's disease, Creutzfeldt-Jakob disease, Alexander's disease, cognitive and / or psychomotor deficits, ataxias, dementias, cerebrovascular diseases, Amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), as well as diseases associated with aging, pathological processes associated with age and progeria.
- ALS Amyotrophic lateral sclerosis
- MS multiple sclerosis
- said neurodegenerative disease is a disease related to neuronal death caused by a neurotoxic substance, for example, a substance that produces endoplasmic reticulum stress, apoptosis, cytoskeleton disorganization, basal ganglia degeneration or mitochondrial damage.
- a neurotoxic substance for example, a substance that produces endoplasmic reticulum stress, apoptosis, cytoskeleton disorganization, basal ganglia degeneration or mitochondrial damage.
- neuronal degeneration and “neuroprotector”, as used herein, refer to the attenuation of the effects of neuronal degeneration or death by any known mechanism or by knowing for example, necrosis, apoptosis, autophagy, excitotoxicity, oxidative damage , mitochondrial damage, endoplasmic reticulum damage, byproduct deposition, loss of cellular architecture, etc., or the disappearance of the effects of degeneration or neuronal death by any known mechanism or by knowing for example, necrosis, apoptosis, autophagy, excitotoxicity , oxidative damage, mitochondrial damage, endoplasmic reticulum damage, byproduct deposition, loss of cellular architecture, etc., or the decrease or disappearance of its side effects.
- subject refers to a member of a mammalian species, and includes, but is not limited to, pets, primates and humans; preferably, the subject is a human being, male or female, of any age or race. In a particular embodiment, said subject is a mammal that suffers, or is susceptible to suffering from a neurodegenerative disease, such as a chronic neurodegenerative disease or a disease associated with aging.
- a neurodegenerative disease such as a chronic neurodegenerative disease or a disease associated with aging.
- salt should be understood as meaning any form of xanthocycline derivatives in which the compound assumes an ionic form, or is charged and coupled with a counterion (a cation or anion) or is in solution. This is why it should be understood also complexes of the active compound with other molecules and ions, and in particular complexes that are complexed through ionic interactions.
- solvate should be understood as meaning any form of the xanthocycline derivative of formula (I) that has another molecule (more likely a solvent) attached through a non-covalent bond.
- solvates include hydrates and alcoholates, for example methanolate.
- the solvates are pharmaceutically acceptable solvates.
- prodrug or “prodrug” is used in its broadest sense and encompasses those derivatives that are converted in vivo into the compounds of the invention. Those skilled in the art would readily produce such derivatives, and include, depending on the functional groups present in the molecule and without limitation, the following derivatives of the present compounds: esters, amino acid esters, phosphate esters, carbamates, amides, etc. Examples of well-known methods for producing a prodrug of a given performance compound are known to those skilled in the art and can be found, for example, in Krogsgaard-Larsen et al, "Textbook of Drugdesign and Discovery” Taylor & Francis (April 2002 ).
- Particularly favorable derivatives or prodrugs are those that increase the bioavailability of the compounds of this invention when such compounds are administered to a patient (for example, allowing a compound administered orally to be more easily absorbed in the blood) or those that increase the administration of the original compound to a biological compartment (for example, the brain or lymphatic system) in relation to the original species.
- pharmaceutically acceptable refers to molecular compositions and entities that are physiologically tolerable and do not normally produce allergic reactions or similar unfavorable reactions such as gastric disorders, dizziness, and reactions of the same style, when administered in humans or animals.
- alkyl refers to a hydrocarbon chain, linear or branched, consisting of carbon and hydrogen atoms, which does not contain unsaturations, and having one to twelve carbon atoms, preferably one to eight carbon atoms, plus preferably one to six carbon atoms, and that is attached to the rest of the molecule through a single bond.
- alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl and hexyl.
- halogen includes fluorine, chlorine, bromine or iodine.
- alkylene in the substituent “O-alkylene-O” refers to a hydrocarbon chain, linear or branched, consisting of carbon and hydrogen atoms, which does not contain unsaturations, and which has one to twelve carbon atoms, preferably from one to eight carbon atoms, more preferably from one to six carbon atoms, and which is attached to the oxygen atoms through a single bond.
- O-alkylene-O examples include O-methylene-0 (0-CH 2 -0), O-ethylene-0 (0-CH 2 -CH 2 0), O-propylene-0 (0-CH 2 -CH 2 -CH 2 0) or O-butylene-0 (0-CH 2 - CH 2 -CH 2 -CH 2 0).
- the present invention relates to a compound of formula (I), as previously defined, or a pharmaceutically acceptable salt, prodrug or solvate, for use in the prevention and / or treatment of neurodegenerative diseases.
- Ri is selected from alkyl, OH and O-alkyl, or Ri is bound to R 2 forming a -O-alkylene-O group.
- R 2 , R 3 and R 4 are independently selected from hydrogen, alkyl, OH and O-alkyl, or R 2 is linked to Ri forming a group - O-alkylene-O, and / or R 3 and R 4 are linked together forming an -O-alkylene-O group.
- R 4 is in the meta position of the aromatic ring.
- Ri is OH, alkyl or form, together with R 2 , a group -O-alkylene-O. More preferably, Ri is OH, methoxy, ethoxy, ethyl, methyl or forms, together with R 2 , a -O-alkylene-O group. Also preferably, R 2 is hydrogen, OH, alkyl or form, together with Ri, a group -O-alkylene-O. More preferably, R 2 is hydrogen, OH, ethyl, methyl or forms, together with Ri, a group -O-alkylene-O.
- R 3 is OH, alkyl or form, together with R 4 , a group -O-alkylene-O. More preferably, R 3 is OH, ethyl, methyl or forms, together with R 4 , a group -O-alkylene-O.
- R 4 is hydrogen, OH, alkyl or form, together with R 3 , a -O-alkylene-O group. More preferably, R 4 is hydrogen, OH, ethyl, methyl or forms, together with R 3 , a group -O-alkylene-O.
- the compound of formula (I) is selected from the following compounds:
- results of the research carried out by the inventors demonstrate that the prevention and / or treatment of neurodegenerative diseases, mild cognitive impairment, cognitive deficits, dementias, diseases associated with aging and / or pathological processes associated with age and progeria with the analogues of Xanthocycins described in the present invention, takes place, at least partially, by neuroprotection, in particular by direct inhibition of neuronal death, that is, by inhibiting the death of neuronal cells of the nervous system. Therefore, this mechanism of action would take place without the involvement of the immune system.
- neurodegenerative diseases are selected from Alzheimer's disease, mild cognitive impairment, Huntingon's disease, Parkinson's disease, Creutzfeldt-Jakob disease, Alexander's disease, cognitive and / or psychomotor deficits, ataxias, dementias, cerebrovascular diseases, amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), as well as diseases associated with aging, pathological processes associated with age and progeria.
- said neurodegenerative disease is Alzheimer's disease.
- the compounds of formula (I) may be in the form of salts, preferably pharmaceutically acceptable salts, in the form of solvates, preferably pharmaceutically acceptable solvates, or in the form of prodrugs.
- Said pharmaceutically acceptable salts, solvates or prodrugs of the compound of formula (I), when administered to the recipient, can provide (directly or indirectly) a compound of formula (I) such as that described herein.
- Pharmaceutically acceptable salts are also within the scope of the invention because they can be useful for preparing pharmaceutically acceptable salts.
- salts and solvates can be carried out by methods known in the art.
- pharmaceutically acceptable salts of compounds provided herein are synthesized from the original compound, which contains one or more basic moieties, by conventional chemical methods.
- such salts are prepared, for example, by reacting the free base forms of these compounds with the appropriate base or acid in water or in an organic solvent or in a mixture of the two.
- non-aqueous media such as ether, ethyl acetate, ethanol, isopropanol or acetonitrile are preferred.
- acid addition salts include inorganic acid addition salts such as, for example, hydrochloride, hydrobromide, iodhydrate, sulfate, nitrate, phosphate, etc., and addition salts of organic acid such as, for example, acetate, maleate, fumarate, citrate, oxalate, succinate, tartrate, malate, mandelate, methanesulfonate, p-toluenesulfonate, etc.
- inorganic acid addition salts such as, for example, hydrochloride, hydrobromide, iodhydrate, sulfate, nitrate, phosphate, etc.
- organic acid such as, for example, acetate, maleate, fumarate, citrate, oxalate, succinate, tartrate, malate, mandelate, methanesulfonate, p-toluenesulfonate, etc.
- a preferred pharmaceutically acceptable form is the crystalline form, including such form in a pharmaceutical composition.
- the additional solvent and ionic residues must also be non-toxic.
- the compounds of the invention can have different polymorphic forms, it is intended that the invention encompasses all these forms.
- any compound that is a prodrug of a compound of formula (I) is within the scope of the invention.
- the compounds of the invention are also intended to include compounds that differ only in the presence of one or more isotopically enriched atoms.
- compounds having the present structures, except for the substitution of a hydrogen for a deuterium or tritium, or the substitution of a carbon for a carbon enriched in 13 C or in 14 C or a nitrogen enriched in 15 N are found within the scope of this invention.
- the compounds of the present invention represented by the formula (I) described above may include isomers such as enantiomers or diastereoisomers depending on the presence of chiral centers.
- the unique isomers, enantiomers or diastereoisomers and mixtures thereof are within the scope of the present invention.
- the xanthocycline analogs of formula (I) may be formulated in a pharmaceutical composition, in a therapeutically effective amount, together with one or more pharmaceutically acceptable carriers or excipients.
- Said pharmaceutical composition may contain one or more analogs of xanthocycins of formula (I) or one or more other drugs, together with one or more pharmaceutically acceptable carriers or excipients.
- said pharmaceutical composition comprises only an xanthocycline derivative of formula (I).
- Said pharmaceutical composition is useful for the treatment of neurodegenerative diseases.
- Pharmaceutical compositions comprising the xanthocycline analogs of formula (I) may be formulated in any pharmaceutical form of administration suitable for administration by the route of administration chosen.
- the pharmaceutical compositions may be formulated in a solid pharmaceutical form for oral administration (eg, granules, tablets, capsules, etc.), in a liquid pharmaceutical form for oral administration (eg, solutions, suspensions, emulsions, etc.), in a pharmaceutical form for parenteral administration (eg, solutions, suspensions, emulsions, etc.).
- a solid pharmaceutical form for oral administration eg, granules, tablets, capsules, etc.
- a liquid pharmaceutical form for oral administration eg, solutions, suspensions, emulsions, etc.
- parenteral administration eg, solutions, suspensions, emulsions, etc.
- the pharmaceutically acceptable carriers and excipients appropriate for the chosen dosage form and route of administration will be chosen, for example, binders, diluents, disintegrants, lubricants, humectants, etc., for the formulation of forms solid administration pharmaceuticals, and buffers, surfactants, etc., for the formulation of liquid pharmaceutical dosage
- Such vehicles and excipients must be pharmaceutically acceptable and pharmacologically tolerable and must be able to be combined with other components of the formulation without exerting any adverse effect on the treated subject.
- Information on said vehicles and excipients, as well as on said pharmaceutical forms of administration of said active ingredient can be found in galenic pharmacy treaties.
- a review of the different pharmaceutical forms of administering drugs, in general, and their methods of preparation can be found in the book "Tratado de Farmacia Galenica", C. Fauli i Trillo of, I Edition, 1993, Luzan 5, SA of Editions.
- the pharmaceutical composition employed in the present invention comprises at least one xanthocycline analog of formula (I) in a therapeutically efficient amount.
- therapeutically efficient amount refers to the amount of drug calculated to produce the desired effect.
- the dose of drug to be administered to a subject may vary within a wide range depending on numerous factors, including the characteristics of the drug used, eg, its activity and biological half-life, the concentration of the drug in the pharmaceutical composition, the clinical situation of the subject, the severity of the pathology, the pharmaceutical form of administration chosen, etc.
- the pharmaceutical composition provided by this invention can be administer one or more times a day for preventive or therapeutic purposes or with other administration guidelines, not necessarily daily but also on a timely, weekly basis, etc.
- the present invention is directed to the use of a compound of formula (I), or a pharmaceutically acceptable salt, prodrug or solvate thereof, for the manufacture of a medicament aimed at the prevention and / or treatment of neurodegenerative diseases. .
- the present invention relates to a method for the prevention or treatment of neurodegenerative diseases, in a subject in need of treatment, which comprises administering to said subject a pharmaceutical composition comprising a therapeutically efficient amount of one or more compounds of formula (I), or a pharmaceutically acceptable salt, prodrug and / or solvate thereof.
- this method of prevention or treatment acts by neuroprotection, in particular by direct inhibition of neuronal death.
- the pharmaceutical composition used for the prevention or treatment of said diseases can be used together with other drugs, for example, drugs useful in the treatment of neurodegenerative diseases, cognitive deficits, dementias or diseases associated with aging, with in order to increase the efficiency of the pharmaceutical composition, thereby generating a combination therapy.
- additional drugs may be part of the same pharmaceutical composition or, alternatively, they may be provided as a separate pharmaceutical composition for administration at the same time (simultaneous administration) as the pharmaceutical composition employed or at different times (sequential administration).
- examples of additional drugs that may be part of the same therapy or pharmaceutical composition together with the xanthocycline analogs of formula (I) are: drugs for the treatment of Alzheimer's (tacrine, rivastigmine, memantine, donepezil, galantamine, statins %), from parkinson's (carbidopa, levodopa, bromocriptine, pramipexole, ropinirole, amantadine, rasagiline Among others, antipsychotics such as haloperidol, antidepressants such as amitriptyline, anxiolytics such as lorazepam, anti-inflammatories such as aspirin, dietary supplements such as vitamins E, C, B, folate or Ginkgo biloba extract or drugs against the rest of neurodegeneratives indicated in the patent.
- the present invention is directed to a compound of formula (II) as previously defined, or to a pharmaceutically acceptable salt, prodrug or solvate thereof. They are excluded from this formula:
- R 2 and R 4 are hydrogen and Ri and R 3 are independently selected from OH and methoxy.
- Ri is selected from methyl, ethyl and ethoxy. In another particular embodiment, Ri is selected from alkyl, OH and O-alkyl, or Ri is bound to R 2 forming a -O-alkylene-O group.
- R 2 , R 3 and R 4 are independently selected from hydrogen, alkyl, OH and O-alkyl, or R 2 is linked to Ri forming a group - O-alkylene-O, and / or R 3 and R 4 are linked together forming an -O-alkylene-O group.
- R 4 is in the meta position of the aromatic ring.
- Ri is OH, O-alkyl, alkyl or form, together with R 2 , a -O-alkylene-O group. More preferably, Ri is OH, methoxy, ethoxy, ethyl, methyl or forms, together with R 2 , a -O-alkylene-O group.
- R 2 is hydrogen, OH, alkyl or form, together with Ri, a group -O-alkylene-O. More preferably, R 2 is hydrogen, OH, ethyl, methyl or forms, together with Ri, a group -O-alkylene-O.
- R 3 is OH, O-alkyl, alkyl or form, together with R 4 , a group -O-alkylene-O. More preferably, R 3 is OH, methoxy, ethoxy, ethyl, methyl or forms, together with R 4 , a -O-alkylene-O group. Also preferably, R 4 is hydrogen, OH, alkyl or form, together with R 3 , a -O-alkylene-O group. More preferably, R 4 is hydrogen, OH, ethyl, methyl or forms, together with R 3 , a group -O-alkylene-O.
- the compound of formula (II) is selected from the following compounds:
- the present invention is directed to a pharmaceutical composition
- a pharmaceutical composition comprising a compound of formula (II), or a pharmaceutically acceptable salt, prodrug or solvate thereof, and a pharmaceutically acceptable carrier.
- vehicle refers to a diluent, adjuvant or excipient with which the active substance is administered.
- Such pharmaceutical vehicles may be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like.
- water or aqueous solutions of saline solution and aqueous solutions of dextrose and glycerol are used as vehicles, particularly for injectable solutions.
- Suitable pharmaceutical vehicles are described in "Remington's Pharmaceutical Sciences” by EW Martin, 1995.
- the vehicles of the invention are approved by the regulatory agency of a state or federal government or are listed in the United States Pharmacopoeia or other pharmacopoeia recognized in general for use in animals, and more particularly in humans.
- Examples of pharmaceutical compositions include any solid composition (tablets, pills, capsules, granules, etc.) or liquid (solutions, suspensions or emulsions) for oral, topical or parenteral administration.
- compositions containing compounds of the invention can be administered by encapsulation in liposomes or nanospheres, in sustained release formulations or by other usual means of administration.
- the formulations can be prepared according to conventional methods such as those described in the Spanish, European or United States Pharmacopoeias, or in similar reference texts, for example "Galenic Pharmacy Treaty", by C. Faul ⁇ i Trillo, 10 Edition, 1993, Luzán 5, SA of Editions.
- the correct dosage of the compounds will vary according to the particular formulation, the mode of application, the site and the particular neurodegenerative disease being treated. Other factors such as age, body weight, sex, diet, administration time, excretion rate, drug combinations, reaction sensitivities and disease severity should also be taken into account. Administration may be carried out continuously or periodically within the maximum tolerated dose.
- the compounds and compositions of this invention can be used with other drugs to provide a combination therapy.
- the other drugs may be part of the same composition, or they may be provided as a separate composition for administration at the same time or at a different time.
- a further aspect of the present invention is a compound of formula (II) as previously described for use in medicine.
- Another additional aspect of the present invention is the use of a compound of formula (II) for the preparation of a medicament.
- the present invention is directed to a process for the preparation of a compound of formula (II) from an extract produced by the Penicillium chrysogenum species.
- said extract is produced by a strain of microorganism of the species Penicillium chrysogenum deposited in the CECT with the registration number 20783.
- a sample is obtained from a marine sponge collected in the area of Cabo de Gata (Almer ⁇ a), from which a strain corresponding to the species Penicillium chrysogenum. Said strain makes it possible to obtain an extract from which, by fractionation and purification, the compounds of formula (II) are obtained, as described in examples 1 and 5 of the present application.
- the compounds of formula (II) can be obtained synthetically by a process comprising:
- R represents an alkyl group
- aryl group includes the substituents Ri to R4 depending on the compound of formula (II) that is desired to be obtained.
- Step a) of the route involves the transformation of an alkyl ester of the aryl propionic acid of formula (III) into its corresponding amide of formula (IV).
- said reaction is carried out by treatment with ammonia.
- the alkyl ester of aryl propionic acid is the methyl ester of aryl propionic acid.
- Step b) of the synthetic route involves a hydrostannination, so that the triple bond of the compound of formula (IV) is reduced, incorporating an alkylstannan group.
- this reaction is carried out in presence of an alkyltin hydride and is catalyzed by a palladium compound.
- the alkyl tin hydride is tributyltin hydride and the catalyst is a complex of Pd and triphenylphosphine, in particular, Pd (PPh 3 ) 4 .
- the Baumgarten oxidation reaction of step c. l) which leads to obtaining the protected carbamate of formula (VI) is carried out using an oxidizing agent, such as Pb (OAc) 4 , in the presence of a silanol, such as for example TMS (CH 2 ) 2 0H (2- Trimethylsilanyl ethanol).
- an oxidizing agent such as Pb (OAc) 4
- OAc oxidizing agent
- silanol such as for example TMS (CH 2 ) 2 0H (2- Trimethylsilanyl ethanol.
- the homoacoupling reaction d. l) is performed using a copper catalyst, for example CuCl 2 and air.
- the stage e. l) of the synthetic route is carried out in two phases, a first one in which formamido groups are incorporated by a formylation reaction in the presence of a strong base and a second one in which the carbamate group protective groups are removed.
- the mentioned incorporation of the formamido groups is carried out with a formic acetic anhydride after treatment with a strong base such as lithium hexamethyldisylilazanide (commonly known as LiHMDS).
- LiHMDS lithium hexamethyldisylilazanide
- l can be carried out using a quaternary ammonium fluoride, in particular tetra - "- butylammonium fluoride, either in the form of a trihydrate or dissolved in THF, since it is a salt commonly used to remove silyl ether protecting groups .
- a quaternary ammonium fluoride in particular tetra - "- butylammonium fluoride, either in the form of a trihydrate or dissolved in THF, since it is a salt commonly used to remove silyl ether protecting groups .
- step c.2 corresponds to step c. 1) and, therefore, is carried out with an oxidizing agent in the presence of a silanol, as mentioned for step c. l).
- Step d.2) of the synthetic route is carried out in two phases, a first in which a formamido group is incorporated by a formylation reaction after treatment with a strong base and a second in which the protective group is removed of the carbamate group.
- the mentioned incorporation of the formamido group is carried out with a formic acetic anhydride after treatment with a strong base such as lithium hexamethyldisylilazanide (commonly known as LiHMDS).
- the carbamate group deprotection phase can lead to made using a quaternary ammonium fluoride, in particular, tetra - "- butylammonium fluoride, either in its trihydrate form or dissolved in THF, since it is a salt commonly used to remove silyl ether protecting groups.
- a quaternary ammonium fluoride in particular, tetra - "- butylammonium fluoride, either in its trihydrate form or dissolved in THF, since it is a salt commonly used to remove silyl ether protecting groups.
- the homocoupling reaction e.2) is also carried out using a copper catalyst, for example CuCl 2 and air, as described for step d. l).
- reaction d.3) of transformation of the carbamate of formula (VI) into the formamide of formula (IX) is carried out in the presence of a reducing agent.
- said reducing agent is a lithium borohydride, preferably lithium triethyl borohydride.
- the homoacoupling reaction e.3) is also carried out using a copper catalyst, for example CuCl 2 and air, as described for step d.1) and e.2).
- a copper catalyst for example CuCl 2 and air, as described for step d.1) and e.2).
- This type of synthetic route allows obtaining the compounds in which the substituents Ri and R 3 and R 2 and P of each aromatic ring are the same.
- a method such as that described in Tetrahedron Letters, 2005, 46, 5017-5020 can be followed.
- a final aspect of the invention refers to a strain of microorganism of the Penicillium chrysogenum species deposited in the CECT with the registration number 20783.
- Said strain was obtained from a sea sponge, as described in example 1 of this document.
- the strain was identified by PCR and sequencing technique as described in example 4 of this document, as well as by microscopic and macroscopic observation. From said strain, it is possible to obtain an extract from which the compounds employed in the present invention are isolated as previously described and as shown in Examples 1 and 5 of this document.
- Sample M082-08 was isolated from a sea sponge taken in Cabo de Gata (Almer ⁇ a) ( Figure 1). To process the sample, a piece of the sponge was extracted with the help of sterile tweezers and scissors and several washings were carried out with Artificial Marine Water (ASW), whose composition in g / L is: KBr 0.1; NaCl 23.48; MgC12 » 6H20 10.61; KC12 » 2H20 1.47; KC1 0.66; SrC12 » 6H20 0.04; Na2S04 3.92; NaHC03 0.19; H3B03 0.03; autoclaved (Presoclave II 75 L, from JP Selecta) at 121 ° C for 20 minutes.
- ASW Artificial Marine Water
- strain 0882 08 was isolated as a pure culture with the help of a sterile planting handle, inoculating it in a 90 mm petri dish with 30 ml of PDA-marine medium after which it is incubated in an oven at 28 ° C ( Figure 2). Once the pure culture was obtained, it was grown in medium inclined agar tubes
- Power whose composition in g / L is: sucrose 15; bacteriological peptone 2,5; lactose 2.5; corn maceration solids 0.5; NaCl 2; NaN03 1; KC1 26.1;
- a spore suspension was prepared with the following procedure: 5 ml of sterile 40% (w / v) glycerol are added to each tube and 10-15 glass beads of 5 mm in diameter The culture is stirred until a homogeneous suspension is achieved and with it the cryovials that are stored at -80 ° C are generated in a freezer (905 -86C ULT Freezer, Thermo Scientific).
- the culture preparation for obtaining the natural extract was carried out by inoculating a 13 ml polypropylene tube with 3 ml of inclined agar of solid YES medium, whose composition in g / L was: sucrose 150; yeast extract 20; MgSO4 » 7H20 0.5; agar 10; with 0.05 ml of the spore suspension stored at -80 ° C.
- the incubation of the tube was carried out in an oven at 28 ° C for 14 days. After that time, 3 mL of ethyl acetate was added to the culture, after which it was vigorously stirred with a vortex for a few seconds.
- the crude extract obtained was resuspended in 800 ⁇ of DMSO for testing on the model of cell death due to oxidative stress.
- This test is performed on cells in SK-N-MC human neuroblastoma culture from "American Type Culture Collection (ATCC, Cod. HTB-10 TM)", following strict sterility standards and handling in class biological safety cabins II that They follow the European standard EN 12469.
- the cells were kept in MEM medium (Minimun Essential Medium Eagle (MEM) supplemented with 1 mM sodium pyruvate, 2 mM L-glutamine, 0.1 mM non-essential amino acids, 0.05 mg / ml gentamicin and 10% bovine serum on these cells, the inhibition produced by the cell death extract caused by treatment with xanthine / xanthine oxidase (XXO) that causes oxidative damage (production of free radicals such as hydrogen peroxide, superoxide anion) was analyzed.
- MEM medium Minimun Essential Medium Eagle (MEM) supplemented with 1 mM sodium pyruvate, 2 mM L-glutamine, 0.1 mM non-essential amino acids, 0.05 mg / ml gentamicin and 10% bovine serum on these cells
- MEM medium Minimun Essential Medium Eagle (MEM) supplemented with 1 mM sodium pyruvate, 2 mM L-glutamine,
- WST-1 (Roche) was added, following the manufacturer's specifications.
- the WST-1 test is based on the measurement of metabolic activity so that cells that are metabolically active (live) reduce the tetrazolium salt of WST-1 to formazan by the mitochondrial respiratory chain succinate-tetrazolium reductase system .
- the formazan produced is detected colorimetrically.
- the results obtained are shown in Figure 3, as the percentage of cell death for each dilution referred to the death produced by the XXO.
- the inventors decided to evaluate the antioxidant capacity in vitro of the extract, for which the TEAC test (absorbance capacity by electron transfer) was used.
- This method is based on the formation of the radical ferryl myoglobin produced by the reaction of metmyoglobin with hydrogen peroxide, followed by oxidation of ABTS reagent [I 2,2' -azino- bis (3-ethylbenzthiazoline-6- sulfonic] by ferril-myoglobin, which produces the cation radical ABTS * +, which can be determined colorimetrically.
- the compounds with antioxidant capacity suppress the production of the radical in a concentration-dependent manner.
- trolox water-soluble vitamin E analogue
- OECD guideline for the testing of chemicals draft proposal for a new guideline: Fish Embryo Toxicity (FET) Test ".
- This test is an alternative method to the acute toxicity test with juvenile and adult fish (OECD Test Guideline 203).
- LC50 Concentration of the test sample that causes the mortality of 50% of the animals.
- NOEC Higher concentration that does not cause mortality.
- LOEC Lower concentration that produces 100% mortality.
- the test methodology was based on the use of a series of concentrations of the compound to be evaluated as well as an appropriate control. The following toxicological parameters were determined in this study.
- Lethal parameters i) determination of the number of coagulated eggs; ii) tail detachment; iii) heart rate (presence or absence); iv) formation of the somites (longitudinal series of the mesoderm that by delamination, fusion and migration become the axial skeleton, the dermis and the dorsal muscles and the wall of the body and the extremities).
- the following sublethal parameters were also studied: i) spontaneous movements; ii) pigmentation; iii) formation of edemas; iv) clot formation.
- EXAMPLE 4 Identification and escalation of strain 0882 08 4.1.
- Strain identification was performed using a PCR that amplifies 560 bp of the 28S gene.
- the PCR mixture carries the following components: PCR buffer, 1.5 mM MgC12, 0.2 mM dNTP mixture, 0.4 ⁇ oligonucleotides (NL1: 5'-gca tat caá taa gcg gag gaa aag-3 '(SEQ ID No: 1) and NL4: 5'-ggt ccg tgt ttc aag acg-3 '(SEQ ID No: 2)), DNA Polymerase PFU (Bioneer) 1 U, DNA extracted from the strain with the Wizard SV Genomic DNA Purification System kit (Promega ) at 1: 50 final dilution.
- the PCR program consisted of: denaturation in 1 cycle of 96 ° C for 5 min; amplification in 30 cycles with three temperature ramps: 94 ° C for 30 sec, 60 ° C for 40 sec and 72 ° C for 1 min; elongation in 1 cycle of 72 ° C for 10 min.
- the characteristics used in the classification were: microscopic observation, growth data, colony morphology and teleomorphic state formation, if any.
- the results of microscopic observation showed fruiting bodies (brushes) of the genus Penicillium. Conidiophores with three branching points (terverticillates) characteristic of the subgenus Penicillium. Stipe with smooth wall. Ampuliform phialides. Spherical to ellipsoidal conidia, smooth.
- the characteristics studied in the macroscopic observation were: size, texture and color of the colonies, production of exudate and diffusible pigment and observation of the reverse.
- the results are the following:
- the molecular level identification was then carried out by the following molecular methods: a) Amplification and sequencing of the ribosomal DNA zone that comprises the ITS 1 and ITS2 intergenic spaces and that includes the 5.8S rDNA gene. b) Amplification and subsequent partial sequencing of the B-Tubulin gene (with two-way readings), with primers Bt2a and Bt2b (Glas & Donaldson, Appl Environ Microb 1995; 61: 1323-30).
- the amplification products were 495 and 477 base pairs respectively.
- 100% similarity was obtained for the ITS-5.8S rDNA zone and 99% for the ⁇ -Tubulin gene with the Penicillium chrysogenum species, CBS strain 306.48.
- cultures were prepared to obtain the natural extract by inoculating with 1.2 ml of spore suspension per plate 25 plates of 14 cm in diameter containing 80 ml of YES medium, whose composition in g / L is: sucrose 150 ; yeast extract 20; MgSO4 » 7H20 0.5; agar 10; and incubating said plates at 28 ° C for 14 days.
- the culture was extracted by crushing with the help of a blender so that it was completely homogeneous, then 2300 mL of ethyl acetate was added and kept under stirring for 6 hours with the help of a stirrer. After this time the supernatant was collected and filtered through a paper funnel. The extraction was repeated by adding 1900 mL of ethyl acetate and kept under stirring for another 4 hours. The supernatant was collected next to the previous one. All this was evaporated to dryness by a rotary evaporator, resulting in 3.3 g of the dried crude extract.
- Fractionation and purification Extract 08 055 C08 was analyzed by analytical HPLC (Agilent 1 100-DAD, Column Zorbax RX-C8 5 ⁇ 4.6X250 mm) with 5-100% acetonitrile / water for 40 min and it was observed that the extract contained metabolites In all polarity ranges, a generic low pressure fractionation by wide-range adsorption / resorption resin (SP207ss) was performed on a Combiflash® automated chromatograph.
- SP207ss wide-range adsorption / resorption resin
- the fractionation was scaled, using preparative HPLC, of the positive fractions with a gradient of 2 to 20% acetonitrile / water with a Zorbax SB-C8 7 ⁇ 21.2 x 250 mm column with a flow of 20 mL / min and detection at 210 and 280 nm.
- the preparative HPLC fractions were tested to find out which peak or peaks of the chromatography exhibited protective death activity.
- ESI-TOF mass spectrum
- Figure 11 the presence in the mass spectrum of ammonium adducts (m / z 358.1365), sodium (m / z 363.0935) and potassium (m / z 379.0676) corroborate the proposed molecular formula.
- the molecule therefore seems to have the same chemical nature as the compound G28, including an additional oxygen atom in its structure.
- Compound G27 obtained in the bioassay chromatography of extract 08 055 C08, therefore has the structure of (lZ, 3Z) -l- (3,4-dihydroxyphenyl) -4- (4-hydroxyphenyl) -2, 3- diformamide-1, 3-butadiene.
- the bibliographic search of the structure also confirmed that it is a new natural product.
- EXAMPLE 6 Protective effect of peaks G27 (or compound NPS0155) and G28 (NPS0156) on neuronal death induced by oxidative stress
- the researchers decided to analyze the neuroprotective effect of the compounds PS0155 and PS0156.
- the assays were performed on cells in SK-N-MC human neuroblastoma culture, maintained as detailed in Example 2.
- the inhibition produced by both compounds of cell death caused by xanthine / xanthine oxidase treatment was analyzed in real time. which produces oxidative damage (generating free radicals such as hydrogen peroxide, superoxide anion, hydroxyl radical) which triggers cell death.
- oxidative damage generating free radicals such as hydrogen peroxide, superoxide anion, hydroxyl radical
- These cells in pass not exceeding 15, were seeded on plates of 16 specific wells for real-time testing with the RTCA system (Real-Time Cell Analyzer, XCelligence, Roche) with a cell concentration of 5x104 cells / well.
- cell treatments were carried out for the control conditions (culture medium); XXO (xanthine 10 ⁇ 7 xanthine oxidase 60 mU / mL); XXO plus G27 or G28 at 10, 40, 100, 400, 1000 or 4000 ng / ml.
- the cells were incubated (at 37 ° C and 5% C02) with these treatments for 72 h, collecting readings every 10 minutes.
- the values obtained are arbitrary units indicated by the cellular index, calculated from the impedance values, which is a magnitude that establishes the relationship between the voltage and the current intensity of the adhered cells and that is used as a measure of cell viability.
- the results obtained for compound PS0155 are shown in Figure 15 as the normalized cell index (A) of each condition analyzed throughout the treatment and as a percentage of cell death (B) for each treatment referred to the death produced by the XXO at 20 h post-treatment. Death protection was observed in the range of 100 to 400 ng / ml of PS0155, the maximum being 27% at 100 ng / ml, so this compound shows a protective effect of the death of human cells of neuronal origin caused Oxidative stress
- the results obtained for compound PS0156 are shown in Figure 16 as the normalized cell index (A) of each condition analyzed throughout the treatment and as a percentage of cell death (B) for each treatment referred to the death produced by the XXO at 20 h post-treatment. Death protection was observed in the range of 10 to 1,000 ng / ml of PS0156, the maximum being 69% at 100 ng / ml, so this compound shows a protective effect of the death of human cells of neuronal origin caused Oxid
- EXAMPLE 7 Antioxidant effect of compounds NPS0155 (G27) and NPS0156 (G2S) Based on the above results, the researchers decided to analyze the antioxidant capacity in vitro of compounds PS0155 and PS0156 using the TEAC test, described in Example 2. To To quantify the antioxidant capacity, a standard curve with increasing concentrations of trolox (water-soluble analogue of vitamin E) was used, so that the results are indicated as a measure of trolox equivalents (TE). The PS0155 test gave a result of 81 ⁇ 19 ⁇ 19 TE ⁇ g compound, indicating that this compound shows antioxidant capacity in vitro. The PS0156 test gave a result of 104 ⁇ 29 ⁇ TE ⁇ g compound, indicating that this compound shows antioxidant capacity in vitro. EXAMPLE 8. Antiapoptotic effect of compounds NPS0155 and NPS0156 in cells with wild and mutated APP
- the researchers decided to analyze the antiapoptotic effect of the compounds PS0155 and PS0156.
- the assays were performed on two cell lines in SK-N-MC human neuroblastoma culture stably transfected with constructs expressing the amyloid precursor protein (APP) gene encoding the mostly expressed isoform in the brain of 695 amino acids , cloned into the pcDNA3.1 expression vector (Invitrogen).
- APP amyloid precursor protein
- One of the lines expresses the wild APP gene (APPwt) and the other expresses the APP gene with the Swedish mutation (APPswe) which is a double mutation in exon 16 of the gene and produces a transversion from G to T resulting in the change of amino acid Lys595Asn and another transversion from A to C that produces the Met596Leu change, said mutation being related to Alzheimer's disease in its senile or hereditary form.
- the cells were maintained as the SK-N-MC parental cells, as detailed in Example 2, using geneticin at 400 ⁇ g / ml as a selection antibiotic.
- DNA fragmentation was analyzed by flow cytometry, produced by treatment with camptothecin (CPT) that inhibits topoisomerase I enzyme, which prevents DNA duplication and triggers apoptotic cell death.
- CPT camptothecin
- the two cell lines in pass not exceeding 10, were seeded on 12 well plates treated for adherent cells with a cell concentration of 4x105 cells / well. After 24 h of incubation of the cells at 37 ° C and 5% C02, the cells were pre-treated with 4 and 10 ⁇ g / mL of NPS0155 or NPS0156 for 24 h; subsequently treated with 50 ⁇ 50 CPT for 6 h.
- the cells were collected together with their culture medium and centrifuged at 300xg for 5 min. The medium was removed, washing with PBS was performed and fixed for 2 minutes with 500 ⁇ ⁇ of 70% ethanol at -20 ° C. Once fixed, they were centrifuged at 400xg for 5 min, washed with PBS and propidium iodide added to 0.05 mg / mL, diluted in a cycle buffer (0.1% sodium citrate, Nonidet P-40 0.3% and RNAse 0.02 mg / mL) and incubated 1 hour at 37 ° C. 18 ha were maintained 4 ° C and, after this time, were analyzed by flow cytometry, comparing the fluorescence of propidium iodide against the amount of DNA.
- a cycle buffer (0.1% sodium citrate, Nonidet P-40 0.3% and RNAse 0.02 mg / mL
- this example shows that compounds PS0155 and PS0156 have a protective effect of apoptosis in human cells of neuronal origin that express wild and mutated APP.
- the carbamate (4) is obtained, which has the appropriate stereochemistry to give the product (5) a homologous reaction catalyzed by palladium.
- This product has the skeleton corresponding to the type of analog of interest. The last two reactions are intended to protect the carbamates and introduce the formamide groups.
- route 3 ⁇ 4 ⁇ 5 ⁇ 6 it can be passed from 3 to isocyanate 7 by oxidation of Baumgarten (without being trapped with silanol), transform 7 into formamide 8 and then perform homocoupling to give 6 (route 3 ⁇ 7 ⁇ 8 ⁇ 6) or also, convert carbamate 4 into formamide 8 and then perform homoacoupling to give 6 (route 3 ⁇ 4 ⁇ 8 ⁇ 6).
- methoxyphenyl 1 or 2 radicals (C, D and E) (eg, 4-methoxyphenyl)
- alkoxyhydroxyphenyl 1 or 2 radicals (L, M or N) (eg, 3-hydroxy-4-methoxyphenyl or 3- hydroxy-4-ethoxyphenyl) • ethoxyphenyl: 1 or 2 radicals (O and P) (eg, 4-ethoxyphenyl)
- the lipophilicity was determined by the value of the CLOGP, defined as the log P of a compound, which is the partition coefficient between n-octanol and water, log (coctanol / cagua).
- Theoretical lipophilicity is essential to predict the passage of blood brain barrier (BHE) by passive diffusion, said step being greater as the value of CLOGP is higher.
- BHE blood brain barrier
- the results of the CLOGP values are presented in Figure 23, and were calculated from the online application Osiris Property Explorer (http: //www.organicchemistry.org/prog/peo/).
- Osiris Property Explorer http: //www.organicchemistry.org/prog/peo/
- the mentioned compound is obtained in quantitative yield (pale yellow solid), after 2 h of reaction at 0 ° C, using 4- methylbenzaldehyde (3.05 g, 25.37 mmol), PPh 3 (29, 94 g, 1,14, 16 mmol) and CBr 4 (20, 19 g, 60.89 mmol) as starting substances.
- the mentioned compound is obtained in 89% yield (pale yellow oil), using l- (2,2-dibromovinyl) -4-methylbenzene (6.93 g, 25.11 mmol), n-BuLi (24 mL, 2.5 M in hexanes; 60.27 mmol) and ClC0 2 Me (2.70 mL, 35, 15 mmol), as starting substances.
- the mentioned compound is obtained in 82% yield (yellow solid), using l- (2,2-dibromovinyl) -4-ethoxybenzene (7.50 g, 24., 0 mmol), n-BuLi (19.6 mL, 2.5 M in hexanes; 49.01 mmol) and ClC0 2 Me (2.66 mL, 34.30 mmol), as starting substances.
- the mentioned compound is obtained in 54% yield (yellow oil), after 2 h of reaction at 0 ° C, using 3 - (3, 4-dimethylphenyl) prop-2-inamide (4.10 g , 28.23 mmol), Bu 3 SnH (9.00 mL, 33.88 mmol) and Pd (PPh 3 ) 4 (0.65 g, 0.56 mmol) as starting substances.
- EXAMPLE 10 Protective effect of cell death of analogs NPS0158 (G + G), NPS0159 (F + F), NPS0160 (P + P) and NPS0161 (H + H).
- the assays were performed on cells in SK-N-MC human neuroblastoma culture, maintained as detailed in Example 2. Inhibition produced by cell death compounds caused by treatment with xanthine / xanthine oxidase (XXO) that produces oxidative damage was analyzed in real time, which triggers cell death.
- the test was performed following the same procedure as described in example 6, testing the analogs at 40, 100, 400 or 1000 ng / ml in the presence of XXO.
- the cells were incubated (at 37 ° C and 5% C0 2 ) with these treatments for 72 h, collecting readings every 10 minutes. The values obtained are arbitrary units indicated by the cellular index, calculated from the impedance values and used as a measure of cell viability.
- Figures 25-28 The results obtained for the analogs are shown in Figures 25-28 as the normalized cell index (A) of each condition analyzed throughout the treatment; and as a percentage of cell death (B) for each treatment referred to the death produced by the XXO at 20 h post-treatment.
- Figures 25, 26, 27 and 28 correspond respectively to the results of analogs PS0158 (G + G), PS0159 (F + F), PS0160 (P + P) and PS0161 (H + H). * Is indicated for the significant difference with respect to XXO treatment according to the Student test (p ⁇ 0.05).
- EXAMPLE 11 Antioxidant effect of analogs NPS0158 (G + G), NPS0159 (F + F), NPS0160 (P + P) and NPS0161 (H + H) in in vitro and cellular models.
- ROS reactive oxygen species
- the ROS measurement test was performed on cells in SK-N-MC human neuroblastoma culture, maintained as detailed in Example 2, subjected to aggression with xanthine / xanthine oxidase (XXO).
- the measurement of ROS is performed by adding a permeable non-fluorescent probe in living cells (2 ', 7'-dichlorodihydrofluorescein diacetate, H 2 DCFDA; Biotium) which is oxidized by the action of ROS, generating 2', 7 ' -dichlorofluorescein (DCF) that can be detected in a fluorimeter at 485 nm excitation and 538 nm emission. Fluorescence results were normalized by cell viability, measured by lactate dehydrogenase (LDH) activity, using Roche's Cytotoxicity Detection Kit (LDH).
- LDH lactate dehydrogenase
- EXAMPLE 13 Passive permeability of analogs NPS0158 (G + G) and NPS0161 (H + H): prediction of theoretical and in vitro blood brain barrier passage.
- BHE blood brain barrier
- lipids derived from pig brain were used, with a phospholipid composition very similar to that which constitutes human BHE, and which is called PBL (Porcine Polar Brain Lipid, Avanti Polar Lipids Inc) which is Prepares on plates with MAIPNTR10 filter (Millipore), with a PVDF membrane and pore size of 45 ⁇ .
- PBL Porcine Polar Brain Lipid, Avanti Polar Lipids Inc
- MAIPNTR10 filter Micropore
- V D donor volume (cm 3 )
- A filter area (cm 2 )
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JP2014556114A JP2015513525A (ja) | 2012-02-07 | 2013-02-06 | 神経保護剤としてのホルミル化キサントシリン類似体 |
IN6536DEN2014 IN2014DN06536A (es) | 2012-02-07 | 2013-02-06 | |
EP13711061.5A EP2813222B1 (en) | 2012-02-07 | 2013-02-06 | Formylated xanthocillin analogues as neuroprotectants |
AU2013217893A AU2013217893A1 (en) | 2012-02-07 | 2013-02-06 | Formylated xanthocillin analogues as neuroprotectants |
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CN114181201B (zh) * | 2020-09-15 | 2023-12-01 | 香港科技大学 | 作为针对各种神经退行性疾病的潜在治疗剂的新化合物 |
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