IE43826B1 - Oximes of nitroacetophenone derivatives - Google Patents
Oximes of nitroacetophenone derivativesInfo
- Publication number
- IE43826B1 IE43826B1 IE570/76A IE57076A IE43826B1 IE 43826 B1 IE43826 B1 IE 43826B1 IE 570/76 A IE570/76 A IE 570/76A IE 57076 A IE57076 A IE 57076A IE 43826 B1 IE43826 B1 IE 43826B1
- Authority
- IE
- Ireland
- Prior art keywords
- formula
- compound
- salts
- oxime
- accompanying drawings
- Prior art date
Links
- 150000002923 oximes Chemical class 0.000 title claims description 28
- JTWHVBNYYWFXSI-UHFFFAOYSA-N 2-nitro-1-phenylethanone Chemical class [O-][N+](=O)CC(=O)C1=CC=CC=C1 JTWHVBNYYWFXSI-UHFFFAOYSA-N 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 91
- 150000003839 salts Chemical class 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052801 chlorine Chemical group 0.000 claims abstract description 8
- 239000005864 Sulphur Chemical group 0.000 claims abstract description 6
- 239000000460 chlorine Chemical group 0.000 claims abstract description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 150000002431 hydrogen Chemical group 0.000 claims abstract 4
- -1 propylthio group Chemical group 0.000 claims description 23
- 239000002253 acid Substances 0.000 claims description 22
- 150000007513 acids Chemical class 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- DPTGZRADVAPUHQ-UHFFFAOYSA-N 1-(4-nitrophenyl)-2-propoxyethanone Chemical compound CCCOCC(=O)C1=CC=C([N+]([O-])=O)C=C1 DPTGZRADVAPUHQ-UHFFFAOYSA-N 0.000 claims description 7
- LQCRSKSCUSXMJH-UHFFFAOYSA-N 1-(4-nitrophenyl)pentan-1-one Chemical compound CCCCC(=O)C1=CC=C([N+]([O-])=O)C=C1 LQCRSKSCUSXMJH-UHFFFAOYSA-N 0.000 claims description 7
- YHUXZWQAYFQBPG-UHFFFAOYSA-N 1-(3-chloro-4-nitrophenyl)-5-methoxypentan-1-one Chemical compound COCCCCC(=O)C1=CC=C([N+]([O-])=O)C(Cl)=C1 YHUXZWQAYFQBPG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical group 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- FMHFXXRKMQWBEP-UHFFFAOYSA-N 1-(3-methyl-4-nitrophenyl)pentan-1-one Chemical compound CCCCC(=O)C1=CC=C([N+]([O-])=O)C(C)=C1 FMHFXXRKMQWBEP-UHFFFAOYSA-N 0.000 claims description 3
- AVMPRGQRQKZCHO-UHFFFAOYSA-N 5-(2-methoxyethoxy)-1-(4-nitrophenyl)pentan-1-one Chemical compound COCCOCCCCC(=O)C1=CC=C([N+]([O-])=O)C=C1 AVMPRGQRQKZCHO-UHFFFAOYSA-N 0.000 claims description 3
- IVLJDGSFPOBAID-UHFFFAOYSA-N 5-methoxy-1-(4-nitrophenyl)pentan-1-one Chemical compound COCCCCC(=O)C1=CC=C([N+]([O-])=O)C=C1 IVLJDGSFPOBAID-UHFFFAOYSA-N 0.000 claims description 3
- 125000006239 protecting group Chemical group 0.000 claims description 3
- PXSLNRQFXCFEAY-UHFFFAOYSA-N 6-methoxy-1-(4-nitrophenyl)hexan-1-one Chemical compound COCCCCCC(=O)C1=CC=C([N+]([O-])=O)C=C1 PXSLNRQFXCFEAY-UHFFFAOYSA-N 0.000 claims description 2
- 241000282414 Homo sapiens Species 0.000 claims description 2
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 125000003544 oxime group Chemical group 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 239000012876 carrier material Substances 0.000 claims 1
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 abstract description 11
- 230000001430 anti-depressive effect Effects 0.000 abstract description 9
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 11
- 235000011152 sodium sulphate Nutrition 0.000 description 11
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- 238000006243 chemical reaction Methods 0.000 description 10
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 9
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- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- QYRFJLLXPINATB-UHFFFAOYSA-N hydron;2,4,5,6-tetrafluorobenzene-1,3-diamine;dichloride Chemical compound Cl.Cl.NC1=C(F)C(N)=C(F)C(F)=C1F QYRFJLLXPINATB-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005905 mesyloxy group Chemical group 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- LAAQSOCEYYDGGG-UHFFFAOYSA-N o-(2-aminopropyl)hydroxylamine;dihydrochloride Chemical compound Cl.Cl.CC(N)CON LAAQSOCEYYDGGG-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- LDCYZAJDBXYCGN-UHFFFAOYSA-N oxitriptan Natural products C1=C(O)C=C2C(CC(N)C(O)=O)=CNC2=C1 LDCYZAJDBXYCGN-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000005424 tosyloxy group Chemical group S(=O)(=O)(C1=CC=C(C)C=C1)O* 0.000 description 1
- 210000001364 upper extremity Anatomy 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/50—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals
- C07C251/58—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C313/08—Sulfenic acids; Derivatives thereof
- C07C313/10—Sulfenic acids; Esters thereof
- C07C313/12—Sulfenic acids; Esters thereof having sulfur atoms of sulfenic groups bound to acyclic carbon atoms
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- Health & Medical Sciences (AREA)
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- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The novel compounds of formula I wherein R is hydrogen, methyl or chlorine, R1 is oxygen or sulphur, R2 is OCH2, CH20CH2, OC2H40CH2, R3 is hydrogen or methyl, n and p are 0 or 1 and n + p is 0 or 1 and salts thereof have a very powerful anti-depressive activity which for a considerable part, and in some substances even entirely, is based on serotonine potentiation. Monoamino oxidase inhibition does not contribute to the anti-depressive effect. The substances have a low toxicity and are substantially free from side effects. The compounds can be synthesized and processed to compositions according to known methods.
Description
The invention relates to oximes of nitroacetophenone derivatives.
Patent Specification No. 33428 discloses a large group of oxime ether compounds having anti-depressive activity, which compounds are derived from alkyl-phenyl-ketone. The compounds have in a phenyl group one or more substituents which are selected from a very large group. Each of the possible substituents may be bound in any position of the phenyl group, but according to said Patent Specification substituents with nitro groups are restricted to the meta-positions.
This suggests that oxime ether compounds which are derived from alkylphenone and which have a nitro-group in a position other than a meta-position, have no anti-depressive activity. The anti-depressive activity of the known compounds is based on monoamino oxidase (MAO) inhibition and/or noradrenaline potentiation.
However, compounds which inhibit monoamino oxidase are particularly difficult to administer. They often have serious side effects and are often incompatible with other medicines and with some nutrients.
Since the regulations governing the use of medicines have become more - 2 stringent, only those compounds which are substantially free from side effects can be considered suitable for administration to human beings.
One object of the present invention is to provide oximes of nitroacetophenone derivatives having a powerful anti-depressive activity which is expressed inter alia in an elevation of mood of the treated patient but which have no component based on MAO inhibition. The compounds in view should be substantially free from side effects.
According to the present invention there are provided oximes of nitroacetophenone of formula I of the accompanying drawings and their salts formed with pharmaceutically acceptable acids in which formula I the symbols have the following meanings: R is hydrogen, methyl or chlorine, R-j is oxygen or sulphur, R2 is 0CH2, CH20CH2> OCgH^OCHg, Rg is hydrogen or methyl, £ and p are 0 and 1 and n + £ is 0 or 1.
It has surprisingly been found that the anti-depressive activity of these compounds is based for a considerable part, and in some compounds even exclusively, on serotonine potentiation, an activity which in a depressive patient results in an elevation of mood. However, most compounds show, in addition to serotonine potentiation, a very powerful noradrenaline potentiation as an antidepressive activity component.
The absence of an activity based on MAO inhibition is surprising especially as the compounds proved to be substantially free from side effects, for example, stomach ulceration and broncho constriction, and have a low toxicity.
In the following table properties of the compounds are compared with those of the closest related known compounds from Patent Specification No. 33428. - 3 CHS, - NHo.HCl CM x o t o II o iZ) fO broncho- constr. i i I i i i ί i 1 I I stomach ulcer. 1 1 1 1 1 1 ( ! 1 1 1 + UO •P- o x g.£ tototOLo ioLOLOtoLoiOLO CM CM CM CM CM CM CM CM CM CM CM Λ Α Λ Λ Λ Λ Λ Λ Λ Α Λ CO CO IO CM A serot. pot. co στ στ co co ι— r^.ccicocMcO'^i'Cor^-o Lft b- CO r- LO co S- Ό · <ΰ -P i. o o o. στ Ο r— b» r— CM CM LO LO «3* i— CO GT LO LO LO O r— ί— ί— σ co CM i— Λ A o co LO IO CO co * * CO CO CO XXXXXXXXXXX O O CJ XXX co If) -σ c ZJ o Cl ε o CJ CM CO co" co * X o o co CO CM CO x x x ο O CM O cm cm co x co co cm co co X O x MX CO X X CMCMO'—*OXOX CM o oxxooooooxo co o o «a· io co co o «3· CM CO O CM CM CM CM CM CM O OJ X CMCMXXXXXX CM X oxxooooooxo <- O O ' --' · --' o co X o *3· LO to CM XXX CM CM O Ο O —- co XXXXXXXr-XXro o o CM CM CM OOO XXX CM CM CM CM CM CM CM CM CM CM CM oo ooooooo oo xxxxzxxxxxx co XXX o o i— CMco^Lntob-cocnot— r- CM co CQ CQ CQ 2 8 3 6 The numbers in this table are EDgg values expressed in mg/kg.
It is remarkable that the compounds 9 and 10 neither potentiate noradrenaline nor inhibit MAO. The anti-depressive activity of these compounds is based entirely on serotonine potentiation.
These compounds therefore and in particular, compound 9 are to be preferred if a very specific serotonine potentiation is endeavoured.
Noradrenaline potentiation and serotonine potentiation in compounds 7 and 8 are of the same order of magnitude. Moreover, the activity is at a high level.
Both noradrenaline potentiation and serotonine potentiation in compound are at a high level but the noradrenaline potentiation is stronger by well over a factor 4.
It appears from the table that the compounds are substantially free from undesired side effects.
Although the knowh compounds BI and B2 have a strong noradrenaline and serotonine potentiating effect, they also have a powerful MAO inhibition. In compound B3 not only both the noradrenaline potentiation and the serotonine potentiation is of quite a different level, in addition the compound gives stomach ulceration. Therefore, none of the known compounds satisfy the object of the invention.
The data recorded in the table were determined by means of the following tests.
The noradrenaline potentiation was determined in the tetrabenazine test.
In this test a quantity of the compound to be tested was administered orally to five male albino mice. After 45 minutes the animals were injected subcutaneously with 80 mg/kg of tetrabenazine. After another 45 minutes the ptosis was determined and compared with the ptosis of animals which had received tetrabenazine alone. The EDgg was determined from the results.
The serotonin potentiation was determined in the 5-hydroxytryptophan test.
For this purpose the compounds to be tested were administered orally in a series of - 5 dosages to isolated male albino mice (5 mice per dosage) 1 hour prior to introperitoneal administration of 150 mg/kg of dl-5-hydroxytryptophan. 30 minutes after this threshold dosage the mice were observed individually and the following parameters were scored: stereotypical shaking of the head, spreading of the hindlegs, tremor, tendency to flee, lordosis and clonic stamping with the front legs. The EDgg value was calculated from the results.
The monoamino oxidase (MAO) inhibiting effect was determined in experiments in which a quantity of the compound to be tested was administered orally to five male albino mice. One hour later the animals were injected subcutaneously with tryptamine hydrochloride in a quantity of 250 mg/kg.
This quantity does nor cause mortality in animals which did not receive the compound to be tested, but did cause mortality in animals to which an active substan had been administered. Eighteen hours after the administration of tryptamine hydrochloride it was determined how many treated animals had died. The ΕΟ^θ was determined from the results.
By means of the method of Metysova, Arneimittelforschung 1_3 1039 (1953) it was determined whether the oral administration of 200 mg of a compound to be tested causes stomach ulceration.
By means of the method by Konzett-Rflssler, Arch. Esp. Path. Pharmakol, 195 71 (1940) it was investigated whether a compound to be tested causes bronchoconstriction after intravenous administration of 3 mg/kg. Reduction of the breathing function as a result of bronchoconstriction is expressed in this method in a smaller volume of air taken in.
On the basis of their properties the compounds of formula I and their salts are particularly suitable for use in the treatment of depressive patients.
This applies in particular to the compounds: 5-(2-methoxyethoxy)-4‘-nitrovalerophenone 0-(2-ami noethyl)oxi me, 4'-ni tro-31-methyl-valerophenone 0-(2-ami noethyl) oxime, 3'-chloro-5-methoxy-4’-nitrovalerophenone 0-(2-aminoethyl)-oxime, 4'nitrovalerophenone 0 - (2-aminopropyl)oxime and 3'-chloro-4'-nitro-5-methoxyvalerophenone 0 - (2-aminopropyl)oxime and their salts. - 5 43836 The quantity, the frequency, and the way in which the compounds are administered may differ for each individual patient and also in accordance with the severity of the disturbance to be treated. In general, an oral daily quantity of 25-500 mg will be chosen, as a rule 50-200 mg.
The compounds are preferably used in the form of tablets, coated tablets, capsules, pills, powders and injection liquids. They can be processed to such compositions according to methods which are known per se.
The invention also relates to compositions having a compound of formula I or a salt thereof formed with a pharmaceutically acceptable acid as an active constituent, and to methods to bring the compounds and their salts in a form suitable for administration, for example, by mixing an active substance with or dissolving it in solid or liquid pharmaceutical carrier materials.
As examples of pharmaceutically acceptable acids with which the bases of formula I can form salts may be mentioned: inorganic acids, for example hydrochloric acid, nitric acid, sulphuric aqid and organic acids, for example, malic acid, citric acid, fumaric acid, maleic acid, tartaric acid and benzoic acid.
The compounds of formula I and their salts can be prepared according to methods which are known for the preparation of this type of compounds and according to methods analogous thereto.
The invention also realtes to the preparation of the compounds.
The compounds can be prepared inter alia by reacting a compound of formula II of the accompanying drawings with a compound of formula III of the accompanying drawings or a salt thereof. In this case is an oxygen atom, an oxime group or an alkylene dioxygroup, for example ethylenedioxy and the symbols R, R-j, Rg, Rg, n. and p are defined as above.
The reaction is preferably carried out in an inert solvent, for example an alcohol, dioxan, dimethyl formamide, tetrahydrofuran or a mixture thereof, at temperatures between room temperature and the boiling point of the mixture and possibly in the presence of an acid binder, for example pyridine. - 7 iS8?-S The compounds are also prepared by converting a compound of formula IV of the accompanying drawings wherein M is a hydrogen atom or an alkali metal atom with a compound of formula V of the accompanying drawings or a salt thereof wherein Hal is a halogen atom, preferably a chlorine atom or a bromine atom.
The reaction is preferably carried out in an inert solvent, for example alcohols, ethers or dimethyl formamide. When M is a hydrogen atom, an acid binder for example an aleoholate is preferably added as well. As a rule the reaction temperature is between 0 and 50°C.
The compounds can also be prepared by reacting a compound of formula VI of the accompanying drawings wherein R5 is a labile group, for example, a mesyloxy group or a tosyloxy group, with ammonia. The reaction is preferably carried out in an inert solvent, for example an alcohol, as a rule at temperatures between room temperature and 150°C.
The compounds of formula VI of the accompanying drawings are prepared by converting a compound of formula IV of the accompanying drawings in ethanol and in the presence of an aleoholate at temperatures up to 60°C. with ethylene oxide or propylene oxide. The reaction product is then converted with mesylchloride or tosylchloride dissolved in methylene chloride.
The compounds can also be obtained by removing a protective group R& by means of hydrolysis from a compound of formula VII of the accompanying drawings. The protective group Rg may be, for example, the trityl group. The reaction is carried out, for example, in a water-miscible solvent in acid conditions at a temperature between room Lemperature and 100°C.
The compounds can also be obtained by converting the para amino (aromatic) group in a compound of formula VIII of the accompanying drawings into a nitro group.
The conversion can be carried out by a reaction with nitrous acid at -10 to +50°C., followed by decomposition of the resulting diazonium compound in the reaction mixture at 20-75° C. in the presence of copper. The conversion of compounds wherein R-| does not represent sulphur may also be carried out with a peroxide, for example hydrogen peroxide or m-chloroperbenzoic acid, in an inert solvent, for example - 8 42S36 methylene chloride or chloroform, at temperatures between room temperature and the boiling point of the mixture.
Compounds of formula I wherein n + jj = 1 can furthermore be prepared by reacting a compound of formula IX of the accompanying drawings with a compound of formula X of the accompanying drawings. In these formulae £ has the value 1, 4 or 5, M1 is an alkali metal atom and R? is a propoxy group, a propylthio group, a methoxy group or a methoxyethoxy group and Hal is a halogen atom, preferably a chlorine atom or a bromine atom. The reaction may be carried out, for example, in aqueous alcohol at temperatures of 0°C. or possibly lower, to room temperature.
Compounds of formula I wherein £ + £ = 1 can also be obtained by reacting a compound of formula XI of the accompanying drawings with a compound of formula XII of the accompanying drawings. In these formulae £ has the value 1, 4 or 5, Rg is an oxygen atom or a sulphur atom, M‘ is an alkali metal atom, R1? is a methyl group, a propyl group or a methoxymethyl group, and Hal is a halogen atom, preferably a chlorine atom or a bromine atom. The reaction may be carried out in a polar aprotic solvent, for example hexamethylphosphortriamide, at a temperature between 0°C, and room temperature. In all formulae the remaining symbols have the same meaning as in formula I.
The invention will now be described in greater detail with reference to the ensuing specific examples. 1) 5-Methoxy-4'-nitrovalerophenone 0-(2-aminoethylJoxime hydrochloride. .35 Mmol (1.27 g) of 5-methoxy-4‘-nitrovalerophenone (melting point 64.5-65.5°C.), 5.35 mmol (0.08 g) of 2- aminoxyethylamine di hydrochloride and 0.34 ml of pyridine were refluxed for 2 hours in 5 ml of absolute ethanol. After evaporating the reaction mixture to dryness in vacuo, 25 ml of water and 10 ml of 2N sodium hydroxide solution were added and extracted with 25 and 10 ml, respectively, of methylene chloride. The extracts were dried over sodium sulphate and then evaporated to dryness in vacuo. Toluene was added another two times to the resulting base which was evaporated in vacuo. The residue was dissolved in absolute ethanol and an equimolar quantity of alcoholic hydrochloric acid was added. After the - 9 45 8 3S addition of diethyl ether, the title compound crystallized. Melting point 121.5 122.5°C. 2) 6-Methoxy-4'-nitrohexanophenone 0-(2-aminoethyl)oxime hydrochloride. t r 135 Mmol (33.7 g) of 6-methoxy-4'-nitrohexaphenone (melting point 50°C.), 135 mmol (20.1 g) of 2-ami noxy-ethyl amine di hydrochloride and 100 ml of pyridine were refluxed for 5 hours in 300 ml of absolute ethanol. The reaction mixture was evaporated to dryness in vacuo and the residue, after having been dissolved in 200 ml of water, was washed twice with 100 ml of petroleum ether 40—60. The aqueous solution was rendered alkaline with 200 ml of 2N sodium hydroxide solution and then extracted four times with 100 ml of ether. The combined ether extracts were washed with 100 ml of water, dried on sodium sulphate and then evaporated to dryness in vacuo. The resulting oil, after the addition of toluene, was evaporated to dryness in vacuo another three times and then dissolved in absolute ethanol. After the addition of an equivalent quantity of alcoholic hydrochloric acid it was evaporatec to dryness in vacuo again. The residue was crystallized from alcohol/ether. The resulting crystals were recrystallized twice from acetonitrile and alcohol/ether, respectively. Melting point 92 - 93°C. 3) 3‘-Methyl-4'-nitrovalerophenone 0-(2-aminoethyl)oxime fumarate (1:1). .7 Mmol of 3'-methyl-4'nitrovalerophenone, 5.7 mmol of 2-aminoxyethylamine dihydrochloride and 0.9 ml of pyridine were refluxed for three hours in 15 ml of absolute ethanol. The base was isolated from the reaction mixture as described in Example 2. It was dissolved in an equimolar quantity of ethanolic fumaric acid. Melting point after recrystallization from ethanol 152.5 - 154°C. 4) 3'-Chloro-5-methoxy-4‘-nitrovalerophenone 0-(2-aminoethyl)oxime fumarate (1:1) In the same manner as described in Example 3, the title compound was obtained from 3'-chioro-5-methoxy-4‘-nitrovalerophenone (melting point 54.5 - 56°C.) and 2aminoxyethylamine di hydrochloride. After recrystallization from ethanol the melting point was 148 - 148.5°C. - 10 5) 4'-hitrovalerophenone-0-(2-aminopropyl)oxinie hydrochloride.
In the same manner as described in Example 2 the title compound was obtained from 4'-nitrovalerophenone (boiling point at 0.03 mm: 128-132°C.) and 2-aminoxy-lmethylethyl amine di hydrochloride. The melting point after recrystallization from acetonitrile/ether was 148-149°C. 6) 4'-Nitro-2-propoxyacetophenone 0-(2-aminopropyl)oxime fumarate (1:1).
In the same manner as described in Example 3 the title compound was obtained from 4'-nitro-2-propoxyacetophenone (melting point 49-50°C.) and 2-aminoxy-lmethylethyl amine di hydrochloride. The melting point after recrystallization from ethanol was 141-142°C. 7) 3'-Chloro-5-methoxy-4‘-nitrovalerophenone 0-(2-aminopropyl)oxime fumarate (1:1).
In the same amnner as described in Example 3 the title compound was obtained from 3'-chloro-5-methoxy-4‘~nitrovalerophenone (melting point 54.5-56°C.) and 2aminoxy-1-methylethylamine di hydrochloride. After crystallization from ethanol/ acetonitrile the melting point was 140-142°C. 8) 4'-Nitrovalerophenone 0-(2-aminoethyl)oxime hydrochloride.
Mmol of 4'-nitrovalerophenone 0-(2-tritylaminoethyl)oxime were dissolved in 50 ml of 90% acetic acid. After standing for three days at room temperature, this reaction mixture was evaporated to dryness in vacuo after which the residue was dissolved in 50 ml of ether. The resulting solution was extracted with 50 ml of 0.2N hydrochloric acid and the extract, after being rendered alkaline with 10 ml of 2N sodium hydroxide solution, was extracted with 50 and 25 ml, respectively, of methylene chloride. After drying on sodium sulphate and evaporating in vacuo the resulting base was converted into the title compound with alcoholic hydrochloric acid. After crystallization and recrystallization from ethanol/ether the melting point was 107-108°C. 9) 4'-Nitro-2-propoxyacetophenone 0-(2-aminoethyl)oxime hydrochloride.
Mmol of 4'-nitro-2-propoxyacetophenone oxime, 10.4 mmol of 2-chloroethyl amine hydrochloride and 1.4 g of powdered potassium hydroxide were added to 25 ml of - 11 42826 dimethyl formamide while stirring at 10°C. After stirring for two days at room temperature the dimethyl formamide was evaporated in vacuo, the residue was brought in water and then 2N hydrochloric acid was added until pH 3. The remaining oxime was removed by means of ether, after which 30 ml of 2N sodium hydroxide solution were added. Then three extractions with ether were carried out. The collected ether layers were washed twice with a 5% sodium bicarbonate solution and then dried on sodium sulphate. After removing the ether in vacuo the residue was dissolved in absolute ethanol and converted into the title compound by means of alcoholic hydrochloric acid. After recrystallization from alcohol/ether the melting point was 128-130°C. ) 4'-Nitro-2-propoxyacetophenone 0-(2-aminoethyl)oxime hydrochloride. a) 2.3 g of ethylene oxide were led into mmol of 4'-nitro-2-propoxyacetophenone oxime in 50 ml of absolute ethanol in which 0.007 g of lithium had been previously dissolved while stirring and at 45°C. by means of a flow of nitrogen, after which stirring at 60°C. was continued for another hour. After the addition of 0.6 ml of acetic acid it was evaporated to dryness in vacuo. The residue was taken up in ether and washed with water. After drying on sodium sulphate and evaporating the ether a residue was obtained which was purified by means of a silica gel column using methylene chloride as an eluent. After evaporation of the solvent the 0-(2-hydroxyethyl) oxime was obtained as an oil. b) To a solution of 22 mmol hereof in 120 ml of methylene chloride 4.5 ml of triethylamine were added while stirring at -5 to -10° C., and then 24 mmol (1.9 ml) of mesyl-chloride were added dropwise in 20 minutes. Stirring was continued for another 30 minutes at 0° C. and the reaction mixture was then washed with water, as sodium bicarbonate solution and a saturated sodium chloride solution. After drying on sodium sulphate the methylene chloride was evaporated in vacuo. In this manner the 0-(2-mesyloxyethyl) oxime was obtained. c) A mixture of 26 mmol thereof in 100 ml of methanol which contained 12 g of ammonia was kept in an autoclave at 80°C. for 16 hours. After cooling, the methanol was removed in vacuo. The residue was stirred with 50 ml of 2N sodium hydroxide - 12 42836 solution and extracted 4 times with ether. The ether layer was washed twice with a 5% sodium bicarbonate solution. After drying on sodium sulphate and distilling off the ether under reduced pressure the resulting oil was converted into the title compound by means of alcoholic hydrochloric acid. After two crystallizations from alcohol/ether the melting point was 128-130°C. 11) 5-(2- Methoxyethoxy)-4'-nitrovalerophenone 0-(2-aminoethyl)oxime fumarate (1:1).
Mmol (3.25 g) of 5-(2-methoxyethoxy)-4'-nitrovalerophenone ethylene ketal, 10 mmol (1.49 g) of 2-aminoxyethylamine di hydrochloride and 10 ml of methanol were refluxed for 6 hours. The resulting residue, after evaporating the methanol, was washed three times with ether after having been dissolved in water.
The aqueous solution was extracted three times with methylene chloride after previously being rendered alkaline with a sodium hydroxide solution. The combined extracts were washed with a 5% sodium bicarbonate solution and then with water.
After drying on sodium sulphate and evaporating the methylene chloride, the free base was obtained, which was converted into the title compound by means of an equimolar quantity of fumaric acid. After crystallization from alcohol the melting point was 134.5 - 135.5°C. 12) 4'-Nitrovalerophenone 0-(2-aminoethyl)oxime hydrochloride.
Mmol (1.23 g) of 4‘-aminovalerophenone 0-(2-aminoethyl)oxime dihydrochloride (melting point 175-177° C.) were converted into the free base by means of 2N sodium hydroxide solution. A solution hereof in 5 ml of methylene chloride was added dropwise while stirring at 25 to 40° C. to 12.3 mmol (2.5 g) of m-chloroperbenzoic acid (85%) in 10 ml of methylene chloride. Stirring at 30 to 35° C., was then continued for another three hours. The precipitate was sucked off and washed with methylene chloride. After the addition of 50 ml of ether to the filtrate and the washing liquid, the mixture was washed three times with 2N sodium hydroxide solution and finally twice with a 5% sodium bicarbonate solution. After drying on sodium sulphate and removing the ether under reduced pressure, the residue was chromatographed over silica gel with methylene chloride as an eluent. The methylene - 13 4S8SG chloride was distilled off from the eluate, after which the residue was converted into the title compound by means of alcoholic hydrochloride acid. After recrystallization from alcohol/ether the melting point was 107-108°C. 13) 4'-Nitro-2-propylthioacetophenone 0-(2-aminoethyl)oxime hydrochloride.
Mmol (0.54 g) of propylmercaptan were added while stirring to a solution of 5 mmol (0.24 g) of sodium hydroxide in 10 ml of 50% alcohol cooled with ice-water. Stirring was continued for another 10 minutes after which 3 mmol (1.0 g) of 2-bromo4'-nitroacetophenone 0-(2-aminoethyl) oxime hydrochloride (melting point 197°C.) were added within 30 minutes while stirring at a temperature between 0 and 5°C. Stirring was continued for another hour at 5°C. and then one hour at room temperature. The reaction mixture was evaporated in vacuo and the residue was washed with water and dissolved in methylene chloride. The solution was washed with water and dried over sodium sulphate. After evaporation, a base was obtained which was converted into the title compound by means of alcoholic hydrochloric acid. After recrystallization from acetonitrile/ether the melting point was 122.5-123.5°C. 14) 4‘-Nitro-2-propoxyacetophenone 0-(2-aminoethyl)oxime hydrochloride. 0.09 g of 55-60% sodium hydride in mineral oil was added to a solution of 2.0 mmol (0.48 g) of 2-hydroxy-4'-nitroacetophenone 0-(2-aminoethyl) oxime (melting point 97-98°C.) in 5 ml of hexamethyl phosphoric acid triamide while stirring at room temperature. After 4 minutes, 0.02 ml of propyl bromide was added while stirring. The reaction mixture was then stirred at room temperature for another 4 hours, diluted with 50 ml of water and extracted two times with 25 ml of ether.
The combined ether extracts were dried on sodium sulphate and evaporated to dryness in vacuo. The residue was chromatographed by means of ethanol/ammonia 95/5 over 15 g of silica gel. The eluate was evaporated to dryness in vacuo and then converted into the title compound by means of alcoholic hydrochloric acid. After crystallization from alcohol-ether the melting point was 128-13O°C.
) Tablet mg of 4'-nitro-31-methylvalerophenone 0-(2-aminoethyl) oxime HC1 335 mg of lactose - 14 42826 rag of potato starch 25 nig of talc mg of magnesium stearate 5 mg of gelatin. 16) Suppository mg of 4'-nitrovalerophenone 0-(2-aminopropyl) oxime HC1 1500 mg of suppository mass. 17) Injection liquid g of 3'-chloro-4'"nitro-5-methoxyvalerophenone 0-(2-aminopropyl) oxime HC1 1.80 g of methyl-p-hydroxybenzoate 0.20 g of propyl-p-hydroxybenzoate 9.0 g of sodium chloride 4.0 g of poly- (oxyethylene)2g sorbitan mono-oleate water to 1000 ml.
Claims (22)
1. Oximes of nitroacetophenone derivatives of formula I of the accompanying drawings and salts thereof with pharmaceutically acceptable acids, in which formula R is hydrogen, chlorine or methyl, R-| is oxygen or sulphur, R 2 is 0CH 2 , CH 2 0CH 2 or OCgH^OCHg, Rg is hydrogen or methyl, £ and £ have the value 0 or 1 and £ + £ is 0 or 1.
2. 4'-Nitrovalerophenone 0-(2-aminoethyl)-oxime and salts thereof formed with pharmaceutically acceptable acids.
3. 4'-Nitro-2-propy1thioacetophenone 0-(2-aminoethyl) oxime and salts thereof formed with pharmaceutically acceptable acids.
4. 4'-Nitro-2-propoxyacetophenone 0-(2-aminoethyl) oxime and salts thereof formed with pharmaceutically acceptable acids.
5. 5-Methoxy-4'-nitrovalerophenone 0-(2-aminoethy1)oxime and salts thereof formed with pharmaceutically acceptable acids.
6. 5-(2-Methoxyethoxy)-4'-nitrovalerophenone 0-(2-aminoethyl)oxime and salts thereof formed with pharmaceutically acceptable acids. - 15
7. 6-Methoxy-4'-nitrohexanophenone 0-(2-aminoethyl)oxime and salts thereof formed with pharmaceutically acceptable acids.
8. 3'-Methyl-4'-nitrovalerophenone 0-(2-aminoethyl) oxime and salts thereof formed with pharmaceutically acceptable acids.
9. 3'-Chloro-5-methoxy-4'-nitrovalerophenone 0-(2-aminoethyl)oxime and salts thereof formed with pharmaceutically acceptable acids.
10. 4'-Nitro-valefOphenone 0-(2-aminopropyl) oxime and salts thereof formed with pharmaceutically acceptable acids.
11. 4'-Nitro-2-propoxyacetophenone 0-(2-aminopropyl) oxime and salts thereof formed with pharmaceutically acceptable acids.
12. 3‘-Chloro-5-methoxy-4'-nitrovalerophenone 0-(2-aminopropyl)oxime and salts thereof formed with pharmaceutically acceptable acids.
13. Pharmaceutical compositions characterized by a content of a compound of formula I of the accompanying drawings or a salt thereof formed with a pharmaceutically acceptable acid in which formula R is hydrogen, chlorine or methyl, Rj is oxygen or sulphur, Rg is OCHg CHgOCHg or OCgH^OCHg and is hydrogen or methyl and n. and £ have the value 0 or 1, while the sum of £ and £ is also 0 or 1 in association with a carrier.
14. A method of preparing pharmaceutical compositions, characterized in that a compound of formula I of the accompanying drawings or a salt thereof formed with a pharmaceutically acceptable acid is brought into a form suitable for administration by mixing the compound with, or dissolving the compound in, solid or liquid carrier materials.
15. A method of preparing oximes of nitroacetophenone derivatives, characterized in that compounds of formula I of the accompanying drawings and their salts formed with pharmaceutically acceptable acids, in which formula R is hydrogen, methyl or chlorine, Rj is oxygen or sulphur, Rg is OCHg, CHgOCHg or OCgH^OCHg and R 3 is hydrogen or methyl, £ and £ have the value 0 or 1 and the sum of £ and £ = 0 or 1, are prepared by reacting a compound of formula II of the accompanying drawings wherein R^ is an oxygen atom, and oxime group or an alkylene dioxy group with a compound of - 16 formula III of the accompanying drawings or a salt thereof.
16. A method as claimed in Claim 15, characterized in that a compound of formula IV of the accompanying drawings wherein M is a hydrogen atom or an alkali metal atom is converted with a compound of formula V or a salt thereof wherein Hal is a halogen atom.
17. A method as claimed in Claim 15, characterized in that a compound of formula VI of the accompanying drawings wherein Rg is a labile group as hereinbefore described which reacts with ammonia to form compounds of formula I.
18. A method as claimed in Claim 15, characterized in that a protective group Rg, wherein R g is a trityl group, in a compound of formula VII of the accompanying drawings is removed by hydrolysis.
19. A method as claimed in Claim 15, characterized in that the para amino (aromatic) group in a compound of formula VIII of the accompanying drawings is converted into a nitro group.
20. A method as claimed in Claim 15, characterized in that compounds of formula I wherein £ + £ = 1 and salts thereof are prepared by reacting a compound of formula IX of the accompanying drawings wherein £ has the value 1, 4 or 5, with a compound of formula X of the accompanying drawings wherein M 1 is an alkali metal atom and R? is a propoxy group, a propylthio group, a methoxy group or a methoxyethoxy group and Hal is a halogen atom.
21. A method as claimed in Claim 15, characterized in that compounds of formula I wherein £ + £ = 1 and salts thereof are prepared by reacting a compound of formula XI of the accompanying drawings wherein £ has the value 1, 4 or 5 and R g is an oxygen atom or a sulphur atom and M‘ is an alkali metal atom with a compound of formula XII of the accompanying drawings wherein Hal is a halogen atom and R'? is a methyl group, a propyl group or a methoxyethyl group.
22. A method of treating non-human animals characterized in that a daily effective dose of a compound of formula I of the accompanying drawings or a salt thereof is administered.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7503307A NL7503307A (en) | 1975-03-20 | 1975-03-20 | ANTIDEPRESSIVE CONNECTIONS. |
Publications (2)
Publication Number | Publication Date |
---|---|
IE43826L IE43826L (en) | 1976-09-20 |
IE43826B1 true IE43826B1 (en) | 1981-06-03 |
Family
ID=19823421
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE570/76A IE43826B1 (en) | 1975-03-20 | 1976-03-18 | Oximes of nitroacetophenone derivatives |
Country Status (21)
Country | Link |
---|---|
JP (1) | JPS51125344A (en) |
AR (2) | AR212811A1 (en) |
AT (1) | AT340894B (en) |
AU (1) | AU502701B2 (en) |
BE (1) | BE839741A (en) |
CA (1) | CA1077964A (en) |
DD (1) | DD128331A5 (en) |
DE (1) | DE2610302A1 (en) |
DK (1) | DK115676A (en) |
ES (1) | ES446189A1 (en) |
FI (1) | FI760696A (en) |
FR (1) | FR2304332A1 (en) |
GB (1) | GB1533063A (en) |
GR (1) | GR60051B (en) |
HU (1) | HU171160B (en) |
IE (1) | IE43826B1 (en) |
IL (1) | IL49236A (en) |
NL (1) | NL7503307A (en) |
PL (3) | PL101882B1 (en) |
SE (1) | SE7603344L (en) |
ZA (1) | ZA761386B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US7256191B2 (en) | 2000-04-24 | 2007-08-14 | Aryx Therapeutics | Materials and methods for the treatment of depression |
US6469064B2 (en) | 2000-04-24 | 2002-10-22 | Aryx Therapeutics | Materials and methods for the treatment of depression |
-
1975
- 1975-03-20 NL NL7503307A patent/NL7503307A/en not_active Application Discontinuation
-
1976
- 1976-03-08 ZA ZA761386A patent/ZA761386B/en unknown
- 1976-03-12 DE DE2610302A patent/DE2610302A1/en not_active Withdrawn
- 1976-03-17 PL PL1976199547A patent/PL101882B1/en unknown
- 1976-03-17 FI FI760696A patent/FI760696A/fi not_active Application Discontinuation
- 1976-03-17 DD DD7600191890A patent/DD128331A5/en unknown
- 1976-03-17 PL PL1976199546A patent/PL100040B1/en unknown
- 1976-03-17 GR GR50330A patent/GR60051B/en unknown
- 1976-03-17 DK DK115676A patent/DK115676A/en unknown
- 1976-03-17 SE SE7603344A patent/SE7603344L/en not_active Application Discontinuation
- 1976-03-17 AT AT195276A patent/AT340894B/en not_active IP Right Cessation
- 1976-03-17 GB GB10706/76A patent/GB1533063A/en not_active Expired
- 1976-03-17 HU HU76PI00000515A patent/HU171160B/en unknown
- 1976-03-17 IL IL49236A patent/IL49236A/en unknown
- 1976-03-17 CA CA248,103A patent/CA1077964A/en not_active Expired
- 1976-03-17 PL PL1976188001A patent/PL100612B1/en unknown
- 1976-03-18 IE IE570/76A patent/IE43826B1/en unknown
- 1976-03-18 AU AU12142/76A patent/AU502701B2/en not_active Expired
- 1976-03-18 ES ES446189A patent/ES446189A1/en not_active Expired
- 1976-03-18 BE BE165313A patent/BE839741A/en unknown
- 1976-03-19 FR FR7608015A patent/FR2304332A1/en active Granted
- 1976-03-19 AR AR262633A patent/AR212811A1/en active
- 1976-03-19 JP JP51029391A patent/JPS51125344A/en active Pending
- 1976-12-07 AR AR265765A patent/AR213298A1/en active
Also Published As
Publication number | Publication date |
---|---|
AU1214276A (en) | 1977-09-22 |
CA1077964A (en) | 1980-05-20 |
GB1533063A (en) | 1978-11-22 |
AT340894B (en) | 1978-01-10 |
PL100612B1 (en) | 1978-10-31 |
FR2304332B1 (en) | 1978-12-08 |
JPS51125344A (en) | 1976-11-01 |
SE7603344L (en) | 1976-09-21 |
DK115676A (en) | 1976-09-21 |
DE2610302A1 (en) | 1976-09-30 |
ZA761386B (en) | 1977-10-26 |
FR2304332A1 (en) | 1976-10-15 |
IE43826L (en) | 1976-09-20 |
ATA195276A (en) | 1977-05-15 |
IL49236A (en) | 1978-08-31 |
AR213298A1 (en) | 1979-01-15 |
GR60051B (en) | 1978-04-04 |
ES446189A1 (en) | 1977-10-01 |
HU171160B (en) | 1977-11-28 |
NL7503307A (en) | 1976-09-22 |
BE839741A (en) | 1976-09-20 |
FI760696A (en) | 1976-09-21 |
PL100040B1 (en) | 1978-08-31 |
PL101882B1 (en) | 1979-02-28 |
AR212811A1 (en) | 1978-10-13 |
DD128331A5 (en) | 1977-11-09 |
AU502701B2 (en) | 1979-08-02 |
IL49236A0 (en) | 1976-05-31 |
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