NO760920L - - Google Patents
Info
- Publication number
- NO760920L NO760920L NO760920A NO760920A NO760920L NO 760920 L NO760920 L NO 760920L NO 760920 A NO760920 A NO 760920A NO 760920 A NO760920 A NO 760920A NO 760920 L NO760920 L NO 760920L
- Authority
- NO
- Norway
- Prior art keywords
- derivative
- stated
- radical
- salt
- guanidinoimino
- Prior art date
Links
- -1 guanidinoimino radical Chemical group 0.000 claims description 74
- 150000004059 quinone derivatives Chemical class 0.000 claims description 46
- 150000003839 salts Chemical class 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 35
- 241001465754 Metazoa Species 0.000 claims description 34
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 31
- 238000002360 preparation method Methods 0.000 claims description 25
- 239000007787 solid Substances 0.000 claims description 19
- 235000005911 diet Nutrition 0.000 claims description 15
- 230000037213 diet Effects 0.000 claims description 15
- 239000003085 diluting agent Substances 0.000 claims description 14
- 150000003254 radicals Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 241000287828 Gallus gallus Species 0.000 claims description 11
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 231100000252 nontoxic Toxicity 0.000 claims description 9
- 230000003000 nontoxic effect Effects 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 6
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical compound O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 claims description 4
- 241000272517 Anseriformes Species 0.000 claims description 4
- 229910002651 NO3 Inorganic materials 0.000 claims description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical class [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 4
- 229910000071 diazene Inorganic materials 0.000 claims description 4
- 239000003651 drinking water Substances 0.000 claims description 4
- 235000020188 drinking water Nutrition 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical class OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 244000144972 livestock Species 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 4
- 235000020183 skimmed milk Nutrition 0.000 claims description 4
- 150000004684 trihydrates Chemical class 0.000 claims description 4
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 3
- SDCAQHPGDHJYER-UHFFFAOYSA-N NC(=N)NN=C1C=CC(C=C1)=NNC(N)=O Chemical group NC(=N)NN=C1C=CC(C=C1)=NNC(N)=O SDCAQHPGDHJYER-UHFFFAOYSA-N 0.000 claims description 3
- 241000282887 Suidae Species 0.000 claims description 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000006227 byproduct Substances 0.000 claims description 3
- MLMFUKWWZIZRHX-UHFFFAOYSA-N chembl2103762 Chemical compound NC(=N)NN=C1C=CC(=NNC(N)=S)C=C1 MLMFUKWWZIZRHX-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004151 quinonyl group Chemical group 0.000 claims description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- 241000283690 Bos taurus Species 0.000 claims description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 claims description 2
- 241000237502 Ostreidae Species 0.000 claims description 2
- 241001494479 Pecora Species 0.000 claims description 2
- 241000286209 Phasianidae Species 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- IXWIAFSBWGYQOE-UHFFFAOYSA-M aluminum;magnesium;oxygen(2-);silicon(4+);hydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Mg+2].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] IXWIAFSBWGYQOE-UHFFFAOYSA-M 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 235000013330 chicken meat Nutrition 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000003840 hydrochlorides Chemical class 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000008101 lactose Substances 0.000 claims description 2
- 235000013372 meat Nutrition 0.000 claims description 2
- 235000020636 oyster Nutrition 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 235000008939 whole milk Nutrition 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 2
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- GEAXLHPORCRESC-UHFFFAOYSA-N chlorocyclohexatriene Chemical compound ClC1=CC=C=C[CH]1 GEAXLHPORCRESC-UHFFFAOYSA-N 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 150000007659 semicarbazones Chemical class 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 239000000243 solution Substances 0.000 description 25
- 238000000354 decomposition reaction Methods 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 241000271566 Aves Species 0.000 description 8
- 239000007952 growth promoter Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- GHNKZLUTOGGWCQ-UHFFFAOYSA-N 1-amino-2-methylguanidine;dihydrochloride Chemical compound Cl.Cl.CNC(=N)NN GHNKZLUTOGGWCQ-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- XQCFHQBGMWUEMY-ZPUQHVIOSA-N Nitrovin Chemical compound C=1C=C([N+]([O-])=O)OC=1\C=C\C(=NNC(=N)N)\C=C\C1=CC=C([N+]([O-])=O)O1 XQCFHQBGMWUEMY-ZPUQHVIOSA-N 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 235000020940 control diet Nutrition 0.000 description 3
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 3
- RNOJZAYWQCKGRK-UHFFFAOYSA-N diazene hydrochloride Chemical compound Cl.N=N RNOJZAYWQCKGRK-UHFFFAOYSA-N 0.000 description 3
- 239000004459 forage Substances 0.000 description 3
- 239000013641 positive control Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- HAZRIBSLCUYMQP-UHFFFAOYSA-N 1,2-diaminoguanidine;hydron;chloride Chemical compound Cl.NN\C(N)=N/N HAZRIBSLCUYMQP-UHFFFAOYSA-N 0.000 description 2
- LHYKTQVFLKHQSR-UHFFFAOYSA-N 1-amino-3-methylurea Chemical compound CNC(=O)NN LHYKTQVFLKHQSR-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- MVTQIFVKRXBCHS-SMMNFGSLSA-N N-[(3S,6S,12R,15S,16R,19S,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentazatricyclo[20.4.0.06,10]hexacosan-15-yl]-3-hydroxypyridine-2-carboxamide (10R,11R,12E,17E,19E,21S)-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),6,12,17,19,25(28)-hexaene-2,8,14,23-tetrone Chemical compound CC(C)[C@H]1OC(=O)C2=CCCN2C(=O)c2coc(CC(=O)C[C@H](O)\C=C(/C)\C=C\CNC(=O)\C=C\[C@H]1C)n2.CC[C@H]1NC(=O)[C@@H](NC(=O)c2ncccc2O)[C@@H](C)OC(=O)[C@@H](NC(=O)[C@@H]2CC(=O)CCN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)[C@@H]2CCCN2C1=O)c1ccccc1 MVTQIFVKRXBCHS-SMMNFGSLSA-N 0.000 description 2
- 108010080702 Virginiamycin Proteins 0.000 description 2
- 239000004188 Virginiamycin Substances 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 244000144977 poultry Species 0.000 description 2
- 235000013594 poultry meat Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000003307 slaughter Methods 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229960003842 virginiamycin Drugs 0.000 description 2
- 235000019373 virginiamycin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- OTXHZHQQWQTQMW-UHFFFAOYSA-N (diaminomethylideneamino)azanium;hydrogen carbonate Chemical compound OC([O-])=O.N[NH2+]C(N)=N OTXHZHQQWQTQMW-UHFFFAOYSA-N 0.000 description 1
- JCTUBDVBFJGKBH-UHFFFAOYSA-N 1,3-bis[[4-(diaminomethylidenehydrazinylidene)cyclohexa-2,5-dien-1-yl]imino]guanidine Chemical compound C1=CC(=NNC(=N)N)C=CC1N=NC(=N)N=NC1C=CC(=NNC(N)=N)C=C1 JCTUBDVBFJGKBH-UHFFFAOYSA-N 0.000 description 1
- AUEFUWQRTOQBOG-UHFFFAOYSA-N 1-amino-2-(4-chlorophenyl)guanidine;dihydrochloride Chemical compound Cl.Cl.NNC(=N)NC1=CC=C(Cl)C=C1 AUEFUWQRTOQBOG-UHFFFAOYSA-N 0.000 description 1
- RKOJUQGKURDYBX-UHFFFAOYSA-N 1-amino-3-benzylurea Chemical compound NNC(=O)NCC1=CC=CC=C1 RKOJUQGKURDYBX-UHFFFAOYSA-N 0.000 description 1
- NSVJAGNNPUQYGA-UHFFFAOYSA-N 1-amino-3-carbamoylurea;hydrochloride Chemical compound Cl.NNC(=O)NC(N)=O NSVJAGNNPUQYGA-UHFFFAOYSA-N 0.000 description 1
- LWPLPMSGDZDOLW-UHFFFAOYSA-N 2-amino-1-nitroguanidine Chemical compound NNC(=N)N[N+]([O-])=O LWPLPMSGDZDOLW-UHFFFAOYSA-N 0.000 description 1
- UJTTUOLQLCQZEA-UHFFFAOYSA-N 9h-fluoren-9-ylmethyl n-(4-hydroxybutyl)carbamate Chemical compound C1=CC=C2C(COC(=O)NCCCCO)C3=CC=CC=C3C2=C1 UJTTUOLQLCQZEA-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 235000019759 Maize starch Nutrition 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GLRFXIUFBYTCRD-UHFFFAOYSA-N [4-amino-2-(diaminomethylideneamino)anilino]thiourea Chemical compound NC(=S)NNC1=CC=C(N)C=C1N=C(N)N GLRFXIUFBYTCRD-UHFFFAOYSA-N 0.000 description 1
- 235000021120 animal protein Nutrition 0.000 description 1
- 235000004251 balanced diet Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- XRDACVXCOKISDA-UHFFFAOYSA-N chembl1162348 Chemical compound NC(=N)NN=C1C=CC(=NNC(N)=N)C=C1 XRDACVXCOKISDA-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- ACFNYGLBKAZUDY-UHFFFAOYSA-N cyclohexa-2,5-diene-1,4-diimine Chemical compound N=C1C=CC(=N)C=C1 ACFNYGLBKAZUDY-UHFFFAOYSA-N 0.000 description 1
- 239000004467 fishmeal Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 description 1
- QMEZUZOCLYUADC-UHFFFAOYSA-N hydrate;dihydrochloride Chemical compound O.Cl.Cl QMEZUZOCLYUADC-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
- 235000021055 solid food Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/16—Compounds containing any of the groups, e.g. aminoguanidine
- C07C281/18—Compounds containing any of the groups, e.g. aminoguanidine the other nitrogen atom being further doubly-bound to a carbon atom, e.g. guanylhydrazones
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/111—Aromatic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/116—Heterocyclic compounds
- A23K20/137—Heterocyclic compounds containing two hetero atoms, of which at least one is nitrogen
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C337/00—Derivatives of thiocarbonic acids containing functional groups covered by groups C07C333/00 or C07C335/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C337/06—Compounds containing any of the groups, e.g. thiosemicarbazides
- C07C337/08—Compounds containing any of the groups, e.g. thiosemicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. thiosemicarbazones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/52—Nitrogen atoms not forming part of a nitro radical with hetero atoms directly attached to said nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Birds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Fodder In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB15854/75A GB1504151A (en) | 1975-04-17 | 1975-04-17 | Methods using and compositions containing quinone derivatives for use in animal husbandry |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO760920L true NO760920L (sv) | 1976-10-19 |
Family
ID=10066720
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO760920A NO760920L (sv) | 1975-04-17 | 1976-03-16 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4112120A (sv) |
| JP (1) | JPS51131862A (sv) |
| AR (1) | AR209158A1 (sv) |
| AU (1) | AU1218176A (sv) |
| BE (1) | BE840889A (sv) |
| DD (1) | DD126626A5 (sv) |
| DE (1) | DE2616646A1 (sv) |
| DK (1) | DK142376A (sv) |
| ES (1) | ES447077A1 (sv) |
| FR (1) | FR2307478A1 (sv) |
| GB (1) | GB1504151A (sv) |
| IE (1) | IE42655B1 (sv) |
| IL (1) | IL49275A0 (sv) |
| NL (1) | NL7604023A (sv) |
| NO (1) | NO760920L (sv) |
| NZ (1) | NZ180331A (sv) |
| SE (1) | SE7603988L (sv) |
| SU (1) | SU668572A3 (sv) |
| ZA (1) | ZA761608B (sv) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU190384B (en) * | 1982-05-04 | 1986-08-28 | Egyt Gyogyszervegyeszeti Gyar,Hu | Process for preparing cycloalkane derivatives and compositions for weight increasing containing such compounds |
| HU190795B (en) * | 1982-05-04 | 1986-11-28 | Egyt Gyogyszervegyeszeti Gyar,Hu | Process for producing carbazinic derivatives and compositions containing them for increasing weight yield |
| DE3366405D1 (en) * | 1983-05-11 | 1986-10-30 | Berlin Chemie Veb | Process for the use of ergotropic agent combinations in the breeding and the fattening of useful animals |
| HU192633B (en) * | 1984-12-12 | 1987-06-29 | Egyt Gyogyszervegyeszeti Gyar | Process for producing carbazinic acid derivatives and compositions containing them for increasing weight-yield |
| US6106869A (en) * | 1998-07-23 | 2000-08-22 | T-Rex Products, Inc. | Method of using a terrarium substrate |
| US6391349B1 (en) * | 1998-07-23 | 2002-05-21 | T-Rex Products, Inc. | Glow-in-the-dark terrarium substrate and method of making and using the same |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1199202A (fr) * | 1952-12-24 | 1959-12-11 | Bayer Ag | Procédé de production de produits de condensation de p-quinones avec les aminoguanidines |
| GB774794A (en) * | 1953-01-30 | 1957-05-15 | Bayer Ag | Quinone condensation products |
| FR2212140A1 (en) * | 1972-12-28 | 1974-07-26 | Rouchy Maurice | Mono-and di-hydrazones of quinones - with antiviral and antihaemorragic activity for human and veterinary use |
-
1975
- 1975-04-17 GB GB15854/75A patent/GB1504151A/en not_active Expired
-
1976
- 1976-03-15 IE IE536/76A patent/IE42655B1/en unknown
- 1976-03-16 NZ NZ180331A patent/NZ180331A/xx unknown
- 1976-03-16 US US05/667,440 patent/US4112120A/en not_active Expired - Lifetime
- 1976-03-16 ZA ZA761608A patent/ZA761608B/xx unknown
- 1976-03-16 NO NO760920A patent/NO760920L/no unknown
- 1976-03-19 AU AU12181/76A patent/AU1218176A/en not_active Expired
- 1976-03-23 IL IL49275A patent/IL49275A0/xx unknown
- 1976-03-30 DK DK142376A patent/DK142376A/da not_active IP Right Cessation
- 1976-04-05 SE SE7603988A patent/SE7603988L/sv unknown
- 1976-04-13 AR AR262870A patent/AR209158A1/es active
- 1976-04-15 DD DD192388A patent/DD126626A5/xx unknown
- 1976-04-15 ES ES447077A patent/ES447077A1/es not_active Expired
- 1976-04-15 NL NL7604023A patent/NL7604023A/xx not_active Application Discontinuation
- 1976-04-15 DE DE19762616646 patent/DE2616646A1/de active Pending
- 1976-04-16 JP JP51043479A patent/JPS51131862A/ja active Pending
- 1976-04-16 FR FR7611490A patent/FR2307478A1/fr active Granted
- 1976-04-16 SU SU762345907A patent/SU668572A3/ru active
- 1976-04-16 BE BE166272A patent/BE840889A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES447077A1 (es) | 1978-03-01 |
| US4112120A (en) | 1978-09-05 |
| ZA761608B (en) | 1977-03-30 |
| IL49275A0 (en) | 1976-06-30 |
| DK142376A (da) | 1976-10-18 |
| IE42655B1 (en) | 1980-09-24 |
| AU1218176A (en) | 1977-09-22 |
| AR209158A1 (es) | 1977-03-31 |
| JPS51131862A (en) | 1976-11-16 |
| FR2307478B1 (sv) | 1980-09-12 |
| IE42655L (en) | 1976-10-17 |
| BE840889A (fr) | 1976-10-18 |
| DD126626A5 (sv) | 1977-08-03 |
| FR2307478A1 (fr) | 1976-11-12 |
| NZ180331A (en) | 1979-01-11 |
| SU668572A3 (ru) | 1979-06-15 |
| DE2616646A1 (de) | 1976-10-28 |
| GB1504151A (en) | 1978-03-15 |
| SE7603988L (sv) | 1976-10-18 |
| NL7604023A (nl) | 1976-10-19 |
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