IL28004A - Derivatives of 6-(6'-oxo-10'-hydroxy-undecyl)-2,4-dihydroxy-benzoic acid lactone - Google Patents
Derivatives of 6-(6'-oxo-10'-hydroxy-undecyl)-2,4-dihydroxy-benzoic acid lactoneInfo
- Publication number
- IL28004A IL28004A IL28004A IL2800467A IL28004A IL 28004 A IL28004 A IL 28004A IL 28004 A IL28004 A IL 28004A IL 2800467 A IL2800467 A IL 2800467A IL 28004 A IL28004 A IL 28004A
- Authority
- IL
- Israel
- Prior art keywords
- compound according
- compound
- ration
- feed
- growth promoting
- Prior art date
Links
- -1 of 6-(6'-oxo-10'-hydroxy-undecyl)-2,4-dihydroxy-benzoic acid lactone Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 39
- 241001465754 Metazoa Species 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 235000015097 nutrients Nutrition 0.000 claims 6
- 230000001737 promoting effect Effects 0.000 claims 6
- 125000002015 acyclic group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 7
- 240000008042 Zea mays Species 0.000 description 5
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 5
- 235000005822 corn Nutrition 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 240000004658 Medicago sativa Species 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 235000013619 trace mineral Nutrition 0.000 description 4
- 239000011573 trace mineral Substances 0.000 description 4
- 241000283690 Bos taurus Species 0.000 description 3
- 241000219823 Medicago Species 0.000 description 3
- 150000002118 epoxides Chemical class 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 235000013379 molasses Nutrition 0.000 description 3
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 235000019483 Peanut oil Nutrition 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 229940036811 bone meal Drugs 0.000 description 2
- 239000002374 bone meal Substances 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000006027 corn-soybean meal Substances 0.000 description 2
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 2
- 229940038472 dicalcium phosphate Drugs 0.000 description 2
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000312 peanut oil Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 235000019155 vitamin A Nutrition 0.000 description 2
- 239000011719 vitamin A Substances 0.000 description 2
- 229940045997 vitamin a Drugs 0.000 description 2
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 235000019737 Animal fat Nutrition 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000283903 Ovis aries Species 0.000 description 1
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical class CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- 229930003316 Vitamin D Natural products 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000021120 animal protein Nutrition 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- IRZRPCGCUMAJRH-UHFFFAOYSA-L calcium;urea;carbonate Chemical compound [Ca+2].NC(N)=O.[O-]C([O-])=O IRZRPCGCUMAJRH-UHFFFAOYSA-L 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229940125797 compound 12 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 230000001076 estrogenic effect Effects 0.000 description 1
- 239000004467 fishmeal Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000004466 pelleted feed Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940046001 vitamin b complex Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- 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
- A23K20/121—Heterocyclic compounds containing oxygen or sulfur as hetero atom
- A23K20/126—Lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
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)
- Fodder In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56140266A | 1966-06-29 | 1966-06-29 | |
| US62026467A | 1967-03-03 | 1967-03-03 | |
| US676079A US3373038A (en) | 1966-06-29 | 1967-10-18 | Estrogenic compounds and animal growth promoters |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL28004A true IL28004A (en) | 1971-08-25 |
Family
ID=27415850
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL28004A IL28004A (en) | 1966-06-29 | 1967-05-18 | Derivatives of 6-(6'-oxo-10'-hydroxy-undecyl)-2,4-dihydroxy-benzoic acid lactone |
| IL30811A IL30811A0 (en) | 1966-06-29 | 1968-10-01 | Estrogenic compounds and animal growth promoters |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL30811A IL30811A0 (en) | 1966-06-29 | 1968-10-01 | Estrogenic compounds and animal growth promoters |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3373038A (en, 2012) |
| BE (2) | BE700218A (en, 2012) |
| DE (1) | DE1801744A1 (en, 2012) |
| FR (2) | FR1564480A (en, 2012) |
| GB (2) | GB1153366A (en, 2012) |
| IL (2) | IL28004A (en, 2012) |
| NL (2) | NL6708986A (en, 2012) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4228079A (en) * | 1978-10-30 | 1980-10-14 | W. R. Grace & Co. | Dialkoxy monorden derivatives |
| US4409392A (en) * | 1981-09-03 | 1983-10-11 | International Minerals & Chemical Corp. | 6' Esters of zearalanol |
| US4849447A (en) * | 1987-10-13 | 1989-07-18 | Pitman-Moore, Inc. | Zearalanol derivatives with anabolic activity |
| ATE328888T1 (de) | 2000-08-25 | 2006-06-15 | Sloan Kettering Inst Cancer | Radicicol und monocillin und ihre analogen und ihre anwendungen |
| CN1652743A (zh) * | 2002-04-17 | 2005-08-10 | 大正制药株式会社 | 毛发生长补剂 |
| US20080108694A1 (en) * | 2003-12-19 | 2008-05-08 | Samuel J Danishefsky | Novel Macrocycles and Uses Thereof |
| WO2008021213A1 (en) | 2006-08-11 | 2008-02-21 | Nicolas Winssinger | Macrocyclic compounds useful as inhibitors of kinases and hsp90 |
| US20110190237A1 (en) * | 2008-01-15 | 2011-08-04 | Nexgenix Pharmaceuticals | Macrocyclic Prodrug Compounds Useful as Therapeutics |
-
0
- FR FR170236A patent/FR96016E/fr not_active Expired
-
1967
- 1967-05-18 IL IL28004A patent/IL28004A/en unknown
- 1967-05-18 GB GB23155/67A patent/GB1153366A/en not_active Expired
- 1967-06-14 FR FR1564480D patent/FR1564480A/fr not_active Expired
- 1967-06-20 BE BE700218D patent/BE700218A/xx unknown
- 1967-06-28 NL NL6708986A patent/NL6708986A/xx unknown
- 1967-10-18 US US676079A patent/US3373038A/en not_active Expired - Lifetime
-
1968
- 1968-10-01 IL IL30811A patent/IL30811A0/xx unknown
- 1968-10-08 DE DE19681801744 patent/DE1801744A1/de active Pending
- 1968-10-10 GB GB1230219D patent/GB1230219A/en not_active Expired
- 1968-10-11 NL NL6814557A patent/NL6814557A/xx unknown
- 1968-10-17 BE BE722455D patent/BE722455A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR96016E (fr) | 1972-05-19 |
| NL6708986A (en, 2012) | 1968-01-02 |
| FR1564480A (en, 2012) | 1969-04-25 |
| BE700218A (en, 2012) | 1967-12-01 |
| US3373038A (en) | 1968-03-12 |
| IL30811A0 (en) | 1968-12-26 |
| GB1153366A (en) | 1969-05-29 |
| NL6814557A (en, 2012) | 1969-04-22 |
| DE1801744A1 (de) | 1969-05-08 |
| BE722455A (en, 2012) | 1969-04-01 |
| GB1230219A (en, 2012) | 1971-04-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3812259A (en) | Animal feed and process | |
| US3373024A (en) | Estrogenic compounds and animal growth promoters | |
| US3338718A (en) | Animal feeds containing maltol | |
| IL28004A (en) | Derivatives of 6-(6'-oxo-10'-hydroxy-undecyl)-2,4-dihydroxy-benzoic acid lactone | |
| US3261687A (en) | Animal feed containing lincomycin and spectinomycin | |
| US3781440A (en) | Animal feed compositions and methods | |
| US5641806A (en) | Growth promotion and feed utilization in swine with Frenolicin B | |
| US3751431A (en) | F.e.s.derivatives | |
| US4622341A (en) | Growth-promoter fodders and feed additives and process for their preparation | |
| US3373030A (en) | Estrogenic compounds and animal growth promoters | |
| US3850987A (en) | Compounds useful as feed supplements | |
| US3373036A (en) | Estrogenic compounds and animal growth promoters | |
| US3373029A (en) | Estrogenic compounds and animal growth promoters | |
| US3144337A (en) | Animal feed containing steroidal sapogenin | |
| PL115472B1 (en) | Fodder appropriated for pigs not being afflicted with dysentery | |
| US3373035A (en) | Estrogenic compounds and animal growth promoters | |
| US3284210A (en) | Feed compositions containing n-substituted aminooxyacetic acid compounds and methods | |
| US3745221A (en) | Methods and compositions for improving feed efficiency of ruminants using poyhydric alkanol haloacetaldehyde hemiacetals | |
| US3373026A (en) | Estrogenic compounds and animal growth promoters | |
| US3803313A (en) | Animal feed and process | |
| US3092496A (en) | Animal feeds | |
| US3778508A (en) | Feed compositions and methods | |
| GB1564187A (en) | Composition and method for promoting animal nutrition | |
| US2971885A (en) | Animal feeds | |
| US3373032A (en) | Estrogenic compounds and animal growth promoters |