MD4274C1 - Азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений - Google Patents
Азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений Download PDFInfo
- Publication number
- MD4274C1 MD4274C1 MDA20130033A MD20130033A MD4274C1 MD 4274 C1 MD4274 C1 MD 4274C1 MD A20130033 A MDA20130033 A MD A20130033A MD 20130033 A MD20130033 A MD 20130033A MD 4274 C1 MD4274 C1 MD 4274C1
- Authority
- MD
- Moldova
- Prior art keywords
- bis
- plants
- iii
- nicotinamide
- cobalt
- Prior art date
Links
- 230000003078 antioxidant effect Effects 0.000 title claims abstract description 15
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 title claims description 16
- 235000005152 nicotinamide Nutrition 0.000 title claims description 8
- 239000011570 nicotinamide Substances 0.000 title claims description 8
- 229960003966 nicotinamide Drugs 0.000 title claims description 6
- 229910017052 cobalt Inorganic materials 0.000 title claims description 4
- 239000010941 cobalt Substances 0.000 title claims description 4
- 150000004683 dihydrates Chemical class 0.000 title claims description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 title 1
- 230000001747 exhibiting effect Effects 0.000 title 1
- GSOLWAFGMNOBSY-UHFFFAOYSA-N cobalt Chemical compound [Co][Co][Co][Co][Co][Co][Co][Co] GSOLWAFGMNOBSY-UHFFFAOYSA-N 0.000 claims description 3
- -1 nitrogenous compound Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 abstract description 10
- 239000003963 antioxidant agent Substances 0.000 abstract description 8
- 241000196324 Embryophyta Species 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 235000006708 antioxidants Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- 238000003359 percent control normalization Methods 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 230000006378 damage Effects 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- WSMYVTOQOOLQHP-UHFFFAOYSA-N Malondialdehyde Chemical compound O=CCC=O WSMYVTOQOOLQHP-UHFFFAOYSA-N 0.000 description 3
- 229910002651 NO3 Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 2
- JGUQDUKBUKFFRO-CIIODKQPSA-N dimethylglyoxime Chemical compound O/N=C(/C)\C(\C)=N\O JGUQDUKBUKFFRO-CIIODKQPSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011708 vitamin B3 Substances 0.000 description 2
- 235000019160 vitamin B3 Nutrition 0.000 description 2
- 108060006004 Ascorbate peroxidase Proteins 0.000 description 1
- 102000016938 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- 241000880490 Leopardus colocolo Species 0.000 description 1
- 102000019197 Superoxide Dismutase Human genes 0.000 description 1
- 108010012715 Superoxide dismutase Proteins 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 235000021466 carotenoid Nutrition 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 229930002868 chlorophyll a Natural products 0.000 description 1
- 229930002869 chlorophyll b Natural products 0.000 description 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Abstract
Изобретение относится к химии, в частности к координационным соединениям которые могут быть использованы в качестве антиоксидантов в сельском хозяйстве.Согласно изобретению, заявляется координационное соединение - азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20130033A MD4274C1 (ru) | 2013-05-27 | 2013-05-27 | Азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20130033A MD4274C1 (ru) | 2013-05-27 | 2013-05-27 | Азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MD4274B1 MD4274B1 (en) | 2014-02-28 |
| MD4274C1 true MD4274C1 (ru) | 2014-09-30 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MDA20130033A MD4274C1 (ru) | 2013-05-27 | 2013-05-27 | Азотат транс бис(диметилглиоксимато)бис(никотинамид)кобальт(III)дигидрат, проявляющий антиоксидантные свойства у растений |
Country Status (1)
| Country | Link |
|---|---|
| MD (1) | MD4274C1 (ru) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD955F1 (en) * | 1997-07-29 | 1998-04-30 | Inst De Chimie Al Academiei De | Hexa-m-acetato(O,O')-m3-oxo-tris (N,N'-diethylnicotinamide)-diûiron(III)cobalt(II) monohydrate having plants growing, vegetation and productivity regulation activity |
| RU2006140961A (ru) * | 2004-05-28 | 2008-07-10 | Юниджен Фармасьютикалз | Диарилалканы в качестве эффективных ингибиторов двухъядерных ферментов |
| US8067394B2 (en) * | 2006-11-17 | 2011-11-29 | Trustees Of Dartmouth College | Synthesis and biological activities of new tricyclic-bis-enones (TBEs) |
| RU2011101380A (ru) * | 2008-06-16 | 2012-07-27 | Эдвин Хенрикус Антониус ХОЛМАН (NL) | Способ возделывания растений |
| US20130131006A1 (en) * | 2010-05-11 | 2013-05-23 | Gachon University Of Industry-Academic Cooperation Foundation | Method for inhibiting the induction of cell death by inhibiting the synthesis or secretion of age-albumin in cells of the mononuclear phagocyte system |
-
2013
- 2013-05-27 MD MDA20130033A patent/MD4274C1/ru not_active IP Right Cessation
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD955F1 (en) * | 1997-07-29 | 1998-04-30 | Inst De Chimie Al Academiei De | Hexa-m-acetato(O,O')-m3-oxo-tris (N,N'-diethylnicotinamide)-diûiron(III)cobalt(II) monohydrate having plants growing, vegetation and productivity regulation activity |
| RU2006140961A (ru) * | 2004-05-28 | 2008-07-10 | Юниджен Фармасьютикалз | Диарилалканы в качестве эффективных ингибиторов двухъядерных ферментов |
| US8067394B2 (en) * | 2006-11-17 | 2011-11-29 | Trustees Of Dartmouth College | Synthesis and biological activities of new tricyclic-bis-enones (TBEs) |
| RU2011101380A (ru) * | 2008-06-16 | 2012-07-27 | Эдвин Хенрикус Антониус ХОЛМАН (NL) | Способ возделывания растений |
| US20130131006A1 (en) * | 2010-05-11 | 2013-05-23 | Gachon University Of Industry-Academic Cooperation Foundation | Method for inhibiting the induction of cell death by inhibiting the synthesis or secretion of age-albumin in cells of the mononuclear phagocyte system |
Non-Patent Citations (1)
| Title |
|---|
| Чиркова Т.В., Новицкая Л.О., Блохина О.Б. Перекисное окисление липидов и активность антиоксидантных систем при аноксии у растений с разной устойчивостью к недостатку кислорода. Физиология растений. 1998. Т. 45. №1. С. 65-73. * |
Also Published As
| Publication number | Publication date |
|---|---|
| MD4274B1 (en) | 2014-02-28 |
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|---|---|---|---|
| FG4A | Patent for invention issued | ||
| KA4A | Patent for invention lapsed due to non-payment of fees (with right of restoration) | ||
| MM4A | Patent for invention definitely lapsed due to non-payment of fees |