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Дорамектин
- английское имяDoramectin
- CAS №117704-25-3
- CBNumberCB4167857
- ФормулаC50H74O14
- мольный вес899.11
- EINECS601-490-4
- номер MDLMFCD00894747
- файл Mol117704-25-3.mol
Температура плавления | 116-1190C |
Температура кипения | 967.4±65.0 °C(Predicted) |
плотность | 1.25±0.1 g/cm3(Predicted) |
давление пара | 0Pa at 20℃ |
температура хранения | Sealed in dry,Store in freezer, under -20°C |
растворимость | methanol: soluble |
форма | solid |
пка | 12.42±0.70(Predicted) |
цвет | white |
ИнЧИКей | QLFZZSKTJWDQOS-YDBLARSUSA-N |
LogP | 4.39-4.43 at 25℃ |
FDA 21 CFR | 556.222 |
FDA UNII | KGD7A54H5P |
Коды опасности | T,N,Xi | |||||||||
Заявления о рисках | 25-50/53-36/37/38 | |||||||||
Заявления о безопасности | 33-45-60-61-36/37-26 | |||||||||
РИДАДР | UN 2811 6.1/PG 3 | |||||||||
WGK Германия | 3 | |||||||||
кода HS | 29419090 | |||||||||
Банк данных об опасных веществах | 117704-25-3(Hazardous Substances Data) | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H302:Вредно при проглатывании.
H362:Может причинить вред детям, находящимся на грудном вскармливании.
H410:Чрезвычайно токсично для водных организмов с долгосрочными последствиями.
H361fd:Предполагается, что данное вещество может отрицательно повлиять на способность к деторождению. Предполагается, что данное вещество может отрицательно повлиять на неродившегося ребенка.
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оператор предупредительных мер
P202:Перед использованием ознакомиться с инструкциями по технике безопасности.
P260:Не вдыхать газ/ пары/ пыль/ аэрозоли/ дым/ туман.
P263:Избегать контакта в период беременности и грудного вскармливания.
P273:Избегать попадания в окружающую среду.
P301+P312:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P308+P313:ПРИ подозрении на возможность воздействия обратиться за медицинской помощью.
Дорамектин химические свойства, назначение, производство
Описание
Doramectin[117704-25-3] is a novel avermectin with a cyclohexyl substituent on the previously inaccessible C-25 position of the molecule; the substitution was facilitated by mutational biosynthesis. The discovery of doramectin involved feeding carboxylic acids or their precursors to a fermentation of Streptomyces avermitilis that lacked branched-chain 2-oxo acid dehydrogenase activity, and then screening the resultant fermentation products for anthelmintic and ectoparasiticidal activity. Two dosage forms of doramectin have been developed for use as an endectocide on cattle, an injectable formulation for subcutaneous administration and a pouron formulation. An injectable formulation is also approved for use on pigs.Химические свойства
White solid or slightly yellow-brown powder with poor water solubility, low stability, easily decomposed and deactivated by sunlight. The remaining drug residue is toxic to fish and aquatic organisms, requiring water source protection.Использование
Doramectin is a biosynthetic avermectin derived from a mutant strain of Streptomyces avermitilis, supplemented with a cyclohexylcaboxylic acid starting unit. Doramectin was developed as an anthelmintic for internal parasite control. The presence of the cyclohexyl group replacing the sec-butyl moiety affords greater hydrophobicity and longer biological half-life compared to avermectin. Like the other milbemycin/avermectins, it selectively binds to parasite glutamate-gated chloride ion channels and disrupts neurotransmission leading to paralysis and death of the parasite.прикладной
Doramectin is a mutational biosynthetic antiparasitic antibiotic structurally related to the avermectins. Avermectins are a group of agents that occurs naturally as a product of fermenting Streptomyces avermitilis, isolated from the soil. Avermectins are composed of a structurally similar 16-membered macrocyclic lactone, and widely used as insecticidal and antiparasitic agents. Doramectin is one of the best of a series of avermectins with antiparasitic activity.Структура и конформация
Doramectin is a macrolide drug of the avermectin family, which is very similar in structure to ivermectin. Doramectin C25 is cyclohexane, and ivermectin is a mixture of several homologues. The C25 of its highly active component B1a (80%) is CH(CH3)C2H5, and the C25 of another component B1b (20%) is CH(CH3)-CH3. Doramectin has a double bond between C22 and C23, while ivermectin has a single bond.использованная литература
1. Production of doramectin by rational engineering of the avermectin biosynthetic pathway. DOI:10.1016/j.bmcl.2011.04.0082. Construction of a doramectin producer mutant from an avermectin-overproducing industrial strain of Streptomyces avermitilis.DOI:10.1139/W09-098
3. An alternative derivatization reaction to the determination of doramectin in bovine milk using spectrofluorimetry.DOI:10.1016/j.saa.2012.02.084
4. Doramectin - a potent novel endectocide. DOI:10.1016/0304-4017(93)90218-C
5. Avermectin derivatives, pharmacokinetics, therapeutic and toxic dosages, mechanism of action, and their biological effects (a review). DOI:10.3390/ph13080196
6. Research progress of avermectin: A minireview based on the structural derivatization of avermectin. DOI:10.1016/j.aac.2022.11.001
7. Positive and negative electrospray LC-MS-MS methods for quantitation of the antiparasitic endectocide drugs, abamectin, doramectin, emamectin, eprinomectin, ivermectin, moxidectin and selamectin in milk. DOI:10.1016/J.JCHROMB.2006.11.014
8. https://www.fda.gov/animal-veterinary/cvm-updates/fda-approves-first-generic-doramectin-topical-solution-treatment-certain-parasites-cattle
Дорамектин поставщик
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+8613812269233 | China | 322 | 58 | ||
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+86-53169958659 +86-13153181156 |
China | 294 | 58 | ||
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+86 13288715578 +8613288715578 |
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+86-17331933971 +86-17331933971 |
China | 2472 | 58 | ||
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