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Paromomycin sulfate salt структурированное изображение

Paromomycin sulfate salt

  • английское имяPAROMOMYCIN SULFATE
  • CAS №1263-89-4
  • CBNumberCB2278832
  • ФормулаC23H47N5O18S
  • мольный вес713.71
  • EINECS215-031-7
  • номер MDLMFCD00079278
  • файл Mol1263-89-4.mol
химическое свойство
Температура плавления 145 °C (decomp)
альфа D25 +50.5° (c = 1.5 in water pH 6)
температура хранения Keep in dark place,Inert atmosphere,Room temperature
растворимость H2O: 50 mg/mL store stock solution at 2-8°C. Stable at 37°C for 5 days.
форма powder
цвет White to Off-White
Растворимость в воде Soluble in water
Мерк 14,7041
БРН 5715182
Стабильность Hygroscopic
ИнЧИКей LJRDOKAZOAKLDU-UDXJMMFXSA-N
Справочник по базе данных CAS 1263-89-4
FDA UNII 845NU6GJPS
Словарь наркотиков NCI Humatin
Система регистрации веществ EPA Paromomycin sulfate (1263-89-4)
Заявления об опасности и безопасности
Коды опасности Xi
Заявления о рисках 23/24/25-36/38-39/23/24/25-61-36/37/38
Заявления о безопасности 26-36/37-45-38-36
WGK Германия 2
RTECS WK2320000
кода HS 2941901010
Токсичность LD50 in mice (mg/kg): ~15,000 orally; 700 s.c.; 110 i.v. (Di Marco, Bertazzoli)

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H315:При попадании на кожу вызывает раздражение.

    H319:При попадании в глаза вызывает выраженное раздражение.

    H335:Может вызывать раздражение верхних дыхательных путей.

  • оператор предупредительных мер

    P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.

    P304+P340:ПРИ ВДЫХАНИИ: Свежий воздух, покой.

    P305+P351+P338:ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.

    P405:Хранить в недоступном для посторонних месте.

Paromomycin sulfate salt химические свойства, назначение, производство

Описание

Paromomycin was found in the culture broth of Streptomyces rimosus forma paromomycinus by Parke Davis & Co. in 1959. In the same year it was found in the culture broth of S. Crestomyceticus by Farmitalia and named amminosidin. Paromomycin is related structurally to neomycin, but it has a hydroxyl group at the 6 position, whereas neomycin has an amino group. Its antibacterial activity is weaker than that of neomycin, but its toxicity is much less. Paromomycin is used by intramuscular injection for therapy of respiratory, urinary, and surgical infections and by oral administration to treat dysentery and salmonellosis.

Химические свойства

PAROMOMYCIN SULFATE is White to Off-White Solid

Использование

PAROMOMYCIN SULFATE is an aminogycoside antibiotic designed to fight intestinal infections such as cryptosporidiosis, amoebiasis, and leishmaniasis. Its antiprotozoal activity makes it an effecive histomonostatic feed addit ive in turkey poults experimentally infected with Histomonas meleagridis.

Определение

ChEBI: An aminoglycoside sulfate salt resulting from the treatment of paromomycin with sulfuric acid. A broad-spectrum antibiotic, it is used for the treatment of acute and chronic intestinal protozoal infections, but is not effective for extraintestinal protozoa infections. It is also used as a therapeutic against visceral leishmaniasis.

Общее описание

Chemical structure: aminoglycoside

Клиническое использование

The isolation of paromomycin (Humatin) was reported in1956 from a fermentation with a Streptomyces sp. (PD04998), a strain said to resemble S. rimosus very closely.The parent organism had been obtained from soil samplescollected in Colombia. Paromomycin, however, moreclosely resembles neomycin and streptomycin in antibioticactivity than it does oxytetracycline, the antibiotic obtainedfrom S. rimosus.
Paromomycin has broad-spectrum antibacterial activityand has been used for the treatment of GI infections causedby Salmonella and Shigella spp., and enteropathogenic E.coli. Currently, however, its use is restricted largely to thetreatment of intestinal amebiasis. Paromomycin is soluble inwater and stable to heat over a wide pH range.

Профиль безопасности

Poison by intravenous,subcutaneous, and intramuscular routes. Mildly toxic byingestion. Mutation data reported. When heated to decomposition it emits very toxic fumesof SOx and NOx.

Методы очистки

Purify it by dissolving it in H2O (0.5g/10mL) and adding excess EtOH, filter or collect and wash with EtOH, then Et2O by centrifugation, and dry it in vacuo. An aqueous solution is stable at 37o for a week but longer at 0-5o. The free base [7542-37-2] is a white amorphous powder which should be stored under N2 because it is strongly basic and can absorb CO2 from the atmosphere. It is soluble in MeOH (less soluble in EtOH) and has [] D 25 +65o (c 1.5, MeOH). It is an antimicrobial against Gram +ve and Gram –ve bacteria and is antiamoebic. It inhibits initiation and peptide elongation during protein synthesis. [Haskell et al. J Am Chem Soc 8 1 , 3480, 3482 1959, Hichens & Rinehart J Am Chem Soc 85 1547 1963, Beilstein 18 III/IV 7534.]

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