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土霉素 二水合物_分子结构_CAS_6153-64-6)
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土霉素 二水合物

产品号 O4636 公司名称 Sigma Aldrich
CAS号 6153-64-6 公司网站 http://www.sigmaaldrich.com
分子式 C22H26N2O10 电 话 1-800-521-8956
分子量 478.44924 传 真
纯 度 ≥99% (TLC) 电子邮件
保 存 Chembase数据库ID: 153449

产品价格信息

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产品别名

标题
Oxytetracycline dihydrate
IUPAC标准名
(4S,4aR,5S,5aR,6S,12aS)-4-(dimethylamino)-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrate
IUPAC传统名
oxytetracycline hydrate

产品登记号

MDL号 MFCD00151234
PubChem SID 24898000
EC号 201-212-8
CAS号 6153-64-6

产品性质

痕量阴离子 chloride (Cl-): ≤0.05%
痕量阴离子 sulfate (SO42-): ≤0.05%
痕量阳离子 Al: ≤0.001%
痕量阳离子 Ca: ≤0.2%
痕量阳离子 Cu: ≤0.0005%
痕量阳离子 Fe: ≤0.002%
痕量阳离子 K: ≤0.005%
痕量阳离子 Mg: ≤0.005%
痕量阳离子 Na: ≤0.01%
痕量阳离子 Pb: ≤0.001%
痕量阳离子 Zn: ≤0.0005%
Empirical Formula (Hill Notation) C22H24N2O9 · 2H2O
燃烧残渣 ≤1.0%
杂质 ≤0.001% Phosphorus (P)
杂质 ≤0.1% Insoluble matter
产品线 BioXtra
纯度 ≥99% (TLC)
溶解度 1 M HCl: soluble0.1 M, clear (yellow to yellow-orange)
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
Antibiotic produced by Streptomyces rimosus.Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Active efflux, ribosome protection, tetracycline inactivation.
Oxytetracycline inhibits translation, which results in cell death. It binds to the 30S ribosomal subunit and prevents the amino-acyl Trna from binding to the A site of the ribosome. The binding is reversible in nature. Oxytetracycline is lipophilic so it can easily pass through a cell membrane and passively diffuses through channels in the bacterial membrane.
Application
Oxytetracycline is a tetracycline analog isolated from the actinomycete Streptomyces rimosus. Oxytetracycline is an antibiotic indicated for treatment of infections caused by Gram positive and Gram negative microorganisms such as Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae, and Diplococcus pneumoniae. It is used in studies on the oxytetracycline-resistance gene (otrA). It is used for fluorescence measurements of hepatocytes1.
详细说明 (简体中文)
Biochem/physiol Actions
Antibiotic produced by Streptomyces rimosus.Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Active efflux, ribosome protection, tetracycline inactivation.
Oxytetracycline inhibits translation, which results in cell death. It binds to the 30S ribosomal subunit and prevents the amino-acyl Trna from binding to the A site of the ribosome. The binding is reversible in nature. Oxytetracycline is lipophilic so it can easily pass through a cell membrane and passively diffuses through channels in the bacterial membrane.
Application
Oxytetracycline is a tetracycline analog isolated from the actinomycete Streptomyces rimosus. Oxytetracycline is an antibiotic indicated for treatment of infections caused by Gram positive and Gram negative microorganisms such as Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae, and Diplococcus pneumoniae. It is used in studies on the oxytetracycline-resistance gene (otrA). It is used for fluorescence measurements of hepatocytes1.

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