推荐产品
生物来源
Streptomyces aureofaciens
质量水平
产品线
BioReagent
方案
≥85.0% (HPLC)
表单
powder or crystals
颜色
faintly yellow to yellow
mp
210-215 °C (dec.) (lit.)
溶解性
H2O: 50 mg/mL
适用性
suitable for fluorescence
抗生素抗菌谱
Gram-negative bacteria
Gram-positive bacteria
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相关类别
一般描述
Chemical structure: tetracycline
应用
Cell-permeable fluorescent probe for Ca2+ for measuring calcium flux in endoplasmic reticulum and other intracellular stores in situ.
生化/生理作用
Chlortetracycline is an antibiotic produced by some strains of Streptomyces aureofaciens.
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.
Antimicrobial spectrum: Gram-positive. Less active against Gram-negative bacteria than tetracycline.
Mode of Resistance: Loss of cell wall permeability.
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.
Antimicrobial spectrum: Gram-positive. Less active against Gram-negative bacteria than tetracycline.
Mode of Resistance: Loss of cell wall permeability.
包装
5 g, 25 g, 100g
质量
Recommended for fluorescent studies of calcium signaling in cells or tissues.
其他说明
Keep container tightly closed in a dry and well-ventilated place.
警示用语：
Warning
危险分类
Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
易制爆化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Sc (OTf) 3-Catalyzed Conjugate Allylation of Alkylidene Meldrum′s Acids
Dumas AM and Fillion E
Organic Letters, 11(9), 1919-1922 (2009)
Palladium-Catalyzed Direct Arylations of Azoles with Aryl Silicon and Tin Reagents
Han W, et al.
Chemistry?A European Journal , 17(25), 6904-6908 (2011)
Allyltriphenylstannane
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Total synthesis of (+)-ambruticin S: probing the pharmacophoric subunit
Hanessian S, et al.
The Journal of Organic Chemistry, 75(16), 5601-5618 (2010)
Journal of the American Chemical Society, 103, 1969-1969 (1981)
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