推荐产品
质量水平
方案
≥95% (GC)
表单
powder
mp
41-42 °C (lit.)
溶解性
pyridine: 50 mg/mL, clear, colorless to faintly yellow
荧光
λex 312 nm in methanol
λex 360 nm; λem 449 nm (Reaction product)
储存温度
−20°C
SMILES字符串
CCCCCCC(=O)Oc1ccc2C(C)=CC(=O)Oc2c1
InChI
1S/C17H20O4/c1-3-4-5-6-7-16(18)20-13-8-9-14-12(2)10-17(19)21-15(14)11-13/h8-11H,3-7H2,1-2H3
InChI key
FFNBFZWIBOIPIV-UHFFFAOYSA-N
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
L Fiksdal et al.
Applied and environmental microbiology, 55(9), 2424-2427 (1989-09-01)
The production of an enzyme, 4-methylumbelliferyl heptanoate hydrolase, in Escherichia coli exposed to enriched and nonenriched seawater was studied. In all media, except for seawater with no or very small amounts of organic material and seawater enriched with peptone, 4-methylumbelliferyl
S Krüger-Krasagakes et al.
Journal of immunological methods, 156(1), 1-8 (1992-11-25)
In order to measure cell mediated cytotoxicity to adherent growing cell lines in vitro more rapidly and conveniently, a fluorometric microassay was developed and results were compared with those obtained by the 51Cr release assay. The fluorometric method is based
E N Dotsika et al.
Journal of immunological methods, 105(1), 55-62 (1987-12-04)
A microplate method for assessing cell growth and viability based on the hydrolysis of fluorogenic substrates by cell esterases has been investigated. Living cells incubated with fluorescein diacetate or 4-methylumbelliferyl heptanoate generate a fluorescent product which is proportional to the
L Virág et al.
Journal of immunological methods, 185(2), 199-208 (1995-09-25)
A fluorimetric method using 4-methylumbelliferyl heptanoate (MUH) has been developed for detecting cell-mediated cytotoxicity and cell proliferation. The assay is based on the hydrolysis of the fluorochrome (MUH) by intracellular esterases of viable cells resulting in the production of highly
C C Zouboulis et al.
Melanoma research, 1(2), 91-95 (1991-06-01)
A simple, rapid and reproducible assay for the determination of melanoma cell proliferation in vitro is described, based on the hydrolysis of a fluorogenic substrate by cell esterases in the cytoplasm of living cells. Human melanoma cells were cultured at
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