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Merck
CN

75092

油酸

purum, natural, ≥98.0% (GC)

别名:

顺式-9-十八碳烯酸, 反油酸

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线性分子式:
CH3(CH2)7CH=CH(CH2)7COOH
化学文摘社编号:
分子量:
282.46
EC Number:
204-007-1
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
1726542
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vapor pressure

1 mmHg ( 176 °C)

grade

purum

assay

≥98.0% (GC)

quality

natural

refractive index

n20/D 1.459

bp

194-195 °C/1.2 mmHg (lit.)

mp

13-14 °C (lit.)

density

0.89 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCCCCCCC\C=C/CCCCCCCC(O)=O

InChI

1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H,19,20)/b10-9-

InChI key

ZQPPMHVWECSIRJ-KTKRTIGZSA-N

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Katerina Brychtova et al.
Bioorganic & medicinal chemistry, 18(24), 8556-8565 (2010-11-09)
Skin penetration enhancers are used in the formulation of transdermal delivery systems for drugs that are otherwise not sufficiently skin-permeable. We generated two series of esters by multi-step synthesis with substituted 6-aminohexanoic acid as potential transdermal penetration enhancers by multi-step
Michael J Bruno et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(23), 9638-9643 (2007-05-31)
At low micromolar concentrations, polyunsaturated fatty acids (PUFAs) alter the function of many membrane proteins. PUFAs exert their effects on unrelated proteins at similar concentrations, suggesting a common mode of action. Because lipid bilayers serve as the common "solvent" for
Haiyan Cai et al.
Bioorganic & medicinal chemistry letters, 20(12), 3675-3679 (2010-05-18)
In this study, a series of small molecule inhibitors of human FABP4 were identified through virtual screening. Compound 1 is the most potent hit against FABP4 with a selectivity of more than 144-fold preferences over human FABP3. In addition, MD
Aaron T Wecksler et al.
Bioorganic & medicinal chemistry, 17(18), 6534-6539 (2009-09-01)
Recently, it has been shown that lipoxygenase (LO) products affect the substrate specificity of human 15-LO. In the current paper, we demonstrate that soybean LO-1 (sLO-1) is not affected by its own products, however, inhibitors which bind the allosteric site
Richard Sulsky et al.
Bioorganic & medicinal chemistry letters, 17(12), 3511-3515 (2007-05-16)
Herein we report the first disclosure of biphenyl azoles that are nanomolar binders of adipocyte fatty acid binding protein (aFABP or aP2) with up to thousand-fold selectivity against muscle fatty acid binding protein and epidermal fatty acid binding protein. In

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