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Methyl phenylacetate Sale

(Synonyms: 苯乙酸甲酯) 目录号 : GC61056

Methylphenylacetate是一种内源性代谢产物。

Methyl phenylacetate Chemical Structure

Cas No.:101-41-7

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500mg
¥450.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Methyl phenylacetate is an endogenous metabolite.

Chemical Properties

Cas No. 101-41-7 SDF
别名 苯乙酸甲酯
Canonical SMILES O=C(OC)CC1=CC=CC=C1
分子式 C9H10O2 分子量 150.17
溶解度 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 6.6591 mL 33.2956 mL 66.5912 mL
5 mM 1.3318 mL 6.6591 mL 13.3182 mL
10 mM 0.6659 mL 3.3296 mL 6.6591 mL
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Research Update

Novel naftopidil derivatives containing Methyl phenylacetate and their blocking effects on α1D/1A-adrenoreceptor subtypes

Bioorg Med Chem Lett 2018 Feb 15;28(4):547-551.PMID:29422390DOI:10.1016/j.bmcl.2018.01.068.

α1-Adrenoceptor (α1-AR) antagonists are considered to be the most effective monotherapy agents for lower urinary tract symptoms associated with benign prostatic hyperplasia (LUTS/BPH). In this study, we synthesized compounds 2-17, which are novel piperazine derivatives that contain Methyl phenylacetate. We then evaluated the vasodilatory activities of these compounds. Among them, we found that compounds 2, 7, 12, which contain 2-OCH3, 2-CH3 or 2, 5-CH3, respectively, exhibited potent α1-blocking activity similar to protype drug naftopidil (1). The antagonistic effects of 2, 7, and 12 on the (-)-noradrenaline-induced contractile response of isolated rat prostatic vas deferens (α1A), spleen (α1B) and thoracic aorta (α1D) were further characterized to assess the sub receptor selectivity. Compared with naftopidil (1) and terazosin, compound 12 showed the most desirable α1D/1A subtype selectivity, especially improved α1A subtype selectivity, and the ratios pA2 (α1D)/pA2 (α1B) and pA2 (α1A)/pA2 (α1B) were 17.0- and 19.5-fold, respectively, indicating less cardiovascular side effects when used to treat LUTS/BPH. Finally, we investigated the chiral pharmacology of 12. We found, however, that the activity of enantiomers (R)-12 and (S)-12 are not significantly different from that of rac-12.

Solvent- or temperature-controlled diastereoselective aldol reaction of Methyl phenylacetate

Org Lett 2012 Sep 7;14(17):4346-9.PMID:22880620DOI:10.1021/ol301782s.

Unlike the enolboration-aldolization of methyl propanoate, the choice of either the solvent or temperature determines the diastereoselectivity during the enolboration-aldolization of Methyl phenylacetate. In CH(2)Cl(2), the reaction favors the anti-pathway at -78 °C and the syn-pathway at rt. Conversely, the reaction produces the anti-isomer up to rt and the syn-isomer at refluxing temperatures in nonpolar solvents.

The scent of Mycobacterium tuberculosis

Tuberculosis (Edinb) 2008 Jul;88(4):317-23.PMID:18296120DOI:10.1016/j.tube.2008.01.002.

Worldwide, tuberculosis (TB) kills nearly 2 million people annually, yet rapid diagnosis still relies on a 100-year-old method of sputum staining for acid-fast bacilli. The advent of solid phase micro-extraction and gas chromatography/mass spectrometry makes it possible to systematically investigate whether volatile metabolites from organisms belonging to the genus Mycobacterium can be used as a rapid and highly selective alternative to the traditional diagnostic methods. We have identified four specific compounds (Methyl phenylacetate, methyl p-anisate, methyl nicotinate and o-phenylanisole) from Mycobacterium tuberculosis and Mycobacterium bovis cultures grown in vitro that are distinctive volatile markers. These compounds are detectable before the visual appearance of colonies, potentially useful as the basis of a non-invasive diagnostic test for TB and have characteristic odors.

Honeybees Apis mellifera can detect the scent of Mycobacterium tuberculosis

Tuberculosis (Edinb) 2011 Jul;91(4):327-8.PMID:21546308DOI:10.1016/j.tube.2011.04.008.

The proboscis extension reflex in honeybees was evaluated for detection of tuberculosis. Restrained bees were tested with Methyl phenylacetate, methyl p-anisate, and methyl nicotinate, previously identified from Mycobacterium tuberculosis cultures, to determine honeybee capacity for signature volatile detection. Methyl p-anisate and Methyl phenylacetate were detectable over eight orders of magnitude, and honeybees showed proboscis extension response down to 0.1 pg loading of methyl p-anisate on filter paper. Potential exists for trained honeybees in non-invasive diagnostic tests for TB.

Assessment of potential causes of falsely positive Mycobacterium tuberculosis breath test

Tuberculosis (Edinb) 2013 May;93(3):312-7.PMID:23499413DOI:10.1016/j.tube.2013.01.005.

A suite of volatiles have previously been identified as specific markers of Mycobacterium tuberculosis metabolism in vitro. These markers - Methyl phenylacetate, methyl p-anisate, methyl nicotinate, o-phenylanisole with the addition of methyl salicylate, may also be derived from other sources and confound development of a breath test for tuberculosis. To identify potential sources of these potential biomarkers food products, cosmetics, TB medication, environmental air and cigarette smoke were analysed for these markers using solid phase microextraction coupled with Gas Chromatography/Mass Spectrometry. Breath from healthy subjects, including smokers was also tested. Methyl salicylate was commonly detected, making this unsuitable as a specific marker for M. tuberculosis. Methyl nicotinate was detected repeatedly in cigarettes. Methyl phenylacetate was detected in 1.7% of healthy subjects and o-phenylanisole in just 1% of healthy breath indicating these may be more suitable for inclusion in the tuberculosis breath test due to their low "background" level. These results justify further clinical studies to further explore these markers as specific indicators of M. tuberculosis infection.