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Nonacosane Sale

(Synonyms: 正二十九烷) 目录号 : GC39125

Nonacosane,从 Baphia massaiensis 分离,对大肠杆菌、枯草杆菌、铜绿假单胞菌和金黄色葡萄球菌的活性较弱。

Nonacosane Chemical Structure

Cas No.:630-03-5

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5mg
¥450.00
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10mg
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20mg
¥1,260.00
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产品描述

Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus[1].

[1]. Ngonye Keroletswe, et al. A New 3-Prenyl-2-flavene and Other Extractives from Baphia massaiensis and Their Antimicrobial Activities. Natural Product Communications.

Chemical Properties

Cas No. 630-03-5 SDF
别名 正二十九烷
Canonical SMILES CCCCCCCCCCCCCCCCCCCCCCCCCCCCC
分子式 C29H60 分子量 408.79
溶解度 Soluble in DMSO 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 2.4462 mL 12.2312 mL 24.4624 mL
5 mM 0.4892 mL 2.4462 mL 4.8925 mL
10 mM 0.2446 mL 1.2231 mL 2.4462 mL
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Research Update

Pedalium murex Linn.: an overview of its phytopharmacological aspects

Asian Pac J Trop Med 2011 Sep;4(9):748-55.PMID:21967701DOI:10.1016/S1995-7645(11)60186-7.

Pedalium murex Linn (family: Pedaliaceae) (P. murex) commonly known as Large Caltrops and Gokhru (India) is a shrub found in the Southern part, Deccan region of India and in some parts of Ceylon. Different parts of the plant are used to treat various ailments like, cough, cold and as an antiseptic. Interestingly, P. murex is reported traditionally to have an excellent cure in patients with reproductive disorders which are mainly impotency in men, nocturnal emissions, gonorrhoea as well as leucorrhoea in women. The plant has also benifited in complications like urinary track disorder as well as gastro intestinal tract disorders. Phytochemically the plant is popular for the presence of a considerable amount of diosgenin and vanillin which are regarded as an important source and useful starting materials for synthesizing steroidal contraceptive drugs and isatin alkaloids. Other phytochemicals reported in the plant includes quercetin, ursolic acid, caffeic acid, amino acids (glycine, histidine, tyrosine, threonine, aspartic acid and glutamic acid) and various classes of fatty acids (triacontanoic acid, Nonacosane, tritriacontane, tetratriacontanyl and heptatriacontan-4-one). Pharmacologically, the plant have been investigated for antiulcerogenic, nephroprotective, hypolipidemic, aphrodisiac, antioxidant, antimicrobial and insecticidal activities. From all these reports it can be concluded that the plant were found to have a better profile with potential natural source for the treatment of various range of either acute or chronic disease. The overall database of our review article was collected from the scientific sources in regards with all the information of the research article for P. murex published so far.

Alkanes in flower surface waxes of Momordica cochinchinensis influence attraction to Aulacophora foveicollis Lucas (Coleoptera: Chrysomelidae)

Neotrop Entomol 2013 Aug;42(4):366-71.PMID:23949856DOI:10.1007/s13744-013-0137-1.

Extraction, thin-layer chromatography, and gas chromatography-mass spectrophotometry analyses revealed 15 alkanes representing 97.14% of the total alkanes in the surface waxes of Momordica cochinchinensis Spreng flowers. Nonacosane was the prevailing alkane followed by hexatriacontane, nonadecane, heptacosane, and hentriacontane, accounting for 39.08%, 24.24%, 13.52%, 6.32%, and 5.12%, respectively. The alkanes from flower surface waxes followed by a synthetic mixture of alkanes mimicking alkanes of flower surface waxes elicited attraction of the female insect, Aulacophora foveicollis Lucas (Coleoptera: Chrysomelidae) between 2 and 10-μg/mL concentrations in a Y-shaped glass tube olfactometer bioassay under laboratory conditions. Synthetic nonadecane from 178.28-891.37 ng, heptacosane from 118.14-590.72 ng, and Nonacosane at 784.73 ng showed attraction of the insect. A synthetic mixture of 534.82 ng nonadecane, 354.43 ng heptacosane, and 2,354.18 ng Nonacosane elicited highest attraction of A. foveicollis.

[Chemical composition of body extracts from Apriona germari and its function in sexual communication]

Ying Yong Sheng Tai Xue Bao 2020 Oct;31(10):3267-3272.PMID:33314814DOI:10.13287/j.1001-9332.202010.031.

To elucidate the composition of semiochemicals of Apriona germari and its function in sexual communication, GC-MS was used to detect the composition of semiochemicals of the overall body and the end abdominal tissue extracts in A. germari. Y-tube olfactometer was used to determine the olfactory response of adult female and male to the standard compounds of the five main extracts. The contact reaction test with male and female adults was performed to the eluted adults that smeared tandard compounds. The results showed that the main ingredients of semiochemicals were alkanes and alkenes with more than 10 carbons. Concentration of (Z)-9-Tricosene was the highest, followed by heptacosane, Nonacosane, nonadecene, octacosane, 9-Hexylheptadecane, aldehyde, and ester. Results of the olfactory reaction showed that Nonacosane had a significant attractivity to both male and female adults, and that heptacosane had a significant attractivity only to female adults. Nonadecene had a extremely significant repellent activity to female adults. 1-docosene and (Z)-9-Tricosene had no evident role to the male and female adults. Results of the contact test showed that male adults had the strongest courtship responses to the eluted adults with 1-docosene, heptacosane and Nonacosane. Female adults had the strongest courtship responses to the eluted adults with Nonacosane. Our results indicated that 1-docosene, heptacosane, and Nonacosane were important component of the sex pheromone of A. germari, which played an important role in the sexual communication.

n-alkane profile of Argemone mexicana leaves

Z Naturforsch C J Biosci 2010 Sep-Oct;65(9-10):533-6.PMID:21138052DOI:10.1515/znc-2010-9-1001.

An n-hexane extract of fresh, mature leaves of Argemone mexicana (Papaveraceae), containing thin-layer epicuticular waxes, has been analysed for the first time by TLC, IR and GLC using standard hydrocarbons. Seventeen long-chain alkanes (n-C18 to n-C34) were identified and quantified. Nonacosane (n-C29) was established as the n-alkane with the highest amount, whilst octadecane (n-C19) was the least abundant component of the extracted wax fraction. The carbon preference index (CPI) calculated for the hydrocarbon sample with the chain lengths between C18 and C34 was 1.2469, showing an odd to even carbon number predominance.

Chemical characterization of Brazilian propolis using automated direct thermal desorption-gas chromatography-mass spectrometry

J Sci Food Agric 2022 Aug 15;102(10):4345-4354.PMID:35066883DOI:10.1002/jsfa.11788.

Background: Propolis, produced by honey bees, is used around the world, displaying several corroborated biological activities. Brazil is one of the leading producers of propolis, with a great diversity of types, each with a characteristically chemical fingerprint influenced by the flora of the local region. The secondary metabolite's composition of propolis strongly impacts its biological properties, and its chemical characterization is of great importance for its quality control. Several chromatographic techniques have been applied to characterize propolis, highlighting the extraction of its volatiles and its analysis through gas chromatography. Fourteen Brazilian propolis samples collected in four states, including brown, green and red propolis types, were chemically characterized using the automated direct thermal desorption-gas chromatography-mass spectrometry (DTD-GC-MS). Results: Red propolis type was characterized by acyclic saturated hydrocarbons, fatty alcohols, terpenes, and phenylpropanoids as Nonacosane, α-copaene, β-amyrin acetate, anethole, and 7-O-methylvestitol. Brown propolis presented hydrocarbons, monoterpenes, and sesquiterpenes, as α-pinene and α-bisabolol. Brazilian green propolis presented polycyclic aromatic hydrocarbons and sesquiterpenes, including 1-methyl-octahydroanthracene, 2,5-dimethyl-γ-oxo-benzenebutanoic acid, nerolidol, and spathulenol. Principal component analysis (PCA) was performed, allowing for clustering brown and red propolis types, indicating a divergence with the chemical composition of the green propolis samples. The hierarchical cluster analysis (HCA) allowed the chemical fingerprint of each propolis type to be differentiated. Conclusion: Red propolis was characterized by sesquiterpenes, pterocarpans, and isoflavans; brown propolis was characterized by hydrocarbons, aldehydes, and monoterpenes, while green propolis samples were characterized by the presence of polycyclic aromatic hydrocarbons, sesquiterpenes, and naphthalene derivatives. © 2022 Society of Chemical Industry.