(-)-Bornyl ferulateCAS# 55511-07-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
| Cas No. | 55511-07-4 | SDF | Download SDF |
| PubChem ID | N/A | Appearance | Powder |
| Formula | C20H26O4 | M.Wt | 330.42 |
| Type of Compound | Monoterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
(-)-Bornyl ferulate Dilution Calculator
(-)-Bornyl ferulate Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.0265 mL | 15.1323 mL | 30.2645 mL | 60.529 mL | 75.6613 mL |
| 5 mM | 0.6053 mL | 3.0265 mL | 6.0529 mL | 12.1058 mL | 15.1323 mL |
| 10 mM | 0.3026 mL | 1.5132 mL | 3.0265 mL | 6.0529 mL | 7.5661 mL |
| 50 mM | 0.0605 mL | 0.3026 mL | 0.6053 mL | 1.2106 mL | 1.5132 mL |
| 100 mM | 0.0303 mL | 0.1513 mL | 0.3026 mL | 0.6053 mL | 0.7566 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
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[Chemical constituents from whole plants of Valeriana hardwickii].[Pubmed:27062818]
Zhongguo Zhong Yao Za Zhi. 2015 Oct;40(20):4007-11.
Chemical investigation of the whole plants of Valeriana hardwickii has led to the isolation of 11 flavones and 2 monoterpe- noids by using various chromatographic techniques including column chromatography on silica gel and Sephadex LH-20, preparative TLC, and preparative HPLC. Their structures were identified by spectroscopic data analysis as syzalterin (1), 6-methylapigenin (2), 5-hydroxy-7,4'-dimethoxyflavone (3), genkwanin (4), acacetin (5), apigenin (6), quercetin (7), tricin (8), (-)-farrerol (9), sosakuranetin (10), 5,3',4'-trihydroxy-7-methoxyflavanone (11), (-)-Bornyl ferulate ( 12) , and (-)-bornyl caffeate ( 13). All compounds were isolated from this plant for the first time, while compounds 1, 9-13 were obtained from this genus for the first time.
[Sesquiterpenes and monoterpene from Aquilaria sinensis].[Pubmed:23019881]
Zhongguo Zhong Yao Za Zhi. 2012 Jul;37(13):1973-6.
The column chromatography on silica gel, semi-preparative HPLC were used to separate and purify the compounds from the petroleum ether and ethanol extract of Aquilaria sinensis. Nine compounds were isolated. On the basis of their spectroscopic data, the structures were identified as 3, 3, 7-trimethyltricycloundecan-8-one (1), longifolene (2), norlongilactone (3), caryophyllenol-II (4), humulene diepoxide A (5), kobusone (6), (-)-Bornyl ferulate (7), (24R) -24-ethylcholesta-4, 22-dien-3-one (8), (24R)-24-3-ono-4-en-sitosterone (9). Compounds 2-9 were isolated from this plant for the first time. compounds 1-6 are sesquiterpenes, compound 7 is a monoterpene derivative, compound 8 and 9 are steroids.
Anti-inflammatory activity of phenyl propanoids from Coreopsis mutica var. mutica.[Pubmed:17253307]
Planta Med. 1998 Oct;64(7):660-1.
The structures of three phenyl propanoids isolated from the aerial parts of Coreopsis mutica var. mutica were established by spectroscopic analysis as (-)-bornyl p-coumarate, (-)-Bornyl ferulate, and (-)-bornyl caffeate. These compounds have been previously isolated from diverse sources. Their complete and assigned 1H- and 13C-NMR data together with an assessment of their anti-inflammatory activities are given.
Differentiation in a rat PC12 cell line induced by ostruthin and (-)-bornyl ferulate, constituents of a Chinese herbal medicine.[Pubmed:10501010]
Biosci Biotechnol Biochem. 1999 Aug;63(8):1501-2.
A search for neuritogenic compounds in Chinese herbs resulted in the isolation of two known substances, ostruthin and (-)-Bornyl ferulate, from Notopterygium incisum (and/or N. forbesii). Both compounds induced comparable neurite-like structures in 20% of rat PC12 cells at 2 micrograms/ml, and showed cytotoxicity at concentrations higher than 3 micrograms/ml.
Anti-inflammatory activity of phenyl propanoids from Coreopsis mutica var. mutica.[Pubmed:9810274]
Planta Med. 1998 Oct;64(7):660-1.
The structures of three phenyl propanoids isolated from the aerial parts of Coreopsis mutica var. mutica were established by spectroscopic analysis as (-)-bornyl p-coumarate (1), (-)-Bornyl ferulate (2), and (-)-bornyl caffeate (3). These compounds have been previously isolated from diverse sources. Their complete and assigned 1H- and 13C-NMR data together with an assessment of their anti-inflammatory activities are given.
5-Lipoxygenase and cyclooxygenase inhibitory active constituents from Qianghuo (Notopterygium incisum).[Pubmed:9265192]
Planta Med. 1997 Jun;63(3):203-6.
The n-hexane extract of Qianghuo (underground parts of Notopterygium incisum Ting x H.T. Chang, Umbelliferae) showed inhibitory activity in vitro in 5-lipoxygenase (5-LO) and cyclooxygenase (COS) assays. Two major constituents, phenethyl ferulate and falcarindiol, and one minor compound (-)-Bornyl ferulate, were identified as the main active principles. The correlation between the content of active constituents and the inhibitory activity of the extracts was examined with seven commercial drug samples from different sources. It was obvious that the content of phenethyl ferulate was mainly responsible for the COX inhibitory activity of the extracts and falcarindiol for 5-LO inhibitory activity. Since the main active constituents phenethyl ferulate and falcarindiol can easily be quantified by HPLC, this is a suitable method for standardization and characterization of the drug.
