Catalogue Number
AV-H13052
Analysis Method
HPLC,NMR,MS
Specification
98%
Storage
2-8°C
Molecular Weight
318.36
Appearance
White crystalline powder
Botanical Source
Dendrobium/Eria carinata
Structure Type
Phenols
Category
Standards;Natural Pytochemical;API
SMILES
COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)OC)OC)O
Synonyms
Phenol, 2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethyl]-/Dihydrocombretatastin A-4/Erianin/2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)-ethyl]-phenol/5-(3,4,5-trimethoxyphenethyl)-2-methoxyphenol/2-Methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethyl]phenol/(E)-2-methoxy-5-(3,4,5-trimethoxyphenylethyl)phenol/3-hydroxy-3',4',4,5'-tetramethoxybibenzyl/2-Methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethyl]benzolol
IUPAC Name
2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethyl]phenol
Applications
Erianin, often used as an antipyretic and analgesic agent, could inhibit IDO-induced tumor angiogenesis.
Density
1.1±0.1 g/cm3
Solubility
Methanol; Chloroform
Flash Point
219.4±27.3 °C
Boiling Point
439.1±40.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C18H22O5/c1-20-15-8-7-12(9-14(15)19)5-6-13-10-16(21-2)18(23-4)17(11-13)22-3/h7-11,19H,5-6H2,1-4H3
InChl Key
UXDFUVFNIAJEGM-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:95041-90-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
19402345
The purpose of the present study was to examine the pharmacokinetic characteristics of erianin (2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)-ethyl]-phenol, CAS 95041-90-0), a nature product extracted from Dendrobium chrysotoxum, having notable antitumour activity, after intravenous injection of erianin fat emulsion to beagle dogs. An HPLC-MS method was developed to analyze the erianin levels in dog plasma and validated in a pharmacokinetic study. Plasma profiles were obtained after intravenous injection of erianin fat emulsion at the doses 7.5, 15 and 30 mg/kg. The elimination half-life (t(1/2)) values for erianin were estimated to be 1.41+/- 0.31, 1.66 +/- 0.19, 1.60 0.28 h, while the mean area under concentration-time curve (AUC(0-infinity)) values were 1021.3 +/- 373.7, 2305.1 +/- 597.0 and 3952.1 +/- 378.2 ng x h/ml, respectively. In conclusion, the present observations indicated that erianin plasma concentrations were clearly dose-proportional for the dose range studied. There was no gender difference in pharmacokinetics for erianin in male and female dogs.
Liquid chromatographic-mass spectrometry analysis and pharmacokinetic studies of erianin for intravenous injection in dogs.
Zhou H1, Yang B, Hong M, Ma R, Sheng L.
2009
30249042
With continuous emergence and widespread of multidrug-resistant Staphylococcus aureus infections, common antibiotics have become ineffective in treating these infections in the clinical setting. Anti-virulence strategies could be novel, effective therapeutic strategies against drug-resistant bacterial infections. Sortase A (srtA), a transpeptidase in gram-positive bacteria, can anchor surface proteins that play a vital role in pathogenesis of these bacteria. SrtA is known as a potential antivirulent drug target to treat bacterial infections. In this study, we found that erianin, a natural bibenzyl compound, could inhibit the activity of srtA in vitro (half maximal inhibitory concentration?IC50 = 20.91 ± 2.31 μg/mL, 65.7 ± 7.2 μM) at subminimum inhibitory concentrations (minimum inhibitory concentrations?MIC = 512 μg/mL against S. aureus). The molecular mechanism underlying the inhibition of srtA by erianin was identified using molecular dynamics simulation: erianin binds to srtA residues Ile182, Val193, Trp194, Arg197, and Ile199, forming a stable bond via hydrophobic interactions. In addition, the activities of S. aureus binding to fibronectin and biofilm formation were inhibited by erianin, when co-culture with S. aureus. In vivo, erianin could improve the survival in mice that infected with S. aureus by tail vein injection. Experimental results showed that erianin is a potential novel therapeutic compound against S. aureus infections via affecting srtA.
sortase A, Staphylococcus aureus, erianin, inhibitor, molecular mechanism
Erianin against Staphylococcus aureus Infection via Inhibiting Sortase A
Ping Ouyang,† Xuewen He,† Zhong-Wei Yuan,† Zhong-Qiong Yin, Hualin Fu, Juchun Lin, Changliang He, Xiaoxia Liang, Cheng Lv, Gang Shu, Zhi-Xiang Yuan, Xu Song, Lixia Li, and Lizi Yin*
2018 Oct;
29843091
In this study, high-efficient phenol-degrading bacterium Bacillus sp. SAS19 which was isolated from activated sludge by resuscitation-promoting factor (Rpf) addition, were immobilized on porous carbonaceous gels (CGs) for phenol degradation. The phenol-degrading capabilities of free and immobilized Bacillus sp. SAS19 were evaluated under various initial phenol concentrations. The obtained results showed that phenol could be removed effectively by both free and immobilized Bacillus sp. SAS19. Furthermore, for degradation of phenol at high concentrations, long-term utilization and recycling were more readily achieved for immobilized bacteria as compared to free bacteria. Immobilized bacteria exhibited significant increase in phenol-degrading capabilities in the third cycle of recycling and reuse, which demonstrated 87.2% and 100% of phenol (1600?mg/L) degradation efficiency at 12 and 24?h, respectively. The present study revealed that immobilized Bacillus sp. SAS19 can be potentially used for enhanced treatment of synthetic phenol-laden wastewater.
Copyright ? 2018 Elsevier Ltd. All rights reserved.
Bacillus sp. SAS19; Carbonaceous gels; Immobilized bacteria; Phenol biodegradation; Resuscitation-promoting factor
Sustainable biodegradation of phenol by immobilized Bacillus sp. SAS19 with porous carbonaceous gels as carriers.
Ke Q1, Zhang Y1, Wu X1, Su X2, Wang Y1, Lin H1, Mei R3, Zhang Y3, Hashmi MZ4, Chen C5, Chen J6.
2018 Sep 15