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6,7-Dimethoxy-2-phenethylchromone

$717

  • Brand : BIOFRON

  • Catalogue Number : BD-P0999

  • Specification : 98.0%(HPLC)

  • CAS number : 84294-87-1

  • Formula : C19H18O4

  • Molecular Weight : 310.344

  • PUBCHEM ID : 5316872

  • Volume : 25mg

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Catalogue Number

BD-P0999

Analysis Method

HPLC,NMR,MS

Specification

98.0%(HPLC)

Storage

2-8°C

Molecular Weight

310.344

Appearance

Powder

Botanical Source

Structure Type

Phenols

Category

SMILES

COC1=C(C=C2C(=C1)C(=O)C=C(O2)CCC3=CC=CC=C3)OC

Synonyms

6,7-dimethoxy-2-(2-phenylethyl)chromen-4-one

IUPAC Name

6,7-dimethoxy-2-(2-phenylethyl)chromen-4-one

Applications

Density

Solubility

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

Flash Point

Boiling Point

Melting Point

InChl

InChI=1S/C19H18O4/c1-21-18-11-15-16(20)10-14(23-17(15)12-19(18)22-2)9-8-13-6-4-3-5-7-13/h3-7,10-12H,8-9H2,1-2H3

InChl Key

MVQOWXHYPYRBOE-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

2933990000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:84294-87-1) 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.

PMID

26977140

Abstract

The zinc(II) complex (C2H6NS)2Zn·ZnCl2 was synthesized with 2-aminoethanethiol hydrochloride and zinc sulfate heptahydrate as the raw materials in aqueous solution. The composition and structure of the complex were characterized by elemental analysis, infrared spectra, single crystal X-ray diffraction, and thermogravimetry. The crystal structure of the zinc(II) complex belongs to monoclinic system, space group P 21/n, with cell parameters of a = 0.84294(4), b = 0.83920(4), c = 1.65787(8) nm, Z = 2, and D = 2.041 g/cm3. In this paper, the interaction of complex with Ct-DNA was investigated by UV-visible and viscosimetric techniques. Upon addition of the complex, important changes were observed in the characteristic UV-Vis bands (hyperchromism) of calf thymus DNA and some changes in specific viscosity. The experimental results showed that the complex is bound to DNA intercalative (intercalation binding).

Title

Synthesis, Crystal Structure, Spectroscopic Properties, and Interaction with Ct-DNA of Zn(II) with 2-Aminoethanethiol Hydrochloride Ligand

Author

Xu-gang Shu, 1 , * Chun-li Wu, 1 Cui-jin Li, 1 Min Zhang, 2 Ke Wan, 2 and Xin Wu 3 ,

Publish date

2016;

PMID

30700932

Abstract

Objective
Liver metastasis, which contributes substantially to high mortality, is the most common recurrent mode of colon carcinoma. Thus, it is necessary to identify genes implicated in metastatic colonization of the liver in colon carcinoma.

Methods
We compared mRNA profiling in 18 normal colon mucosa (N), 20 primary tumors (T) and 19 liver metastases (M) samples from the dataset GSE49355 and GSE62321 of Gene Expression Omnibus (GEO) database. Gene ontology (GO) and pathways of the identified genes were analyzed. Co-expression network and protein-protein interaction (PPI) network were employed to identify the interaction relationship. Survival analyses based on The Cancer Genome Atlas (TCGA) database were used to further screening. Then, the candidate genes were validated by our data.

Results
We identified 22 specific genes related to liver metastasis and they were strongly associated with cell migration, adhesion, proliferation and immune response. Simultaneously, the results showed that C-X-C motif chemokine ligand 14 (CXCL14) might be a favorable prediction factor for survival of patients with colon carcinoma. Importantly, our validated data further suggested that lower CXCL14 represented poorer outcome and contributed to metastasis. Gene set enrichment analysis (GSEA) showed that CXCL14 was negatively related to the regulation of stem cell proliferation and epithelial to mesenchymal transition (EMT).

Conclusions
CXCL14 was identified as a crucial anti-metastasis regulator of colon carcinoma for the first time, and might provide novel therapeutic strategies for colon carcinoma patients to improve prognosis and prevent metastasis.

KEYWORDS

Colon carcinoma, liver metastasis, mRNA profiling, functions annotation

Title

Identification of liver metastasis-associated genes in human colon carcinoma by mRNA profiling

Author

Jianling Liu,1,2,* Dan Wang,1,2,* Chaoqi Zhang,1,2,* Zhen Zhang,1,2 Xinfeng Chen,1,2 Jingyao Lian,1,2 Jinbo Liu,4 Guixian Wang,4 Weitang Yuan,4 Zhenqiang Sun,4 Weijia Wang,1,2 Mengjia Song,1,2 Yaping Wang,5 Qian Wu,1,2 Ling Cao,1,2 Dong Wang,1,2 and Yi Zhang*,1,2,3

Publish date

2018 Dec;

PMID

25885887

Abstract

Background
Smoking in pregnancy is known to be associated with a range of adverse pregnancy outcomes, yet there is a high prevalence of smoking among pregnant women in many countries, and it remains a major public health concern. We have conducted a systematic review and meta-analysis to provide contemporary estimates of the association between maternal smoking in pregnancy and the risk of stillbirth.

Methods
We searched four databases namely MEDLINE, EMBASE, Psych Info and Web of Science for all relevant original studies published until 31st December 2012. We included observational studies that measured the association between maternal smoking during pregnancy and the risk of stillbirth.

Results
1766 studies were screened for title analysis, of which 34 papers (21 cohorts, 8 case controls and 5 cross sectional studies) met the inclusion criteria. In meta-analysis smoking during pregnancy was significantly associated with a 47% increase in the odds of stillbirth (OR 1.47, 95% CI 1.37, 1.57, p < 0.0001). In subgroup analysis, smoking 1-9 cig/day and ≥10 cig/day was associated with an 9% and 52% increase in the odds of stillbirth respectively. Subsequently, studies defining stillbirth at ≥ 20 weeks demonstrated a 43% increase in odds for smoking mothers compared to mothers who do not smoke, (OR 1.43, 95% CI 1.32, 1.54, p < 0.0001), whereas studies with stillbirth defined at ≥ 24 weeks and ≥ 28 weeks showed 58% and 33% increase in the odds of stillbirth respectively. Conclusion Our review confirms a dose-response effect of maternal smoking in pregnancy on risk of stillbirth. To minimise the risk of stillbirth, reducing current smoking prevalence in pregnancy should continue to be a key public health high priority. Electronic supplementary material The online version of this article (doi:10.1186/s12889-015-1552-5) contains supplementary material, which is available to authorized users.

Title

Maternal smoking and the risk of still birth: systematic review and meta-analysis

Author

Takawira C Marufu, Anand Ahankari, Tim Coleman, and Sarah Lewiscorresponding author

Publish date

2015