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Qingyangshengenin

$692

  • Brand : BIOFRON

  • Catalogue Number : BN-O0015

  • Specification : 98%(HPLC)

  • CAS number : 84745-94-8

  • Formula : C28H36O8

  • Molecular Weight : 500.6

  • PUBCHEM ID : 90476678

  • Volume : 5mg

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Catalogue Number

BN-O0015

Analysis Method

Specification

98%(HPLC)

Storage

-20℃

Molecular Weight

500.6

Appearance

Cryst.

Botanical Source

This product is isolated and purified from the roots of Cynanchum otophyllum

Structure Type

Category

SMILES

CC(=O)C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C5=CC=C(C=C5)O)C)O)O

Synonyms

IUPAC Name

Applications

Density

1.4±0.1 g/cm3

Solubility

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

Flash Point

226.2±25.0 °C

Boiling Point

686.4±55.0 °C at 760 mmHg

Melting Point

InChl

InChl Key

IMRGSWAJVVVYOW-ZCARJHNXSA-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#:84745-94-8) 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

28547345

Abstract

Increasing physical activity (PA) at the population level requires appropriately targeting intervention development. Identifying the locations in which participants with various sociodemographic, body weight, and geographic characteristics tend to engage in varying intensities of PA as well as locations these populations underutilize for PA may facilitate this process. A visual location-coding protocol was developed and implemented in Google Fusion Tables and Maps using data from participants (N = 223, age 18-85) in five states. Participants concurrently wore ActiGraph GT1M accelerometers and Qstarz BT-Q1000X GPS units for 3 weeks to identify locations of moderate-to-vigorous (MVPA) or vigorous (VPA) bouts. Cochran-Mantel-Haenzel general association tests examined usage differences by participant characteristics (sex, age, race/ethnicity, education, body mass index (BMI), and recruitment city). Homes and roads encompassed >40% of bout-based PA minutes regardless of PA intensity. Fitness facilities and schools were important for VPA (19 and 12% of bout minutes). Parks were used for 13% of MVPA bout minutes but only 4% of VPA bout minutes. Hispanics, those without a college degree, and overweight/obese participants frequently completed MVPA bouts at home. Older adults often used roads for MVPA bouts. Hispanics, those with ≤high school education, and healthy/overweight participants frequently had MVPA bouts in parks. Applying a new location-coding protocol in a diverse population showed that adult PA locations varied by PA intensity, sociodemographic characteristics, BMI, and geographic location. Although homes, roads, and parks remain important locations for demographically targeted PA interventions, observed usage patterns by participant characteristics may facilitate development of more appropriately targeted interventions.

KEYWORDS

Health behavior, Accelerometry, Global positioning system, Location-coding protocol

Title

Where Are Adults Active? An Examination of Physical Activity Locations Using GPS in Five US Cities

Author

Katelyn M. Holliday,corresponding author1 Annie Green Howard,2 Michael Emch,1,3 Daniel A. Rodriguez,4 Wayne D. Rosamond,1 and Kelly R. Evenson1

Publish date

2017 Aug;

PMID

30881116

Abstract

Objective
Cholangiocarcinoma (CCA) is a devastating disease. Interferon α-inducible protein 27 (IFI27), originally known to involve in innate immunity, is later found to intervene in cell proliferation, leading to inventive studies regarding the role of IFI27 in cancer treatment. We aimed to investigate the role of IFI27 in CCA.

Materials and methods
Cell proliferation, migration, and invasion assays, Western blot, gene transfection and knockdown, immunofluorescent and immunohistochemical stains, and xenograft animal model were applied.

Results
IFI27 knockdown in CCA cells induced cell cycle arrest in S phase, resulting in lower cell proliferative rate in vitro and in vivo. IFI27 knockdown attenuated CCA cell migration and invasion through inhibition of epithelial-mesenchymal transition, which was supported by increased E-cadherin and decreased N-cadherin and fibronectin. Filamentous actin level was also reduced. IFI27 knockdown further repressed expression and secretion of vascular endothelial growth factor (VEGF-A), a strong stimulator of angiogenesis, through downregulation of c-jun and c-fos, which was supported in vitro by the finding that human vascular endothelial cells grew more slowly in conditioned medium of IFI27 knockdown on CCA cells and in vivo by the lower erythropoietin concentration found in the xenografted tumors derived from IFI27 knockdown on CCA cells. In addition, anti-VEGF-A antibody treatment was able to repress CCA cell growth. To the contrary, IFI27 overexpression could increase CCA cell proliferation, migration, and invasion. Clinically, higher IFI27 expression was linked to inferior overall survival of CCA patients.

Conclusion
Our data strongly suggest that IFI27 could be deemed as a potential target for CCA treatment.

KEYWORDS

IFI27, cholangiocarcinoma, oncogene, angiogenesis, VEGF-A, metastasis, tumor growth, cell cycle

Title

Interferon α-inducible protein 27 is an oncogene and highly expressed in cholangiocarcinoma patients with poor survival

Author

Kun-Chun Chiang,1 Sheng-Teng Huang,2 Ren-Chin Wu,3 Shih-Chiang Huang,3 Ta-Sen Yeh,4 Ming-Huang Chen,5 Jun-Te Hsu,4 Li-Wei Chen,6 Sheng-Fong Kuo,7 Ho-Yen Chueh,8 Horng-Heng Juang,9 Shuen-Iu Hung,10 Chun-Nan Yeh,4 and Jong-Hwei S Pang11,12

Publish date

2019;

PMID

17583932

Abstract

The composition of zymogen granules from rat pancreas was determined by LC-MS/MS. Enriched intragranular content, peripheral membrane and integral membrane protein fractions were analyzed after one-dimensional SDS/PAGE and tryptic digestion of gel slices. A total of 371 proteins were identified with high confidence, including 84 previously identified granule proteins. The 287 remaining proteins included 37 GTP-binding proteins and effectors, 8 tetraspan membrane proteins, and 22 channels and transporters. Seven proteins – pantophysin, cyclic nucleotide phosphodiesterase, carboxypeptidase D, ecto-nucleotide phosphodiesterase 3, aminopeptidase N, ral, and the potassium channel TWIK-2 – were confirmed by immunofluorescence microscopy or by immunoblotting to be new zymogen granule membrane proteins.

KEYWORDS

proteomics, mass spectrometry, LC-MS/MS, pancreas, zymogen granules, acinar cells

Title

Proteomic Analysis of Pancreatic Zymogen Granules: Identification of New Granule Proteins

Author

Michael J. Rindler,+* Chong-feng Xu,§ Iwona Gumper,+ Nora N. Smith,+ and Thomas A. Neubert§

Publish date

2008 Nov 10.