Catalogue Number
BN-O1480
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
232.2
Appearance
Cryst.
Botanical Source
This product is isolated and purified from the leaves of Senna siamea
Structure Type
Chromones
Category
Standards;Natural Pytochemical;API
SMILES
CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C
Synonyms
5-acetonyl-7-hydroxy-2-methylchromone/7-Hydroxy-2-methyl-5-(2-oxopropyl)-4H-chromen-4-one/4H-1-Benzopyran-4-one, 7-hydroxy-2-methyl-5-(2-oxopropyl)-/Cassiachromone/Chromone,5-acetonyl-7-hydroxy-2-methyl/2-Methyl-5-acetonyl-7-hydroxychromone
IUPAC Name
7-hydroxy-2-methyl-5-(2-oxopropyl)chromen-4-one
Density
1.3±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
174.8±22.2 °C
Boiling Point
444.7±45.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C13H12O4/c1-7(14)3-9-5-10(15)6-12-13(9)11(16)4-8(2)17-12/h4-6,15H,3H2,1-2H3
InChl Key
YMCXDPKFRCHLPK-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#:28955-30-8) 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.
23696738
Botulinum neurotoxin serotype A (BoNT/A) causes transient muscle paralysis by entering motor nerve terminals (MNTs) where it cleaves the SNARE protein Synaptosomal-associated protein 25 (SNAP25206) to yield SNAP25197. Cleavage of SNAP25 results in blockage of synaptic vesicle fusion and inhibition of the release of acetylcholine. The specific uptake of BoNT/A into pre-synaptic nerve terminals is a tightly controlled multistep process, involving a combination of high and low affinity receptors. Interestingly, the C-terminal binding domain region of BoNT/A, HC/A, is homologous to fibroblast growth factors (FGFs), making it a possible ligand for Fibroblast Growth Factor Receptors (FGFRs). Here we present data supporting the identification of Fibroblast Growth Factor Receptor 3 (FGFR3) as a high affinity receptor for BoNT/A in neuronal cells. HC/A binds with high affinity to the two extra-cellular loops of FGFR3 and acts similar to an agonist ligand for FGFR3, resulting in phosphorylation of the receptor. Native ligands for FGFR3; FGF1, FGF2, and FGF9 compete for binding to FGFR3 and block BoNT/A cellular uptake. These findings show that FGFR3 plays a pivotal role in the specific uptake of BoNT/A across the cell membrane being part of a larger receptor complex involving ganglioside- and protein-protein interactions.
Identification of Fibroblast Growth Factor Receptor 3 (FGFR3) as a Protein Receptor for Botulinum Neurotoxin Serotype A (BoNT/A)
Birgitte P. S. Jacky, Patton E. Garay, Jerôme Dupuy, Jeremy B. Nelson, Brian Cai, Yanira Molina, Joanne Wang, Lance E. Steward, Ron S. Broide, Joseph Francis, K. Roger Aoki, Raymond C. Stevens, Ester Fernandez-Salas
2013 May;
31321269
The present article provides water quality data collected from three South Texas Estuaries (Guadalupe, Nueces and Lavaca-Colorado Estuaries) during frequent drought from 2011 to 2014. The data described here are presented in the research article “The relationship between suspended solids and nutrients with variable hydrologic flow regimes” Paudel et al., 2019. Quarterly (i.e. four times a year) surface water quality data presented here were collected from various stations lie along river-estuary mouth to oceanic salinity gradient. Followings are the water quality data provided from Texas estuaries at different river flow regimes: pH, DO, TSS, salinity, chlorophyll-a, secchi disc reading, and nutrients (dissolved nitrogen, dissolved phosphorus and dissolved silicate). Surface inflow was obtained by adding gauged, modeled and return flow.
Estuaries, Hydrologic flow, Salinity, TSS, Nutrients
Water quality data from estuarine variable hydrologic flow regimes during frequent drought
Bhanu Paudel,a,∗ Paul A. Montagna,b and Leslie Adamsb
2019 Aug;
32233133
Porcine epidemic diarrhea virus (PEDV) emerged into Canada in January 2014, primarily affecting sow herds. Subsequent epidemiological analyses suggested contaminated feed was the most likely transmission pathway. The primary objective of this study was to describe general biosecurity and management practices implemented in PEDV-positive sow herds and matched control herds at the time the virus emerged. The secondary objective was to determine if any of these general biosecurity and farm management practices were important in explaining PEDV infection status from January 22, 2014 to March 1, 2014. A case herd was defined as a swine herd with clinical signs and a positive test result for PEDV. A questionnaire was used to a gather 30-day history of herd management practices, animal movements on/off site, feed management practices, semen deliveries and biosecurity practices for case (n = 8) and control (n = 12) herds, primarily located in Ontario. Data was analyzed using descriptive statistics and random forests (RFs). Case herds were larger in size than control herds. Case herds had more animal movements and non-staff movements onto the site. Also, case herds had higher quantities of pigs delivered, feed deliveries and semen deliveries on-site. The biosecurity practices of case herds were considered more rigorous based on herd management, feed deliveries, transportation and truck driver practices than control herds. The RF model found that the most important variables for predicting herd status were related to herd size and feed management variables. Nonetheless, predictive accuracy of the final RF model was 72%.
Swine, biosecurity, porcine epidemic diarrhea, random forests, Canada
A descriptive study of on-farm biosecurity and management practices during the incursion of porcine epidemic diarrhea into Canadian swine herds, 2014
Amanda M. Perri,1 Zvonimir Poljak,1 Cate Dewey,1 John CS. Harding,2 Terri L. O'Sullivancorresponding author1
2020 Mar