Catalogue Number
BN-O1127
Analysis Method
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
275.14
Appearance
Botanical Source
Structure Type
Category
SMILES
C1=CC=C(C=C1)CC(=O)C2=CC=C(C=C2)Br
Synonyms
1-(4-Bromophenyl)-2-phenylethanone/4'-Bromo-2-phenylacetophenone/2-phenyl-4'-bromoacetophenone/Benzyl 4-Bromophenyl Ketone/4-bromophenylbenzylmethanone/1-(4-bromophenyl)-2-phenylethan-1-one/4-Bromodesoxybenzoin/Ethanone, 1-(4-bromophenyl)-2-phenyl-
IUPAC Name
1-(4-bromophenyl)-2-phenylethanone
Density
1.4±0.1 g/cm3
Solubility
Flash Point
84.6±10.5 °C
Boiling Point
383.2±25.0 °C at 760 mmHg
Melting Point
112-116 °C(lit.)
InChl
InChl Key
MOSIKPSTRPODHQ-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#:2001-29-8) 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.
11806778
The recent scientific session of the American College of Cardiology (ACC), held in Orlando, provided a forum for ongoing cardiovascular clinical trials from around the world. The high point was clearly the first ever release of results from the CURE study. The Late-Breaking Clinical Trials sessions also featured results and interim data from other trials such as MIRACLE, CAPRICORN, SVG WRIST, RITZ 2, SoS and PRINCE. New applications for data from the OPUS-TIMI16 trial were discussed and promising results from initial studies into the experimental drug ALT-711 showed the way for further studies.
cardiology, clinical trials, congress, meeting report
Selected highlights from the 50th Annual Scientific Session of the American College of Cardiology, Orlando, USA, 18-21 March 2001
Joanna Lyfordcorresponding author1
2001;
11737945
Background
Recombinant inbred (RI) strains of mice are an important resource used to map and analyze complex traits. They have proved particularly effective in multidisciplinary genetic studies. Widespread use of RI strains has been hampered by their modest numbers and by the difficulty of combining results derived from different RI sets.
Results
We have increased the density of typed microsatellite markers two- to five-fold in each of several major RI sets that share C57BL/6 as a parental strain (AXB, BXA, BXD, BXH and CXB). A common set of 490 markers was genotyped in just over 100 RI strains. Genotypes of around 1,100 additional microsatellites in one or more RI sets were generated, collected and checked for errors. Consensus RI maps that integrate genotypes of approximately 1,600 microsatellite loci were assembled. The genomes of individual strains typically incorporate 45-55 recombination breakpoints. The collected RI set – termed the BXN set – contains approximately 5,000 breakpoints. The distribution of recombinations approximates a Poisson distribution and distances between breakpoints average about 0.5 centimorgans (cM). Locations of most breakpoints have been defined with a precision of < 2 cM. Genotypes deviate from Hardy-Weinberg equilibrium in only a small number of intervals.
Conclusions
Consensus maps derived from RI strains conform almost exactly to theoretical expectation and are close to the length predicted by the Haldane-Waddington equation (x3.6 for a 2-3 cM interval between markers). Non-syntenic associations between different chromosomes introduce predictable distortions in quantitative trait locus (QTL) datasets that can be partly corrected using two-locus correlation matrices.
The genetic structure of recombinant inbred mice: high-resolution consensus maps for complex trait analysis
Robert W Williams,corresponding author1,2,3 Jing Gu,1,3 Shuhua Qi,2,3 and Lu Lu1,2,3
2001;
11707603
Using the yeast two-hybrid system with syntaxin-1A as bait, we isolated soluble NSF attachment protein (SNAP)-29 from a human brain cDNA library. Synaptosomal fractionation and immunocytochemical staining of hippocampal neurons in culture showed that SNAP-29 is present at synapses and is predominantly associated with synaptic vesicles. The interaction of SNAP-29 with syntaxin-1 was further confirmed with immunoprecipitation analysis. Binding competition studies with SNAP-29 demonstrated that it could compete with α-SNAP for binding to synaptic SNAP receptors (SNAREs) and consequently inhibit disassembly of the SNARE complex. Introduction of SNAP-29 into presynaptic superior cervical ganglion neurons in culture significantly inhibited synaptic transmission in an activity-dependent manner. Although SNAP-29 has been suggested to be a general SNARE component in membrane trafficking, our findings suggest that it may function as a regulator of SNARE complex disassembly and modulate the process of postfusion recycling of the SNARE components.
SNAP-29: A general SNARE protein that inhibits SNARE disassembly and is implicated in synaptic transmission
Qingning Su,* Sumiko Mochida,† Jin-Hua Tian,* Rashi Mehta,* and Zu-Hang Sheng*‡
2001 Nov 20;
Description :
Empty ...