This entity has been manually annotated by the ChEBI Team. Note that translated names are available at this time only for substances which have a harmonised C&L or which are approved Biocidal active substances. In order to overcome such drawbacks, many researchers have sought to develop innovative solutions for eliminating the unfavorable nonspecifically bound proteins, termed background proteins. The CLP Regulation makes sure that the hazards presented by chemicals are clearly communicated to workers and consumers in the European Union. Applicant’s summary and conclusion – Interpretation of results. 1 000 g will be displayed as 1 kg. After adjustment to pH 0 (1 M HCl), the preparation is applied to a XAD-2 column, equilibrated as described above. The column is then washed with 100 mL HCl (1 M) and 140 mL H2O. Two cases of immuno-chemo-proteomics have been utilized in target-fishing studies of bisindolyl maleimide III (Bis-III): a protein kinase Cα (PKCα) and a glycogen synthase kinase 3β (GSK3β) inhibitor.41,42 The first scenario was used to compare the effects of peptide-based immuno-chemo-proteomics and traditional solid support matrix-based chemical proteomics on searching target proteins of Bis-III in high-salt HeLa cell lysates.41 Both traditional chemical proteomics techniques and immuno-chemo-proteomics captured several identical proteins, including PKCα, GSK3α/β, CaMKII-γ, NQO2, VDAC, and prohibitin; however, the FLAG-coupled–Bis-III probes exhibited raised activity levels in enriching proteins with lower binding affinity. Processable data is prioritised by the toxicity descriptor type (see list below) and subsequently further prioritised by duration (longer prioritised over shorter).
EC10 / LC10 or NOEC for marine water plants provides substance information on the substance’s effect concentration/lethal concentration for 10% of the tested marine water plants or the no observed effect concentration for marine water plants. The information is aggregated from REACH registered dossiers provided by industry through a use descriptor system based on five separate descriptor lists which in combination with each other form a brief description of use and exposure for certain life cycle stage. Close Find out more on how we use cookies.
Koc at 20°C provides substance information on the substance’s Koc adsorption at a temperature 20 °C. Substances may have impurities and additives that lead to different classifications. Due to the number of the substances and the associated information, substance data is processed and aggregated in an automatic process. A novel yet simple tactic for discriminating target proteins from the nonspecific binding of irrelevant proteins is a comparison-based target-fishing method that introduces blank control of affinity matrices without immobilized parent ligand or negative control of affinity matrices that contain a nonbioactive analog sharing structural similarities to the parent ligand.28,43 Due to the vast structural diversity and complexity of biologically active small molecules, the production of such a nonbioactive analog would involve arduous work to modify or remove functional groups necessary for drug activity. 1.6), oxidising: maximum burning rate equal or higher than reference mixture, oxidising: vigorous reaction in preliminary test. If more than one result is available per endpoint, the range of results (min-max) and range of experimental conditions will be presented (RANGE method). If so, the data provided is not processed for the Brief Profile. European Food Safety Authority (EFSA) reference(s): Flavouring Group Evaluation 6, Revision 1 (FGE.06Rev1) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC), Flavouring Group Evaluation 2, Revision 1 (FGE.02) : Branched- and straight-chain aliphatic saturated primary alcohols and related esters of primary alcohols and straight-chain carboxylic acids and one straight-chain aldehyde from chemical groups 1 and 2 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC), Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species.
Then, the solution is dried with anhydrous MgSO4 and concentrated under reduced pressure. 'IUPAC name' is the generic field by which substance names are provided in various data submission tools. In ‘Malwana Special Selection’ and ‘Malaysian Red’ the SSC remains between 18–19% at color stage 6 (commercial maturity).
Park, in Coffee in Health and Disease Prevention, 2015.
Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. Figure 115.2. The dark blue bar illustrates the percentage of matching substance classifications provided by manufacturers and importers in a REACH registration dossier. Extremely destructive to mucous membranes, upper respiratory tract, skin, and eyes. The mixture is again refluxed at 78 °C for 16 h. After cooling to room temperature, the solution is acidified with HCl to a pH < 1.
Another key factor for high product formation rates would be substrate transport inside the cell to reach the cascade enzymes (Jeon etal.,2016), because the cellular membranes, in particular the outer leaflet of outer membrane of E. coli, which consists mostly of lipopolysaccharides, was reported as a major barrier for the transport of hydrophobic compounds into E. coli (Nikaido,2003). This section provides a listing of alternate names for this chemical,
ECHA maintains the C&L Inventory, but does not review or verify the accuracy of the information. Registrants can choose from the following picklist endpoint conclusions/effect levels: This section displays the values related to sensitisation from all registered dossiers for the substance. The resulting crystals are filtered and recrystallized using the same solvents. The availability of additional data beyond the five results displayed is indicated by (…). If the substance has no EC number attributed, ECHA will attribute a list number. It is used as a selectable marker for plant transformation (Table 13.3). There are a number of ways to increase mass transport efficiency of fatty acids into microbial cells (Jeon etal.,2016; Julsing etal., 2012; Van Nuland etal.,2016). Oral route provides substance information on the substance’s acute toxicity via the oral route.