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Lipoxygenase-catalyzed peroxidative decomposition of unsaturated fatty acids occurs within seconds when diatoms are crushed or eaten, producing alkyls. DDA is a prominent member of this class of reactive compounds. Common omega-6 fatty acids such as linoleic acid, dihomo-omega-linolenic acid, and arachidonic acid can give rise to DDA. DDA reduces the hatching rate and has a strong teratogenic effect on the eggs of pelagic copepods, at concentrations around 1 µM. In human carcinoma Caco2 cells, DDA induces cell growth arrest at around 15 µM. DDA appears to be a natural defensive chemical designed to limit the reproductive success of copepods, the main predators of diatoms. It may also be a more general inducer of apoptosis.Formal Name: 2E,4E-decadienal. CAS Number: 25152-84-5. Synonyms: Decadienealdehyde, trans-2,4-Decadien-1-al. Molecular Formula: C10H16O. Formula Weight: 152.2. Purity: >98%. Formulation: (Request formulation change), A liquid. Solubility: DMF: 10 mg/ml, DMSO: 10 mg/ml, Ethanol: 10 mg/ml, Ethanol:PBS (pH 7.2) (1:2): .15 mg/ml. lambdamax: 273 nm. SMILES: CCCCC\C=C\C=C/C=O. InChi Code: InChI=1S/C10H16O/c1-2-3-4-5-6-7-8-9-10-11/h6-10H,2-5H2,1H3/b7-6+,9-8+. InChi Key: JZQKTMZYLHNFPL-BLHCBFLLSA-N. Origin: Synthetic.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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