trans-2-Decenoic acid
| Overview | |
| Catalog # | bs-76193c-100mg |
| Product Name | trans-2-Decenoic acid |
| Specifications | |
| Storage Buffer | Oil |
| Storage Condition | Stable for 2 years after receipt when stored at -20°C. |
| Target | |
| Product Information | CAS Number: 334-49-6 Molecular formula: C10H18O2 Molecular weight: 170.25 Purity: >95% (NMR) Appearance: Viscous oil. Solubility: Soluble in DMSO, DMF (both 30mg/ml) or ethanol (20mg/ml). InChiKey: WXBXVVIUZANZAU-CMDGGOBGSA-N SMILES: CCCCCCC/C=C/C(O)=O SMILES: CCCCCCC\C=C\C(O)=O |
| Description | trans-2-Decenoic acid is an unsaturated short chain fatty acid that is secreted by S. mutans. It is a novel interkingdom-signaling molecule (from a Gram-positive organism) that inhibits hyphal formation of the dimorphic fungus C. albicans by blocking the yeast-to-hyphal morphological transition. It might play a critical role in regulating the disintegration of aerobic granules. As in other parts of the body, Streptococci and Candida coexist in the mouth and compete for the same substrate. In a mixed species environment such as the oral cavity the quantitative and qualitative nature of the bacteria modulates the biofilm formation of C. albicans. trans-2-Decenoic acid is structurally similar to undecylenic acid, the active ingredient of Desenex, a widely used antifungal agent. In addition, trans-2-Decenoic acid inhibited the luciferase reporter activity and therefore the bioluminescence of the Gram-negative marine bacteria Vibrio harveyi. trans-2-Decenoic acid is found in royal jelly produced from the hypopharyngeal and mandibular gland secretions of honeybees. Demonstrates weak estrogenic activity, inhibiting binding of 17beta-estradiol to estrogen receptor beta. |