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Chemodex
trans-2-Decenoic acid
Product Details | |
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Synonyms | (E)-2-Decenoic Acid; trans-2-Decylenic Acid; Streptococcus Diffusible Signal Factor; SDSF |
Product Type | Chemical |
Properties | |
Formula |
C10H18O2 |
MW | 170.25 |
CAS | 334-49-6 |
Source/Host Chemicals | Synthetic. |
Purity Chemicals | ≥95% (NMR) |
Appearance | Viscous oil. |
Solubility | Soluble in DMSO, DMF (both 30mg/ml) or ethanol (20mg/ml). |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | WXBXVVIUZANZAU-CMDGGOBGSA-N |
Smiles | CCCCCCC/C=C/C(O)=O |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +4°C |
Long Term Storage | -20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at -20°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
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 17β-estradiol to estrogen receptor β.
(1) K.M. Suzuki, et al.; Evid. Based Complement. Alternat. Med. 5, 295 (2008) | (2) D.G. Davies & C.N.H. Marques; J. Bateriol. 191, 1393 (2009) | (3) R. Vilchez, et al.; ChemBioChem 11, 1552 (2010) | (4) P.-J. Cai, et al.; Biores. Technol. 182, 823 (2013)