Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H18O2 |
Molecular Weight | 170.2487 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC\C=C\C(O)=O
InChI
InChIKey=WXBXVVIUZANZAU-CMDGGOBGSA-N
InChI=1S/C10H18O2/c1-2-3-4-5-6-7-8-9-10(11)12/h8-9H,2-7H2,1H3,(H,11,12)/b9-8+
Molecular Formula | C10H18O2 |
Molecular Weight | 170.2487 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
(E)-2-decenoic acid is a stereoisomer of the corresponding medium-chain fatty acid in the trans configuration. This compound excreted by the caries bacterium Streptococcus mutants and inhibits the morphological transition from yeast to hyphae, an important virulence trait, in the opportunistic fungus Candida albicans. As a component of royal jelly it exhibits estrogenic effect by activation of estrogen receptor beta. Ethyl ester of trans-2-decenoic acid exerts neurotrophin-like neurotrophic activities in animal models of stress-induced anxiety-like, cerebral infarction and spinal cord injury.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P46593 Gene ID: 3645372|||3645386 Gene Symbol: HWP1 Target Organism: Candida albicans (strain SC5314 / ATCC MYA-2876) (Yeast) Sources: https://www.ncbi.nlm.nih.gov/pubmed/20572249 |
|||
Target ID: CHEMBL242 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18830443 |
17.0 µM [IC50] | ||
Target ID: GO:0038179 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21187649 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Estrogenic activities of Fatty acids and a sterol isolated from royal jelly. | 2008 Sep |
|
2-Decenoic acid ethyl ester possesses neurotrophin-like activities to facilitate intracellular signals and increase synapse-specific proteins in neurons cultured from embryonic rat brain. | 2010 Dec |
|
Streptococcus mutans inhibits Candida albicans hyphal formation by the fatty acid signaling molecule trans-2-decenoic acid (SDSF). | 2010 Jul 26 |
|
2-decenoic acid ethyl ester, a compound that elicits neurotrophin-like intracellular signals, facilitating functional recovery from cerebral infarction in mice. | 2012 |
|
Anxiolytic-like effect of trans-2-decenoic acid ethyl ester in stress-induced anxiety-like model mice. | 2013 |
|
Disintegration of aerobic granules induced by trans-2-decenoic acid. | 2013 Jan |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18830443
Starting at post-natal day 20, the female
rats were injected subcutaneously with trans-2-decenoic acid 1g/kg per day
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18830443
trans-2-decenoic acid increased the rate of proliferation of MCF-7 cells at concentrations of 0.01-0.1 mM
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:45:16 GMT 2023
by
admin
on
Fri Dec 15 18:45:16 GMT 2023
|
Record UNII |
332T8TH7B1
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
JECFA EVALUATION |
(E)-2-DECENOIC ACID
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID20904657
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
C052476
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
332T8TH7B1
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
5282724
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
334-49-6
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
1371
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
206-378-5
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY | |||
|
50467
Created by
admin on Fri Dec 15 18:45:16 GMT 2023 , Edited by admin on Fri Dec 15 18:45:16 GMT 2023
|
PRIMARY |