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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
Structure of 2-DECENOIC ACID, (E)-

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+

HIDE SMILES / InChI

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.

CNS Activity

Curator's Comment: Ethyl ester of trans-2-decenoic acid exerts neurotrophin-like neurotrophic activities in animal models. No human data available.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P46593
Gene ID: 3645372|||3645386
Gene Symbol: HWP1
Target Organism: Candida albicans (strain SC5314 / ATCC MYA-2876) (Yeast)
17.0 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
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

Patents

Sample Use Guides

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
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 Fri Dec 15 18:45:16 GMT 2023
Edited
by admin
on Fri Dec 15 18:45:16 GMT 2023
Record UNII
332T8TH7B1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-DECENOIC ACID, (E)-
Common Name English
2-DECENOIC ACID, TRANS-
Common Name English
(E)-2-DECENOIC ACID
FHFI  
Systematic Name English
FEMA NO. 3913
Code English
(E)-2-DECENOIC ACID [FHFI]
Common Name English
2-DECENOIC ACID, (2E)-
Systematic Name English
TRANS-2-DECENOIC ACID
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
EPA CompTox
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
MESH
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
FDA UNII
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
PUBCHEM
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
CAS
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
JECFA MONOGRAPH
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
ECHA (EC/EINECS)
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
CHEBI
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