106983-36-2 Usage
Description
N-DECANOYL-DL-HOMOSERINE LACTONE is a synthetic molecule that belongs to the class of homoserine lactones, which are known for their role as quorum-sensing molecules in certain bacteria. It is characterized by its unique structure, where a decanoyl group is attached to a homoserine lactone moiety. N-DECANOYL-DL-HOMOSERINE LACTONE has gained interest in various research and industrial applications due to its ability to modulate bacterial communication and behavior.
Uses
Used in Application Test:
N-DECANOYL-DL-HOMOSERINE LACTONE is used as an inducer for violacein expression in a Chromobacterium violaceum mutant that is typically unable to produce homoserine lactones. This application is crucial for studying the effects of quorum-sensing molecules on bacterial behavior and communication, as well as for developing potential antibacterial agents that can interfere with these processes.
Biochem/physiol Actions
N-Decanoyl-DL-homoserine lactone (N-C10-HSL) is among a group of homoserine lactones that includes; N-octanoyl-homoserine lactone (N-C8-HSL), N-(3-oxodecanoyl) homoserine-L-lactone (3-oxo-C10 HSL), N-(3-oxododecanoyl)homoserine-L-lactone (3-oxo-C12-HSL), N-(3-Oxotetradecanoyl)-L-homoserine lactone (3-oxo-C14-HSL, N-(3-hydroxydecanoyl)-L-homoserine lactone, and N-(3-hydroxyoctanoyl)-L-homoserine lactone involved in the processes of bacterial quorum sensing. These N-acyl-homoserine lactones are used to study the processes and mechanisms of bacterial quorum sensing.
Check Digit Verification of cas no
The CAS Registry Mumber 106983-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106983-36:
(8*1)+(7*0)+(6*6)+(5*9)+(4*8)+(3*3)+(2*3)+(1*6)=142
142 % 10 = 2
So 106983-36-2 is a valid CAS Registry Number.
106983-36-2Relevant articles and documents
A solid-phase synthetic route to N-acylated α-alkyl-D,L-homoserine lactones
Ali, Ahmed I. M.,O'Donnell, Martin J.,Samaritoni, J. Geno,Scott, William L.
supporting information, (2020/09/04)
A synthetic route to N-acylated α-alkyl-D,L-homoserine lactones was established using solid-phase unnatural peptide synthesis (UPS) and combinatorial chemistry. The application of UPS methodology allowed access to racemic N-acylated homoserine lactones (D,L-AHLs) and their α-alkyl structural analogs (α-R1-D,L-AHLs). The synthesis and characterization of a library of five D,L-AHLs and ten α-R1-D,L-AHLs prepared from resin-bound amino acids is reported.
