N-(3-(4-bromophenyl)-propanoyl)-L-homoserine lactone - ≥95%, high purity , CAS No.959613-39-9

  • ≥95%
Item Number
N463511
Grouped product items
SKUSizeAvailabilityPrice Qty
N463511-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$369.90

Basic Description

Specifications & Purity≥95%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Description

AHL analog is a strong, broad-spectrum inhibitor of numerous LuxR-type receptors (e.g.: LuxR fromVibrio fischeri, LasR fromP. aeruginosa, and TraR fromAgrobacterium tumefaciens). This compound represents a good choice for initial testing of LuxR-type receptor inhibition.

Associated Targets(non-human)

luxR Transcriptional activator protein luxR (400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
traR Transcriptional activator protein traR (147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lasR Transcriptional activator protein lasR (432 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
phzR PhzR (76 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 3-(4-bromophenyl)-N-[(3S)-2-oxooxolan-3-yl]propanamide
INCHI InChI=1S/C13H14BrNO3/c14-10-4-1-9(2-5-10)3-6-12(16)15-11-7-8-18-13(11)17/h1-2,4-5,11H,3,6-8H2,(H,15,16)/t11-/m0/s1
InChi Key SGDZSJUYCLTPRG-NSHDSACASA-N
Canonical SMILES C1COC(=O)C1NC(=O)CCC2=CC=C(C=C2)Br
Isomeric SMILES C1COC(=O)[C@H]1NC(=O)CCC2=CC=C(C=C2)Br
PubChem CID 24179234
Molecular Weight 312.16

Certificates

Certificate of Analysis(COA)

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Safety and Hazards(GHS)

RIDADR NONHforallmodesoftransport

Related Documents

References

1. Grant D Geske, Jennifer C O'Neill, David M Miller, Margrith E Mattmann, Helen E Blackwell.  (2008-01-29)  Comparative analyses of N-acylated homoserine lactones reveal unique structural features that dictate their ability to activate or inhibit quorum sensing..  Chembiochem : a European journal of chemical biology,  ((3)): ( 389-400 ).  [PMID:18224645]

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