LMFA08030032
  LIPID_MAPS_STRUCTURE_DATABASE

 14 14  0     0  0            999 V2000
    1.8124    0.2478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6274   -0.3385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4389    0.2509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1270    1.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213    1.2045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5658   -0.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    0.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8138   -0.2679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0616    0.2383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9426   -0.2577    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6335   -1.2509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0557    1.2509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4389    0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    1.2284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0     0  0
  2  3  1  0     0  0
  3  4  1  0     0  0
  6  7  1  0     0  0
  7  8  1  0     0  0
  4  5  1  0     0  0
  8  9  1  0     0  0
  9 10  1  0     0  0
  1 10  1  1     0  0
  5  1  1  0     0  0
  2 11  2  0     0  0
  9 12  2  0     0  0
  6 13  1  0     0  0
  7 14  1  0     0  0
M  END
> <LM_ID>
LMFA08030032

> <COMMON_NAME>
N-(3-hydroxy-pentanoyl)-homoserine lactone

> <SYSTEMATIC_NAME>
N-(3-hydroxy-pentanoyl)-homoserine lactone

> <FORMULA>
C9H15NO4

> <MASS>
201.10

> <CATEGORY>
Fatty Acyls [FA]

> <MAIN_CLASS>
Fatty amides [FA08]

> <SUB_CLASS>
Fatty acyl homoserine lactones [FA0803]

> <CLASS_LEVEL4>
-

> <SYNONYMS>
3-hydroxy-C5:0-HSL; 3OH-C5-HSL

> <KEGG_ID>
-

> <HMDB_ID>
-

> <YMDB_ID>
-

> <CHEBI_ID>
-

> <CAYMAN_ID>
-

> <PLANTFA_ID>
-

> <SWISSLIPIDS_ID>
-

> <ALT_CLASSES>
-

> <METABOLOMICS_ID>
-

> <PUBCHEM_COMPOUND_ID>
10241919

> <LIPIDBANK_ID>
-

> <LIPIDAT_ID>
-

> <STATUS>
Active

> <REFS>
Synthesis of N-Acyl Homoserine Lactone Analogues Reveals Strong Activators of SdiA, the Salmonella enterica Serovar Typhimurium LuxR Homologue. Joost C. A. Janssens, Kristine Metzger, Ruth Daniels, Dave Ptacek, Tine Verhoeven, Lothar W. Habel, Jos Vanderleyden, Dirk E. De Vos and Sigrid C. J. De Keersmaecker. Applied and Environmental Microbiology. Volume 73. No. 2, 2007, p. 535–544. doi:10.1128/AEM.01451-06
<a href=https://aem.asm.org/content/73/2/535.long> https://aem.asm.org/content/73/2/535.long<a/>

> <LIPID_MAPS_URL>
https://lipidmaps.org/databases/lmsd/LMFA08030032

$$$$