Structure Database (LMSD)

Common Name
N-arachidonoyl taurine
Systematic Name
N-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-taurine
Synonyms
  • NAT
LM ID
LMFA08020075
Formula
Exact Mass
Calculate m/z
411.24433
Sum Composition
Status
Curated

Classification

Biological Context

N-Arachidonoyl taurine is an arachidonoyl amino acid.1 It is oxygenated by 12(S)- and 15(S)-lipoxygenase and is converted to 12-HETE-taurine (12-HETE-T) in murine resident peritoneal macrophages.2 N-Arachidonoyl taurine is an activator of the transient receptor potential vanilloid (TRPV) channels TRPV1 and TRPV4 (EC50s = 28 and 21 µM, respectively).1 It increases calcium flux in HIT-T15 pancreatic β-cells and INS-1 rat islet cells when used at a concentration of 10 µM and increases insulin secretion from 832/13 INS-1 pancreatic β-cells.3 The levels of N-arachidonoyl taurine are changed in mouse brain following administration of Δ9-tetrahydrocannabinol (Δ9-THC).4

This information has been provided by Cayman Chemical

References

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Mus musculus (#10090)
Mammalia (#40674)
A FAAH-regulated class of N-acyl taurines that activates TRP ion channels.,
Biochemistry, 2006
Pubmed ID: 16866345

String Representations

InChiKey (Click to copy)
YUNYSWCRLRYOPO-DOFZRALJSA-N
InChi (Click to copy)
InChI=1S/C22H37NO4S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(24)23-20-21-28(25,26)27/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-21H2,1H3,(H,23,24)(H,25,26,27)/b7-6-,10-9-,13-12-,16-15-
SMILES (Click to copy)
C(CNC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)S(O)(=O)=O

Other Databases

CHEBI ID
PubChem CID
Cayman ID

Calculated Physicochemical Properties

Heavy Atoms 28
Rings 0
Aromatic Rings 0
Rotatable Bonds 17
Van der Waals Molecular Volume 440.63
Topological Polar Surface Area 83.47
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 4
logP 6.96
Molar Refractivity 118.72

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Updated at
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