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
3D model of N-arachidonoyl taurine
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
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
Biochemistry, 2006
Pubmed ID:
16866345
DOI:
10.1021/bi0608008
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
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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