| Identification | Back Directory | [Name]
2[(1-OXOOCTADECYL)AMINO]-ETHANESULFONIC ACID | [CAS]
63155-80-6 | [Synonyms]
N-STEAROYL TAURINE
LMIJIHJZVURGQK-UHFFFAOYSA-N
2[(1-OXOOCTADECYL)AMINO]-ETHANESULFONIC ACID
Ethanesulfonic acid, 2-[(1-oxooctadecyl)amino]- | [Molecular Formula]
C20H41NO4S | [MDL Number]
MFCD08062156 | [MOL File]
63155-80-6.mol | [Molecular Weight]
391.61 |
| Chemical Properties | Back Directory | [Melting point ]
240 °C (approx, decomp) | [density ]
1.022±0.06 g/cm3(Predicted) | [solubility ]
DMF: 1.5 mg/ml; DMSO: 1.5 mg/ml | [form ]
Liquid | [pka]
1.42±0.50(Predicted) | [color ]
Colorless to light yellow |
| Hazard Information | Back Directory | [Description]
Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain. During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered. This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels. N-Stearoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling. | [Uses]
N-Stearoyl Taurine is a prominent amino-acyl endocannabinoid. | [Definition]
ChEBI: N-stearoyltaurine is a fatty acid-taurine conjugate derived from stearic acid. It has a role as a mouse metabolite. It is functionally related to an octadecanoic acid. It is a conjugate acid of a N-stearoyltaurine(1-). | [References]
[1] SUNDERLAND D, UZOIGWE G N. Personal Communication[J]. Communications in Africa, 1880–1939, 2018, 73 1: 0. DOI: 10.4324/9781351112277-85
[2] ALAN SAGHATELIAN. A FAAH-Regulated Class of N-Acyl Taurines That Activates TRP Ion Channels?[J]. Biochemistry Biochemistry, 2006, 45 30: 9007-9015. DOI: 10.1021/bi0608008 |
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