ChemicalBook--->CAS DataBase List--->6036-76-6

6036-76-6

6036-76-6 Structure

6036-76-6 Structure
IdentificationBack Directory
[Name]

L-ERYTHRO-DIHYDROSPHINGOSINE
[CAS]

6036-76-6
[Synonyms]

SPC-103980
L-ERYTHRO-SPHINGANINE
L-ERYTHRO-DIHYDROSPHINGOSINE
L-erythro Sphinganine (d18:0)
(2R,3S)-2-Amino-1,3-octadecanediol
1,3-Octadecanediol, 2-amino-, (2R,3S)-
[Molecular Formula]

C18H39NO2
[MDL Number]

MFCD00274349
[MOL File]

6036-76-6.mol
[Molecular Weight]

301.51
Chemical PropertiesBack Directory
[Boiling point ]

446.2±25.0 °C(Predicted)
[density ]

0.927±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

DMSO: 25 mg/mL warm
[form ]

A solid
[pka]

12.57±0.45(Predicted)
[color ]

white
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

L-erythro Sphinganine (d18:0) is a synthetic bioactive sphingolipid and stereoisomer of sphinganine (d18:0) and D-threo sphinganine . It induces autophagy in HCT116 cells when used at a concentration of 12 μM. L-erythro Sphinganine induces cell cycle arrest of 7R4-LCB1 yeast cells. It is metabolized via sphinganine N-acyltransferase and sphinganine kinase in vivo in rat liver. [Matreya, LLC. Catalog No. 1846]
[Uses]

L-erythro-Dihydrosphingosine is an ester product.
[Definition]

ChEBI: Erythro-dihydrosphingosine is an amino alcohol.
[storage]

Store at -20°C
[References]

[1] JESSE COWARD. Safingol (L-threo-sphinganine) induces autophagy in solid tumor cells through inhibition of PKC and the PI3-kinase pathway.[J]. Autophagy, 2009, 5 2: 184-193. DOI: 10.4161/auto.5.2.7361
[2] G M JENKINS  Y A H. Role for de novo sphingoid base biosynthesis in the heat-induced transient cell cycle arrest of Saccharomyces cerevisiae.[J]. The Journal of Biological Chemistry, 2001, 276 11: 8574-8581. DOI: 10.1074/jbc.m007425200
[3] W STOFFEL  K B. Stereospecificities in the metabolic reactions of the four isomeric sphinganines (dihydrosphingosines) in rat liver.[J]. Hoppe-Seyler’s Zeitschrift fur physiologische Chemie, 1973, 354 2: 169-181. DOI: 10.1515/bchm2.1973.354.1.169
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