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474943-05-0

474943-05-0 Structure

474943-05-0 Structure
IdentificationBack Directory
[Name]

N-[12-[(7-NITRO-2-1,3-BENZOXADIAZOL-4-YL)AMINO]DODECANOYL]-SPHINGANINE
[CAS]

474943-05-0
[Synonyms]

NBD-C12-SAFINGOL
C12 NBD SAFINGOL
C12 NBD SPHINGANINE
N-ACYL-SPHINGANINE (C12 NBD)
N-(NBD-AMINOLAUROYL)SAFINGOL
N-(NBD-AMINOLAUROYL)SPHINGANINE
C12 NBD dihydro Ceramide (d18:0/12:0)
N-[12-[(7-NITRO-2-1,3-BENZOXADIAZOL-4-YL)AMINO]DODECANOYL]-SPHINGANINE
N-[6-[(7-NITRO-2-1,3-BENZOXADIAZOL-4-YL)AMINO]DODECANOYL]-L-THREO-SPHINGANINE
N-[12-[(7-NITRO-2-1,3-BENZOXADIAZOL-4-YL)AMINO]DODECANOYL]-L-THREO-SPHINGANINE
N-Dodecanoyl-NBD-D-erythro-dihydrosphingosine, Fluorescent C12:0-dihydrosphingosine analog
N-[12-[(7-NITRO-2-1,3-BENZOXADIAZOL-4-YL)AMINO]DODECANOYL]-SPHINGANINE;C12-NBD SPHINGANINE
C12-NBD Sphinganine, N-[12-[(7-Nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-sphinganine
NBD-C12-Safingol, N-[6-[(7-Nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-L-threo-sphinganine
Dodecanamide, N-[(1S,2R)-2-hydroxy-1-(hydroxymethyl)heptadecyl]-12-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-
[Molecular Formula]

C36H63N5O6
[MDL Number]

MFCD02259241
[MOL File]

474943-05-0.mol
[Molecular Weight]

661.92
Chemical PropertiesBack Directory
[density ]

1.095±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

DMF: 30 mg/ml; DMSO: 20 mg/ml; Ethanol: 20 mg/ml
[form ]

A solid
[pka]

14.30±0.20(Predicted)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-38-40-48/20/22
[Safety Statements ]

36/37
[RIDADR ]

UN 1888 6.1/PG 3
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

C-12 NBD-dihydro-Ceramide is a fluorescent ceramidase substrate. C-12 NBD-dihydro-Ceramide compound is a fluorescent ceramide analog which contains a saturated bond in the C4-C5 position of the sphingosine backbone. It can be used for the measurement of alkaline and neutral ceramidase activity from a variety of sources. C-12 NBD-dihydro-ceramide may exhibit reduced activity in ceramidase assays compared to C-12 NBD ceramide. This is based on the observation that saturation of the C4-C5 sphingosine bond in C16-ceramide results in approximately a 10-fold reduction in efficiency as a substrate for rat brain ceramidase compared to the unsaturated substrate. Yet, experimental characterization of C-12 NBD-dihydro-ceramide as a ceramidase substrate needs to be performed.
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