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ChemicalBook--->CAS DataBase List--->666860-59-9

666860-59-9

666860-59-9 Structure

666860-59-9 Structure
IdentificationBack Directory
[Name]

CarbaMic acid, [3-[trans-5-(6-Methoxy-1-naphthalenyl)-1,3-dioxan-2-yl]propyl]-, 2-aMino-2-oxoethyl ester
[CAS]

666860-59-9
[Synonyms]

CarbaMic acid, [3-[trans-5-(6-Methoxy-1-naphthalenyl)-1,3-dioxan-2-yl]propyl]-, 2-aMino-2-oxoethyl ester
Carbamic acid, N-[3-[trans-5-(6-methoxy-1-naphthalenyl)-1,3-dioxan-2-yl]propyl]-, 2-amino-2-oxoethyl ester
[EINECS(EC#)]

682-612-3
[Molecular Formula]

C21H26N2O6
[MDL Number]

MFCD34469332
[MOL File]

666860-59-9.mol
[Molecular Weight]

402.44
Chemical PropertiesBack Directory
[Boiling point ]

648.0±55.0 °C(Predicted)
[density ]

1.228±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

12.38±0.46(Predicted)
[color ]

White to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Warning
[Hazard statements ]

H361
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501
Hazard InformationBack Directory
[Biological Activity]

SSR411298 is an orally active, selective and reversible fatty acid amide hydrolase (FAAH) inhibitor. SSR411298 has the potential for post-traumatic stress disorder research[1]. SSR411298 (0.1, 1, 10, 100, 1000, 10000 nM) inhibits mouse brain FAAH in a concentration-dependent manner[1]. SSR411298 produces maximal inhibition of FAAH between 0.3 and 30 mg/kg in the ex-vivo experiment[1]. SSR411298 (0.3, 1, 3 mg/kg; p.o.; twice a day during 2 days; 60 minutes before pretest, immediately after, and 60 minutes before the second session of testing) produces robust antidepressant-like activity in the rat forced-swimming test and in the mouse chronic mild stress model, restoring notably the development of inadequate coping responses to chronic stress in male Wistar rats weighing 235-290 g[1]. SSR411298 (0.3, 1, 3, 10 mg/kg; po; single dose; two hours prior to sacrifice) produces a significant global increase of tissular AEA, PEA and OEA levels in the hippocampus, but not of 2-AG levels[1].
[References]

[1]. Guy Griebel, et al. The selective reversible FAAH inhibitor, SSR411298, restores the development of maladaptive behaviors to acute and chronic stress in rodents. Sci Rep. 2018 Feb 5;8(1):2416.
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