ChemicalBook--->CAS DataBase List--->2101517-69-3

2101517-69-3

2101517-69-3 Structure

2101517-69-3 Structure
IdentificationBack Directory
[Name]

(2R)-2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)-N-(2,4-difluorophenyl)-2-phenylacetamide
[CAS]

2101517-69-3
[Synonyms]

BL 918 NEW
BL-918 (BL918)
(2R)-2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)-N-(2,4-difluorophenyl)-2-phenylacetamide
[EINECS(EC#)]

825-946-9
[Molecular Formula]

C23H15F8N3OS
[MDL Number]

MFCD31693829
[MOL File]

2101517-69-3.mol
[Molecular Weight]

533.437
Questions And AnswerBack Directory
[Uses]

BL 918 is a potent small-molecule activator of UNC-51-like kinase 1 (ULK1), a serine-threonine kinase involved in autophagy. Promotes cytoprotective autophagy in MPP+-treated SH-SY5Y cells, via the ULK complex. Improves motor dysfunction and reduces loss of dopaminergic neurons, mediated by MPTP, in in vivo models of Parkinson’s disease.
Chemical PropertiesBack Directory
[density ]

1.508±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: ≥ 250 mg/mL (468.66 mM)
[form ]

A solid
[pka]

11.13±0.70(Predicted)
[color ]

White to off-white
[InChIKey]

BDBWQANRZRCMMD-DETXXQSHNA-N
[SMILES]

C(NC1=CC=C(F)C=C1F)(=O)[C@H](NC(=S)NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1)C1=CC=CC=C1 |&1:11,r|
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

(2R)-2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)-N-(2,4-difluorophenyl)-2-phenylacetamide(2101517-69-3)1HNMR
Hazard InformationBack Directory
[in vivo]

BL-918 (compound 33i; 20, 40, or 80 mg/kg/day; oral gavage; began 2 days before the first injection of saline/MPTP and continuously maintained for 5 days after the last injection of saline/MPTP) attenuates the loss of DA and its metabolites. BL-918 obviously decreases the levels of dopamine (DA), 3,4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA)[1].

Animal Model:Male C57BL/6 mice (eight-week old) weighing between 20 and 25 g[1]
Dosage:20, 40, or 80 mg/kg
Administration:Oral gavage; daily; began 2 days before the first injection of saline/MPTP and continuously maintained for 5 days after the last injection of saline/MPTP
Result:Attenuated the loss of DA and its metabolites.
[IC 50]

ULK1: 24.14 nM (EC50); ULK1: 0.719 μM (Kd)
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