ChemicalBook--->CAS DataBase List--->1155877-97-6

1155877-97-6

1155877-97-6 Structure

1155877-97-6 Structure
IdentificationBack Directory
[Name]

1-(4-((3'-Chloro-6-Methoxy-[1,1'-biphenyl]-3-yl)Methyl)phenyl)urea
[CAS]

1155877-97-6
[Synonyms]

D159687
D159687; D-159687; D 159687
1-(4-((3'-chloro-6-methoxybiphenyl-3-yl)methyl)phenyl)urea
1-(4-((3'-Chloro-6-Methoxy-[1,1'-biphenyl]-3-yl)Methyl)phenyl)urea
Urea, N-[4-[(3'-chloro-6-methoxy[1,1'-biphenyl]-3-yl)methyl]phenyl]-
[Molecular Formula]

C21H19ClN2O2
[MDL Number]

MFCD26793458
[MOL File]

1155877-97-6.mol
[Molecular Weight]

366.84
Chemical PropertiesBack Directory
[Boiling point ]

502.0±50.0 °C(Predicted)
[density ]

1.263±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO : 150 mg/mL (408.90 mM)
[form ]

Solid
[pka]

14.48±0.50(Predicted)
[color ]

White to off-white
[InChI]

1S/C21H19ClN2O2/c1-26-20-10-7-15(12-19(20)16-3-2-4-17(22)13-16)11-14-5-8-18(9-6-14)24-21(23)25/h2-10,12-13H,11H2,1H3,(H3,23,24,25)
[InChIKey]

RJJLUTWHJUDZFP-UHFFFAOYSA-N
[SMILES]

Clc1cc(ccc1)c2c(ccc(c2)Cc3ccc(cc3)NC(=O)N)OC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

D-159687 is a selective inhibitor of cyclic AMP phosphodiesterase 4D (PDE4D).
[Biological Activity]

D159687 is a brain-penetrantorally availablehighly potent and selective negative allosteric modulator (NAM) against phosphodiesterase 4 (PDE4) subtype PDE4D (hPDE4D7 IC50 = 27 nM; PDE4A1/B1/C1 IC50 = 2.50/1.47/6.80 μM; IC50 ≥29 μM against PDE1/2/3/5/7/8/9/10/11 subtypes). Comparing to RolipramD159678 offers similar in vivo efficacy on long-term memory formation by novel object recognition test (MED = 3 μg/kg mouse iv.1 μg/kg r at p.o.)while being more effective in the scopolamine-impaired Y-maze tests (D159678/Rolipram MED = 0.1/1 μg/kg mouse iv. or 30/100 μg/kg mouse p.o.) and much less emetic in shrews/dog/monkeys (by 100-/3000-/500-fold).
[in vivo]

D159687 (0.05-5 mg/kg; oral daily for a week) shows a potential recruitment or enhancement of synaptic function with increased task difficulty in female Cynomolgus macaques[2].

Animal Model:Female Cynomolgus macaques (4–6 year old) [2]
Dosage:0.05, 0.5, 5 mg/kg
Administration:Oral daily for a week
Result:A potential recruitment or enhancement of synaptic function with increased task difficulty.
[IC 50]

PDE4
Spectrum DetailBack Directory
[Spectrum Detail]

1-(4-((3'-Chloro-6-Methoxy-[1,1'-biphenyl]-3-yl)Methyl)phenyl)urea(1155877-97-6)1HNMR
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