ChemicalBook--->CAS DataBase List--->103253-15-2

103253-15-2

103253-15-2 Structure

103253-15-2 Structure
IdentificationBack Directory
[Name]

L-655,240
[CAS]

103253-15-2
[Synonyms]

L-655,240
JLPYLHLUHJOPNL-UHFFFAOYSA-N
1-(4-Chlorobenzyl)-5-fluoro-α,α,3-trimethyl-1H-indole-2-propanoic acid
1-[(4-Chlorophenyl)methyl]-5-fluoro-α,α,3-trimethyl-1H-indole-2-propanoic acid
1-[(4-CHLOROPHENYL)METHYL]-5-FLUORO-A,A,3-TRIMETHYL-1H-INDOLE-2-PROPANOIC ACID
3-[1-(4-CHLOROBENZYL)-5-FLUORO-3-METHYL-INDOL-2-YL]-2,2-DIMETHYL PROPANOIC ACID
1-((4-Chlorophenyl)methyl)-5-fluoro-alpha,alpha-3-trimethyl-(1H)-indole-2-propanoicacid
[Molecular Formula]

C21H21ClFNO2
[MDL Number]

MFCD04040005
[MOL File]

103253-15-2.mol
[Molecular Weight]

373.85
Chemical PropertiesBack Directory
[Boiling point ]

548.7±50.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

DMSO: 30 mg/mL
[form ]

solid
[pka]

4.82±0.10(Predicted)
[color ]

off-white
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

36/37/39
[WGK Germany ]

3
Hazard InformationBack Directory
[Biological Activity]

Potent and selective thromboxane A 2 /prostaglandin endoperoxide receptor antagonist. pA 2 values are 8-8.4 in guinea pig smooth muscle; IC 50 = 7 nM for inhibition of human platelet aggregation. Orally active in vivo .
[Uses]

L-655,240 is a selective and potent thromboxane and prostaglandin endoperoxide antagonist. Also used in the structure-based and ligand-based drug design for microsomal prostaglandins E synthase-1 inhibitors.
[Definition]

ChEBI: 3-[1-[(4-chlorophenyl)methyl]-5-fluoro-3-methyl-2-indolyl]-2,2-dimethylpropanoic acid is a methylindole.
[in vivo]

L 655240 (0.3 mg/kg; i.v.; single dose) changes heat rate, arterial and pulmonary arterial blood pressure, and cardiac output in canine model[1].

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