ChemicalBook--->CAS DataBase List--->909725-62-8

909725-62-8

909725-62-8 Structure

909725-62-8 Structure
IdentificationBack Directory
[Name]

[(3R)-3-Amino-4-[(3-hexylphenyl)amino]-4-oxobutyl]-phosphonic acid mono(trifluoroacetate)
[CAS]

909725-62-8
[Synonyms]

W146
(R)-3-AMino-(3-hexylphenylaMino)-4-oxobutylphosphonic acid (TFA salt)
(R)-3-AMINO-(3-HEXYLPHENYLAMINO)-4-OXOBUTYLPHOSPHONIC ACID (TFA SALT);W146
[(3R)-3-Amino-4-[(3-hexylphenyl)amino]-4-oxobutyl]-phosphonic acid mono(trifluoroacetate)
[Molecular Formula]

C18H28F3N2O6P
[MDL Number]

MFCD21602904
[MOL File]

909725-62-8.mol
[Molecular Weight]

456.394
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Methanol: 0.1 mg/ml
[form ]

A crystalline solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

W146 is a selective antagonists of spingosine-1-phosphate receptor subtype 1.
[Biological Activity]

W146 acts as an orthosteric antagonist. It is linked to blood lymphopenia and lung edema in mice.
[in vivo]

W146 (5 mg/kg, ip, prior to AMD3100 administration) pre-treatment shows approximately 8-fold increase of KSL-HSPC mobilization, measured by the CFU-G/M colony forming assays, compared to that in mice treated with AMD3100 alone[3]
The W146-mediated augmentation of KSL-HSPC mobilization is specific, because pretreatment of mice with W140 is unable to produce any effect on AMD3100-stimulated KSL-HSPC mobilization. Injections of W146, W140, JTE013, or Cay10444 do not alter the basal WBC count in mice[3].

Animal Model:Mice (4-6-week-old)[3]
.
Dosage:5 mg/kg.
Administration:IP, 1 hour prior to AMD3100 (ADM) administration.
Result:Significantly increased in KSL-HSPC mobilization compared to that in mice pretreated with dextran followed by AMD3100 administration.
[storage]

Store at -20°C
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