ChemicalBook--->CAS DataBase List--->1050670-85-3

1050670-85-3

1050670-85-3 Structure

1050670-85-3 Structure
IdentificationBack Directory
[Name]

Ro 51
[CAS]

1050670-85-3
[Synonyms]

Ro 51
2-((4-Amino-5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidin-2-yl)amino)propane-1,3-diol
2-[[4-amino-5-(5-iodo-4-methoxy-2-propan-2-ylphenoxy)pyrimidin-2-yl]amino]propane-1,3-diol
2-[[4-Amino-5-[5-iodo-4-methoxy-2-(1-methylethyl)phenoxy]-2-pyrimidinyl]amino]-1,3-propanediol
1,3-Propanediol,2-[[4-amino-5-[5-iodo-4-methoxy-2-(1-methylethyl)phenoxy]-2-pyrimidinyl]amino]-
2-[[4-Amino-5-[5-iodo-4-methoxy-2-(1-methylethyl)phenoxy]-2,4-pyrimidinyl]amino]-1,3-propanediol
[Molecular Formula]

C17H23IN4O4
[MOL File]

1050670-85-3.mol
[Molecular Weight]

474.29
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble to 100 mM in DMSO and to 100 mM in ethanol
[form ]

Powder
Hazard InformationBack Directory
[Uses]

Ro 51 is a potent and selective dual antagonist of purinoceptor subtypes P2X3 and P2X2/3. P2X3 and P2X2/3 have been shown to play a pivotal role in models of various pain conditions making Ro 51 a pot ential option in the treatment of pain.
[Uses]

Ro 51 is a potent and selective dual antagonist of purinoceptor subtypes P2X3 and P2X2/3. P2X3 and P2X2/3 have been shown to play a pivotal role in models of various pain conditions making Ro 51 a potential option in the treatment of pain.
[in vivo]

Ro-51 suffers rapid clearance, short half-lives, and high protein binding in rat[1].

Animal Model:Rat[1]
Dosage:2 mg/kg (Pharmacokinetic Analysis)
Administration:Oral administration
Result:AUC= 237 ng/h/mL, T 1/2 =1.52 h
[storage]

Store at -20°C
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