| Identification | Back Directory | [Name]
3,4-Dehydro Cilostazol-d11 | [CAS]
1073608-13-5 | [Synonyms]
OPC 13015-d11
3,4-Dehydro Cilostazol-d11
Cilostazol Impurity 12-d11
[2H11]-3,4-Dehydro Cilostazol
6-[4-(1-Cyclohexyl-d11-1H-tetrazol-5-yl)butoxy]-2(1H)-quinolinone | [Molecular Formula]
C20H25N5O2 | [MOL File]
1073608-13-5.mol | [Molecular Weight]
367.445 |
| Chemical Properties | Back Directory | [Melting point ]
177-180°C | [storage temp. ]
-20°C Freezer | [solubility ]
DMSO (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [color ]
White |
| Hazard Information | Back Directory | [Uses]
A labelled metabolite of Cilostazol. | [in vivo]
3,4-Dehydro Cilostazol (OPC-13015; Oral; 1 mg/kg GLZ and 10 mg/kg CLZ) has a T1/2 of 3.94 hours, a Cmax of 1.39 μM and an AUC0-24 of 4.69 μg?h/ml. The plasma concentration time profiles of GLZ, CLZ & its active metabolite DCLZ are traceable up to 24 h, 12 h and 12 h respectively by oral administration at 1 mg/kg dose of GLZ and 10 mg/kg CLZ[2].
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Medical Isotopes
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