1246641-05-3
1246641-05-3
Chemical Structure
Cilostazol-d6
Synonym(s): OPC 13013-d6
- CAS. Nr.: 1246641-05-3
- Formula:C20H21D6N5O2
- Molecular Weight:375.50
InChIKey: RRGUKTPIGVIEKM-NMFSSPJFSA-N
SMILES: O=C1NC2=CC=C(OCCCCC3=NN=NN3C4CC([2H])(C([2H])(C([2H])(C4)[2H])[2H])[2H])C=C2CC1
Biological Activity: Cilostazol-d6 (OPC 13013-d6) is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM[1][2].
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Cilostazol-d6 | Cilostazol-d6 (OPC 13013-d6) is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | |||||||||||||||||||||
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Cilostazol (Standard) | ≥98% | Cilostazol (Standard) is the analytical standard of Cilostazol. This product is intended for research and analytical applications. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | ||||||||||||||||||||
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Cilostazol-d11 | Cilostazol-d11 is the deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | |||||||||||||||||||||
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Cilostazol-d4 | Cilostazol-d4 is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | |||||||||||||||||||||
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Cilostazol-d2 | Cilostazol-d2 (OPC 13013-d2) is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | |||||||||||||||||||||
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Cilostazol | 99.77% | Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM. | ||||||||||||||||||||
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3,4-Dehydro Cilostazol (Standard) | 98.34% | 3,4-Dehydro Cilostazol (Standard) is the analytical standard of 3,4-Dehydro Cilostazol. This product is intended for research and analytical applications. 3,4-Dehydro Cilostazol (OPC-13015) is an active metabolite of Cilostazol (CLZ; HY-17464). 3,4-Dehydro Cilostazol is used for pharmacokinetic study. | ||||||||||||||||||||
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Aripiprazole impurity 22 | Aripiprazole impurity 22 is an impurity of Aripiprazole. | |||||||||||||||||||||
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4'-trans-Hydroxy Cilostazol | 97.04% | 4'-trans-Hydroxy Cilostazol is a metabolite of Cilostazol. | ||||||||||||||||||||
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OPC 3911 | OPC 3911 is a highly selective inhibitor of cGMP-inhibited cAMP phosphodiesterase (cGI-PDE/PDE3) and a vasodilator, with an IC50 of 0.042 μM against rat cGI-PDE. OPC 3911 upregulates the expression of Osteopontin. OPC 3911 mediates vasodilation of arterial smooth muscle, induces vasodilatory responses in isolated rat arteriovenous tissues, and exhibits additive vasodilatory effects with Isoprenaline (HY-108353) and Forskolin (HY-15371). OPC 3911 can be used in studies related to congestive heart failure and insulin resistance. | |||||||||||||||||||||
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Aripiprazole impurity 32 | Aripiprazole impurity 32 (Deschloroaripiprazole) is an impurity of Aripiprazole. | |||||||||||||||||||||
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Aripiprazole impurity 33 | Aripiprazole impurity 33 is an impurity of Aripiprazole. | |||||||||||||||||||||
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