15 Results for "

Cilostazol

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "Cilostazol" in MCE Product Catalog:

6
6 Cited Publications
Cat. No.: HY-17464
CAS No.: 73963-72-1
Synonyms: OPC 13013
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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Cat. No.: HY-135910
CAS No.: 73963-62-9
Purity:  98.09%
Synonyms: OPC-13015
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease Cancer

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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Cat. No.: HY-17464S1
CAS No.: 1215541-47-1
Synonyms: OPC-13013-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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Cat. No.: HY-135910R
CAS No.: 73963-62-9
Synonyms: OPC-13015 (Standard)
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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Cat. No.: HY-135910S
CAS No.: 1073608-13-5
Synonyms: OPC-13015-d11
3,4-Dehydro Cilostazol-d11 is deuterated labeled 3,4-Dehydro Cilostazol (HY-135910). 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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Cat. No.: HY-137215
CAS No.: 87153-04-6
Purity:  97.04%
Target:  

Drug Metabolite

Research Areas:  

Others

4'-trans-Hydroxy Cilostazol is a metabolite of Cilostazol .
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Cat. No.: HY-17464S
CAS No.: 1073608-02-2
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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Cat. No.: HY-137215S2
4'-trans-Hydroxy Cilostazol-d4 is deuterated labeled 4'-trans-Hydroxy Cilostazol (HY-137215). 4'-trans-Hydroxy Cilostazol is a metabolite of Cilostazol .
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Cat. No.: HY-137215S1
4-cis-Hydroxy Cilostazol-d5 is the deuterium labeled 4'-trans-Hydroxy Cilostazol[1].
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Cat. No.: HY-17464R
CAS No.: 73963-72-1
Synonyms: OPC 13013 (Standard)
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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Cat. No.: HY-17464S2
CAS No.: 1073608-03-3
Synonyms: OPC 13013-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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Cat. No.: HY-19249
CAS No.: 146731-14-8
Z-335 sodium is an orally active thromboxane a2 (TXA2) receptor antagonist, with IC50 values of 29.9 nM and 32.5 nM for human and Guinea pig platelets, respectively .
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Cat. No.: HY-111219
CAS No.: 139145-84-9
Synonyms: NM-702; NT-702
Research Areas:  

Others

Parogrelil (hydrochloride) (NM-702) is a phosphodiesterase inhibitor with activity in inhibiting intermittent claudication. Parogrelil (hydrochloride) selectively inhibits PDE3, inhibits human platelet aggregation in vitro and rat aortic contraction, and improves walking distance and plantar surface temperature in the rat femoral artery ligation model, with better effects than cilostazol.
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Cat. No.: HY-137215S
4'-trans-Hydroxy Cilostazol-d5 is the deuterium labeled 4'-trans-Hydroxy Cilostazol.
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Cat. No.: HY-17464S3
CAS No.: 1246641-05-3
Synonyms: OPC 13013-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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